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Connexin 26 expression and mutation analysis in epidermal disease.
Di WL, Common JE, Kelsell DP. Di WL, et al. Cell Commun Adhes. 2001;8(4-6):415-8. doi: 10.3109/15419060109080763. Cell Commun Adhes. 2001. PMID: 12064628
A heterozygous null mutation combined with the G1258A polymorphism of SPINK5 causes impaired LEKTI function and abnormal expression of skin barrier proteins.
Di WL, Hennekam RC, Callard RE, Harper JI. Di WL, et al. Br J Dermatol. 2009 Aug;161(2):404-12. doi: 10.1111/j.1365-2133.2009.09231.x. Epub 2009 May 12. Br J Dermatol. 2009. PMID: 19438860
Multiple epidermal connexins are expressed in different keratinocyte subpopulations including connexin 31.
Di WL, Rugg EL, Leigh IM, Kelsell DP. Di WL, et al. J Invest Dermatol. 2001 Oct;117(4):958-64. doi: 10.1046/j.0022-202x.2001.01468.x. J Invest Dermatol. 2001. PMID: 11676838
AKT1-mediated Lamin A/C degradation is required for nuclear degradation and normal epidermal terminal differentiation.
Naeem AS, Zhu Y, Di WL, Marmiroli S, O'Shaughnessy RF. Naeem AS, et al. Among authors: di wl. Cell Death Differ. 2015 Dec;22(12):2123-32. doi: 10.1038/cdd.2015.62. Epub 2015 Jun 5. Cell Death Differ. 2015. PMID: 26045045 Free PMC article.
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss.
Houseman MJ, Ellis LA, Pagnamenta A, Di WL, Rickard S, Osborn AH, Dahl HH, Taylor GR, Bitner-Glindzicz M, Reardon W, Mueller RF, Kelsell DP. Houseman MJ, et al. Among authors: di wl. J Med Genet. 2001 Jan;38(1):20-5. doi: 10.1136/jmg.38.1.20. J Med Genet. 2001. PMID: 11134236 Free PMC article.
Connexin mutations in skin disease and hearing loss.
Kelsell DP, Di WL, Houseman MJ. Kelsell DP, et al. Among authors: di wl. Am J Hum Genet. 2001 Mar;68(3):559-68. doi: 10.1086/318803. Epub 2001 Jan 25. Am J Hum Genet. 2001. PMID: 11179004 Free PMC article. Review. No abstract available.
Aberrant gating, but a normal expression pattern, underlies the recessive phenotype of the deafness mutant Connexin26M34T.
Skerrett IM, Di WL, Kasperek EM, Kelsell DP, Nicholson BJ. Skerrett IM, et al. Among authors: di wl. FASEB J. 2004 May;18(7):860-2. doi: 10.1096/fj.03-0763fje. Epub 2004 Mar 19. FASEB J. 2004. PMID: 15033936
Oestriol and oestradiol increase cell to cell communication and connexin43 protein expression in human myometrium.
Di WL, Lachelin GC, McGarrigle HH, Thomas NS, Becker DL. Di WL, et al. Mol Hum Reprod. 2001 Jul;7(7):671-9. doi: 10.1093/molehr/7.7.671. Mol Hum Reprod. 2001. PMID: 11420391
Human Mesenchymal Stromal Cells Engineered to Express Collagen VII Can Restore Anchoring Fibrils in Recessive Dystrophic Epidermolysis Bullosa Skin Graft Chimeras.
Petrova A, Georgiadis C, Fleck RA, Allison L, McGrath JA, Dazzi F, Di WL, Qasim W. Petrova A, et al. Among authors: di wl. J Invest Dermatol. 2020 Jan;140(1):121-131.e6. doi: 10.1016/j.jid.2019.05.031. Epub 2019 Jul 19. J Invest Dermatol. 2020. PMID: 31326396
Further evidence for heterozygote advantage of GJB2 deafness mutations: a link with cell survival.
Common JE, Di WL, Davies D, Kelsell DP. Common JE, et al. Among authors: di wl. J Med Genet. 2004 Jul;41(7):573-5. doi: 10.1136/jmg.2003.017632. J Med Genet. 2004. PMID: 15235031 Free PMC article. No abstract available.
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