日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

SLC4A1 mutations that cause distal renal tubular acidosis alter cytoplasmic pH and cellular autophagy.

导致远端肾小管酸中毒的 SLC4A1 突变会改变细胞质 pH 值和细胞自噬。

Essuman Grace, Rizvi Midhat, Almomani Ensaf, Ullah Shahid A K M, Hasib Sarder M A, Chelangarimiyandoab Forough, Mungara Priyanka, Schmitt Manfred J, Hureaux Marguerite, Vargas-Poussou Rosa, Touret Nicolas, Cordat Emmanuelle

Case Report: Abnormally low hemoglobin A1c in a diabetic patient with SLC4A1 gene mutation

病例报告:SLC4A1基因突变糖尿病患者糖化血红蛋白A1c异常偏低

Ye, Lili; Ren, Qian; Ba, Tianhao; Wu, Jing; Han, Xueyao; Ji, Linong

SLC4A10 impedes atherosclerosis by diminishing IFN-γ/GZMB levels of CD8(+) T cells via the MAPK pathway

SLC4A10 通过 MAPK 通路降低 CD8(+) T 细胞中 IFN-γ/GZMB 的水平,从而抑制动脉粥样硬化。

Chen, Bo; Zhu, Lei; Lin, Xueguang; Kwan, Kristine J S; Wang, Jie; Lu, Yijie; Li, Jialong; Deng, Ying; Jiang, Shuai; Tang, Jingdong; Yu, Bo

Alteration of Bone Microarchitecture in Hereditary Distal RTA Patients With SLC4A1 Gene Mutation: Assessed by HR-pQCT

遗传性远端肾小管酸中毒伴SLC4A1基因突变患者的骨微结构改变:高分辨率外周定量CT评估

Chen, Rong; Cui, Lijia; Du, Juan; Zhang, Shujie; Jiang, Yan; Li, Mei; Xing, Xiaoping; Wang, Ou; Xia, Weibo

SLC4A11 Revisited: Isoforms, Expression, Functions, and Unresolved Questions

SLC4A11 再探:异构体、表达、功能及未解之谜

Kovaleva, Polina Alekseevna; Kotova, Elena Sergeevna; Sharova, Elena Ivanovna; Skorodumova, Liubov Olegovna

Elevated SLC4A11 expression promotes OV progression via interaction with EGFR

SLC4A11表达升高通过与EGFR相互作用促进卵巢癌进展。

Peng, Qihua; Sun, Yixuan; Wang, Ruiwen; Zhang, Shiyu; Hu, Lipeng; Teng, Yincheng; Zhu, Xiaolu

Antioxidant MitoQ increases viability of human corneal endothelial cells with congenital hereditary endothelial dystrophy-associated SLC4A11 mutations

抗氧化剂MitoQ可提高携带先天性遗传性内皮营养不良相关SLC4A11突变的人类角膜内皮细胞的存活率。

Peshkar-Kulkarni, Saloni; Chung, Doug D; Aldave, Anthony J

Biallelic variants in SLC4A10 encoding a sodium-dependent bicarbonate transporter lead to a neurodevelopmental disorder

编码钠依赖性碳酸氢盐转运蛋白的SLC4A10基因的双等位基因变异会导致神经发育障碍

Maroofian, Reza; Zamani, Mina; Kaiyrzhanov, Rauan; Liebmann, Lutz; Karimiani, Ehsan Ghayoor; Vona, Barbara; Huebner, Antje K; Calame, Daniel G; Misra, Vinod K; Sadeghian, Saeid; Azizimalamiri, Reza; Mohammadi, Mohammad Hasan; Zeighami, Jawaher; Heydaran, Sogand; Toosi, Mehran Beiraghi; Akhondian, Javad; Babaei, Meisam; Hashemi, Narges; Schnur, Rhonda E; Suri, Mohnish; Setzke, Jonas; Wagner, Matias; Brunet, Theresa; Grochowski, Christopher M; Emrick, Lisa; Chung, Wendy K; Hellmich, Ute A; Schmidts, Miriam; Lupski, James R; Galehdari, Hamid; Severino, Mariasavina; Houlden, Henry; Hübner, Christian A

NH(3)/NH(4) (+) allosterically activates SLC4A11 by causing an acidic shift in the intracellular pK that governs H(+)(OH(-)) conductance

NH(3)/NH(4) (+) 通过引起细胞内 pK 的酸性变化来变构激活 SLC4A11,从而控制 H(+)(OH(-)) 电导。

Pasternack, Richard A; Quade, Bianca N; Marshall, Aniko; Parker, Mark D

Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells

研究 CHED 和 FECD4 相关 SLC4A11 突变对人角膜内皮细胞功能的影响

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