Results 131 to 140 of about 854 (148)
Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypes
Experimental Dermatology, 2011 Mutations in connexin26, a cutaneous gap junction protein, cause a wide variety of skin disorders including keratitis-ichthyosis-deafness syndrome (KID).
Carla Graziadio, Paulo R G Zen
exaly +2 more sources
Connexin26 Mutations Associated With Nonsyndromic Hearing Loss †
Laryngoscope, 2000 OBJECTIVE: Mutations in the GJB2 gene are a major cause of autosomal recessive and sporadic types of congenital deafness. The 35delG mutation is the most frequent type of mutation in white populations.
Keehyun Park +2 more
exaly +2 more sources
International Journal of Molecular Sciences, 2016 Connexin26 (Cx26, encoded by GJB2) mutations are the most common cause of non-syndromic deafness. GJB2 is thought to be involved in noise-induced hearing loss (NIHL). However, the role of Cx26 in NIHL is still obscure.
Weijia Kong, Xi Lin, Yu Sun
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Intrinsic Oncogenic Function of Intracellular Connexin26 Protein in Head and Neck Squamous Cell Carcinoma Cells [PDF]
International Journal of Molecular Sciences, 2018 It has long been known that the gap junction is down-regulated in many tumours. One of the downregulation mechanisms is the translocation of connexin, a gap junction protein, from cell membrane into cytoplasm, nucleus, or Golgi apparatus.
Yohei Kawasaki +2 more
exaly +4 more sources
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Mouse Horizontal Cells do not Express Connexin26 or Connexin36
Cell Communication and Adhesion, 2001Michael R Deans, David L Paul
exaly
Targeted connexin26 ablation arrests postnatal development of the organ of Corti
Biochemical and Biophysical Research Communications, 2009Huawei Li, Yunfeng Wang, Wenxue Tang
exaly