Generation of human induced pluripotent stem cell lines derived from four DiGeorge syndrome patients with 22q11.2 deletion-Reference-Cited by-同舟云学术

Generation of human induced pluripotent stem cell lines derived from four DiGeorge syndrome patients with 22q11.2 deletion

Published:2022-05 Issue: Volume:61 Page:102744
ISSN:1873-5061
Container-title:Stem Cell Research
language:en
Short-container-title:Stem Cell Research

Author:

Shimizu Tomoya,Matsuo-Takasaki Mami,Luijkx Dorian,Takami Miho,Arai Yutaka,Noguchi Michiya,Nakamura Yukio,Hayata Tadayoshi,Saito Megumu K.,Hayashi Yohei^ORCID

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. Generation of MBP-tdTomato reporter human induced pluripotent stem cell line for live myelin visualization;Stem Cell Research;2024-09

2. Patient-derived and gene-edited pluripotent stem cells lacking NPHP1 recapitulate juvenile nephronophthisis in abnormalities of primary cilia and renal cyst formation;Frontiers in Cell and Developmental Biology;2024-06-26

3. Generation of human induced pluripotent stem cell lines derived from four Rett syndrome patients with MECP2 mutations;Stem Cell Research;2024-06

4. 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

5. A CRISPR-engineered isogenic model of the 22q11.2 A-B syndromic deletion;Scientific Reports;2023-05-11