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Kv1.1 Potassium Channel
Known as:
Kv1.1 Potassium Channel [Chemical/Ingredient]
, Potassium Channel, Kv1.1
, KCNA1 Potassium Channel
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A delayed rectifier subtype of shaker potassium channels that is commonly mutated in human episodic ATAXIA and MYOKYMIA.
National Institutes of Health
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Related topics
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9 relations
In Blood
KCNA1 gene
Process of secretion
agonists
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Megalencephalic leukoencephalopathy with subcortical cysts: A personal biochemical retrospective.
R. Estévez
,
Xabier Elorza-Vidal
,
+14 authors
V. Nunes
European Journal of Medical Genetics
2018
Corpus ID: 41586557
2012
2012
Identification of Selective Inhibitors of the Potassium Channel Kv1.1–1.2(3) by High-Throughput Virtual Screening and Automated Patch Clamp
S. Wacker
,
W. Jurkowski
,
+6 authors
B. L. de Groot
ChemMedChem
2012
Corpus ID: 11416999
Two voltage‐dependent potassium channels, Kv1.1 (KCNA1) and Kv1.2 (KCNA2), are found to co‐localize at the juxtaparanodal region…
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Highly Cited
2004
Highly Cited
2004
Tonotopic Gradients of Membrane and Synaptic Properties for Neurons of the Chicken Nucleus Magnocellularis
I. Fukui
,
H. Ohmori
Journal of Neuroscience
2004
Corpus ID: 16365471
Nucleus magnocellularis (NM) is a division of the avian cochlear nucleus that extracts the timing of auditory signals. We…
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2003
2003
Hyperexcitability of CA3 Pyramidal Cells in Mice Lacking the Potassium Channel Subunit Kv1.1
V. Lopantsev
,
B. Tempel
,
P. Schwartzkroin
Epilepsia
2003
Corpus ID: 19819136
Summary: Purpose: To investigate further the membrane properties and postsynaptic potentials of the CA3 pyramidal cells in mice…
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2002
2002
Episodic Ataxia Type 1 Mutations in the Human Kv1.1 Potassium Channel Alter hKvβ1-Induced N-Type Inactivation
Brooke Maylie
,
Erinne Bissonnette
,
Michael S. Virk
,
J. Adelman
,
J. Maylie
Journal of Neuroscience
2002
Corpus ID: 37873287
Episodic ataxia type 1 (EA1) is an autosomal dominant neurological disorder affecting both central and peripheral nerve function…
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Highly Cited
2000
Highly Cited
2000
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability
L. Eunson
,
R. Rea
,
+9 authors
A. Spauschus
Annals of Neurology
2000
Corpus ID: 1691004
Episodic ataxia type 1 (EA1) is an autosomal dominant central nervous system potassium channelopathy characterized by brief…
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Review
1999
Review
1999
Developmental Seizure Susceptibility of Kv1.1 Potassium Channel Knockout Mice
J. Rho
,
P. Szot
,
B. Tempel
,
P. Schwartzkroin
Developmental Neuroscience
1999
Corpus ID: 9737126
Potassium channels play a critical role in limiting neuronal excitability. Mutations in certain voltage-gated potassium channels…
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Highly Cited
1999
Highly Cited
1999
Protein kinase C inhibits Kv1.1 potassium channel function.
L. M. Boland
,
K. A. Jackson
American Journal of Physiology - Cell Physiology
1999
Corpus ID: 4474163
The regulation by protein kinase C (PKC) of recombinant voltage-gated potassium (K) channels in frog oocytes was studied. Phorbol…
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1999
1999
Protein kinase C inhibits Kv1.1 potassium channel function.
L. M. Boland
,
K. A. Jackson
American Journal of Physiology
1999
Corpus ID: 20624833
The regulation by protein kinase C (PKC) of recombinant voltage-gated potassium (K) channels in frog oocytes was studied. Phorbol…
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Highly Cited
1998
Highly Cited
1998
Characterization of three episodic ataxia mutations in the human Kv1.1 potassium channel
P. Zerr
,
J. Adelman
,
J. Maylie
FEBS Letters
1998
Corpus ID: 26761264
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