Rothmund-Thomson Syndrome-Like RECQL4 Truncating Mutations Cause a Haploinsufficient Low-Bone-Mass Phenotype in Mice

Author:

Castillo-Tandazo Wilson12ORCID,Frazier Ann E.34ORCID,Sims Natalie A.12ORCID,Smeets Monique F.12ORCID,Walkley Carl R.125ORCID

Affiliation:

1. St. Vincent’s Institute of Medical Research, Fitzroy, VIC, Australia

2. Department of Medicine, St. Vincent’s Hospital, The University of Melbourne, Fitzroy, VIC, Australia

3. Murdoch Children’s Research Institute, Royal Children's Hospital, Parkville, VIC, Australia

4. Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia

5. Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, VIC, Australia

Abstract

Rothmund-Thomson syndrome (RTS) is an autosomal recessive disorder characterized by defects in the skeletal system, such as bone hypoplasia, short stature, low bone mass, and an increased incidence of osteosarcoma. RTS type 2 patients have germ line compound biallelic protein-truncating mutations of RECQL4 .

Funder

Mito Foundation

U.S. Department of Defense

State Government of Victoria

University of Melbourne

Department of Health, Australian Government | National Health and Medical Research Council

Victorian Cancer Agency

Australian Government

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

Cited by 6 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. A Chinese patient with Rothmund–Thomson syndrome;Molecular Genetics & Genomic Medicine;2023-12-22

2. Rothmund-Thomson syndrome, a disorder far from solved;Frontiers in Aging;2023-11-10

3. Salicylic acid directly binds to ribosomal protein S3 and suppresses CDK4 expression in colorectal cancer cells;Biochemical and Biophysical Research Communications;2022-11

4. Molecular Mechanisms of the RECQ4 Pathogenic Mutations;Frontiers in Molecular Biosciences;2021-11-18

5. Molecular pathology of rare progeroid diseases;Trends in Molecular Medicine;2021-09

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