Zobrazeno 1 - 10
of 623
pro vyhledávání: '"O'Brien, W E"'
Autor:
Chang, Jianjun1 (AUTHOR), Li, Zijie1 (AUTHOR), Yuan, Hui2 (AUTHOR), Wang, Xuejiao1 (AUTHOR), Xu, Jingyi3 (AUTHOR), Yang, Pingting3 (AUTHOR) yangpingtingting@163.com, Qin, Ling2 (AUTHOR) qinlingling@yahoo.com
Publikováno v:
Communications Biology. 11/13/2024, Vol. 7 Issue 1, p1-17. 17p.
Autor:
O'Brien, W. E.
Publikováno v:
America Magazine: The Jesuit Review of Faith & Culture. 6/11/1955, Vol. 93 Issue 11, p287-289. 3p.
Publikováno v:
American journal of human genetics. 47(4)
The common mutation causing cystic fibrosis is a deletion of phenylalanine 508 (delta F508), which occurs in a putative nucleotide-binding fold of the gene product. We report two additional mutations, substitution of cysteine for phenylalanine 508 (F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::531a67854d5bb6a9e53186d522a0f184
https://pubmed.ncbi.nlm.nih.gov/1384326
https://pubmed.ncbi.nlm.nih.gov/1384326
Autor:
BOYLU, Olena1 lenaboylu@gmail.com
Publikováno v:
Gaziantep University Journal of Social Sciences. 2024, Vol. 23 Issue 1, p155-164. 10p.
Autor:
Vlasova, Violetta V.1 (AUTHOR) violetbaudelaire73@gmail.com, Shmagel, Konstantin V.1 (AUTHOR)
Publikováno v:
Biochemistry (00062979). Nov2023, Vol. 88 Issue 11, p1857-1873. 17p.
Autor:
Gu, Xia, Mo, Wenhui, Zhuang, Guiying, Shi, Congcong, Wei, Tao, Zhang, Jinze, Tu, Chiaowen, Cai, Yao, Liao, Biwen, Hao, Hu
Publikováno v:
Frontiers in Molecular Biosciences; 2024, p1-10, 10p
Autor:
Suchy, Sharon F., Lin, Ti, Horwitz, Juli A., O'Brien, William E., Nussbaum, Robert L., Suchy, S F, Lin, T, Horwitz, J A, O'Brien, W E, Nussbaum, R L
Publikováno v:
Prenatal Diagnosis; Nov1998, Vol. 18 Issue 11, p1117-1121, 5p
Publikováno v:
Prenatal Diagnosis; Apr1995, Vol. 15 Issue 4, p329-338, 10p
Publikováno v:
Clinica Chimica Acta; 2001, Vol. 308 Issue: 1 p173-178, 6p