Resultats de la cerca - Mathias Herr
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Clinical Heterogeneity in Patients With <i>FOXP3</i> Mutations Presenting With Permanent Neonatal Diabetes per Oscar Rubio‐Cabezas, Jayne A.L. Minton, Richard Caswell, Julian Hamilton‐Shield, Dorothee Deiss, Zdenĕk Šumnı́k, Amely Cayssials, Mathias Herr, Anja Loew, Vaughan E Lewis, Sian Ellard, Andrew T. Hattersley
Publicat 2008Artigo -
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Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease per Hironori Ueda, Joanna M. M. Howson, Laura Esposito, J. M. Heward, Snook, Giselle Chamberlain, Daniel B. Rainbow, Kara Hunter, Annabel N. Smith, Gianfranco Di Genova, Mathias Herr, Ingrid Dahlman, Felicity Payne, Deborah J. Smyth, Christopher Lowe, Rebecca C.J. Twells, Sarah Howlett, Barry Healy, Sarah Nutland, Helen Rance, Vin Everett, Luc J Smink, Alexander Lam, Heather J. Cordell, Neil Walker, Cristina Bordin, John S. Hulme, Costantino Motzo, Francesco Cucca, J. Fred Hess, Michael L. Metzker, Jane Rogers, Simon G. Gregory, Amit Allahabadia, Ratnasingam Nithiyananthan, Eva Tuomilehto‐Wolf, Jaakko Tuomilehto, Polly J. Bingley, Kathleen M. Gillespie, Dag E. Undlien, Kjersti S. Rønningen, Cristian Guja, C Ionescu-Tîrgovişte, David A. Savage, Alexander P. Maxwell, D. J. Carson, C. C. Patterson, Jayne A. Franklyn, David Clayton, Laurence B. Peterson, Linda S. Wicker, John A. Todd, Stephen Gough
Publicat 2003Artigo
Eines de cerca:
Matèries relacionades
Antigen
Autoimmunity
Biology
Disease
Gene
Genetics
Human leukocyte antigen
Immune system
Immunology
Medicine
Allele
Alternative splicing
Antibody
Association mapping
Autoimmune disease
Chromosome
Complete linkage
Computational biology
Cytotoxic T cell
Diabetes mellitus
Endocrinology
Enteropathy
Exon
FOXP3
Gastroenterology
Gene mapping
Genetic association
Genetic linkage
Genotype
Immune dysregulation