Mitchell-Riley syndrome iPSCs exhibit reduced pancreatic endoderm differentiation due to a mutation in

Autor:	Jamie, Trott, Yunus, Alpagu, Ee Kim, Tan, Mohammad, Shboul, Yousif, Dawood, Michael, Elsy, Heike, Wollmann, Vincent, Tano, Carine, Bonnard, Shermaine, Eng, Gunaseelan, Narayanan, Seetanshu, Junnarkar, Stephen, Wearne, James, Strutt, Aakash, Kumar, Lucian B, Tomaz, Pierre-Alexis, Goy, Slim, Mzoughi, Rachel, Jennings, Jaco, Hagoort, Ascia, Eskin, Hane, Lee, Stanley F, Nelson, Fawaz, Al-Kazaleh, Mohammad, El-Khateeb, Rajaa, Fathallah, Harsha, Shah, Jonathan, Goeke, Sarah R, Langley, Ernesto, Guccione, Neil, Hanley, Bernadette S, De Bakker, Bruno, Reversade, N Ray, Dunn
Rok vydání:	2020
Předmět:	Male Base Sequence Transcription Genetic Genome Human Endoderm Induced Pluripotent Stem Cells Intestinal Atresia Embryonic Development Cell Differentiation Regulatory Factor X Transcription Factors Gallbladder Diseases X-Ray Microtomography Embryo Mammalian Chromatin Pedigree Consanguinity Mutation Diabetes Mellitus Humans Family Female Transcriptome Pancreas Alleles
Zdroj:	Development (Cambridge, England). 147(21)
ISSN:	1477-9129
Popis:	Mitchell-Riley syndrome (MRS) is caused by recessive mutations in the regulatory factor X6 gene (
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::5f977b2d81a6d953ebaae742dbb2a49d https://pubmed.ncbi.nlm.nih.gov/33033118 Zobrazit plný text záznamu