Pages that link to "Q48913945"
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The following pages link to Characterization of a mouse Cx50 mutation associated with the No2 mouse cataract. (Q48913945):
Displaying 27 items.
- A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract. (Q33323353) (← links)
- Exchange of gating properties between rat cx46 and chicken cx45.6. (Q34187324) (← links)
- Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract (Q34530828) (← links)
- Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study. (Q34628639) (← links)
- A novel GJA8 mutation (p.V44A) causing autosomal dominant congenital cataract (Q34724585) (← links)
- A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family (Q34912741) (← links)
- Different consequences of cataract-associated mutations at adjacent positions in the first extracellular boundary of connexin50 (Q34979286) (← links)
- The connexin46 mutant, Cx46T19M, causes loss of gap junction function and alters hemi-channel gating (Q34990414) (← links)
- Another evidence for a D47N mutation in GJA8 associated with autosomal dominant congenital cataract (Q35209179) (← links)
- Lens gap junctions in growth, differentiation, and homeostasis. (Q36233134) (← links)
- A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin (Q36479042) (← links)
- A novel connexin 50 gene (gap junction protein, alpha 8) mutation associated with congenital nuclear and zonular pulverulent cataract (Q36766108) (← links)
- Properties of two cataract-associated mutations located in the NH2 terminus of connexin 46. (Q36836123) (← links)
- Novel mutation in the gamma-S crystallin gene causing autosomal dominant cataract. (Q37116152) (← links)
- Connexin mutation that causes dominant congenital cataracts inhibits gap junctions, but not hemichannels, in a dominant negative manner (Q37116451) (← links)
- Cataracts are caused by alterations of a critical N-terminal positive charge in connexin50 (Q37222714) (← links)
- Connexin50D47A decreases levels of fiber cell connexins and impairs lens fiber cell differentiation. (Q37328881) (← links)
- A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts. (Q37373627) (← links)
- Functional effects of Cx50 mutations associated with congenital cataracts. (Q37575363) (← links)
- Gap junctions or hemichannel-dependent and independent roles of connexins in cataractogenesis and lens development. (Q37811014) (← links)
- Loss of function and impaired degradation of a cataract-associated mutant connexin50. (Q40640625) (← links)
- A mutant connexin50 with enhanced hemichannel function leads to cell death (Q42699037) (← links)
- Dense cataract and microphthalmia (dcm) in BALB/c mice is caused by mutations in the GJA8 locus. (Q42879143) (← links)
- The cataract causing Cx50-S50P mutant inhibits Cx43 and intercellular communication in the lens epithelium (Q43143798) (← links)
- Connexin hemichannels mediate glutathione transport and protect lens fiber cells from oxidative stress. (Q52682485) (← links)
- Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract (Q62127831) (← links)
- Chemical chaperone treatment improves levels and distributions of connexins in Cx50D47A mouse lenses (Q89138157) (← links)