TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome-Reference-Cited by-同舟云学术

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TALEN-mediated single-base-pair editing identification of an intergenic mutation upstream of BUB1B as causative of PCS (MVA) syndrome

Published:2013-12-16 Issue:4 Volume:111 Page:1461-1466
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Ochiai H.,Miyamoto T.,Kanai A.,Hosoba K.,Sakuma T.,Kudo Y.,Asami K.,Ogawa A.,Watanabe A.,Kajii T.,Yamamoto T.,Matsuura S.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference31 articles.

1. Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B

2. MonoallelicBUB1B mutations and defective mitotic-spindle checkpoint in seven families with premature chromatid separation (PCS) syndrome

3. Targeted Genome Editing Across Species Using ZFNs and TALENs

4. Targeted gene disruption in somatic zebrafish cells using engineered TALENs

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1. Mosaic variegated aneuploidy in development, ageing and cancer;Nature Reviews Genetics;2024-08-21

2. BUB1B monoallelic germline variants contribute to prostate cancer predisposition by triggering chromosomal instability;Journal of Biomedical Science;2024-07-16

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5. Elucidation of the etiological mechanisms underlying rare hereditary cilia/centrosome disorders using genome editing technology;Gene and Genome Editing;2022-12

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