PMC Links for Nucleotide (Select 1520687295) - PMC

Select item 64257031.

A novel mutation in the OAR domain of PITX3 associated with congenital posterior subcapsular cataract

Qi Fan, Dan Li, Lei Cai, Xiaodi Qiu, Zhennan Zhao, Jihong Wu, Jin Yang, Yi Lu

BMC Med Genet. 2019; 20: 42. Published online 2019 Mar 20. doi: 10.1186/s12881-019-0782-2

PMCID:: PMC6425703

Select item 64235732.

PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population

Zehua Wu, Delong Meng, Chengbo Fang, Jian Li, Xiujie Zheng, Jiansuo Lin, Haijiang Zeng, Sihan Lv, Zhenning Zhang, Bing Luan, Zilin Zhong, Jianjun Chen

Mol Med Rep. 2019 Apr; 19(4): 3123–3131. Published online 2019 Feb 26. doi: 10.3892/mmr.2019.9989

PMCID:: PMC6423573

Abstract Article PDF–1.3M

Select item 17358533.

Recurrent 17 bp duplication in PITX3 is primarily associated with posterior polar cataract (CPP4)

V Berry, Z Yang, P Addison, P Francis, A Ionides, G Karan, L Jiang, W Lin, J Hu, R Yang, A Moore, K Zhang, S Bhattacharya

J Med Genet. 2004 Aug; 41(8): e109. doi: 10.1136/jmg.2004.020289

PMCID:: PMC1735853

Summary PDF–273K

Select item 58399894.

Mutation Update of Transcription Factor Genes FOXE3, HSF4, MAF and PITX3 Causing Cataracts and Other Developmental Ocular Defects

Deepti Anand, Smriti A. Agrawal, Anne Slavotinek, Salil A. Lachke

Hum Mutat. Author manuscript; available in PMC 2019 Apr 1.

Published in final edited form as: Hum Mutat. 2018 Apr; 39(4): 471–494. Published online 2018 Jan 16. doi: 10.1002/humu.23395

PMCID:: PMC5839989

Abstract Article PDF–2.6M

Select item 48193095.

Targeted Genes Sequencing Identified a Novel 15 bp Deletion on GJA8 in a Chinese Family with Autosomal Dominant Congenital Cataracts

Han-Yi Min, Peng-Peng Qiao, Asan, Zhi-Hui Yan, Hui-Feng Jiang, Ya-Ping Zhu, Hui-Qian Du, Qin Li, Jia-Wei Wang, Jie Zhang, Jun Sun, Xin Yi, Ling Yang

Chin Med J (Engl) 2016 Apr 5; 129(7): 860–867. doi: 10.4103/0366-6999.178966

PMCID:: PMC4819309

Abstract Article PDF–2.8M

Select item 45185496.

Direct conversion of human fibroblasts to induced serotonergic neurons

Z Xu, H Jiang, P Zhong, Z Yan, S Chen, J Feng

Mol Psychiatry. 2016 Jan; 21(1): 62–70. Published online 2015 Jul 28. doi: 10.1038/mp.2015.101

PMCID:: PMC4518549

Abstract Article PDF–960K

Select item 45160867.

NEUROPROTECTIVE PROPERTIES OF MARROW-ISOLATED ADULT MULTILINEAGE INDUCIBLE CELLS IN RAT HIPPOCAMPUS FOLLOWING GLOBAL CEREBRAL ISCHEMIA ARE ENHANCED WHEN COMPLEXED TO BIOMIMETIC MICROCARRIERS

E. Garbayo, A.P. Raval, K.M. Curtis, D. Della-Morte, L.A. Gomez, G. D'Ippolito, T. Reiner, C. Perez-Stable, G.A. Howard, M.A. Perez-Pinzon, C.N. Montero-Menei, P.C. Schiller

J Neurochem. Author manuscript; available in PMC 2015 Jul 27.

Published in final edited form as: J Neurochem. 2011 Dec; 119(5): 972–988. Published online 2011 May 13. doi: 10.1111/j.1471-4159.2011.07272.x

PMCID:: PMC4516086

Abstract Article PDF–1.4M

Select item 33408568.

Epidemiology and molecular genetics of congenital cataracts

Jun Yi, Jun Yun, Zhi-Kui Li, Chang-Tai Xu, Bo-Rong Pan

Int J Ophthalmol. 2011; 4(4): 422–432. Published online 2011 Aug 18. doi: 10.3980/j.issn.2222-3959.2011.04.20

PMCID:: PMC3340856

Abstract Article PDF–3.1M

Select item 30620099.

A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly

Lance Doucette, Jane Green, Bridget Fernandez, Gordon J Johnson, Patrick Parfrey, Terry-Lynn Young

Eur J Hum Genet. 2011 Mar; 19(3): 293–299. Published online 2010 Dec 8. doi: 10.1038/ejhg.2010.210

PMCID:: PMC3062009

Abstract Article PDF–452K

Select item 302157710.

Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese family

Ke Yao, Jinyu Li, Chongfei Jin, Wei Wang, Yanan Zhu, Xingchao Shentu, Qiwei Wang

Mol Vis. 2011; 17: 144–152. Published online 2011 Jan 13.

PMCID:: PMC3021577

Abstract Article PDF–741K

Select item 287395711.

A Data Integration Approach to Mapping OCT4 Gene Regulatory Networks Operative in Embryonic Stem Cells and Embryonal Carcinoma Cells

Marc Jung, Hedi Peterson, Lukas Chavez, Pascal Kahlem, Hans Lehrach, Jaak Vilo, James Adjaye

PLoS One. 2010; 5(5): e10709. Published online 2010 May 21. doi: 10.1371/journal.pone.0010709

PMCID:: PMC2873957

Abstract Article PDF–1.8M

Select item 280571012.

Microphthalmia in Texel Sheep Is Associated with a Missense Mutation in the Paired-Like Homeodomain 3 (PITX3) Gene

Doreen Becker, Jens Tetens, Adrian Brunner, Daniela Bürstel, Martin Ganter, James Kijas, for the International Sheep Genomics Consortium, Cord Drögemüller

PLoS One. 2010; 5(1): e8689. Published online 2010 Jan 13. doi: 10.1371/journal.pone.0008689

PMCID:: PMC2805710

Abstract Article PDF–523K

Select item 228848713.

Congenital Cataracts and their Molecular Genetics

J. Fielding Hejtmancik

Semin Cell Dev Biol. Author manuscript; available in PMC 2009 Apr 1.

Published in final edited form as: Semin Cell Dev Biol. 2008 Apr; 19(2): 134–149. Published online 2007 Oct 10. doi: 10.1016/j.semcdb.2007.10.003

PMCID:: PMC2288487

Abstract Article PDF–611K

Select item 150909914.

Radiation hybrid mapping of cataract genes in the dog

Linda S. Hunter, Duska J. Sidjanin, Jennifer L. Johnson, Barbara Zangerl, Francis Galibert, Catherine Andre, Ewen Kirkness, Elijah Talamas, Gregory M. Acland, Gustavo D. Aguirre

Mol Vis. Author manuscript; available in PMC 2006 Jul 16.

Published in final edited form as: Mol Vis. 2006 May 24; 12: 588–596. Published online 2006 May 24.

PMCID:: PMC1509099

Abstract Article PDF–457K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 14

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity