囊性纤维变性跨膜调节器基因突变对男性生殖的影响
周晨曦， 王曦， 王子栋， 黄宜定 - 中国病理生理杂志, 2001 - cqvip.com
Large number of cystic fibrosis transmembrane conductance regulator (CFTR) gene
mutations are responsible for a wide spectrum of disease expressions in CF (cystic fibrosis) …
mutations are responsible for a wide spectrum of disease expressions in CF (cystic fibrosis) …
Effect of cystic fibrosis transmembrane conductance regulator gene mutation on male fertility
C Zhou, X Wang, Z Wang… - Chinese Journal of …, 1986 - pesquisa.bvsalud.org
Large number of cystic fibrosis transmembrane conductance regulator (CFTR) gene
mutations are responsible for a wide spectrum of disease expressions in CF (cystic fibrosis) …
mutations are responsible for a wide spectrum of disease expressions in CF (cystic fibrosis) …
CFTR 基因突变对生殖系统影响的研究进展
吕涛， 魏睦新 - 现代中西医结合杂志, 2009 - cqvip.com
囊性纤维化(cystic fibrosis, CF) 是一种致命的常染色体隐性遗传疾病, 病变主要影响呼吸道,
消化道和生殖道等. 1995 年陈柏华等首次采用PCR-SSCR 方法检测到囊性纤维化跨膜传导调节 …
消化道和生殖道等. 1995 年陈柏华等首次采用PCR-SSCR 方法检测到囊性纤维化跨膜传导调节 …
CFTR 基因与无精子症关系研究进展
杨慧敏， 胡蓉， 裴秀英 - 发育医学电子杂志, 2019 - cqvip.com
囊性纤维跨膜传导调节因子(cystic fibers transmembrane regulators, CFTR)
是完整的跨膜蛋白, 也是腺苷-3', 5'-环化一磷酸(cyclic adenosine monophosphate, cAMP) …
是完整的跨膜蛋白, 也是腺苷-3', 5'-环化一磷酸(cyclic adenosine monophosphate, cAMP) …
囊性纤维化跨膜转导调节因子的生物学特性及与妇科疾病的关系
梅又文， 彭雪， 李金科， 胡丽娜 - 现代妇产科进展, 2011 - cqvip.com
囊性纤维化跨膜转导调节因子(cystic fibrosis transmembrane conductance regulator, CFTR)
是囊性纤维化(CF, cystic fibrosis) 基因编码的cAMP 依赖的氯离子通道. 它在多种组织器官的 …
是囊性纤维化(CF, cystic fibrosis) 基因编码的cAMP 依赖的氯离子通道. 它在多种组织器官的 …
先天性单侧输精管缺如患者CFTR 基因突变研究
曾国华， 梅骅， 庄广伦， 李满 - 中华医学遗传学杂志, 2000 - cqvip.com
目的探讨囊性纤维跨膜转运调节物(cystic fibrosis transmembrane conductance regulator,
CFTR) 基因在中国人先天性单侧输精管缺如(congenital unilateral asenceof the vas deferens …
CFTR) 基因在中国人先天性单侧输精管缺如(congenital unilateral asenceof the vas deferens …
CFTR 基因多态性对男性生殖影响的研究进展
胡春风， 刘红英 - 中国男科学杂志, 2016 - cqvip.com
囊性纤维化(cystic fibrosis, CF) 是白种人中常见的致死性常染色体隐性遗传病,
是由囊性纤维化跨膜转导调节因子(cystic fibrisis transmembrane conductance regulator …
是由囊性纤维化跨膜转导调节因子(cystic fibrisis transmembrane conductance regulator …
MP52-19 NOVEL MUTATIONS OF THE CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE IN CHINESE PATIENTS WITH CONGENITAL …
Y Zhang, P Yuan, X Yang, Q Sun, X Wu… - The Journal of …, 2015 - auajournals.org
METHODS We have characterized 19 CAVD patients including congenital bilateral absence
of vas deferens (CBAVD), congenital unilateral absence of vas deferens (CUAVD) and …
of vas deferens (CBAVD), congenital unilateral absence of vas deferens (CUAVD) and …
[HTML][HTML] Genetics of CFTR and male infertility
JM Bieniek, CD Lapin, KA Jarvi - Translational andrology and …, 2021 - ncbi.nlm.nih.gov
Cystic fibrosis (CF) is a rare autosomal-recessive disorder manifested as multisystem organ
dysfunction. The cystic fibrosis transmembrane conductance regulator (CFTR) protein …
dysfunction. The cystic fibrosis transmembrane conductance regulator (CFTR) protein …
Compound heterozygous mutations in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree
L Li, X Qu, C Cui, K Feng, Y Xia, F Wan… - … Genetics & Genomic …, 2024 - Wiley Online Library
Background Cystic fibrosis (CF) is an autosomal recessive disorder rarely found in Asian
populations. Most males with CF are infertile because of obstructive azoospermia (OA) …
populations. Most males with CF are infertile because of obstructive azoospermia (OA) …