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Items: 1 to 20 of 41

1.
Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells
Doug D. Chung, Angela C. Chen, Charlene H. Choo, Wenlin Zhang, Dominic Williams, Christopher G. Griffis, Paul Bonezzi, Kavya Jatavallabhula, Alapakkam P. Sampath, Anthony J. Aldave
PLoS One. 2024; 19(1): e0296928. Published online 2024 Jan 22. doi: 10.1371/journal.pone.0296928
PMCID:
PMC10802951
AbstractArticlePDF–3.6M
2.
Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophy
Tianjiao Zhen, Ya Li, Qingge Guo, Shun Yao, Ya You, Bo Lei
Transl Vis Sci Technol. 2023 Oct; 12(10): 1. Published online 2023 Oct 3. doi: 10.1167/tvst.12.10.1
PMCID:
PMC10561774
AbstractArticlePDF–8.1M
3.
Structural insights into the conformational changes of BTR1/SLC4A11 in complex with PIP2
Yishuo Lu, Peng Zuo, Hongyi Chen, Hui Shan, Weize Wang, Zonglin Dai, He Xu, Yayu Chen, Ling Liang, Dian Ding, Yan Jin, Yuxin Yin
Nat Commun. 2023; 14: 6157. Published online 2023 Oct 3. doi: 10.1038/s41467-023-41924-0
PMCID:
PMC10547724
AbstractArticlePDF–3.5M
4.
Corneal dystrophy mutations R125H and R804H disable SLC4A11 by altering the extracellular pH dependence of the intracellular pK that governs H+(OH−) transport
Bianca N. Quade, Aniko Marshall, Mark D. Parker
Am J Physiol Cell Physiol. 2022 Oct 1; 323(4): C990–C1002. Published online 2022 Aug 22. doi: 10.1152/ajpcell.00221.2022
PMCID:
PMC9484998
AbstractArticle
5.
Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy
Mohd Salman, Anshuman Verma, Sunita Chaurasia, Deeksha Prasad, Chitra Kannabiran, Vivek Singh, Muralidhar Ramappa
Orphanet J Rare Dis. 2022; 17: 361. Published online 2022 Sep 17. doi: 10.1186/s13023-022-02521-4
Correction in:
Orphanet J Rare Dis. 2023; 18: 170.
PMCID:
PMC9482203
AbstractArticlePDF–2.3M
6.
Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan
Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor
PLoS One. 2022; 17(8): e0273685. Published online 2022 Aug 29. doi: 10.1371/journal.pone.0273685
Correction in:
PLoS One. 2023; 18(10): e0293769.
PMCID:
PMC9423612
AbstractArticlePDF–1.2M
7.
Histone deacetylase inhibitors inhibit cervical cancer growth through Parkin acetylation-mediated mitophagy
Xin Sun, Yuhan Shu, Guiqin Ye, Caixia Wu, Mengting Xu, Ruilan Gao, Dongsheng Huang, Jianbin Zhang
Acta Pharm Sin B. 2022 Feb; 12(2): 838–852. Published online 2021 Jul 21. doi: 10.1016/j.apsb.2021.07.003
PMCID:
PMC8897022
AbstractArticlePDF–3.0M
8.
pH dependence of the Slc4a11-mediated H+ conductance is influenced by intracellular lysine residues and modified by disease-linked mutations
Bianca N. Quade, Aniko Marshall, Mark D. Parker
Am J Physiol Cell Physiol. 2020 Aug 1; 319(2): C359–C370. Published online 2020 Jun 10. doi: 10.1152/ajpcell.00128.2020
PMCID:
PMC7500215
AbstractArticle
9.
Systematic bromodomain protein screens identify homologous recombination and R-loop suppression pathways involved in genome integrity
Jae Jin Kim, Seo Yun Lee, Fade Gong, Anna M. Battenhouse, Daniel R. Boutz, Aarti Bashyal, Samantha T. Refvik, Cheng-Ming Chiang, Blerta Xhemalce, Tanya T. Paull, Jennifer S. Brodbelt, Edward M. Marcotte, Kyle M. Miller
Genes Dev. 2019 Dec 1; 33(23-24): 1751–1774. doi: 10.1101/gad.331231.119
PMCID:
PMC6942044
AbstractArticlePDF–10M
10.
IPSC-Derived Corneal Endothelial-like Cells Act as an Appropriate Model System to Assess the Impact of SLC4A11 Variants on Pre-mRNA Splicing
Kristyna Brejchova, Lubica Dudakova, Pavlina Skalicka, Robert Dobrovolny, Petr Masek, Martina Putzova, Mariya Moosajee, Stephen J. Tuft, Alice E. Davidson, Petra Liskova
Invest Ophthalmol Vis Sci. 2019 Jul; 60(8): 3084–3090. doi: 10.1167/iovs.19-26930
PMCID:
PMC6645617
AbstractArticlePDF–695K
11.
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies
Darpan Malhotra, Sampath K. Loganathan, Anthony M. Chiu, Chris M. Lukowski, Joseph R. Casey
Sci Rep. 2019; 9: 9681. Published online 2019 Jul 4. doi: 10.1038/s41598-019-46094-y
PMCID:
PMC6609610
AbstractArticlePDF–2.4M
12.
R125H, W240S, C386R, and V507I SLC4A11 Mutations Associated with Corneal Endothelial Dystrophy Affect the Transporter Function but not Trafficking in PS120 cells
Shimin Li, Karmjot Singh Hundal, Xingjuan Chen, Moonjung Choi, Diego G. Ogando, Alexander G. Obukhov, Joseph A. Bonanno
Exp Eye Res. Author manuscript; available in PMC 2020 Mar 1.
Published in final edited form as: Exp Eye Res. 2019 Mar; 180: 86–91. Published online 2018 Dec 14. doi: 10.1016/j.exer.2018.12.003
PMCID:
PMC6389376
AbstractArticlePDF–896K
13.
Histone Interaction Landscapes Visualized by Crosslinking Mass Spectrometry in Intact Cell Nuclei
Domenico Fasci, Hugo van Ingen, Richard A. Scheltema, Albert J. R. Heck
Mol Cell Proteomics. 2018 Oct; 17(10): 2018–2033. Published online 2018 Jul 18. doi: 10.1074/mcp.RA118.000924
PMCID:
PMC6166682
AbstractArticlePDF–3.8M
14.
High SLC4A11 expression is an independent predictor for poor overall survival in grade 3/4 serous ovarian cancer
Lianzhi Qin, Ting Li, Yuhua Liu
PLoS One. 2017; 12(11): e0187385. Published online 2017 Nov 1. doi: 10.1371/journal.pone.0187385
PMCID:
PMC5665559
AbstractArticlePDF–14M
15.
SLC4A11 depletion impairs NRF2 mediated antioxidant signaling and increases reactive oxygen species in human corneal endothelial cells during oxidative stress
Sanjukta Guha, Sunita Chaurasia, Charanya Ramachandran, Sanhita Roy
Sci Rep. 2017; 7: 4074. Published online 2017 Jun 22. doi: 10.1038/s41598-017-03654-4
PMCID:
PMC5481427
AbstractArticlePDF–4.7M
16.
Mouse Slc4a11 expressed in Xenopus oocytes is an ideally selective H+/OH− conductance pathway that is stimulated by rises in intracellular and extracellular pH
Evan J. Myers, Aniko Marshall, Michael L. Jennings, Mark D. Parker
Am J Physiol Cell Physiol. 2016 Dec 1; 311(6): C945–C959. Published online 2016 Sep 28. doi: 10.1152/ajpcell.00259.2016
PMCID:
PMC5206308
AbstractArticle
17.
Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies
Sampath K. Loganathan, Hans-Peter Schneider, Patricio E. Morgan, Joachim W. Deitmer, Joseph R. Casey
Am J Physiol Cell Physiol. 2016 Nov 1; 311(5): C735–C748. Published online 2016 Aug 24. doi: 10.1152/ajpcell.00078.2016
PMCID:
PMC5130586
AbstractArticle
18.
Multifunctional ion transport properties of human SLC4A11: comparison of the SLC4A11-B and SLC4A11-C variants
Liyo Kao, Rustam Azimov, Xuesi M. Shao, Ricardo F. Frausto, Natalia Abuladze, Debra Newman, Anthony J. Aldave, Ira Kurtz
Am J Physiol Cell Physiol. 2016 Nov 1; 311(5): C820–C830. Published online 2016 Aug 31. doi: 10.1152/ajpcell.00233.2016
PMCID:
PMC5130583
AbstractArticle
19.
Delayed onset of congenital hereditary endothelial dystrophy due to compound heterozygous SLC4A11 mutations
Babu Lal Kumawat, Ranjan Gupta, Arundhati Sharma, Seema Sen, Shikha Gupta, Radhika Tandon
Indian J Ophthalmol. 2016 Jul; 64(7): 492–495. doi: 10.4103/0301-4738.190100
PMCID:
PMC5026072
AbstractArticlePDF–814K
20.
Analysis of SLC4A11, ZEB1, LOXHD1, COL8A2 and TCF4 gene sequences in a multi-generational family with late-onset Fuchs corneal dystrophy
HUI TANG, WEN ZHANG, XIN-MIN YAN, LIN-PING WANG, HONG DONG, TAO SHOU, HUO LEI, QIANG GUO
Int J Mol Med. 2016 Jun; 37(6): 1487–1500. Published online 2016 Apr 20. doi: 10.3892/ijmm.2016.2570
PMCID:
PMC4866966
AbstractArticlePDF–1.4M

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