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

Castillo-Tandazo, Wilson; Frazier, Ann E; Sims, Natalie A; Smeets, Monique F; Walkley, Carl R

Castillo-Tandazo, Wilson; Frazier, Ann E; Sims, Natalie A; Smeets, Monique F; Walkley, Carl R.

Afiliação

Castillo-Tandazo W; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.
Frazier AE; Department of Medicine, St. Vincent's Hospital, The University of Melbourne, Fitzroy, VIC, Australia.
Sims NA; Murdoch Children's Research Institute, Royal Children's Hospital, Parkville, VIC, Australia.
Smeets MF; Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia.
Walkley CR; St. Vincent's Institute of Medical Research, Fitzroy, VIC, Australia.

Mol Cell Biol ; 41(3): e0059020, 2021 Feb 23.

Article em En | MEDLINE | ID: mdl-33361189

Palavras-chave

RECQL4; RecQ; Rothmund-Thomson syndrome; familial cancer syndrome; mouse models; myeloid cells; osteoblast; osteoporosis; osteosarcoma; tumor suppressor

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article