Crispr-Cas9 engineered osteogenesis imperfecta type V leads to severe skeletal deformities and perinatal lethality in mice-Reference-Cited by-同舟云学术

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Crispr-Cas9 engineered osteogenesis imperfecta type V leads to severe skeletal deformities and perinatal lethality in mice

Published:2018-02 Issue: Volume:107 Page:131-142
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Rauch Frank,Geng Yeqing,Lamplugh Lisa,Hekmatnejad Bahareh,Gaumond Marie-Hélène,Penney Janice,Yamanaka Yojiro,Moffatt Pierre

Funder

Shriners Hospital

Shriners of North America

Canadian Institutes of Health Research

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference61 articles.

1. Osteogenesis imperfecta;Forlino;Lancet,2016

2. DNA sequence analysis in 598 individuals with a clinical diagnosis of osteogenesis imperfecta: diagnostic yield and mutation spectrum;Bardai;Osteoporos. Int.,2016

3. New perspectives on osteogenesis imperfecta;Forlino;Nat. Rev. Endocrinol.,2011

4. Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.-14C>T mutation in all patients;Rauch;J. Med. Genet.,2013

5. Type V osteogenesis imperfecta: a new form of brittle bone disease;Glorieux;J. Bone Miner. Res.,2000

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4. Identification of a family with van der Hoeve’s syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs;Human Cell;2024-02-20

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