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Items: 1 to 20 of 44

1.
Connexins in Cancer, the Possible Role of Connexin46 as a Cancer Stem Cell-Determining Protein
Isidora M. León-Fuentes, María G. Salgado-Gil, María S. Novoa, Mauricio A. Retamal
Biomolecules. 2023 Oct; 13(10): 1460. Published online 2023 Sep 27. doi: 10.3390/biom13101460
PMCID:
PMC10604234
ArticlePDF–1.7M
2.
Connexin46 Expression Enhances Cancer Stem Cell and Epithelial-to-Mesenchymal Transition Characteristics of Human Breast Cancer MCF-7 Cells
Rodrigo A. Acuña, Manuel Varas-Godoy, Diego Herrera-Sepulveda, Mauricio A. Retamal
Int J Mol Sci. 2021 Nov; 22(22): 12604. Published online 2021 Nov 22. doi: 10.3390/ijms222212604
PMCID:
PMC8624448
ArticlePDF–2.4M
3.
Connexin-46 Contained in Extracellular Vesicles Enhance Malignancy Features in Breast Cancer Cells
Rodrigo A. Acuña, Manuel Varas-Godoy, Viviana M. Berthoud, Ivan E. Alfaro, Mauricio A. Retamal
Biomolecules. 2020 May; 10(5): 676. Published online 2020 Apr 28. doi: 10.3390/biom10050676
PMCID:
PMC7277863
ArticlePDF–5.0M
4.
Analysis of the dominant mutation N188T of human connexin46 (hCx46) using concatenation and molecular dynamics simulation
Patrik Schadzek, Yannick Stahl, Matthias Preller, Anaclet Ngezahayo
FEBS Open Bio. 2019 May; 9(5): 840–850. Published online 2019 Mar 23. doi: 10.1002/2211-5463.12624
PMCID:
PMC6487695
ArticlePDF–1.2M
5.
Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract
Vanita Berry, Alexander C. W. Ionides, Nikolas Pontikos, Ismail Moghul, Anthony T. Moore, Michael E. Cheetham, Michel Michaelides
Eye (Lond) 2018 Oct; 32(10): 1661–1668. Published online 2018 Jun 22. doi: 10.1038/s41433-018-0154-8
PMCID:
PMC6189195
ArticlePDF–1.0M
6.
Identification of a novel GJA3 mutation in a large Chinese family with congenital cataract using targeted exome sequencing
Yihua Yao, Xuedong Zheng, Xianglian Ge, Yanghui Xiu, Liu Zhang, Weifang Fang, Junzhao Zhao, Feng Gu, Yihua Zhu
PLoS One. 2017; 12(9): e0184440. Published online 2017 Sep 6. doi: 10.1371/journal.pone.0184440
PMCID:
PMC5587237
ArticlePDF–5.8M
7.
Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract
Li Wang, Yuhong Chen, Xueli Chen, Xinghuai Sun
Indian J Ophthalmol. 2016 Jul; 64(7): 508–512. doi: 10.4103/0301-4738.190139
PMCID:
PMC5026076
ArticlePDF–896K
8.
Cataract-Causing Mutation of Human Connexin 46 Impairs Gap Junction, but Increases Hemichannel Function and Cell Death
Qian Ren, Manuel A. Riquelme, Ji Xu, Xiang Yan, Bruce J. Nicholson, Sumin Gu, Jean X. Jiang
PLoS One. 2013; 8(9): e74732. Published online 2013 Sep 3. doi: 10.1371/journal.pone.0074732
PMCID:
PMC3760834
ArticlePDF–1.7M
9.
The N-terminal half of the connexin protein contains the core elements of the pore and voltage gates
Jack Kronengold, Miduturu Srinivas, Vytas K. Verselis
J Membr Biol. Author manuscript; available in PMC 2013 Aug 6.
Published in final edited form as: J Membr Biol. 2012 Aug; 245(8): 453–463. Published online 2012 Jul 24. doi: 10.1007/s00232-012-9457-z
PMCID:
PMC3735448
ArticlePDF–2.4M
10.
Properties of two cataract-associated mutations located in the NH2 terminus of connexin 46
Jun-Jie Tong, Bonnie C. H. Sohn, Anh Lam, D. Eric Walters, Barbara M. Vertel, Lisa Ebihara
Am J Physiol Cell Physiol. 2013 May 1; 304(9): C823–C832. Published online 2013 Jan 9. doi: 10.1152/ajpcell.00344.2012
PMCID:
PMC3651606
Article
11.
A novel insertional mutation in the connexin 46 (gap junction alpha 3) gene associated with autosomal dominant congenital cataract in a Chinese family
Dingan Zhou, Hongyun Ji, Zhiyun Wei, Luo Guo, Yanpeng Li, Teng Wang, Yu Zhu, Xingran Dong, Yang Wang, Lin He, Qinghe Xing, Lirong Zhang
Mol Vis. 2013; 19: 789–795. Published online 2013 Apr 5.
PMCID:
PMC3626289
ArticlePDF–2.9M
12.
A novel mutation in GJA3 associated with congenital Coppock-like cataract in a large Chinese family
Lu Zhang, Xin Qu, Sheng Su, Linan Guan, Ping Liu
Mol Vis. 2012; 18: 2114–2118. Published online 2012 Jul 26.
PMCID:
PMC3413429
ArticlePDF–1.8M
13.
A novel p.F206I mutation in Cx46 associated with autosomal dominant congenital cataract
Kai Jie Wang, Si Quan Zhu
Mol Vis. 2012; 18: 968–973. Published online 2012 Apr 18.
PMCID:
PMC3339038
ArticlePDF–1.1M
14.
Coralliform cataract caused by a novel connexin46 (GJA3) mutation in a Chinese family
Xiaohui Zhang, Lina Wang, Jun Wang, Bing Dong, Yang Li
Mol Vis. 2012; 18: 203–210. Published online 2012 Jan 25.
PMCID:
PMC3272055
ArticlePDF–699K
15.
A recurrent missense mutation in GJA3 associated with autosomal dominant cataract linked to chromosome 13q
Thomas M. Bennett, Alan Shiels
Mol Vis. 2011; 17: 2255–2262. Published online 2011 Aug 20.
PMCID:
PMC3164684
ArticlePDF–881K
16.
A novel role of gap junction connexin46 protein to protect breast tumors from hypoxia
Debarshi Banerjee, Gunjan Gakhar, Dan Madgwick, Amy Hurt, Dolores Takemoto, Thu Annelise Nguyen
Int J Cancer. Author manuscript; available in PMC 2011 Aug 15.
Published in final edited form as: Int J Cancer. 2010 Aug 15; 127(4): 839–848. doi: 10.1002/ijc.25107
PMCID:
PMC3150590
ArticlePDF–1.2M
17.
A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree
Xuchen Ding, Binbin Wang, Yongfeng Luo, Shanshan Hu, Guangkai Zhou, Zhou Zhou, Jing Wang, Xu Ma, Yanhua Qi
Mol Vis. 2011; 17: 1343–1349. Published online 2011 May 20.
PMCID:
PMC3107996
ArticlePDF–560K
18.
A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
Guoxing Yang, Baogang Xing, Guangcai Liu, Xiangqing Lu, Xingang Jia, Xiangqing Lu, Xiuli Wang, Hongyan Yu, Yanjiang Fu, Jialiang Zhao
Mol Vis. 2011; 17: 1070–1073. Published online 2011 Apr 27.
PMCID:
PMC3086624
ArticlePDF–414K
19.
Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3)
Zhou Zhou, Shanshan Hu, Binbin Wang, Nan Zhou, Shiyi Zhou, Xu Ma, Yanhua Qi
Mol Vis. 2010; 16: 713–719. Published online 2010 Apr 21.
PMCID:
PMC2861125
ArticlePDF–2.3M
20.
A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene
Kamlesh Guleria, Vanita Vanita, Daljit Singh, Jai Rup Singh
Mol Vis. 2007; 13: 797–803. Published online 2007 Jun 4.
PMCID:
PMC2768755
ArticlePDF–840K

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