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*Clone Cells 3T3 Cells 5' Untranslated Regions Abnormalities Acrylic Resins/*chemistry Action Potentials Activating Transcription Factor 4 Adipocytes Adolescent Adult African Continental Ancestry Group Age of Onset albinism Alleles Alpha-Globulins/*genetics/metabolism Alternative Splicing alternative technology Alternative treatments Amino Acid Sequence analysis Animals Anobium punctatum Anticoagulants Antigens AP3 complex AP3δ arachnophobia Base Sequence beclometasone dipropionate bed bugs Binding bio-predators Biopredators Blotting Body fluid identification boron Bottleneck Building Conservation buildings Carrier Proteins/*genetics/metabolism Cell Proliferation/drug effects chemical treatments Chemical treatments for timber Child Chromosome Mapping common furniture beetle congenital Consanguinity conservation decay Drug Carriers/analysis/*metabolism ecology exome sequencing Female flagellin Forensic Genetics Genetic Genetic Markers/genetics green building gut epithelium Hermansky-Pudlak syndrome historic buildings in-vitro dose emission Infant infection susceptibility infestation inflammation inflammatory skin diseases interferon γ Ly/*genetics malaria metabolites metered dose inhalers Missense mosquitoes mRNA Multiple/genetics/*pathology mutations myeloid differentiation factor 88 (MyD88) nanoparticles Nanoparticles/analysis/*metabolism Nanotoxicology neurodevelopmental delay neutropenia Newborn permethrin pest control pesticides Pholcus phalangioides poison Psoriasis Real-Time PCR relative lung bioavailability seizures Selection signal transducer and activator of transcription (STAT) Skin spacers spiders sustainability SYBR Green Timber timber products traditional buildings urinary excretion VKORC1 Western woodworm
Number of items at this level: 150.

*Clone Cells

Shao, K., Koch, C., Gupta, M.K., Lin, Q., Lenz, M., Laufs, S., Denecke, B., Schmidt, M., Linke, M., Hennies, H.C., Hescheler, J., Zenke, M., Zechner, U., Saric, T. and Wagner, W. (2013) Induced pluripotent mesenchymal stromal cell clones retain donor-derived differences in DNA methylation profiles. Molecular Therapy—Nucleic Acids, 21 (1). pp. 240-250. ISSN 2162-2531

3T3 Cells

Eckl, K.M., Weindl, G., Ackermann, K., Küchler, S., Casper, R., Radowski, M.R., Haag, R., Hennies, H.C. and Schäfer-Korting, M. (2014) Increased cutaneous absorption reflects impaired barrier function of reconstructed skin models mimicking keratinisation disorders. Experimental dermatology, 23 (4). pp. 286-288. ISSN 1600-0625

5' Untranslated Regions

Vanita, V., Hejtmancik, J.F., Hennies, H.C., Guleria, K., Nürnberg, P., Singh, D., Sperling, K. and Singh, J.R. (2006) Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin. Molecular Vision, 12. pp. 93-99. ISSN 1090-0535

Abnormalities

Gruber, R., Sugarman, J.L., Crumrine, D., Hupe, M., Mauro, T.M., Mauldin, E.A., Thyssen, J.P., Brandner, J.M., Hennies, H.C., Schmuth, M. and Elias, P.M. (2015) Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiency. The American Journal of Pathology, 185 (4). pp. 1012-1021. ISSN 0002-9440

Hennies, H.C., Kornak, U., Zhang, H., Egerer, J., Zhang, X., Seifert, W., Kühnisch, J., Budde, B., Natebus, M., Brancati, F., Wilcox, W.R., Muller, D., Kaplan, P.B., Rajab, A., Zampino, G., Fodale, V., Dallapiccola, B., Newman, W., Metcalfe, K., Clayton-Smith, J., Tassabehji, M., Steinmann, B., Barr, F.A., Nürnberg, P., Wieacker, P. and Mundlos, S. (2008) Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin. Nature Genetics, 40 (12). pp. 1410-1412. ISSN 1061-4036

Seifert, W., Holder-Espinasse, M., Spranger, S., Hoeltzenbein, M., Rossier, E., Dollfus, H., Lacombe, D., Verloes, A., Chrzanowska, K.H., Maegawa, G.H., Chitayat, D., Kotzot, D., Huhle, D., Meinecke, P., Albrecht, B., Mathijssen, I., Leheup, B., Raile, K., Hennies, H.C. and Horn, D. (2006) Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome. Journal of Medical Genetics, 43 (5). ISSN 0022-2593

Todt, I., Hennies, H.C., Küster, W., Smolle, J., Rademacher, G., Mutze, S., Basta, D., Eisenschenk, A. and Ernst, A. (2006) Neurotological and neuroanatomical changes in the connexin-26-related HID/KID syndrome. Audiology Neurotology, 11 (4). pp. 242-248. ISSN 1420-3030

Utsch, B., Sayer, J.A., Attanasio, M., Pereira, R.R., Eccles, M., Hennies, H.C., Otto, E.A. and Hildebrandt, F. (2006) Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome. Pediatric Nephrology, 21 (1). pp. 32-35. ISSN 0931-041X

Vanita, V., Singh, J.R., Hejtmancik, J.F., Nürnberg, P., Hennies, H.C., Singh, D. and Sperling, K. (2006) A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family. Molecular Vision, 12. pp. 518-522. ISSN 1090-0535

Acrylic Resins/*chemistry

Witting, M., Molina, M., Obst, K., Plank, R., Eckl, K.M., Hennies, H.C., Calderon, M., Friess, W. and Hedtrich, S. (2015) Thermosensitive dendritic polyglycerol-based nanogels for cutaneous delivery of biomacromolecules. Nanomedicine, 11 (5). pp. 1179-1187. ISSN 1549-9634

Action Potentials

Fatima, A., Xu, G., Shao, K., Papadopoulos, S., Lehmann, M., Arnaiz-Cot, J.J., Rosa, A.O., Nguemo, F., Matzkies, M., Dittmann, S., Stone, S.L., Linke, M., Zechner, U., Beyer, V., Hennies, H.C., Rosenkranz, S., Klauke, B., Parwani, A.S., Haverkamp, W., Pfitzer, G., Farr, M., Cleemann, L., Morad, M., Milting, H., Hescheler, J. and Saric, T. (2011) In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cells. Cellular Physiology and Biochemistry, 28 (4). pp. 579-592. ISSN 1015-8987

Activating Transcription Factor 4

Sayer, J.A. et al. (2006) The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nature Genetics, 38 (6). pp. 674-681. ISSN 1061-4036

Adipocytes

Fürstenberger, G., Epp, N., Eckl, K.M., Hennies, H.C., Jorgensen, C., Hallenborg, P., Kristiansen, K. and Krieg, P. (2006) Role of epidermis-type lipoxygenases for skin barrier function and adipocyte differentiation. Prostaglandins Other Lipid Mediators, 82 (1-4). pp. 128-134.

Adolescent

Basel-Vanagaite, L., Sarig, O., Hershkovitz, D., Fuchs-Telem, D., Rapaport, D., Gat, A., Isman, G., Shirazi, I., Shohat, M., Enk, C.D., Birk, E., Kohlhase, J., Matysiak-Scholze, U., Maya, I., Knopf, C., Peffekoven, A., Hennies, H.C., Bergman, R., Horowitz, M., Ishida-Yamamoto, A. and Sprecher, E. (2009) RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome. American Journal of Human Genetics, 85 (2). pp. 254-263. ISSN 1537-6605

Ellinor, P.T., Sasse-Klaassen, S., Probst, S., Gerull, B., Shin, J.T., Toeppel, A., Heuser, A., Michely, B., Yoerger, D.M., Song, B.S., Pilz, B., Krings, G., Coplin, B., Lange, P.E., Dec, G.W., Hennies, H.C., Thierfelder, L. and MacRae, C.A. (2006) A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26. Journal of the American College of Cardiology, 48 (1). pp. 106-111. ISSN 0735-1097

Oji, V., Hautier, J.M., Ahvazi, B., Hausser, I., Aufenvenne, K., Walker, T., Seller, N., Steijlen, P.M., Küster, W., Hovnanian, A., Hennies, H.C. and Traupe, H. (2006) Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype. Human Molecular Genetics, 15 (21). pp. 3083-3097. ISSN 0964-6906

Oji, V., Tadini, G., Akiyama, M., Blanchet, Bardon C., Bodemer, C., Bourrat, E., Coudiere, P., DiGiovanna, J.J., Elias, P., Fischer, J., Fleckman, P., Gina, M., Harper, J., Hashimoto, T., Hausser, I., Hennies, H.C., Hohl, D., Hovnanian, A., Ishida-Yamamoto, A., Jacyk, W.K., Leachman, S., Leigh, I., Mazereeuw-Hautier, J., Milstone, L., Morice-Picard, F., Paller, A.S., Richard, G., Schmuth, M., Shimizu, H., Sprecher, E., Van, Steensel M., Taieb, A., Toro, J.R., Vabres, P., Vahlquist, A., Williams, M. and Traupe, H. (2010) Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Soreze 2009. Journal of American Academy of Dermatology, 63 (4). pp. 607-641. ISSN 0190-9622

Vago, B., Hausser, I., Hennies, H.C., Enk, A. and Jappe, U. (2007) Hyalinosis cutis et mucosae. Journal der Deutschen Dermatologischen Gesellschaft, 5 (5). pp. 401-405. ISSN 1610-0379

Adult

Becker, K., Tinschert, S., Lienert, A., Bleuler, P.E., Staub, F., Meinel, A., Rössler, J., Wach, W., Hoffmann, R., Kühnel, F., Damert, H.G., Nick, H.E., Spicher, R., Lenze, W., Langer, M., Nürnberg, P. and Hennies, H.C. (2015) The importance of genetic susceptibility in Dupuytren's disease. Clinical Genetics, 87 (5). pp. 483-487. ISSN 0009-9163

Gruber, R., Börnchen, C., Rose, K., Daubmann, A., Volksdorf, T., Wladykowski, E., Vidal, Y.Sy S., Peters, E.M., Danso, M., Bouwstra, J.A., Hennies, H.C., Moll, I., Schmuth, M. and Brandner, J.M. (2015) Diverse regulation of claudin-1 and claudin-4 in atopic dermatitis. American Journal of Physical Anthropology, 185 (10). pp. 2777-2789. ISSN 0002-9483

Hillmer, A.M., Flaquer, A., Hanneken, S., Eigelshoven, S., Kortum, A.K., Brockschmidt, F.F., Golla, A., Metzen, C., Thiele, H., Kolberg, S., Reinartz, R., Betz, R.C., Ruzicka, T., Hennies, H.C., Kruse, R. and Nöthen, M.M. (2008) Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26. American Journal of Human Genetics, 82 (3). pp. 737-743. ISSN 1537-6605

Moosbrugger-Martinz, V., Jalili, A., Schossig, A.S., Jahn-Bassler, K., Zschocke, J., Schmuth, M., Stingl, G., Eckl, K.M., Hennies, H.C. and Gruber, R. (2015) Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss-of-function mutation in CSTA. British Journal of Dermatology, 172 (6). pp. 1628-1632. ISSN 0007-0963

African Continental Ancestry Group

Trindade, F., Fiadeiro, T., Torrelo, A., Hennies, H.C., Hausser, I. and Traupe, H. (2010) Bathing suit ichthyosis. European Journal Dermatology, 20 (4). pp. 447-450. ISSN 1167-1122

Age of Onset

Arweiler-Harbeck, D., Horsthemke, B., Jahnke, K. and Hennies, H.C. (2011) Genetic Aspects of Familial Meniere's Disease. Otology and Neurotology, 32 (4). pp. 695-700. ISSN 1531-7129

albinism

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

Alleles

Forstbauer, L.M., Brockschmidt, F.F., Moskvina, V., Herold, C., Redler, S., Herzog, A., Hillmer, A.M., Meesters, C., Heilmann, S., Albert, F., Alblas, M., Hanneken, S., Eigelshoven, S., Giehl, K.A., Jagielska, D., Blume-Peytavi, U., Garcia Bartels, N., Kuhn, J., Hennies, H.C., Goebeler, M., Jung, A., Peitsch, W.K., Kortüm, A.K., Moll, I., Kruse, R., Lutz, G., Wolff, H., Blaumeiser, B., Böhm, M., Kirov, G., Becker, T., Nöthen, M.M. and Betz, R.C. (2011) Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata. European Journal of Human Genetics, 20 (3). pp. 326-332. ISSN 1018-4813

Alpha-Globulins/*genetics/metabolism

Hennies, H.C. (2015) All is balanced: inter-alpha-trypsin inhibitors as unseen extracellular matrix proteins in epidermal morphology and differentiation. Experimental dermatology, 24 (9). pp. 661-662. ISSN 1600-0625

Alternative Splicing

Seifert, W., Holder-Espinasse, M., Kühnisch, J., Kahrizi, K., Tzschach, A., Garshasbi, M., Najmabadi, H., Walter, Kuss A., Kress, W., Laureys, G., Loeys, B., Brilstra, E., Mancini, G.M., Dollfus, H., Dahan, K., Apse, K., Hennies, H.C. and Horn, D. (2008) Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1. Human Mutation, 30 (2). pp. 404-420. ISSN 1059-7794

alternative technology

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

Alternative treatments

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Amino Acid Sequence

Blaydon, D.C., Etheridge, S.L., Risk, J.M., Hennies, H.C., Gay, L.J., Carroll, R., Plagnol, V., McRonald, F.E., Stevens, H.P., Spurr, N.K., Bishop, D.T., Ellis, A., Jankowski, J., Field, J.K., Leigh, I.M., South, A.P. and Kelsell, D.P. (2012) RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome. The American Journal of Human Genetics, 90 (2). pp. 340-346. ISSN 0002-9297

Blaydon, D.C., Nitoiu, D., Eckl, K.M., Cabral, R.M., Bland, P., Hausser, I., van Heel, D.A., Rajpopat, S., Fischer, J., Oji, V., Zvulunov, A., Traupe, H., Hennies, H.C. and Kelsell, D.P. (2011) Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion. The American Journal of Human Genetics, 89 (4). pp. 564-571. ISSN 0002-9297

analysis

Aufenvenne, K., Oji, V., Walker, T., Becker-Pauly, C., Hennies, H.C., Stöcker, W. and Traupe, H. (2009) Transglutaminase-1 and bathing suit ichthyosis: molecular analysis of gene/environment interactions. Journal of Investigative Dermatology, 129 (8). pp. 2068-2071. ISSN 0022-202X

Cichon, S., Martin, L., Hennies, H.C., Muller, F., Van Driessche, K., Karpushova, A., Stevens, W., Colombo, R., Renne, T., Drouet, C., Bork, K. and Nöthen, M.M. (2006) Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III. American Journal of Human Genetics, 79 (6). pp. 1098-1104. ISSN 1537-6605

Dolmans, G.H., Werker, P.M., Hennies, H.C., Furniss, D., Festen, E.A., Franke, L., Becker, K., van der Vlies, P., Wolffenbuttel, B.H., Tinschert, S., Toliat, M.R., Nothnagel, M., Franke, A., Klopp, N., Wichmann, H.E., Nürnberg, P., Giele, H., Ophoff, R.A. and Wijmenga, C. (2011) Wnt signaling and Dupuytren's disease. New England Journal of Medicine, 365 (4). pp. 307-317. ISSN 0028-4793

Eckl, K.M., de Juanes, S., Kurtenbach, J., Natebus, M., Lugassy, J., Oji, V., Traupe, H., Preil, M.L., Martinez-Vidal, F., Smolle, J., Harel, A., Krieger, P., Sprecher, E. and Hennies, H.C. (2009) Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: Evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B. Journal of Investigative Dermatology, 129 (6). pp. 1421-1428. ISSN 0022-202X

Gedicke, M.M., Traupe, H., Fischer, B., Tinschert, S. and Hennies, H.C. (2006) Towards characterization of palmoplantar keratoderma caused by gain-of-function mutation in loricrin: analysis of a family and review of the literature. British Journal of Dermatology, 154 (1). pp. 167-171. ISSN 0007-0963

Lugassy, J., Itin, P., Ishida-Yamamoto, A., Holland, K.R., Huson, S., Geiger, D., Hennies, H.C., Indelman, M., Bercovich, D., Uitto, J., Bergman, R., McGrath, J.A., Richard, G. and Sprecher, E. (2006) Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14. American Journal of Human Genetics, 79 (4). pp. 724-730. ISSN 1537-6605

Mizrachi-Koren, M., Shemer, S., Morganti, M., Indelman, M., Khamaysi, Z., Petronius, D., Bitterman-Deutsch, O., Hennies, H.C., Bergman, R. and Sprecher, E. (2006) Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations. Journal of American Academy of Dermatology, 55 (3). pp. 393-401. ISSN 0190-9622

Oji, V., Eckl, K.M., Aufenvenne, K., Natebus, M., Tarinski, T., Ackermann, K., Seller, N., Metze, D., Nürnberg, G., Fölster-Holst, R., Schäfer-Korting, M., Hausser, I., Traupe, H. and Hennies, H.C. (2010) Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease. American Journal of Human Genetics, 87 (2). pp. 274-281. ISSN 1537-6605

Vanita, V., Hennies, H.C., Singh, D., Nürnberg, P., Sperling, K. and Singh, J.R. (2006) A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin. Molecular Vision, 12:121. pp. 1217-1222. ISSN 1090-0535

Wolf, M.T., Mucha, B.E., Hennies, H.C., Attanasio, M., Panther, F., Zalewski, I., Karle, S.M., Otto, E.A., Deltas, C.C., Fuchshuber, A. and Hildebrandt, F. (2006) Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing. Human Genetics, 119 (6). pp. 649-658. ISSN 0340-6717

Animals

Aufenvenne, K., Rice, R.H., Hausser, I., Oji, V., Hennies, H.C., Rio, M.D., Traupe, H. and Larcher, F. (2012) Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model, and insights from proteomic studies. Journal of Investigative Dermatology, 132 (7). pp. 1918-1921. ISSN 0022-202X

Eckl, K.M., Tidhar, R., Thiele, H., Oji, V., Hausser, I., Brodesser, S., Preil, M.L., Önal-Akan, A., Stock, F., Muller, D., Becker, K., Casper, R., Nürnberg, G., Altmüller, J., Nürnberg, P., Traupe, H., Futerman, A.H. and Hennies, H.C. (2013) Impaired epidermal ceramide synthesis causes autosomal recessive congenital ichthyosis and reveals the importance of ceramide acyl chain length. Journal of Investigative Dermatology, 133 (9). pp. 2202-2211. ISSN 0022-202X

Hinkes, B. et al. (2006) Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nature Genetics, 38 (12). pp. 1397-1405. ISSN 1061-4036

Seifert, W., Kühnisch, J., Maritzen, T., Lommatzsch, S., Hennies, H.C., Bachmann, S., Horn, D. and Haucke, V. (2015) Cohen syndrome-associated protein COH1 physically and functionally interacts with the small GTPase RAB6 at the Golgi complex and directs neurite outgrowth. Journal of Biological Chemistry, 290 (6). pp. 3349-3358. ISSN 0021-9258

Anobium punctatum

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Anticoagulants

Haniza, Mohd Z.H., Adams, Sally, Jones, Eleanor P., MacNicoll, Alan, Mallon, Eamonn B., Smith, Robert H. and Lambert, Mark S. (2015) Large-scale structure of brown rat (Rattus norvegicus) populations in England: effects on rodenticide resistance. PeerJ, 3. e1458. ISSN 2167-8359

Antigens

Nellen, R.G., Steijlen, P.M., Hennies, H.C., Fischer, J., Munro, C.S., Jonkman, M.F., van Steensel, M.A. and van Geel, M. (2013) Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene. British Journal of Dermatology, 168 (6). pp. 1372-1374. ISSN 0007-0963

AP3 complex

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

AP3δ

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

arachnophobia

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Base Sequence

Kalay, E., Uzumcu, A., Krieger, E., Caylan, R., Uyguner, O., Ulubil-Emiroglu, M., Erdol, H., Kayserili, H., Hafiz, G., Baserer, N., Heister, A.J., Hennies, H.C., Nürnberg, P., Basaran, S., Brunner, H.G., Cremers, C.W., Karaguzel, A., Wollnik, B. and Kremer, H. (2007) MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation. American Journal of Medical Genetics. Part A, 143A (20). pp. 2382-2389. ISSN 1552-4825

beclometasone dipropionate

Said, Amira (2011) Urinary Pharmacokinetic Methodology to Determine the Relative Lung Bioavailability of Inhaled Beclometasone. Doctoral thesis, University of Huddersfield.

bed bugs

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

Binding

Zur Stadt, U., Rohr, J., Seifert, W., Koch, F., Grieve, S., Pagel, J., Strauss, J., Kasper, B., Nürnberg, G., Becker, C., Maul-Pavicic, A., Beutel, K., Janka, G., Griffiths, G., Ehl, S. and Hennies, H.C. (2009) Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11. American Journal of Human Genetics, 85 (4). pp. 482-492. ISSN 1537-6605

bio-predators

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Biopredators

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

Blotting

Fuchs-Telem, D., Stewart, H., Rapaport, D., Nousbeck, J., Gat, A., Gini, M., Lugassy, Y., Emmert, S., Eckl, K.M., Hennies, H.C., Sarig, O., Goldsher, D., Meilik, B., Ishida-Yamamoto, A., Horowitz, M. and Sprecher, E. (2011) CEDNIK syndrome results from loss-of-function mutations in SNAP29. British Journal of Dermatology, 164 (3). pp. 610-616. ISSN 0007-0963

Body fluid identification

Connolly, Jo-Ann and Williams, Graham (2011) Evaluating an MRNA based body fluid identification test using sybr green fluorescent dye and real-time PCR. International Journal of Criminal Investigation, 1 (4). pp. 177-185. ISSN 2247-0271

boron

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Bottleneck

Haniza, Mohd Z.H., Adams, Sally, Jones, Eleanor P., MacNicoll, Alan, Mallon, Eamonn B., Smith, Robert H. and Lambert, Mark S. (2015) Large-scale structure of brown rat (Rattus norvegicus) populations in England: effects on rodenticide resistance. PeerJ, 3. e1458. ISSN 2167-8359

Building Conservation

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

buildings

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

Carrier Proteins/*genetics/metabolism

Hussain, M.S., Baig, S.M., Neumann, S., Nürnberg, G., Farooq, M., Ahmad, I.A., Alef, T., Hennies, H.C., Technau, M., Altmüller, J., Frommolt, P., Thiele, H., Noegel, A.A. and Nürnberg, P. (2012) A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function. The American Journal of Human Genetics, 90 (5). pp. 871-878. ISSN 0002-9297

Cell Proliferation/drug effects

Jansen, P.A., van den Bogaard, E.H., Kersten, F.F., Oostendorp, C., van Vlijmen-Willems, I.M., Oji, V., Traupe, H., Hennies, H.C., Schalkwijk, J. and Zeeuwen, P.L. (2012) Cystatin M/E knockdown by lentiviral delivery of shRNA impairs epidermal morphogenesis of human skin equivalents. Experimental dermatology, 21 (11). pp. 889-891. ISSN 1600-0625

chemical treatments

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

Chemical treatments for timber

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Child

Zur Stadt, U., Beutel, K., Kolberg, S., Schneppenheim, R., Kabisch, H., Janka, G. and Hennies, H.C. (2005) Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A. Human Mutation, 27 (1). pp. 62-68. ISSN 1059-7794

Chromosome Mapping

Uyguner, O., Kayserili, H., Li, Y., Karaman, B., Nürnberg, G., Hennies, H.C., Becker, C., Nürnberg, P., Basaran, S., Apak, M.Y. and Wollnik, B. (2007) A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3. Clinical Genetics, 71 (3). pp. 212-219. ISSN 0009-9163

common furniture beetle

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

congenital

Eckl, K.M., Alef, T., Torres, S. and Hennies, H.C. (2011) Full-Thickness Human Skin Models for Congenital Ichthyosis and Related Keratinization Disorders. Journal of Investigative Dermatology, 131 (9). pp. 1938-1942. ISSN 0022-202X

Consanguinity

Lugassy, J., Hennies, H.C., Indelman, M., Khamaysi, Z., Bergman, R. and Sprecher, E. (2008) Rapid detection of homozygous mutations in congenital recessive ichthyosis. Archives of Dermatological Research, 300 (2). pp. 81-85. ISSN 0340-3696

conservation

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

decay

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

Drug Carriers/analysis/*metabolism

Alnasif, N., Zoschke, C., Fleige, E., Brodwolf, R., Boreham, A., Ruhl, E., Eckl, K.M., Merk, H.F., Hennies, H.C., Alexiev, U., Haag, R., Küchler, S. and Schäfer-Korting, M. (2014) Penetration of normal, damaged and diseased skin--an in vitro study on dendritic core-multishell nanotransporters. Journal of Controlled Release, 185. pp. 45-50. ISSN 0168-3659

ecology

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

exome sequencing

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

Female

Pasternack, S.M., Refke, M., Paknia, E., Hennies, H.C., Franz, T., Schäfer, N., Fryer, A., van Steensel, M., Sweeney, E., Just, M., Grimm, C., Kruse, R., Ferrandiz, C., Nöthen, M.M., Fischer, U. and Betz, R.C. (2013) Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex. The American Journal of Human Genetics, 92 (1). pp. 81-87. ISSN 0002-9297

flagellin

Bannon, Ciara, Davies, Pam J., Collett, Andrew and Warhurst, Geoff (2009) Potentiation of flagellin responses in gut epithelial cells by interferon-γ is associated with STAT-independent regulation of MyD88 expression. Biochemical Journal, 423 (1). pp. 119-128. ISSN 0264-6021

Forensic Genetics

Connolly, Jo-Ann and Williams, Graham (2011) Evaluating an MRNA based body fluid identification test using sybr green fluorescent dye and real-time PCR. International Journal of Criminal Investigation, 1 (4). pp. 177-185. ISSN 2247-0271

Genetic

Dolmans, G.H. and Hennies, H.C. (2011) The genetic basis of Dupuytren's disease. In: Morbus Dupuytren and related hyperproliferative disorders. Springer, Heidelberg, pp. 89-91. ISBN 978-3-642-22696-0

Genetic Markers/genetics

Schiller, S., Seebode, C., Hennies, H.C., Giehl, K. and Emmert, S. (2014) Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease. Journal der Deutschen Dermatologischen Gesellschaft, 12 (9). pp. 781-788. ISSN 1610-0379

green building

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

gut epithelium

Bannon, Ciara, Davies, Pam J., Collett, Andrew and Warhurst, Geoff (2009) Potentiation of flagellin responses in gut epithelial cells by interferon-γ is associated with STAT-independent regulation of MyD88 expression. Biochemical Journal, 423 (1). pp. 119-128. ISSN 0264-6021

Hermansky-Pudlak syndrome

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

historic buildings

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

in-vitro dose emission

Said, Amira (2011) Urinary Pharmacokinetic Methodology to Determine the Relative Lung Bioavailability of Inhaled Beclometasone. Doctoral thesis, University of Huddersfield.

Infant

Eckl, K.M., Tidhar, R., Thiele, H., Oji, V., Hausser, I., Brodesser, S., Preil, M.L., Önal-Akan, A., Stock, F., Muller, D., Becker, K., Casper, R., Nürnberg, G., Altmüller, J., Nürnberg, P., Traupe, H., Futerman, A.H. and Hennies, H.C. (2013) Impaired epidermal ceramide synthesis causes autosomal recessive congenital ichthyosis and reveals the importance of ceramide acyl chain length. Journal of Investigative Dermatology, 133 (9). pp. 2202-2211. ISSN 0022-202X

Fuchs-Telem, D., Stewart, H., Rapaport, D., Nousbeck, J., Gat, A., Gini, M., Lugassy, Y., Emmert, S., Eckl, K.M., Hennies, H.C., Sarig, O., Goldsher, D., Meilik, B., Ishida-Yamamoto, A., Horowitz, M. and Sprecher, E. (2011) CEDNIK syndrome results from loss-of-function mutations in SNAP29. British Journal of Dermatology, 164 (3). pp. 610-616. ISSN 0007-0963

Hennies, H.C., Kornak, U., Zhang, H., Egerer, J., Zhang, X., Seifert, W., Kühnisch, J., Budde, B., Natebus, M., Brancati, F., Wilcox, W.R., Muller, D., Kaplan, P.B., Rajab, A., Zampino, G., Fodale, V., Dallapiccola, B., Newman, W., Metcalfe, K., Clayton-Smith, J., Tassabehji, M., Steinmann, B., Barr, F.A., Nürnberg, P., Wieacker, P. and Mundlos, S. (2008) Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin. Nature Genetics, 40 (12). pp. 1410-1412. ISSN 1061-4036

Hinkes, B. et al. (2006) Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nature Genetics, 38 (12). pp. 1397-1405. ISSN 1061-4036

Oji, V., Hautier, J.M., Ahvazi, B., Hausser, I., Aufenvenne, K., Walker, T., Seller, N., Steijlen, P.M., Küster, W., Hovnanian, A., Hennies, H.C. and Traupe, H. (2006) Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype. Human Molecular Genetics, 15 (21). pp. 3083-3097. ISSN 0964-6906

Oji, V., Tadini, G., Akiyama, M., Blanchet, Bardon C., Bodemer, C., Bourrat, E., Coudiere, P., DiGiovanna, J.J., Elias, P., Fischer, J., Fleckman, P., Gina, M., Harper, J., Hashimoto, T., Hausser, I., Hennies, H.C., Hohl, D., Hovnanian, A., Ishida-Yamamoto, A., Jacyk, W.K., Leachman, S., Leigh, I., Mazereeuw-Hautier, J., Milstone, L., Morice-Picard, F., Paller, A.S., Richard, G., Schmuth, M., Shimizu, H., Sprecher, E., Van, Steensel M., Taieb, A., Toro, J.R., Vabres, P., Vahlquist, A., Williams, M. and Traupe, H. (2010) Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Soreze 2009. Journal of American Academy of Dermatology, 63 (4). pp. 607-641. ISSN 0190-9622

Oji, V., Tadini, G., Akiyama, M., Blanchet, Bardon C., Bodemer, C., Bourrat, E., Coudiere, P., DiGiovanna, J.J., Elias, P., Fischer, J., Fleckman, P., Gina, M., Harper, J., Hashimoto, T., Hausser, I., Hennies, H.C., Hohl, D., Hovnanian, A., Ishida-Yamamoto, A., Jacyk, W.K., Leachman, S., Leigh, I., Mazereeuw-Hautier, J., Milstone, L., Morice-Picard, F., Paller, A.S., Richard, G., Schmuth, M., Shimizu, H., Sprecher, E., Van, Steensel M., Taieb, A., Toro, J.R., Vabres, P., Vahlquist, A., Williams, M. and Traupe, H. (2010) Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Soreze 2009. Journal of American Academy of Dermatology, 63 (4). pp. 607-641. ISSN 0190-9622

Trindade, F., Fiadeiro, T., Torrelo, A., Hennies, H.C., Hausser, I. and Traupe, H. (2010) Bathing suit ichthyosis. European Journal Dermatology, 20 (4). pp. 447-450. ISSN 1167-1122

Zur Stadt, U., Rohr, J., Seifert, W., Koch, F., Grieve, S., Pagel, J., Strauss, J., Kasper, B., Nürnberg, G., Becker, C., Maul-Pavicic, A., Beutel, K., Janka, G., Griffiths, G., Ehl, S. and Hennies, H.C. (2009) Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11. American Journal of Human Genetics, 85 (4). pp. 482-492. ISSN 1537-6605

infection susceptibility

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

infestation

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

inflammation

Bannon, Ciara, Davies, Pam J., Collett, Andrew and Warhurst, Geoff (2009) Potentiation of flagellin responses in gut epithelial cells by interferon-γ is associated with STAT-independent regulation of MyD88 expression. Biochemical Journal, 423 (1). pp. 119-128. ISSN 0264-6021

inflammatory skin diseases

Hennies, H.C. (2015) All is balanced: inter-alpha-trypsin inhibitors as unseen extracellular matrix proteins in epidermal morphology and differentiation. Experimental dermatology, 24 (9). pp. 661-662. ISSN 1600-0625

interferon γ

Bannon, Ciara, Davies, Pam J., Collett, Andrew and Warhurst, Geoff (2009) Potentiation of flagellin responses in gut epithelial cells by interferon-γ is associated with STAT-independent regulation of MyD88 expression. Biochemical Journal, 423 (1). pp. 119-128. ISSN 0264-6021

Ly/*genetics

Nellen, R.G., Steijlen, P.M., Hennies, H.C., Fischer, J., Munro, C.S., Jonkman, M.F., van Steensel, M.A. and van Geel, M. (2013) Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene. British Journal of Dermatology, 168 (6). pp. 1372-1374. ISSN 0007-0963

malaria

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

metabolites

Said, Amira (2011) Urinary Pharmacokinetic Methodology to Determine the Relative Lung Bioavailability of Inhaled Beclometasone. Doctoral thesis, University of Huddersfield.

metered dose inhalers

Said, Amira (2011) Urinary Pharmacokinetic Methodology to Determine the Relative Lung Bioavailability of Inhaled Beclometasone. Doctoral thesis, University of Huddersfield.

Missense

Gruber, R., Hennies, H.C., Romani, N. and Schmuth, M. (2011) A Novel Homozygous Missense Mutation in SLURP1 Causing Mal de Meleda With an Atypical Phenotype. Archives of Dermatology, 147 (6). pp. 748-750. ISSN 0003-987X

mosquitoes

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

mRNA

Connolly, Jo-Ann and Williams, Graham (2011) Evaluating an MRNA based body fluid identification test using sybr green fluorescent dye and real-time PCR. International Journal of Criminal Investigation, 1 (4). pp. 177-185. ISSN 2247-0271

Multiple/genetics/*pathology

Gruber, R., Sugarman, J.L., Crumrine, D., Hupe, M., Mauro, T.M., Mauldin, E.A., Thyssen, J.P., Brandner, J.M., Hennies, H.C., Schmuth, M. and Elias, P.M. (2015) Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiency. The American Journal of Pathology, 185 (4). pp. 1012-1021. ISSN 0002-9440

mutations

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

myeloid differentiation factor 88 (MyD88)

Bannon, Ciara, Davies, Pam J., Collett, Andrew and Warhurst, Geoff (2009) Potentiation of flagellin responses in gut epithelial cells by interferon-γ is associated with STAT-independent regulation of MyD88 expression. Biochemical Journal, 423 (1). pp. 119-128. ISSN 0264-6021

nanoparticles

Eckl, K.M., Weindl, G., Ackermann, K., Küchler, S., Casper, R., Radowski, M.R., Haag, R., Hennies, H.C. and Schäfer-Korting, M. (2014) Increased cutaneous absorption reflects impaired barrier function of reconstructed skin models mimicking keratinisation disorders. Experimental dermatology, 23 (4). pp. 286-288. ISSN 1600-0625

Nanoparticles/analysis/*metabolism

Alnasif, N., Zoschke, C., Fleige, E., Brodwolf, R., Boreham, A., Ruhl, E., Eckl, K.M., Merk, H.F., Hennies, H.C., Alexiev, U., Haag, R., Küchler, S. and Schäfer-Korting, M. (2014) Penetration of normal, damaged and diseased skin--an in vitro study on dendritic core-multishell nanotransporters. Journal of Controlled Release, 185. pp. 45-50. ISSN 0168-3659

Nanotoxicology

Alnasif, N., Zoschke, C., Fleige, E., Brodwolf, R., Boreham, A., Ruhl, E., Eckl, K.M., Merk, H.F., Hennies, H.C., Alexiev, U., Haag, R., Küchler, S. and Schäfer-Korting, M. (2014) Penetration of normal, damaged and diseased skin--an in vitro study on dendritic core-multishell nanotransporters. Journal of Controlled Release, 185. pp. 45-50. ISSN 0168-3659

neurodevelopmental delay

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

neutropenia

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

Newborn

Eckl, K.M., Tidhar, R., Thiele, H., Oji, V., Hausser, I., Brodesser, S., Preil, M.L., Önal-Akan, A., Stock, F., Muller, D., Becker, K., Casper, R., Nürnberg, G., Altmüller, J., Nürnberg, P., Traupe, H., Futerman, A.H. and Hennies, H.C. (2013) Impaired epidermal ceramide synthesis causes autosomal recessive congenital ichthyosis and reveals the importance of ceramide acyl chain length. Journal of Investigative Dermatology, 133 (9). pp. 2202-2211. ISSN 0022-202X

Oji, V., Tadini, G., Akiyama, M., Blanchet, Bardon C., Bodemer, C., Bourrat, E., Coudiere, P., DiGiovanna, J.J., Elias, P., Fischer, J., Fleckman, P., Gina, M., Harper, J., Hashimoto, T., Hausser, I., Hennies, H.C., Hohl, D., Hovnanian, A., Ishida-Yamamoto, A., Jacyk, W.K., Leachman, S., Leigh, I., Mazereeuw-Hautier, J., Milstone, L., Morice-Picard, F., Paller, A.S., Richard, G., Schmuth, M., Shimizu, H., Sprecher, E., Van, Steensel M., Taieb, A., Toro, J.R., Vabres, P., Vahlquist, A., Williams, M. and Traupe, H. (2010) Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Soreze 2009. Journal of American Academy of Dermatology, 63 (4). pp. 607-641. ISSN 0190-9622

permethrin

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

pest control

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

pesticides

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Pholcus phalangioides

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

poison

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Psoriasis

Nousbeck, J., Ishida-Yamamoto, A., Bidder, M., Fuchs, D., Eckl, K.M., Hennies, H.C., Sagiv, N., Gat, A., Gini, M., Filip, I., Matz, H., Goldberg, I., Enk, C.D., Sarig, O., Meilik, B., Aberdam, D., Gilhar, A. and Sprecher, E. (2011) IGFBP7 as a Potential Therapeutic Target in Psoriasis. Journal of Investigative Dermatology, 131 (8). pp. 1767-1770. ISSN 0022-202X

Real-Time PCR

Connolly, Jo-Ann and Williams, Graham (2011) Evaluating an MRNA based body fluid identification test using sybr green fluorescent dye and real-time PCR. International Journal of Criminal Investigation, 1 (4). pp. 177-185. ISSN 2247-0271

relative lung bioavailability

Said, Amira (2011) Urinary Pharmacokinetic Methodology to Determine the Relative Lung Bioavailability of Inhaled Beclometasone. Doctoral thesis, University of Huddersfield.

seizures

Ammann, S., Schulz, A., Krägeloh-Mann, I., Dieckmann, N.M., Niethammer, K., Fuchs, S., Eckl, K.M., Plank, R., Werner, R., Altmüller, J., Thiele, H., Nürnberg, P., Bank, J., Strauss, A., von Bernuth, H., Zur Stadt, U., Grieve, S., Griffiths, G.M., Lehmberg, K., Hennies, H.C. and Ehl, S. (2016) Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome. Blood, 127 (8). pp. 997-1006. ISSN 0006-4971

Selection

Haniza, Mohd Z.H., Adams, Sally, Jones, Eleanor P., MacNicoll, Alan, Mallon, Eamonn B., Smith, Robert H. and Lambert, Mark S. (2015) Large-scale structure of brown rat (Rattus norvegicus) populations in England: effects on rodenticide resistance. PeerJ, 3. e1458. ISSN 2167-8359

signal transducer and activator of transcription (STAT)

Bannon, Ciara, Davies, Pam J., Collett, Andrew and Warhurst, Geoff (2009) Potentiation of flagellin responses in gut epithelial cells by interferon-γ is associated with STAT-independent regulation of MyD88 expression. Biochemical Journal, 423 (1). pp. 119-128. ISSN 0264-6021

Skin

Eckl, K.M. and Hennies, H.C. (2009) Disease-specific skin models: In vitro models for the development of treatment approaches to inherited disorders of cornification as illustrated by congenital ichthyosis. Medizinische Genetik, 21 (4). pp. 487-492. ISSN 0936-5931

Küchler, S., Henkes, D., Eckl, K.M., Ackermann, K., Plendl, J., Korting, H.C., Hennies, H.C. and Schäfer-Korting, M. (2011) Hallmarks of atopic skin in vitro - Mimicked by the means of a skin disease model based on FLG knock down. Alternatives to Laboratory Animals, 39 (5). pp. 471-480. ISSN 0261-1929

spacers

Said, Amira (2011) Urinary Pharmacokinetic Methodology to Determine the Relative Lung Bioavailability of Inhaled Beclometasone. Doctoral thesis, University of Huddersfield.

spiders

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

sustainability

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

SYBR Green

Connolly, Jo-Ann and Williams, Graham (2011) Evaluating an MRNA based body fluid identification test using sybr green fluorescent dye and real-time PCR. International Journal of Criminal Investigation, 1 (4). pp. 177-185. ISSN 2247-0271

Timber

Hippisley-Cox, Charles (2012) Spiders as Potential Bio-Predators for Controlling Woodworm Infestation. Building Engineer, 87 (04). pp. 28-30. ISSN 0969-8213

timber products

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

traditional buildings

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

urinary excretion

Said, Amira (2011) Urinary Pharmacokinetic Methodology to Determine the Relative Lung Bioavailability of Inhaled Beclometasone. Doctoral thesis, University of Huddersfield.

VKORC1

Haniza, Mohd Z.H., Adams, Sally, Jones, Eleanor P., MacNicoll, Alan, Mallon, Eamonn B., Smith, Robert H. and Lambert, Mark S. (2015) Large-scale structure of brown rat (Rattus norvegicus) populations in England: effects on rodenticide resistance. PeerJ, 3. e1458. ISSN 2167-8359

Western

Fuchs-Telem, D., Stewart, H., Rapaport, D., Nousbeck, J., Gat, A., Gini, M., Lugassy, Y., Emmert, S., Eckl, K.M., Hennies, H.C., Sarig, O., Goldsher, D., Meilik, B., Ishida-Yamamoto, A., Horowitz, M. and Sprecher, E. (2011) CEDNIK syndrome results from loss-of-function mutations in SNAP29. British Journal of Dermatology, 164 (3). pp. 610-616. ISSN 0007-0963

woodworm

Hippisley-Cox, Charles (2013) Come into my parlour... Architectural Technology (107). p. 11. ISSN 1361-326X

Hippisley-Cox, Charles (2015) Traditional buildings as ecosystems with spiders as biocontrol for woodworm. The Bulletin of the British Ecological Society, 46 (4). pp. 40-41.

This list was generated on Wed Jul 27 13:29:17 2016 UTC.

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