The dentin phosphoprotein repeat region and inherited defects of dentin-Reference-Cited by-全球学者库

The dentin phosphoprotein repeat region and inherited defects of dentin

Published:2015-09-07 Issue:1 Volume:4 Page:28-38
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Yang Jie¹²,Kawasaki Kazuhiko³,Lee Moses⁴,Reid Bryan M.¹,Nunez Stephanie M.¹,Choi Murim⁴,Seymen Figen⁵,Koruyucu Mine⁵,Kasimoglu Yelda⁵,Estrella‐Yuson Ninna⁶,Lin Brent P. J.⁷,Simmer James P.¹,Hu Jan C.‐C.¹

Affiliation:

1. Department of Biologic and Materials Sciences University of Michigan School of Dentistry 1210 Eisenhower Place Ann Arbor Michigan

2. Department of Pediatric Dentistry School and Hospital of Stomatology Peking University 22 South Avenue Zhongguancun Haidian District Beijing 100081 China

3. Department of Anthropology Pennsylvania State University University Park Pennsylvania 16802

4. Department of Biomedical Sciences Seoul National University College of Medicine 275‐1 Yongon‐dong, Chongno‐gu Seoul 110‐768 Korea

5. Department of Pedodontics Faculty of Dentistry Istanbul University Istanbul Turkey

6. Department of Paediatric Dentistry Women's and Children's Hospital 72 King William Road North Adelaide South Australia 5006 Australia

7. Department of Pediatric Dentistry School of Dentistry University of California San Francisco California

Funder

Ministry of Education, Science and Technology

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.176

Reference54 articles.

1. Predicting functional effect of human missense mutations using PolyPhen‐2;Adzhubei I.;Curr. Protoc. Hum. Genet.,2013

2. Mapping of the Human Dentin Matrix Acidic Phosphoprotein Gene (DMP1) to the Dentinogenesis Imperfecta Type II Critical Region at Chromosome 4q21

3. Median-joining networks for inferring intraspecific phylogenies

4. Phenotypic Variation in Dentinogenesis Imperfecta/Dentin Dysplasia Linked to 4q21

5. Resolving the complexity of the human genome using single-molecule sequencing

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