Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Katherine Gowan"'
Publikováno v:
Journal of Investigative Dermatology. 130:798-803
Generalized vitiligo is a common disorder in which patchy loss of skin and hair pigmentation principally appears to result from autoimmune loss of melanocytes from affected regions. We previously characterized a unique founder population in an isolat
Autor:
Fei Bao, Katherine Gowan, George S. Eisenbarth, Christine M. Roberts, Allison K. Martin, Pamela R. Fain, Sunanda R. Babu
Publikováno v:
Annals of the New York Academy of Sciences. 1005:340-343
The IDDM 17 locus was mapped to an 8-cM interval at chromosome 10q25.1 based on linkage in a large Bedouin Arab family with 19 affected relatives. Caspase 7 (CASP7), an apoptosis-related cysteine protease, is one of the few known genes in this region
Autor:
Albert Wolkerstorfer, Stanca A. Birlea, Jo Lambert, Anthony P. Weetman, Alain Taieb, Nanette B. Silverberg, E. Helen Kemp, Andreas Overbeck, Margaret R. Wallace, Paulene J. Holland, Mauro Picardo, J.P. Wietze van der Veen, Wayne T. McCormack, Gerold Schuler, Thomas Jouary, Nanja van Geel, Richard A. Spritz, Katherine Gowan, Giovanni Leone, Ying Jin, Rosalie M. Luiten, Joanne B. Cole, Songtao Ben, Dorothy C. Bennett, Tracey M. Ferrara, A. Hartmann, Saskia Eichner, David J. Gawkrodger, Khaled Ezzedine, Sheri L. Riccardi, Pamela R. Fain
Publikováno v:
Nature genetics
Nature genetics, 44(6), 676-U94. Nature Publishing Group
Nature genetics, 44(6), 676-U94. Nature Publishing Group
We previously reported a genome-wide association study (GWAS) identifying 14 susceptibility loci for generalized vitiligo. We report here a second GWAS (450 individuals with vitiligo (cases) and 3,182 controls), an independent replication study (1,44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6f8df3973a2c0c5c1972bdc7dc64698
Autor:
Elise Eller, Gavin C. Conant, Sunanda R. Babu, Pnina Vardi, George S. Eisenbarth, Katherine Gowan, Pamela R. Fain, Christine M. Roberts
Publikováno v:
Annals of the New York Academy of Sciences. 1037
IDDM17 on chromosome 10 was identified in an initial genome screen of 13 members (10 affected) of a large Bedouin Arab family that had 19 relatives affected with type 1 diabetes. Two more children have now been diagnosed with the disease. A second ge
Autor:
Katherine Gowan, Allison K. Martin, Pamela R. Fain, George S. Eisenbarth, Sunanda R. Babu, Christine M. Roberts, Fei Bao
Publikováno v:
Annals of the New York Academy of Sciences. 1005
Type 1 diabetes is an autoimmune disease caused by a combination of genetic and environmental factors. On the basis of a genomic search for linkage in a Bedouin Arab family with 19 members with type 1 diabetes, we previously mapped the IDDM 17 locus
Publikováno v:
Journal of Investigative Dermatology. (3):774-783
Generalized vitiligo is the most common pigmentation disorder, the result of autoimmune loss of melanocytes from the skin and hair, with a high frequency of other autoimmune diseases in vitiligo patients and their relatives. We previously reported th