Bone health and SATB2 -associated syndrome-Reference-Cited by-同舟云学术

Bone health and SATB2 -associated syndrome

Published:2017-12-27 Issue:3 Volume:93 Page:588-594
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Zarate Y.A.¹^ORCID,Steinraths M.²,Matthews A.²³,Smith W.E.⁴,Sun A.⁵,Wilson L.C.⁶,Brain C.⁷,Allgove J.⁷,Jacobs B.⁸,Fish J.L.⁹,Powell C.M.¹⁰¹¹,Wasserman W.W.²³,van Karnebeek C.D.³¹²¹³,Wakeling E.L.¹⁴,Ma N.S.¹⁵

Affiliation:

1. Section of Genetics and Metabolism; University of Arkansas for Medical Sciences; Little Rock Arkansas

2. Department of Medical Genetics; University of British Columbia; Vancouver Canada

3. Centre for Molecular Medicine and Therapeutics; British Columbia Children's Hospital Research Institute; Vancouver Canada

4. Department of Pediatrics, The Barbara Bush Children's Hospital; Maine Medical Center; Portland Maine

5. Division of Genetic Medicine, Department of Pediatrics; University of Washington; Seattle Washington

6. Department of Genetics; Great Ormond Street for Children NHS Foundation Trust; London UK

7. Department of Endocrinology; Great Ormond Street for Children NHS Foundation Trust; London UK

8. Department of Pediatrics; Royal National Orthopaedic Hospital NHS Trust; London UK

9. Department of Biological Sciences; University of Massachusetts Lowell; Lowell Massachusetts

10. Department of Pediatrics; University of North Carolina at Chapel Hill; Chapel Hill North Carolina

11. Department of Genetics; University of North Carolina at Chapel Hill; Chapel Hill North Carolina

12. Department of Pediatrics; University of British Columbia; Vancouver Canada

13. Department of Pediatrics and Clinical Genetics, Emma Children's Hospital; Academic Medical Centre; Amsterdam The Netherlands

14. North West Thames Regional Genetics Service; London North West Healthcare NHS Trust; Harrow UK

15. Division of Endocrinology, Boston Children's Hospital; Harvard Medical School; Boston Massachusetts

Funder

BCCH Foundation as “1st Collaborative Area of Innovation”

Canadian Institutes for Health Research

Genome BC and Genome Canada (ABC4DE Project)

Michael Smith Foundation for Health Research Scholar Award

BCCH Research Institute fellowship

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13121/fullpdf

Reference24 articles.

1. SATB2-associated syndrome: mechanisms, phenotype, and practical recommendations;Zarate;Am J Med Genet A,2017

2. Clinical and molecular consequences of disease-associated de novo mutations in SATB2;Bengani;Genet Med,2017

3. SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation;Dobreva;Cell,2006

4. Lentiviral-mediated expression of SATB2 promotes osteogenic differentiation of bone marrow stromal cells in vitro and in vivo;Gong;Eur J Oral Sci,2014

5. Roles of SATB2 in osteogenic differentiation and bone regeneration;Zhang;Tissue Eng Part A,2011

Cited by 15 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. Progress of epigenetic modification of SATB2 gene in the pathogenesis of non-syndromic cleft lip and palate;Asian Journal of Surgery;2024-01

2. Bone health in SATB2‐associated syndrome: Results from a large prospective cohort and recommendations for surveillance;American Journal of Medical Genetics Part A;2023-10-02

3. Application and Molecular Mechanisms of Extracellular Vesicles Derived from Mesenchymal Stem Cells in Osteoporosis;Current Issues in Molecular Biology;2022-12-15

4. The dental phenotype of primary dentition in SATB2-associated syndrome: a report of three cases and literature review;BMC Oral Health;2022-11-22

5. SATB2 Expression in Undifferentiated Pleomorphic Sarcomas of Bone;American Journal of Clinical Pathology;2022-03-21