Veal CD - Search Results

1

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.

Tarpey P, Thomas S, Sarvananthan N, Mallya U, Lisgo S, Talbot CJ, Roberts EO, Awan M, Surendran M, McLean RJ, Reinecke RD, Langmann A, Lindner S, Koch M, Jain S, Woodruff G, Gale RP, Bastawrous A, Degg C, Droutsas K, Asproudis I, Zubcov AA, Pieh C, Veal CD, Machado RD, Backhouse OC, Baumber L, Constantinescu CS, Brodsky MC, Hunter DG, Hertle RW, Read RJ, Edkins S, O'Meara S, Parker A, Stevens C, Teague J, Wooster R, Futreal PA, Trembath RC, Stratton MR, Raymond FL, Gottlob I. Tarpey P, et al. Among authors: veal cd. Nat Genet. 2006 Nov;38(11):1242-4. doi: 10.1038/ng1893. Epub 2006 Oct 1. Nat Genet. 2006. PMID: 17013395 Free PMC article.

2

A defect in the regional deposition of adipose tissue (partial lipodystrophy) is encoded by a gene at chromosome 1q.

Jackson SN, Pinkney J, Bargiotta A, Veal CD, Howlett TA, McNally PG, Corral R, Johnson A, Trembath RC. Jackson SN, et al. Among authors: veal cd. Am J Hum Genet. 1998 Aug;63(2):534-40. doi: 10.1086/301971. Am J Hum Genet. 1998. PMID: 9683602 Free PMC article.

3

Identification of a novel psoriasis susceptibility locus at 1p and evidence of epistasis between PSORS1 and candidate loci.

Veal CD, Clough RL, Barber RC, Mason S, Tillman D, Ferry B, Jones AB, Ameen M, Balendran N, Powis SH, Burden AD, Barker JN, Trembath RC. Veal CD, et al. J Med Genet. 2001 Jan;38(1):7-13. doi: 10.1136/jmg.38.1.7. J Med Genet. 2001. PMID: 11134234 Free PMC article.

4

Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus.

Veal CD, Capon F, Allen MH, Heath EK, Evans JC, Jones A, Patel S, Burden D, Tillman D, Barker JN, Trembath RC. Veal CD, et al. Am J Hum Genet. 2002 Sep;71(3):554-64. doi: 10.1086/342289. Epub 2002 Jul 29. Am J Hum Genet. 2002. PMID: 12148091 Free PMC article.

5

Genetic association analysis using data from triads and unrelated subjects.

Epstein MP, Veal CD, Trembath RC, Barker JN, Li C, Satten GA. Epstein MP, et al. Among authors: veal cd. Am J Hum Genet. 2005 Apr;76(4):592-608. doi: 10.1086/429225. Epub 2005 Feb 14. Am J Hum Genet. 2005. PMID: 15712104 Free PMC article.

6

Genetic association of the serotonin transporter in pulmonary arterial hypertension.

Machado RD, Koehler R, Glissmeyer E, Veal C, Suntharalingam J, Kim M, Carlquist J, Town M, Elliott CG, Hoeper M, Fijalkowska A, Kurzyna M, Thomson JR, Gibbs SR, Wilkins MR, Seeger W, Morrell NW, Gruenig E, Trembath RC, Janssen B. Machado RD, et al. Am J Respir Crit Care Med. 2006 Apr 1;173(7):793-7. doi: 10.1164/rccm.200509-1365OC. Epub 2006 Jan 6. Am J Respir Crit Care Med. 2006. PMID: 16399993

7

A non-HLA gene within the MHC in psoriasis.

Allen MH, Veal C, Faassen A, Powis SH, Vaughan RW, Trembath RC, Barker JN. Allen MH, et al. Lancet. 1999 May 8;353(9164):1589-90. doi: 10.1016/S0140-6736(99)01618-9. Lancet. 1999. PMID: 10334264 No abstract available.

8

Characterization of the major susceptibility region for psoriasis at chromosome 6p21.3.

Balendran N, Clough RL, Arguello JR, Barber R, Veal C, Jones AB, Rosbotham JL, Little AM, Madrigal A, Barker JN, Powis SH, Trembath RC. Balendran N, et al. J Invest Dermatol. 1999 Sep;113(3):322-8. doi: 10.1046/j.1523-1747.1999.00710.x. J Invest Dermatol. 1999. PMID: 10469328 Free article.

9

A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium.

Machado RD, Pauciulo MW, Fretwell N, Veal C, Thomson JR, Vilariño Güell C, Aldred M, Brannon CA, Trembath RC, Nichols WC. Machado RD, et al. Genomics. 2000 Sep 1;68(2):220-8. doi: 10.1006/geno.2000.6291. Genomics. 2000. PMID: 10964520

10

A Crohn's disease-associated insertion polymorphism (3020insC) in the NOD2 gene is not associated with psoriasis vulgaris, palmo-plantar pustular psoriasis or guttate psoriasis.

Young C, Allen MH, Cuthbert A, Ameen M, Veal C, Leman J, Burden AD, Kirby B, Griffiths CE, Trembath RC, Mathew CG, Barker JN. Young C, et al. Exp Dermatol. 2003 Aug;12(4):506-9. doi: 10.1034/j.1600-0625.2002.120420.x. Exp Dermatol. 2003. PMID: 12930309

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