KCNJ10 Mutations Display Differential Sensitivity to Heteromerisation with KCNJ16-Reference-Cited by-同舟云学术

KCNJ10 Mutations Display Differential Sensitivity to Heteromerisation with KCNJ16

Published:2013 Issue:3-4 Volume:123 Page:7-14
ISSN:1660-2137
Container-title:Nephron Physiology
language:en
Short-container-title:Nephron Physiol

Author:

Parrock Sophie,Hussain Sofia,Issler Naomi,Differ Ann-Marie,Lench Nicholas,Guarino Stefano,Oosterveld Michiel J.S.,Keijzer-Veen Mandy,Brilstra Eva,van Wieringen Hester,Konijnenberg A. Yvette,Amin-Rasip Sarah,Dumitriu Simona,Klootwijk Enriko,Knoers Nine,Bockenhauer Detlef,Kleta Robert,Zdebik Anselm A.

Publisher

S. Karger AG

Subject

Physiology (medical),Nephrology,General Medicine,Physiology

Reference35 articles.

1. Bartter Syndromes and Other Salt-Losing Tubulopathies

2. Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, andKCNJ10Mutations

3. Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

4. Molecular Basis of Decreased Kir4.1 Function in SeSAME/EAST Syndrome

5. Subunit positional effects revealed by novel heteromeric inwardly rectifying K+ channels.

Cited by 35 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Role of Kir4.1 Channel in Auditory Function: Impact on Endocochlear Potential and Hearing Loss;Applied Sciences;2024-06-07

2. Inward rectifier potassium (Kir) channels in the retina: living our vision;American Journal of Physiology-Cell Physiology;2022-09-01

3. Inwardly rectifying K⁺ channels 4.1 and 5.1 (Kir4.1/Kir5.1) in the renal distal nephron;American Journal of Physiology-Cell Physiology;2022-08-01

4. EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- and Kir5.1-Associated Channelopathies;Frontiers in Physiology;2022-03-15

5. Calcium Signaling in the Cerebellar Radial Glia and Its Association with Morphological Changes during Zebrafish Development;International Journal of Molecular Sciences;2021-12-16