In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations-Reference-Cited by-同舟云学术

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In Vitro Modeling Using Ciliopathy-Patient-Derived Cells Reveals Distinct Cilia Dysfunctions Caused by CEP290 Mutations

Published:2017-07 Issue:2 Volume:20 Page:384-396
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Shimada Hiroko,Lu Quanlong,Insinna-Kettenhofen Christine,Nagashima Kunio,English Milton A.,Semler Elizabeth M.,Mahgerefteh Jacklyn,Cideciyan Artur V.,Li Tiansen,Brooks Brian P.,Gunay-Aygun Meral,Jacobson Samuel G.,Cogliati Tiziana,Westlake Christopher J.,Swaroop Anand

Funder

National Eye Institute

National Human Genome Research Institute

Japan Society for the Promotion of Science

Joubert Syndrome and Related Disorders Foundation

National Cancer Institute

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference67 articles.

1. Mechanisms regulating cilia growth and cilia function in endothelial cells;Abdul-Majeed;Cell. Mol. Life Sci.,2012

2. Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome;Aguilar;Proc. Natl. Acad. Sci. USA,2012

3. Meckel-Gruber syndrome and the role of primary cilia in kidney, skeleton, and central nervous system development;Barker;Organogenesis,2014

4. Passaging and colony expansion of human pluripotent stem cells by enzyme-free dissociation in chemically defined culture conditions;Beers;Nat. Protoc.,2012

5. A cost-effective and efficient reprogramming platform for large-scale production of integration-free human induced pluripotent stem cells in chemically defined culture;Beers;Sci. Rep.,2015

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