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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1978 2
1979 2
1984 2
1986 2
1987 1
1988 1
1989 2
1991 2
1992 3
1993 1
1994 1
1995 2
1996 2
1997 1
1998 1
1999 1
2000 3
2001 3
2002 3
2003 2
2004 2
2006 1
2007 1
2008 2
2009 1
2010 1
2012 1
2013 1
2024 0

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47 results

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Page 1
The keratins and their disorders.
Rugg EL, Leigh IM. Rugg EL, et al. Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):4-11. doi: 10.1002/ajmg.c.30029. Am J Med Genet C Semin Med Genet. 2004. PMID: 15452838 Review.
Keratin 16 and keratin 17 mutations cause pachyonychia congenita.
McLean WH, Rugg EL, Lunny DP, Morley SM, Lane EB, Swensson O, Dopping-Hepenstal PJ, Griffiths WA, Eady RA, Higgins C, et al. McLean WH, et al. Among authors: rugg el. Nat Genet. 1995 Mar;9(3):273-8. doi: 10.1038/ng0395-273. Nat Genet. 1995. PMID: 7539673
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa.
Smith FJ, Eady RA, Leigh IM, McMillan JR, Rugg EL, Kelsell DP, Bryant SP, Spurr NK, Geddes JF, Kirtschig G, Milana G, de Bono AG, Owaribe K, Wiche G, Pulkkinen L, Uitto J, McLean WH, Lane EB. Smith FJ, et al. Among authors: rugg el. Nat Genet. 1996 Aug;13(4):450-7. doi: 10.1038/ng0896-450. Nat Genet. 1996. PMID: 8696340
A functional "knockout" of human keratin 14.
Rugg EL, McLean WH, Lane EB, Pitera R, McMillan JR, Dopping-Hepenstal PJ, Navsaria HA, Leigh IM, Eady RA. Rugg EL, et al. Genes Dev. 1994 Nov 1;8(21):2563-73. doi: 10.1101/gad.8.21.2563. Genes Dev. 1994. PMID: 7525407 Free article.
47 results