A Deafness-Associated Mutant Human Connexin 26 Improves the Epithelial Barrier In Vitro

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

David P. Kelsell, John Dunlop, Howard P. Stevens et al. · Nature · 1997 · 1.5K citations

Mendelian Disorder, Developmental Biology, Genetic Disorder +2

Human Keratinocytes That Express hTERT and Also Bypass a p16^INK4a-Enforced Mechanism That Limits Life Span Become Immortal yet Retain Normal Growth and Differentiation Characteristics

Mark A. Dickson, William C. Hahn, Yasushi Ino et al. · Molecular and Cellular Biology · 2000 · 1.1K citations

Retain Normal Growth, Telomerase Expression, Skin Development +13

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 635 citations · Full text

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 551 citations · Full text

Genetic Disorder, Genetics, Audiology +9

Keratins (Kl6 and Kl7) as markers of keratinocyte hyperproliferation in psoriasis in vivo and in vitro

Irene M. Leigh, Harshad Navsaria, Patricia E. Purkis et al. · British Journal of Dermatology · 1995 · 329 citations