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Mutations of the Connexin43 gap-junction gene in patients with heart malformations and defects of laterality.
Britz-Cunningham SH, Shah MM, Zuppan CW, Fletcher WH. Britz-Cunningham SH, et al. Among authors: fletcher wh. N Engl J Med. 1995 May 18;332(20):1323-9. doi: 10.1056/NEJM199505183322002. N Engl J Med. 1995. PMID: 7715640 Free article.
The highly conserved Gln49 and Ser50 of mammalian connexin43 are present in chick connexin43 and essential for functional gap junction channels.
Sokolova IV, Martinez AM, Fletcher WH. Sokolova IV, et al. Among authors: fletcher wh. Cell Commun Adhes. 2002 Mar-Apr;9(2):75-86. doi: 10.1080/15419060214149. Cell Commun Adhes. 2002. PMID: 12487409
Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE).
Dasgupta C, Martinez AM, Zuppan CW, Shah MM, Bailey LL, Fletcher WH. Dasgupta C, et al. Among authors: fletcher wh. Mutat Res. 2001 Aug 8;479(1-2):173-86. doi: 10.1016/s0027-5107(01)00160-9. Mutat Res. 2001. PMID: 11470490
Misregulation of connexin43 gap junction channels and congenital heart defects.
Dasgupta C, Escobar-Poni B, Shah M, Duncan J, Fletcher WH. Dasgupta C, et al. Among authors: fletcher wh. Novartis Found Symp. 1999;219:212-21; discussion 221-5. doi: 10.1002/9780470515587.ch13. Novartis Found Symp. 1999. PMID: 10207906 Review.
Regulation of cell-cell communication mediated by connexin 43 in rabbit myometrial cells.
Nnamani C, Godwin A, Ducsay CA, Longo LD, Fletcher WH. Nnamani C, et al. Among authors: fletcher wh. Biol Reprod. 1994 Feb;50(2):377-89. doi: 10.1095/biolreprod50.2.377. Biol Reprod. 1994. PMID: 8142555
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