Coleman CM - Search Results

1

A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophy.

Irvine AD, Coleman CM, Moore JE, Swensson O, Morgan SJ, McCarthy JH, Smith FJ, Black GC, McLean WH. Irvine AD, et al. Among authors: coleman cm. Br J Ophthalmol. 2002 Jul;86(7):729-32. doi: 10.1136/bjo.86.7.729. Br J Ophthalmol. 2002. PMID: 12084738 Free PMC article.

2

A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy.

Coleman CM, Hannush S, Covello SP, Smith FJ, Uitto J, McLean WH. Coleman CM, et al. Am J Ophthalmol. 1999 Dec;128(6):687-91. doi: 10.1016/s0002-9394(99)00317-7. Am J Ophthalmol. 1999. PMID: 10612503

3

Epidermolytic palmoplantar keratoderma due to a novel type of keratin mutation, a 3-bp insertion in the keratin 9 helix termination motif.

Coleman CM, Munro CS, Smith FJ, Uitto J, McLean WH. Coleman CM, et al. Br J Dermatol. 1999 Mar;140(3):486-90. doi: 10.1046/j.1365-2133.1999.02715.x. Br J Dermatol. 1999. PMID: 10233272

4

Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1.

Smith FJ, Del Monaco M, Steijlen PM, Munro CS, Morvay M, Coleman CM, Rietveld FJ, Uitto J, McLean WH. Smith FJ, et al. Among authors: coleman cm. Br J Dermatol. 1999 Dec;141(6):1010-6. doi: 10.1046/j.1365-2133.1999.03198.x. Br J Dermatol. 1999. PMID: 10606845

5

A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1.

Smith FJ, McKenna KE, Irvine AD, Bingham EA, Coleman CM, Uitto J, McLean WH. Smith FJ, et al. Among authors: coleman cm. Exp Dermatol. 1999 Apr;8(2):109-14. doi: 10.1111/j.1600-0625.1999.tb00356.x. Exp Dermatol. 1999. PMID: 10232400

6

A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2.

Smith FJ, Jonkman MF, van Goor H, Coleman CM, Covello SP, Uitto J, McLean WH. Smith FJ, et al. Among authors: coleman cm. Hum Mol Genet. 1998 Jul;7(7):1143-8. doi: 10.1093/hmg/7.7.1143. Hum Mol Genet. 1998. PMID: 9618173

7

Novel keratin 17 mutations in pachyonychia congenita type 2.

Smith FJ, Coleman CM, Bayoumy NM, Tenconi R, Nelson J, David A, McLean WH. Smith FJ, et al. Among authors: coleman cm. J Invest Dermatol. 2001 May;116(5):806-8. doi: 10.1046/j.1523-1747.2001.01335.x. J Invest Dermatol. 2001. PMID: 11348474 Free article.

8

The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.

van Steensel M, Smith FJ, Steijlen PM, Kluijt I, Stevens HP, Messenger A, Kremer H, Dunnill MG, Kennedy C, Munro CS, Doherty VR, McGrath JA, Covello SP, Coleman CM, Uitto J, McLean WH. van Steensel M, et al. Among authors: coleman cm. Am J Hum Genet. 1999 Aug;65(2):413-9. doi: 10.1086/302506. Am J Hum Genet. 1999. PMID: 10417283 Free PMC article.

9

The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21.

Whittock NV, Coleman CM, McLean WH, Ashton GH, Acland KM, Eady RA, McGrath JA. Whittock NV, et al. Among authors: coleman cm. J Invest Dermatol. 2000 Oct;115(4):694-8. doi: 10.1046/j.1523-1747.2000.00097.x. J Invest Dermatol. 2000. PMID: 10998145 Free article.

10

Per- and polyfluoroalkyl substances (PFAS), perceived stress, and depressive symptoms in a prospective cohort study of black women.

Schildroth S, Claus Henn B, Vines AI, Geller RJ, Lovett SM, Coleman CM, Bethea TN, Botelho JC, Calafat AM, Milando C, Baird DD, Wegienka G, Wise LA. Schildroth S, et al. Among authors: coleman cm. Sci Total Environ. 2024 Jun 15;929:172445. doi: 10.1016/j.scitotenv.2024.172445. Epub 2024 Apr 19. Sci Total Environ. 2024. PMID: 38642767

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