of the main causes of infertility in women; however, the mechanism underlying the formation of hydrosalpinx fluid (HF) remains elusive. The present study investigated the possible involvement of cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-dependent chloride channel, in the pathogenesis of hydrosalpinx. METHODS: Masson’s trichrome staining was used to characterize epithelial transformation in human HSP; RT– PCR, immunohistochemistry and immunofluorescence staining were used for CFTR expression and localization. RESULTS: Masson’s trichrome staining showed areas of epithelial transformation, focally attenuated and pseudos-tratified. Immunostaining showed enhanced CFTR immunoreactivity in the focally attenuated and pseudo...
Cystic Fibrosis (CF) is caused by ∼1,900 mutations in the CF transmembrane conductance regulator (CF...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-activated Cl- channel that ...
To verify the hypothesis that cystic fibrosis transmembrane conductance regulator (CFTR) is expresse...
Background: Hydrosalpinx (HSP), characterized by abnormal fluid accumulation in the Fallopian tube, ...
BACKGROUND: As a cAMP-regulated Cl2 channel, cystic fibrosis transmembrane conductance regulator (CF...
The adverse effects of hydrosalpinx on the outcome of IVF have been well documented; however, the ca...
Background: As a cAMP-regulated Cl- channel, cystic fibrosis transmembrane conductance regulator (CF...
The cystic fibrosis transmembrane conductance regulator (CFTR) is an important protein that acts as ...
The cystic fibrosis transmembrane conductance regulator (CFTR) is an important protein that acts as ...
BACKGROUND: The cystic fibrosis transmembrane conductance regulator (CFTR) plays a critical role in ...
The cystic fibrosis transmembrane conductance regulator mediates transepithelial fluid secretion by ...
Abstract Background Hydrosalpinx are associated with infertility, due to reduced rates of implantati...
To establish whether cystic fibrosis transmembrane conductance regulator (CFTR) is functionally expr...
Cystic fibrosis, an autosomal recessive disorder caused by a mutation in a gene encoding the cystic ...
Cystic fibrosis, an autosomal recessive disorder caused by a mutation in a gene encoding the cystic ...
Cystic Fibrosis (CF) is caused by ∼1,900 mutations in the CF transmembrane conductance regulator (CF...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-activated Cl- channel that ...
To verify the hypothesis that cystic fibrosis transmembrane conductance regulator (CFTR) is expresse...
Background: Hydrosalpinx (HSP), characterized by abnormal fluid accumulation in the Fallopian tube, ...
BACKGROUND: As a cAMP-regulated Cl2 channel, cystic fibrosis transmembrane conductance regulator (CF...
The adverse effects of hydrosalpinx on the outcome of IVF have been well documented; however, the ca...
Background: As a cAMP-regulated Cl- channel, cystic fibrosis transmembrane conductance regulator (CF...
The cystic fibrosis transmembrane conductance regulator (CFTR) is an important protein that acts as ...
The cystic fibrosis transmembrane conductance regulator (CFTR) is an important protein that acts as ...
BACKGROUND: The cystic fibrosis transmembrane conductance regulator (CFTR) plays a critical role in ...
The cystic fibrosis transmembrane conductance regulator mediates transepithelial fluid secretion by ...
Abstract Background Hydrosalpinx are associated with infertility, due to reduced rates of implantati...
To establish whether cystic fibrosis transmembrane conductance regulator (CFTR) is functionally expr...
Cystic fibrosis, an autosomal recessive disorder caused by a mutation in a gene encoding the cystic ...
Cystic fibrosis, an autosomal recessive disorder caused by a mutation in a gene encoding the cystic ...
Cystic Fibrosis (CF) is caused by ∼1,900 mutations in the CF transmembrane conductance regulator (CF...
The cystic fibrosis transmembrane conductance regulator (CFTR) is a cAMP-activated Cl- channel that ...
To verify the hypothesis that cystic fibrosis transmembrane conductance regulator (CFTR) is expresse...