Generation of human induced pluripotent stem cell lines derived from four DiGeorge syndrome patients with 22q11.2 deletion
Author:
Funder
Japan Society for the Promotion of Science
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
1. A more efficient method to generate integration-free human iPS cells;Okita;Nat. Methods,2011
2. Generation of two human induced pluripotent stem cell lines derived from two juvenile nephronophthisis patients with NPHP1 deletion;Arai;Stem Cell Res.,2020
3. 22q11.2 deletion syndrome;McDonald-McGinn;Nat. Rev. Dis. Primers,2015
4. Teratoma formation by human embryonic stem cells is site dependent and enhanced by the presence of Matrigel;Prokhorova;Stem Cells Dev.,2009
5. Studying abnormal chromosomal diseases using patient-derived induced pluripotent stem cells;Hayashi;Front. Cell. Neurosci.,2020
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1. Establishment of induced pluripotent stem cells derived from patients and healthy siblings of a nevoid basal cell carcinoma syndrome family;In Vitro Cellular & Developmental Biology - Animal;2023-06
2. A CRISPR-engineered isogenic model of the 22q11.2 A-B syndromic deletion;Scientific Reports;2023-05-11
3. A CRISPR-engineered Isogenic Model Reveals Altered Neuronal Phenotypes of the 22q11.2 A-B Syndromic Deletion;2022-06-24
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