Elucidation of the etiological mechanisms underlying rare hereditary cilia/centrosome disorders using genome editing technology-Reference-Cited by-同舟云学术

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Elucidation of the etiological mechanisms underlying rare hereditary cilia/centrosome disorders using genome editing technology

Published:2022-12 Issue: Volume:3-4 Page:100016
ISSN:2666-3880
Container-title:Gene and Genome Editing
language:en
Short-container-title:Gene and Genome Editing

Author:

Morita Tomoka,Hosoba Kosuke,Miyamoto Tatsuo^ORCID

Publisher

Elsevier BV

Subject

General Medicine

Reference25 articles.

1. NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations;Tomioka;Sci Rep,2021

2. Updated summary of genome editing technology in human cultured cells linked to human genetics studies;Miyamoto;J Hum Genet,2018

3. The microtubule-depolymerizing activity of a mitotic kinesin protein KIF2A drives primary cilia disassembly coupled with cell proliferation;Miyamoto;Cell Rep,2015

4. Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly;Poirier;Nat Genet,2013

5. Obligate ligation-gated recombination (ObLiGaRe): custom-designed nuclease-mediated targeted integration through nonhomologous end joining;Maresca;Genome Res,2013

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