The cystic fibrosis transmembrane conductance regulator (Cftr) modulates the timing of puberty in mice.
about
Murine model for cystic fibrosis bone disease demonstrates osteopenia and sex-related differences in bone formation.Infertility in females with cystic fibrosis is multifactorial: evidence from mouse modelsGeneration of a conditional null allele for Cftr in mice.Growth in Prepubertal Children With Cystic Fibrosis Treated With IvacaftorCystic fibrosis: a clinical view.Pathogen and autoantigen homologous regions within the cystic fibrosis transmembrane conductance regulator (CFTR) protein suggest an autoimmune treatable component of cystic fibrosis.Peripheral quantitative computed tomography (pQCT) bone measurements in children with cystic fibrosis.
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P2860
The cystic fibrosis transmembrane conductance regulator (Cftr) modulates the timing of puberty in mice.
description
2006 nî lūn-bûn
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2006年の論文
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name
The cystic fibrosis transmembr ...... the timing of puberty in mice.
@en
The cystic fibrosis transmembrane conductance regulator
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type
label
The cystic fibrosis transmembr ...... the timing of puberty in mice.
@en
The cystic fibrosis transmembrane conductance regulator
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prefLabel
The cystic fibrosis transmembr ...... the timing of puberty in mice.
@en
The cystic fibrosis transmembrane conductance regulator
@nl
P2093
P2860
P356
P1476
The cystic fibrosis transmembr ...... the timing of puberty in mice.
@en
P2093
P2860
P356
10.1136/JMG.2005.032839
P407
P577
2006-06-01T00:00:00Z