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Showing 1-9 of 9 results for "sab4200730" within Papers
Syndromic and non-syndromic disease-linked Cx43 mutations
Laird DW
Febs Letters, 588(8), 1339-1348 (2014)
Connexin 43 a check-point component of cell proliferation implicated in a wide range of human testis diseases
Chevallier D, et al.
Cellular and Molecular Life Sciences, 70(7), 1207-1220 (2013)
A case of oculodentodigital dysplasia syndrome with novel GJA1 gene mutation
Himi M, et al.
Japanese Journal of Ophthalmology, 53(5), 541-541 (2009)
Structural organization of gap junction channels
Sosinsky GE and Nicholson BJ
Biochimica et Biophysica Acta - Biomembranes, 1711(2), 99-125 (2005)
Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE)
Dasgupta C, et al.
Mutation Research. Fundamental and Molecular Mechanisms of Mutagenesis, 479(1), 173-186 (2001)
Yan Zeng et al.
Cell & bioscience, 12(1), 191-191 (2022-12-03)
Mechanical loading promotes bone formation and osteocytes are a major mechanosensory cell in the bone. Both Piezo1 channels and connexin 43 hemichannels (Cx43 HCs) in osteocytes are important players in mechanotransduction and anabolic function by mechanical loading. However, the mechanism
Channel-independent influence of connexin 43 on cell migration
Kameritsch P, et al.
Biochimica et Biophysica Acta - Biomembranes, 1818(8), 1993-2001 (2012)
The gap junction channel protein connexin 43 is covalently modified and regulated by SUMOylation
Kjenseth A, et al.
The Journal of Biological Chemistry, 287(19), 15851-15861 (2012)
Dominant de novo mutations in GJA1 cause erythrokeratodermia variabilis et progressiva, without features of oculodentodigital dysplasia
Boyden LM, et al.
The Journal of Investigative Dermatology, 135(6), 1540-1547 (2015)
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