Authors:
Imrie, H
Vaidya, B
Perros, P
Kelly, WF
Toft, AD
Young, ET
Kendall-Taylor, P
Pearce, SHS
Citation: H. Imrie et al., Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population, J CLIN END, 86(2), 2001, pp. 626-630
Authors:
Satyamoorthy, K
Li, G
Vaidya, B
Patel, D
Herlyn, M
Citation: K. Satyamoorthy et al., Insulin-like growth factor-1 induces survival and growth of biologically early melanoma cells through both the mitogen-activated protein kinase and beta-catenin pathways, CANCER RES, 61(19), 2001, pp. 7318-7324
Authors:
Simmons, NJ
Chin, KOA
Harnisch, JA
Vaidya, B
Trahanovsky, WS
Porter, MD
Angelici, RJ
Citation: Nj. Simmons et al., Synthesis and characterization of a catechol-terminated alkanethiolate monolayer adsorbed on gold, J ELEC CHEM, 482(2), 2000, pp. 178-187
Citation: B. Vaidya et al., Recent advances in the molecular genetics of congenital and acquired primary adrenocortical failure, CLIN ENDOCR, 53(4), 2000, pp. 403-418
Authors:
Vaidya, B
Imrie, H
Geatch, DR
Perros, P
Ball, SG
Baylis, PH
Carr, D
Hurel, SJ
James, RA
Kelly, WF
Kemp, EH
Young, ET
Weetman, AP
Kendall-Taylor, P
Pearce, SHS
Citation: B. Vaidya et al., Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease, J CLIN END, 85(2), 2000, pp. 688-691
Authors:
Vaidya, B
Imrie, H
Perros, P
Dickinson, J
McCarthy, MI
Kendall-Taylor, P
Pearce, SHS
Citation: B. Vaidya et al., Cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism confers susceptibility to thyroid associated orbitopathy, LANCET, 354(9180), 1999, pp. 743-744
Authors:
Vaidya, B
Coffey, R
Coyle, B
Trembath, R
San Lazaro, C
Reardon, W
Kendall-Taylor, P
Citation: B. Vaidya et al., Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiterin one family, J CLIN END, 84(8), 1999, pp. 2736-2738
Authors:
Pearce, SHS
Vaidya, B
Imrie, H
Perros, P
Kelly, WF
Toft, AD
McCarthy, MI
Young, ET
Kendall-Taylor, P
Citation: Shs. Pearce et al., Further evidence for a susceptibility locus on chromosome 20q13.11 in families with dominant transmission of Graves disease, AM J HU GEN, 65(5), 1999, pp. 1462-1465
Authors:
Pearce, SHS
Cheetham, T
Imrie, H
Vaidya, B
Barnes, ND
Bilous, RW
Carr, D
Meeran, K
Shaw, NJ
Smith, CS
Toft, AD
Williams, G
Kendall-Taylor, P
Citation: Shs. Pearce et al., A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1, AM J HU GEN, 63(6), 1998, pp. 1675-1684