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Year Number of Results
1952 1
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2002 4
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150 results

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Page 1
Showing results for fain p[au]
Your search for Faion P[au] retrieved no results
Alport syndrome--clinical phenotypes, incidence, and pathology.
Gregory MC, Terreros DA, Barker DF, Fain PN, Denison JC, Atkin CL. Gregory MC, et al. Among authors: fain pn. Contrib Nephrol. 1996;117:1-28. doi: 10.1159/000424804. Contrib Nephrol. 1996. PMID: 8801040 Review. No abstract available.
Genetics of type 1A diabetes.
Redondo MJ, Fain PR, Eisenbarth GS. Redondo MJ, et al. Among authors: fain pr. Recent Prog Horm Res. 2001;56:69-89. doi: 10.1210/rp.56.1.69. Recent Prog Horm Res. 2001. PMID: 11237226 Review.
The genetics of autoimmune polyendocrine syndrome type II.
Robles DT, Fain PR, Gottlieb PA, Eisenbarth GS. Robles DT, et al. Among authors: fain pr. Endocrinol Metab Clin North Am. 2002 Jun;31(2):353-68, vi-vii. doi: 10.1016/s0889-8529(01)00015-9. Endocrinol Metab Clin North Am. 2002. PMID: 12092455 Review.
Genetics of type 1A (immune mediated) diabetes.
Melanitou E, Fain P, Eisenbarth GS. Melanitou E, et al. Among authors: fain p. J Autoimmun. 2003 Sep;21(2):93-8. doi: 10.1016/s0896-8411(03)00097-0. J Autoimmun. 2003. PMID: 12935776 Review.
Major association of vitiligo with HLA-A*02:01 in Japanese.
Jin Y, Hayashi M, Fain PR, Suzuki T, Fukai K, Oiso N, Tanemura A, Holcomb CL, Rastrou M, Erlich HA, Spritz RA. Jin Y, et al. Among authors: fain pr. Pigment Cell Melanoma Res. 2015 May;28(3):360-2. doi: 10.1111/pcmr.12356. Epub 2015 Feb 17. Pigment Cell Melanoma Res. 2015. PMID: 25645285 Free PMC article. No abstract available.
Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.
Jin Y, Birlea SA, Fain PR, Ferrara TM, Ben S, Riccardi SL, Cole JB, Gowan K, Holland PJ, Bennett DC, Luiten RM, Wolkerstorfer A, van der Veen JP, Hartmann A, Eichner S, Schuler G, van Geel N, Lambert J, Kemp EH, Gawkrodger DJ, Weetman AP, Taïeb A, Jouary T, Ezzedine K, Wallace MR, McCormack WT, Picardo M, Leone G, Overbeck A, Silverberg NB, Spritz RA. Jin Y, et al. Among authors: fain pr. Nat Genet. 2012 May 6;44(6):676-80. doi: 10.1038/ng.2272. Nat Genet. 2012. PMID: 22561518 Free PMC article.
SASH1 Is Involved in an Autosomal Dominant Lentiginous Phenotype.
Shellman YG, Lambert KA, Brauweiler A, Fain P, Spritz RA, Martini M, Janssen KP, Box NF, Terzian T, Rewers M, Horvath A, Stratakis CA, Robinson WA, Robinson SE, Norris DA, Artinger KB, Pacheco TR. Shellman YG, et al. Among authors: fain p. J Invest Dermatol. 2015 Dec;135(12):3192-3194. doi: 10.1038/jid.2015.292. Epub 2015 Jul 23. J Invest Dermatol. 2015. PMID: 26203640 Free PMC article. No abstract available.
Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.
Birlea SA, Jin Y, Bennett DC, Herbstman DM, Wallace MR, McCormack WT, Kemp EH, Gawkrodger DJ, Weetman AP, Picardo M, Leone G, Taïeb A, Jouary T, Ezzedine K, van Geel N, Lambert J, Overbeck A, Fain PR, Spritz RA. Birlea SA, et al. Among authors: fain pr. J Invest Dermatol. 2011 Feb;131(2):371-81. doi: 10.1038/jid.2010.337. Epub 2010 Nov 18. J Invest Dermatol. 2011. PMID: 21085187 Free PMC article.
NALP1 in vitiligo-associated multiple autoimmune disease.
Jin Y, Mailloux CM, Gowan K, Riccardi SL, LaBerge G, Bennett DC, Fain PR, Spritz RA. Jin Y, et al. Among authors: fain pr. N Engl J Med. 2007 Mar 22;356(12):1216-25. doi: 10.1056/NEJMoa061592. N Engl J Med. 2007. PMID: 17377159 Free article.
Genetic susceptibility to lung cancer.
Miller YE, Fain P. Miller YE, et al. Among authors: fain p. Semin Respir Crit Care Med. 2003 Apr;24(2):197-204. doi: 10.1055/s-2003-39018. Semin Respir Crit Care Med. 2003. PMID: 16088539
150 results