<p>(A) Animals at days 1 and 24 postnatal. (B) Results of PCR genotyping from a representative litter. (C) Western blot indicating expression of CFTR in wild-type rats and absence of CFTR protein from lungs of CFTR<sup>−/−</sup> animals. Arrow - CFTR. (D) Body weight values (mean ± SD) from wild-type and CFTR<sup>−/−</sup> rats from 12 to 44 days postnatal. (E) Survival curve for CFTR<sup>−/−</sup> rats from postnatal day 1 to 44 (p<0.05 for all groups, n = 12–67 animals/group).</p
Animal models of cystic fibrosis (CF) are essential for investigating disease mechanisms and trialin...
<p>The transcript levels of each target gene were normalized to the G3PDH gene expression level and ...
<p>(<b>A</b>) Genotyping. The <i>ter</i> mutation disrupts a <i>Kpn</i>I restriction site used for g...
Representative RT-PCR gels are shown for lung CFTR and GAPDH (internal standard) mRNA.<p><b>Copyrigh...
<p><b>(</b>A) <i>Cftr-/-</i> rats are notably smaller in size compared to their wild type (WT) litte...
<p>(A) Wild-type rats (left) have yellowish-brown enamel while CFTR<sup>−/−</sup> rats (right) exhib...
AbstractThe collecting duct epithelium originates from the embryonic ureter by branching morphogenes...
Animal models for cystic fibrosis (CF) have contributed significantly to our understanding of diseas...
<p>Comparison of postnatal growth rates between control rats transplanted with neonatal ovary (COT) ...
Reduced growth and osteopenia are common in individuals with cystic fibrosis (CF). Additionally, imp...
Animal models for cystic fibrosis (CF) have contributed significantly to our understanding of diseas...
Abstract One of the mechanisms by which adult disease can arise from a fetal origin is by in utero d...
<p>A. CF mice homozygous for a null <i>Cftr</i> allele (<i>Cftr</i><sup>−/−</sup>) and wild-type for...
<p>The survival curves of offspring rats were displayed at PND 35 (control group, n=12; 5 min HIE gr...
International audienceBackground:Genetically engineered animals are essential for gaining a proper u...
Animal models of cystic fibrosis (CF) are essential for investigating disease mechanisms and trialin...
<p>The transcript levels of each target gene were normalized to the G3PDH gene expression level and ...
<p>(<b>A</b>) Genotyping. The <i>ter</i> mutation disrupts a <i>Kpn</i>I restriction site used for g...
Representative RT-PCR gels are shown for lung CFTR and GAPDH (internal standard) mRNA.<p><b>Copyrigh...
<p><b>(</b>A) <i>Cftr-/-</i> rats are notably smaller in size compared to their wild type (WT) litte...
<p>(A) Wild-type rats (left) have yellowish-brown enamel while CFTR<sup>−/−</sup> rats (right) exhib...
AbstractThe collecting duct epithelium originates from the embryonic ureter by branching morphogenes...
Animal models for cystic fibrosis (CF) have contributed significantly to our understanding of diseas...
<p>Comparison of postnatal growth rates between control rats transplanted with neonatal ovary (COT) ...
Reduced growth and osteopenia are common in individuals with cystic fibrosis (CF). Additionally, imp...
Animal models for cystic fibrosis (CF) have contributed significantly to our understanding of diseas...
Abstract One of the mechanisms by which adult disease can arise from a fetal origin is by in utero d...
<p>A. CF mice homozygous for a null <i>Cftr</i> allele (<i>Cftr</i><sup>−/−</sup>) and wild-type for...
<p>The survival curves of offspring rats were displayed at PND 35 (control group, n=12; 5 min HIE gr...
International audienceBackground:Genetically engineered animals are essential for gaining a proper u...
Animal models of cystic fibrosis (CF) are essential for investigating disease mechanisms and trialin...
<p>The transcript levels of each target gene were normalized to the G3PDH gene expression level and ...
<p>(<b>A</b>) Genotyping. The <i>ter</i> mutation disrupts a <i>Kpn</i>I restriction site used for g...