Assessing the consistency of iPSC and animal models in cystic fibrosis modelling: A meta-analysis

<h3>Introduction</h3><p dir="ltr">Cystic fibrosis (CF) is a hereditary autosomal recessive disorder caused by a range of mutations in the CF Transmembrane Conductance Regulator (CFTR) gene. This gene encodes the CFTR protein, which acts as a chloride channel activated by...

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Main Author:	Toqa Darwish (13222230) (author)
Other Authors:	Azhar Al-Khulaifi (13222233) (author), Menatalla Ali (13222236) (author), Rana Mowafy (13222239) (author), Abdelilah Arredouani (10914455) (author), Suhail A. Doi (9552474) (author), Mohamed M. Emara (9913215) (author)
Published:	2022
Subjects:	Biological sciences Genetics Zoology Biomedical and clinical sciences Cardiovascular medicine and haematology Medical biochemistry and metabolomics Medical biotechnology Mathematical sciences Statistics Cystic Fibrosis (CF) Autosomal recessive disorder CFTR gene CFTR protein Respiratory disease Pathogens Respiratory failure Liver, pancreas, small bowel Molecular mechanisms Disease modeling Animal models iPSC (Induced Pluripotent Stem Cells) Amyotrophic lateral sclerosis (ALS) Spinal muscular atrophy (SMA) Parkinson’s disease (PD) Alzheimer’s disease (AD) Drug responses Chloride channel function
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Assessing the consistency of iPSC and animal models in cystic fibrosis modelling: A meta-analysis

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