Establishment of EHMT1 mutant induced pluripotent stem cell (iPSC) line from a 11-year-old Kleefstra syndrome (KS) patient with autism and normal intellectual performance-Reference-Cited by-同舟云学术

Establishment of EHMT1 mutant induced pluripotent stem cell (iPSC) line from a 11-year-old Kleefstra syndrome (KS) patient with autism and normal intellectual performance

Published:2016-11 Issue:3 Volume:17 Page:531-533
ISSN:1873-5061
Container-title:Stem Cell Research
language:en
Short-container-title:Stem Cell Research

Author:

Varga Eszter,Nemes Csilla,Táncos Zsuzsanna,Bock István,Berzsenyi Sára,Lévay György,Román Viktor,Kobolák Julianna,Dinnyés András

Funder

IDPBYNMR

Anistem

ERNYO

Research Centre of Excellence

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,General Medicine

Reference5 articles.

1. Targeted next generation sequencing of a panel of autism-related genes identifies an EHMT1 mutation in a Kleefstra syndrome patient with autism and normal intellectual performance;Bock;Gene,2016

2. Characterization and differentiation of human embryonic stem cells;Carpenter;Cloning Stem Cells,2003

3. Efficient induction of transgene-free human pluripotent stem cells using a vector based on Sendai virus, an RNA virus that does not integrate into the host genome;Fusaki;Proc. Jpn. Acad. Ser. B Phys. Biol. Sci.,2009

4. Differentiation of human embryonic stem cells into embryoid bodies compromising the three embryonic germ layers;Itskovitz-Eldor;Mol. Med.,2000

5. iPSC Reprogramming From Human Peripheral Blood Using Sendai Virus Mediated Gene Transfer;Yang,2008

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Establishment of Human Pluripotent Stem Cell-derived Cortical Neurosphere Model to Study Pathomechanisms and Drug Sensitivity in Kleefstra Syndrome;2024-04-25

2. The occurrence and development of induced pluripotent stem cells;Frontiers in Genetics;2024-04-18

3. Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals;Journal of Medical Genetics;2024-01-30

4. Arrhythmias including atrial fibrillation and congenital heart disease in Kleefstra syndrome: a possible epigenetic link;Europace;2023-12-28

5. Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome;Molecular Psychiatry;2020-04-28