HuGE Literature Finder
Records 1-10
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Role of C1858T polymorphism of Lymphoid Tyrosine Phosphatase in Egyptian children and adolescents with type 1 diabetes.
Current diabetes reviews 2018 Jul . El Fotoh Wafaa Moustafa M Abo, El Razek Midan Dina Abd, El Shalakany Abeer Ham |
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A polymorphism in a phosphotyrosine signalling motif of CD229 (Ly9, SLAMF3) alters SH2 domain binding and T-cell activation.
Immunology 2015 Jul . Margraf Stefanie, Garner Lee I, Wilson Timothy J, Brown Marion |
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Non-synonymous single nucleotide polymorphisms in genes for immunoregulatory galectins: association of galectin-8 (F19Y) occurrence with autoimmune diseases in a Caucasian population.
Biochimica et biophysica acta 2012 Oct 1820 (10): 1512-8. Pál Zsuzsanna, Antal Péter, Srivastava Sanjeev Kumar, Hullám Gábor, Semsei Agnes F, Gál János, Svébis Mihály, Soós Györgyi, Szalai Csaba, André Sabine, Gordeeva Elena, Nagy György, Kaltner Herbert, Bovin Nicolai V, Molnár Mária Judit, Falus András, Gabius Hans-Joachim, Buzás Edit Ir |
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Shared molecular amino acid signature in the HLA-DR peptide binding pocket predisposes to both autoimmune diabetes and thyroiditis.
Proceedings of the National Academy of Sciences of the United States of America 2010 Sep 107 (39): 16899-903. Menconi Francesca, Osman Roman, Monti Maria C, Greenberg David A, Concepcion Erlinda S, Tomer Yar |
Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.
The New England journal of medicine 2010 May 362 (18): 1686-97. Jin Ying, Birlea Stanca A, Fain Pamela R, Gowan Katherine, Riccardi Sheri L, Holland Paulene J, Mailloux Christina M, Sufit Alexandra J D, Hutton Saunie M, Amadi-Myers Anita, Bennett Dorothy C, Wallace Margaret R, McCormack Wayne T, Kemp E Helen, Gawkrodger David J, Weetman Anthony P, Picardo Mauro, Leone Giovanni, Taïeb Alain, Jouary Thomas, Ezzedine Khaled, van Geel Nanny, Lambert Jo, Overbeck Andreas, Spritz Richard |
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Mutations in the hemochromatosis gene (HFE) and multiple sclerosis.
Neuroscience letters 2005 Aug 383 (3): 301-4. Risti? Smiljana, Lovreci? Luca, Brajenovi?-Mili? Bojana, Starcevi?-Cizmarevi? Nada, Jazbec Sasa Sega, Sepci? Juraj, Kapovi? Miljenko, Peterlin Bor |
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Susceptibility and outcome in MS: associations with polymorphisms in pigmentation-related genes.
Neurology 2004 Jun 62 (12): 2323-5. Partridge J M, Weatherby S J M, Woolmore J A, Highland D J, Fryer A A, Mann C L A, Boggild M D, Ollier W E R, Strange R C, Hawkins C |
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The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.
Journal of medical genetics 2004 Jan 41 (1): 6-10. Livesey K J, Wimhurst V L C, Carter K, Worwood M, Cadet E, Rochette J, Roberts A G, Pointon J J, Merryweather-Clarke A T, Bassett M L, Jouanolle A-M, Mosser A, David V, Poulton J, Robson K J |
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Nitric oxide synthase 2 promoter polymorphisms and systemic lupus erythematosus in african-americans.
The Journal of rheumatology 2003 Jan 30 (1): 60-7. Oates Jim C, Levesque Marc C, Hobbs Maurine R, Smith Erica Grace, Molano Ivan D, Page Grier P, Hill Bruce S, Weinberg J Brice, Cooper Glinda S, Gilkeson Gary |
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Polymorphism in the TNF-alpha gene promoter at position -1031 is associated with increased circulating levels of TNF-alpha, myeloperoxidase and nitrotyrosine in primary Sjögren's syndrome.
Clinical and experimental rheumatology 0 30 (6): 843-9. Cay H Fatih, Sezer Ilhan, Dogan Serdar, Felek Rasih, Aslan Mut |
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- Page last updated:Apr 06, 2020
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