Pages that link to "Q40542422"
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The following pages link to Transport and function of cx26 mutants involved in skin and deafness disorders. (Q40542422):
Displaying 13 items.
- Life cycle of connexins in health and disease (Q24541428) (← links)
- Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease (Q24682835) (← links)
- Human connexin26 and connexin30 form functional heteromeric and heterotypic channels (Q28235511) (← links)
- Gap-junction channels dysfunction in deafness and hearing loss (Q30490087) (← links)
- Post-translational modifications of connexin26 revealed by mass spectrometry (Q33506159) (← links)
- Intercellular redistribution of cAMP underlies selective suppression of cancer cell growth by connexin26. (Q35061520) (← links)
- Connexinopathies: a structural and functional glimpse (Q36031035) (← links)
- Managing the complexity of communication: regulation of gap junctions by post-translational modification (Q37246555) (← links)
- Connexin-26 mutations in deafness and skin disease. (Q37638797) (← links)
- Gap junctions in inherited human disease (Q37689002) (← links)
- GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss (Q38006692) (← links)
- Role of gamma carboxylated Glu47 in connexin 26 hemichannel regulation by extracellular Ca²⁺: insight from a local quantum chemistry study. (Q38552774) (← links)
- Differentiation of organotypic epidermis in the presence of skin disease-linked dominant-negative Cx26 mutants and knockdown Cx26. (Q40105775) (← links)