Publications by authors named "Xiaobei Yin"

9Publications

A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa.

Hum Genet 2016 12 21;135(12):1375-1387. Epub 2016 Sep 21.

Key Laboratory of Vision Loss and Restoration, Department of Ophthalmology, Ministry of Education, Peking University Third Hospital, Beijing, People's Republic of China.

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http://dx.doi.org/10.1007/s00439-016-1730-2DOI Listing
December 2016

Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy.

Exp Eye Res 2016 05 10;146:154-62. Epub 2016 Mar 10.

Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing 100005, PR China. Electronic address:

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http://dx.doi.org/10.1016/j.exer.2016.03.007DOI Listing
May 2016

Dependable and Efficient Clinical Molecular Diagnosis of Chinese RP Patient with Targeted Exon Sequencing.

PLoS One 2015 23;10(10):e0140684. Epub 2015 Oct 23.

Department of Ophthalmology, Peking University Third Hospital, Key Laboratory of Vision Loss and Restoration, Ministry of Education, Beijing, P. R. China.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0140684PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4619688PMC
June 2016

SPATA4 Counteracts Etoposide-Induced Apoptosis via Modulating Bcl-2 Family Proteins in HeLa Cells.

Biol Pharm Bull 2015 ;38(10):1458-63

MOE Key Laboratory of Protein Sciences, Department of Pharmacology, School of Medicine, Tsinghua University.

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http://dx.doi.org/10.1248/bpb.b15-00117DOI Listing
July 2016

[The anomalies of choroidal and retinal blood flow in retinitis pigmentosa patients].

Zhonghua Yan Ke Za Zhi 2014 Jul;50(7):518-22

Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology & Visual Sciences Key Lab, Beijing 100730, China. Email:

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July 2014

Novel mutations of CRB1 in Chinese families presenting with retinal dystrophies.

Mol Vis 2014 26;20:359-67. Epub 2014 Mar 26.

Department of Ophthalmology, Peking University Third Hospital, Key Laboratory of Vision Loss and Restoration, Ministry of Education, Beijing, P. R. China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976687PMC
September 2014

Novel mutations of RPGR in Chinese retinitis pigmentosa patients and the genotype-phenotype correlation.

PLoS One 2014 15;9(1):e85752. Epub 2014 Jan 15.

Department of Ophthalmology, Peking University Third Hospital, Key Laboratory of Vision Loss and Restoration, Ministry of Education, Beijing, P. R. China.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0085752PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893273PMC
September 2014

Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families.

BMJ Open 2013 Nov 7;3(11):e004030. Epub 2013 Nov 7.

Department of Ophthalmology, Peking University Third Hospital, Key Laboratory of Vision Loss and Restoration, Ministry of Education, Beijing, P. R. China.

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http://dx.doi.org/10.1136/bmjopen-2013-004030DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822309PMC
November 2013

Construction of a eukaryotic expression plasmid for human retina-derived neurotrophin-3.

Neural Regen Res 2013 Apr;8(11):1031-40

Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Beijing 100730, China.

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http://dx.doi.org/10.3969/j.issn.1673-5374.2013.11.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145883PMC
April 2013