Bowcock AM - Search Results

1

AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.

Agarwal AK, Arioglu E, De Almeida S, Akkoc N, Taylor SI, Bowcock AM, Barnes RI, Garg A. Agarwal AK, et al. Among authors: bowcock am. Nat Genet. 2002 May;31(1):21-3. doi: 10.1038/ng880. Epub 2002 Apr 22. Nat Genet. 2002. PMID: 11967537

2

Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22.

Peters JM, Barnes R, Bennett L, Gitomer WM, Bowcock AM, Garg A. Peters JM, et al. Among authors: bowcock am. Nat Genet. 1998 Mar;18(3):292-5. doi: 10.1038/ng0398-292. Nat Genet. 1998. PMID: 9500556

3

A gene for congenital generalized lipodystrophy maps to human chromosome 9q34.

Garg A, Wilson R, Barnes R, Arioglu E, Zaidi Z, Gurakan F, Kocak N, O'Rahilly S, Taylor SI, Patel SB, Bowcock AM. Garg A, et al. Among authors: bowcock am. J Clin Endocrinol Metab. 1999 Sep;84(9):3390-4. doi: 10.1210/jcem.84.9.6103. J Clin Endocrinol Metab. 1999. PMID: 10487716

4

Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene.

Garg A, Speckman RA, Bowcock AM. Garg A, et al. Among authors: bowcock am. Am J Med. 2002 May;112(7):549-55. doi: 10.1016/s0002-9343(02)01070-7. Am J Med. 2002. PMID: 12015247

5

Risk factors for diabetes in familial partial lipodystrophy, Dunnigan variety.

Haque WA, Oral EA, Dietz K, Bowcock AM, Agarwal AK, Garg A. Haque WA, et al. Among authors: bowcock am. Diabetes Care. 2003 May;26(5):1350-5. doi: 10.2337/diacare.26.5.1350. Diabetes Care. 2003. PMID: 12716787

6

Mutational and haplotype analyses of families with familial partial lipodystrophy (Dunnigan variety) reveal recurrent missense mutations in the globular C-terminal domain of lamin A/C.

Speckman RA, Garg A, Du F, Bennett L, Veile R, Arioglu E, Taylor SI, Lovett M, Bowcock AM. Speckman RA, et al. Among authors: bowcock am. Am J Hum Genet. 2000 Apr;66(4):1192-8. doi: 10.1086/302836. Am J Hum Genet. 2000. PMID: 10739751 Free PMC article.

7

Detection of a polymorphism within the pepsinogen C gene with PCR: construction of a linkage map around PGC from 6p11-6p21.3.

Bowcock AM, Azuma T, Barnes RI, Wu SH, Bell GI, Taggart RT. Bowcock AM, et al. Genomics. 1992 Oct;14(2):398-402. doi: 10.1016/s0888-7543(05)80232-0. Genomics. 1992. PMID: 1427855

8

Dinucleotide repeat polymorphism at the D1S167 locus.

Bowcock A, Osborne-Lawrence S, Barnes R, Weiss L, Dunn G. Bowcock A, et al. Hum Mol Genet. 1992 May;1(2):138. doi: 10.1093/hmg/1.2.138. Hum Mol Genet. 1992. PMID: 1301153 No abstract available.

9

Phenotypic heterogeneity in patients with familial partial lipodystrophy (dunnigan variety) related to the site of missense mutations in lamin a/c gene.

Garg A, Vinaitheerthan M, Weatherall PT, Bowcock AM. Garg A, et al. Among authors: bowcock am. J Clin Endocrinol Metab. 2001 Jan;86(1):59-65. doi: 10.1210/jcem.86.1.7121. J Clin Endocrinol Metab. 2001. PMID: 11231979

10

Dinucleotide repeat polymorphism at the D6S223 locus.

Bowcock A, Osborne-Lawrence S, Barnes R, Weiss L, Dunn G. Bowcock A, et al. Hum Mol Genet. 1992 Apr;1(1):66. doi: 10.1093/hmg/1.1.66. Hum Mol Genet. 1992. PMID: 1301141 No abstract available.

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