Compton JG - Search Results

1

Concurrence between the molecular overlap regions in keratin intermediate filaments and the locations of keratin mutations in genodermatoses.

Steinert PM, Yang JM, Bale SJ, Compton JG. Steinert PM, et al. Among authors: compton jg. Biochem Biophys Res Commun. 1993 Dec 15;197(2):840-8. doi: 10.1006/bbrc.1993.2555. Biochem Biophys Res Commun. 1993. PMID: 7505575

2

The two size alleles of human keratin 1 are due to a deletion in the glycine-rich carboxyl-terminal V2 subdomain.

Korge BP, Compton JG, Steinert PM, Mischke D. Korge BP, et al. Among authors: compton jg. J Invest Dermatol. 1992 Dec;99(6):697-702. doi: 10.1111/1523-1747.ep12614149. J Invest Dermatol. 1992. PMID: 1281859 Free article.

3

Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.

Compton JG, DiGiovanna JJ, Santucci SK, Kearns KS, Amos CI, Abangan DL, Korge BP, McBride OW, Steinert PM, Bale SJ. Compton JG, et al. Nat Genet. 1992 Jul;1(4):301-5. doi: 10.1038/ng0792-301. Nat Genet. 1992. PMID: 1284546

4

A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis.

Chipev CC, Korge BP, Markova N, Bale SJ, DiGiovanna JJ, Compton JG, Steinert PM. Chipev CC, et al. Among authors: compton jg. Cell. 1992 Sep 4;70(5):821-8. doi: 10.1016/0092-8674(92)90315-4. Cell. 1992. PMID: 1381288

5

Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevus.

Richard G, De Laurenzi V, Didona B, Bale SJ, Compton JG. Richard G, et al. Among authors: compton jg. Nat Genet. 1995 Dec;11(4):453-5. doi: 10.1038/ng1295-453. Nat Genet. 1995. PMID: 7493031

6

Mutations in the H1 and 1A domains in the keratin 1 gene in epidermolytic hyperkeratosis.

Yang JM, Chipev CC, DiGiovanna JJ, Bale SJ, Marekov LN, Steinert PM, Compton JG. Yang JM, et al. Among authors: compton jg. J Invest Dermatol. 1994 Jan;102(1):17-23. doi: 10.1111/1523-1747.ep12371725. J Invest Dermatol. 1994. PMID: 7507151 Free article.

7

Preferential sites in keratin 10 that are mutated in epidermolytic hyperkeratosis.

Chipev CC, Yang JM, DiGiovanna JJ, Steinert PM, Marekov L, Compton JG, Bale SJ. Chipev CC, et al. Among authors: compton jg. Am J Hum Genet. 1994 Feb;54(2):179-90. Am J Hum Genet. 1994. PMID: 7508181 Free PMC article.

8

A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma.

Kimonis V, DiGiovanna JJ, Yang JM, Doyle SZ, Bale SJ, Compton JG. Kimonis V, et al. Among authors: compton jg. J Invest Dermatol. 1994 Dec;103(6):764-9. doi: 10.1111/1523-1747.ep12412771. J Invest Dermatol. 1994. PMID: 7528239 Free article.

9

A highly conserved lysine residue on the head domain of type II keratins is essential for the attachment of keratin intermediate filaments to the cornified cell envelope through isopeptide crosslinking by transglutaminases.

Candi E, Tarcsa E, Digiovanna JJ, Compton JG, Elias PM, Marekov LN, Steinert PM. Candi E, et al. Among authors: compton jg. Proc Natl Acad Sci U S A. 1998 Mar 3;95(5):2067-72. doi: 10.1073/pnas.95.5.2067. Proc Natl Acad Sci U S A. 1998. PMID: 9482839 Free PMC article.

10

Mapping of the associated phenotype of an absent granular layer in ichthyosis vulgaris to the epidermal differentiation complex on chromosome 1.

Compton JG, DiGiovanna JJ, Johnston KA, Fleckman P, Bale SJ. Compton JG, et al. Exp Dermatol. 2002 Dec;11(6):518-26. doi: 10.1034/j.1600-0625.2002.110604.x. Exp Dermatol. 2002. PMID: 12473059

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