The Mutation of the Ap3b1 Gene Causes Uterine Hypoplasia in Pearl Mice-Reference-Cited by-同舟云学术

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The Mutation of the Ap3b1 Gene Causes Uterine Hypoplasia in Pearl Mice

Published:2020-01 Issue:1 Volume:27 Page:182-191
ISSN:1933-7191
Container-title:Reproductive Sciences
language:en
Short-container-title:Reprod. Sci.

Author:

Jing Renwei,Kong Yu,Han Gang,Zhang Jingye,Li Kailin,Dong Xuan,Yan Jie,Zhang Haiqing,Han Jia,Feng Lijun

Publisher

Springer Science and Business Media LLC

Subject

Obstetrics and Gynecology

Link

http://link.springer.com/content/pdf/10.1007/s43032-019-00006-7.pdf

Reference34 articles.

1. Hermansky F, Pudlak P. Albinism associated with hemorrhagic diathesis and unusual pigmented reticular cells in the bone marrow: report of two cases with histochemical studies. Blood. 1959;14(2):162–9.

2. Feng L, Seymour AB, Jiang S, To A, Peden AA, Novak EK, et al. The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness. Hum Mol Genet. 1999;8(2):323–30.

3. Vallejo MO, Niemeyer GP, Vaglenov A, Hock T, Urie B, Christopherson P, et al. Decreased hematopoietic progenitor cell mobilization in pearl mice. Exp Hematol. 2013;41(10):848–57.

4. Vicary GW, Vergne Y, Santiago-Cornier A. Pulmonary fibrosis in Hermansky-Pudlak syndrome. Ann Am Thorac Soc. 2016;13(10):1839–46.

5. Huizing M, Helip-Wooley A, Westbroek W, Gunay-Aygun M, Gahl WA. Disorders of lysosome-related organelle biogenesis: clinical and molecular genetics. Annu Rev Genomics Hum Genet. 2008;9:359–86.

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