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KCNC1 gene
Known as:
KCNC1
, KV3.1
, NGK2
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
Three cases of progressive myoclonic epilepsy caused by KCNC1 gene mutations and literature review
Jing Zhang
,
Yuehua Zhang
,
Jiaoyang Chen
,
Ying Yang
,
Q. Zeng
,
Xiaoling Yang
2019
Corpus ID: 219818496
Objective To summarize the clinical phenotype and genotype features of 3 children with progre-ssive myoclonic epilepsy (PME…
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2017
2017
Functional alterations of the praxis network underlying limb kinetic apraxia in Parkinson’s disease
S. Kübel
,
K. Stegmayer
,
+7 authors
S. Bohlhalter
2017
Corpus ID: 51731573
Abstract Autism spectrum disorders (ASD) comprise a number of heterogeneous neurodevelopmental diseases characterized by core…
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2015
2015
Mass spectrometry study of N-alkylbenzenesulfonamides with potential antagonist activity to potassium channels
Carina C. Martins
,
C. A. Z. Bassetto
,
+4 authors
E. González
Amino Acids
2015
Corpus ID: 18679452
Herein, we report the synthesis and mass spectrometry studies of several N-alkylbenzenesulfonamides structurally related to…
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2013
2013
Evolutionary Conservation of Kv3.1 in the Barn Owl Tyto alba
Lars Kullmann
,
Tina Schlüter
,
H. Wagner
,
H. Nothwang
Brain, Behavior and Evolution
2013
Corpus ID: 20455479
For prey capture in the dark, the barn owl Tyto alba has evolved into an auditory specialist with an exquisite capability of…
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2005
2005
Single Amino Acid Substitutions Within the Ion Permeation Pathway Alter Single-Channel Conductance of the Human L-type Cardiac Ca 21 Channel
A. Yatani
,
A. Bahinski
,
G. Mikala
,
Satoshi Yamamoto
,
A. Schwartz
2005
Corpus ID: 16043699
Voltage-dependent L-type Ca2' channels select for Ca2' and other divalent cations by high-affinity Ca2' binding and ion-ion…
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1997
1997
Usher's Syndrome Type IC: Clinical Studies and Fine-Mapping the Disease Locus
J. Marietta
,
K. Walters
,
+5 authors
Richard J. H. Smith
Annals of Otology, Rhinology and Laryngology
1997
Corpus ID: 38084288
Usher's syndrome type I is a heterogeneous group of diseases characterized by severe to profound sensorineural hearing loss…
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1995
1995
Microheterogeneity in heteromultimeric assemblies formed by Shaker (Kv1) and Shaw (Kv3) subfamilies of voltage-gated K+ channels
M. Shahidullah
,
N. Hoshi
,
S. Yokoyama
,
Haruhiro Higasida
Proceedings of the Royal Society of London…
1995
Corpus ID: 34430421
Single K+ channels were recorded in Xenopus oocytes injected with a 1:1 mixture of mRNAs coding for NGK1 (Kvl. 2) and NGK2 (Kv3…
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1995
1995
Slow inactivation conserved in heteromultimeric voltage‐dependent K+ channels between Shaker (Kv1) and Shaw (Kv3) subfamilies
M. Shahidullah
,
N. Hoshi
,
S. Yokoyama
,
T. Kawamura
,
H. Higashida
FEBS Letters
1995
Corpus ID: 23546125
1995
1995
Whole-cell analysis of NGK2 (mKv3.1a) K+ channels stably expressed in mouse fibroblast cells
T. Kawamura
,
K. Enomoto
,
S. Yokoyama
,
N. Hoshi
,
Junkoh Yamashita
,
H. Higashida
Neuroscience Letters
1995
Corpus ID: 20382453
1992
1992
Expression of the H-ras oncogene induces potassium conductance and neuron-specific potassium channel mRNAs in the AtT20 cell line
LM Hemmick
,
T. Perney
,
RE Flamm
,
L. Kaczmarek
,
NC Birnberg
Journal of Neuroscience
1992
Corpus ID: 24470118
Expression of the EJ-ras oncogene in the AtT20 cell line results in several changes in their properties that correspond to a…
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