Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens.
about
Longevity and plasticity of CFTR provide an argument for noncanonical SNP organization in hominid DNATransforming growth factor-β1 impairs CFTR-mediated anion secretion across cultured porcine vas deferens epithelial monolayer via the p38 MAPK pathwayA unique case of segmental vasal atresiaHeterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.The diagnosis of male infertility: an analysis of the evidence to support the development of global WHO guidance-challenges and future research opportunities.Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.
P2860
Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens.
description
2010 nî lūn-bûn
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2010年の論文
@ja
2010年学术文章
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2010年学术文章
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2010年学术文章
@zh-cn
2010年学术文章
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2010年学术文章
@zh-my
2010年学术文章
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2010年學術文章
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2010年學術文章
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name
Association of cystic fibrosis ...... l absence of the vas deferens.
@en
Association of cystic fibrosis ...... l absence of the vas deferens.
@nl
type
label
Association of cystic fibrosis ...... l absence of the vas deferens.
@en
Association of cystic fibrosis ...... l absence of the vas deferens.
@nl
prefLabel
Association of cystic fibrosis ...... l absence of the vas deferens.
@en
Association of cystic fibrosis ...... l absence of the vas deferens.
@nl
P2093
P2860
P50
P1476
Association of cystic fibrosis ...... l absence of the vas deferens.
@en
P2093
Ahmet Sahin
Didem Dayangac
Eric J Sorscher
Lluis Bassas
Mario Sousa
Peter N Kolettis
Steven M Rowe
Teresa Casals
Viktoria Havasi
P2860
P304
P356
10.1016/J.FERTNSTERT.2009.11.044
P407
P577
2010-01-25T00:00:00Z