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Items: 1 to 20 of 38

1.
CYP4V2 rs56413992 C > T was associated with the risk of coronary heart disease in the Chinese Han population: a case–control study
Kang Huang, Tianyi Ma, Qiang Li, Zanrui Zhong, Yilei Zhou, Wei Zhang, Ting Qin, Shilin Tang, Jianghua Zhong, Shijuan Lu
BMC Med Genomics. 2023; 16: 322. Published online 2023 Dec 8. doi: 10.1186/s12920-023-01737-y
PMCID:
PMC10709878
AbstractArticlePDF–1.7M
2.
An In-Depth Single-Gene Worldwide Carrier Frequency and Genetic Prevalence Analysis of CYP4V2 as the Cause of Bietti Crystalline Dystrophy
Mor Hanany, Richard Rui Yang, Chun Man Lam, Avigail Beryozkin, Yogapriya Sundaresan, Dror Sharon
Transl Vis Sci Technol. 2023 Feb; 12(2): 27. Published online 2023 Feb 16. doi: 10.1167/tvst.12.2.27
PMCID:
PMC9940774
AbstractArticlePDF–4.1M
3.
Structural Investigation of Beta-Cyclodextrin Complexes with Cannabidiol and Delta-9-Tetrahydrocannabinol in 1:1 and 2:1 Host-Guest Stoichiometry: Molecular Docking and Density Functional Calculations
Nat Triamchaisri, Pisanu Toochinda, Luckhana Lawtrakul
Int J Mol Sci. 2023 Jan; 24(2): 1525. Published online 2023 Jan 12. doi: 10.3390/ijms24021525
PMCID:
PMC9865391
AbstractArticlePDF–3.1M
4.
CYP4 subfamily V member 2 (CYP4V2) polymorphisms were associated with ischemic stroke in Chinese Han population
Faqing Long, Desheng Wang, Qingjie Su, Yuhui Zhang, Jianhong Li, Shiliang Xia, Hailun Wang, Yongping Wu, Qiumin Qu
BMC Med Genomics. 2022; 15: 246. Published online 2022 Nov 28. doi: 10.1186/s12920-022-01393-8
PMCID:
PMC9703829
AbstractArticlePDF–894K
5.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
6.
Genome-wide CRISPR screening reveals genetic modifiers of mutant EGFR dependence in human NSCLC
Hao Zeng, Johnny Castillo-Cabrera, Mika Manser, Bo Lu, Zinger Yang, Vaik Strande, Damien Begue, Raffaella Zamponi, Shumei Qiu, Frederic Sigoillot, Qiong Wang, Alicia Lindeman, John S Reece-Hoyes, Carsten Russ, Debora Bonenfant, Xiaomo Jiang, Youzhen Wang, Feng Cong
eLife. 2019; 8: e50223. Published online 2019 Nov 19. doi: 10.7554/eLife.50223
PMCID:
PMC6927754
AbstractArticlePDF–5.1M
7.
Novel mutations in CYP4V2 in Bietti corneoretinal crystalline dystrophy: Next-generation sequencing technology and genotype-phenotype correlations
Xiao Hong Meng, Yan He, Tong Tao Zhao, Shi Ying Li, Yong Liu, Zheng Qin Yin
Mol Vis. 2019; 25: 654–662. Published online 2019 Oct 31.
PMCID:
PMC6828992
AbstractArticlePDF–846K
8.
Association of the CYP4V2 polymorphism rs13146272 with venous thromboembolism in a Chinese population
Yongjian Yue, Qing Sun, Chiwai Man, Yingyun Fu
Clin Exp Med. 2019; 19(1): 159–166. Published online 2018 Oct 1. doi: 10.1007/s10238-018-0529-y
PMCID:
PMC6394589
AbstractArticlePDF–1.2M
9.
Longitudinal characterisation of function and structure of Bietti crystalline dystrophy: report on a novel homozygous mutation in CYP4V2
Catherine M Lockhart, Travis B Smith, Paul Yang, Malini Naidu, Allan E Rettie, Abhinav Nath, Richard Weleber, Edward J Kelly
Br J Ophthalmol. Author manuscript; available in PMC 2019 Feb 1.
Published in final edited form as: Br J Ophthalmol. 2018 Feb; 102(2): 187–194. Published online 2017 Jul 11. doi: 10.1136/bjophthalmol-2016-309696
PMCID:
PMC6208130
AbstractArticlePDF–1.8M
10.
Comprehensive screening of CYP4V2 in a cohort of Chinese patients with Bietti crystalline dystrophy
Xiaohui Zhang, Ke Xu, Bing Dong, Xiaoyan Peng, Qian Li, Feng Jiang, Yue Xie, Lu Tian, Yang Li
Mol Vis. 2018; 24: 700–711. Published online 2018 Oct 26.
PMCID:
PMC6204257
AbstractArticlePDF–3.0M
11.
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper
Nature. Author manuscript; available in PMC 2017 Nov 17.
Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366
PMCID:
PMC5531611
AbstractArticlePDF–2.7M
12.
Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing
Teng Fei, Yiwen Chen, Tengfei Xiao, Wei Li, Laura Cato, Peng Zhang, Maura B. Cotter, Michaela Bowden, Rosina T. Lis, Shuang G. Zhao, Qiu Wu, Felix Y. Feng, Massimo Loda, Housheng Hansen He, X. Shirley Liu, Myles Brown
Proc Natl Acad Sci U S A. 2017 Jun 27; 114(26): E5207–E5215. Published online 2017 Jun 13. doi: 10.1073/pnas.1617467114
PMCID:
PMC5495225
AbstractArticlePDF–1.3M
13.
Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy
Xiaodong Jiao, Anren Li, Zi-Bing Jin, Xinjing Wang, Alessandro Iannaccone, Elias I Traboulsi, Michael B Gorin, Francesca Simonelli, J Fielding Hejtmancik
Eur J Hum Genet. 2017 Apr; 25(4): 461–471. Published online 2017 Jan 4. doi: 10.1038/ejhg.2016.184
PMCID:
PMC5386409
AbstractArticlePDF–1.3M
14.
Detailed Functional and Structural Phenotype of Bietti Crystalline Dystrophy Associated with Mutations in CYP4V2 Complicated by Choroidal Neovascularization
Nicole M. Fuerst, Leona Serrano, Grace Han, Jessica I. W. Morgan, Albert M. Maguire, Bart P. Leroy, Benjamin J. Kim, Tomas S. Aleman
Ophthalmic Genet. Author manuscript; available in PMC 2017 Dec 1.
Published in final edited form as: Ophthalmic Genet. 2016 Dec; 37(4): 445–452. Published online 2016 Mar 30. doi: 10.3109/13816810.2015.1126616
PMCID:
PMC5149010
AbstractArticlePDF–1.9M
15.
Bietti Crystalline Retinopathy Confirmed by Mutation of CYP4V2 Gene in a Korean Patient
Young Joo Park, Duck Jin Hwang, Moon-Woo Seong, Sung Sup Park, Se Joon Woo
Korean J Ophthalmol. 2016 Feb; 30(1): 81–83. Published online 2016 Jan 21. doi: 10.3341/kjo.2016.30.1.81
PMCID:
PMC4742652
ArticlePDF–7.7M
16.
Identification of novel CYP4V2 gene mutations in 92 Chinese families with Bietti’s crystalline corneoretinal dystrophy
Xiao Hong Meng, Hong Guo, Hai Wei Xu, Qi You Li, Xin Jin, Yun Bai, Shi Ying Li, Zheng Qin Yin
Mol Vis. 2014; 20: 1806–1814. Published online 2014 Dec 31.
PMCID:
PMC4287718
AbstractArticlePDF–1.3M
17.
Protein interaction discovery using parallel analysis of translated ORFs (PLATO)
Jian Zhu, H. Benjamin Larman, Geng Gao, Romel Somwar, Zijuan Zhang, Uri Laserson, Alberto Ciccia, Natalya Pavlova, George Church, Wei Zhang, Santosh Kesari, Stephen J. Elledge
Nat Biotechnol. Author manuscript; available in PMC 2014 Jul 25.
Published in final edited form as: Nat Biotechnol. 2013 Apr; 31(4): 331–334. Published online 2013 Mar 17. doi: 10.1038/nbt.2539
PMCID:
PMC4110636
AbstractArticlePDF–585K
18.
Molecular Analysis and Phenotypic Study in 14 Chinese Families with Bietti Crystalline Dystrophy
Houfa Yin, Chongfei Jin, Xiaoyun Fang, Qi Miao, Yingying Zhao, Zhiqing Chen, Zhaoan Su, Panpan Ye, Yao Wang, Jinfu Yin
PLoS One. 2014; 9(4): e94960. Published online 2014 Apr 16. doi: 10.1371/journal.pone.0094960
PMCID:
PMC3989252
AbstractArticlePDF–2.1M
19.
Clinical and genetic features in Italian Bietti crystalline dystrophy patients
Settimio Rossi, Francesco Testa, Anren Li, Fulya Yaylacioğlu, Carlo Gesualdo, J Fielding Hejtmancik, Francesca Simonelli
Br J Ophthalmol. 2013 Feb; 97(2): 174–179. Published online 2012 Dec 6. doi: 10.1136/bjophthalmol-2012-302469
PMCID:
PMC3582089
AbstractArticlePDF–417K
20.
CYP4V2 in Bietti's Crystalline Dystrophy: Ocular Localization, Metabolism of ω-3-Polyunsaturated Fatty Acids, and Functional Deficit of the p.H331P Variant
Mariko Nakano, Edward J. Kelly, Constanze Wiek, Helmut Hanenberg, Allan E. Rettie
Mol Pharmacol. 2012 Oct; 82(4): 679–686. doi: 10.1124/mol.112.080085
PMCID:
PMC3463217
AbstractArticlePDF–882K

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