Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
about
Mutant mouse tottering: selective increase of locus ceruleus axons in a defined single-locus mutationAblation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunitMutational ataxia resulting from abnormal vestibular acquisition and processing is partially compensated forDecreased calretinin expression in cerebellar granule cells in the leaner mouse.Animal models of generalized dystonia.GABAA Receptor Expression in the Forebrain of Ataxic Rolling Nagoya MiceAbnormal excitability and episodic low-frequency oscillations in the cerebral cortex of the tottering mouse.Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control.Differential cerebellar GABAA receptor expression in mice with mutations in CaV2.1 (P/Q-type) calcium channels.Altered functional expression of Purkinje cell calcium channels precedes motor dysfunction in tottering mice.Spontaneous shaker rat mutant - a new model for X-linked tremor/ataxia.Low-frequency oscillations in the cerebellar cortex of the tottering mouse.Mouse forward genetics in the study of the peripheral nervous system and human peripheral neuropathyThe ataxic Cacna1a-mutant mouse rolling nagoya: an overview of neuromorphological and electrophysiological findings.Synchronous hippocampal bursting reveals network excitability defects in an epilepsy gene mutation.A role for cerebellum in the hereditary dystonia DYT1.From mice to men: lessons from mutant ataxic mice.The Role of Calcium Channels in Epilepsy.STD-dependent and independent encoding of input irregularity as spike rate in a computational model of a cerebellar nucleus neuron.Upregulation of L-type calcium channels in colonic inhibitory motoneurons of P/Q-type calcium channel-deficient mice.Enhanced G protein-dependent modulation of excitatory synaptic transmission in the cerebellum of the Ca2+ channel-mutant mouse, tottering.Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits.Impact of the leaner P/Q-type Ca2+ channel mutation on excitatory synaptic transmission in cerebellar Purkinje cells.Motor deficits in homozygous and heterozygous p/q-type calcium channel mutants.
P2860
Q28589781-C0363239-9495-4232-B567-CDD0E93CABCAQ28592875-95C0911E-ADCF-4621-BAFB-AADA3D5B5F60Q30512203-8BEBDB3E-55E3-4713-AD25-5A70B687D9DDQ31099420-F299B67C-9A7C-4A10-8D95-EE896951EAD5Q33844755-75A5B88E-6FF8-456D-A526-552894329945Q34314614-F1E7CEAF-05CE-462D-B957-A1513C49F7CFQ35307681-AD599FBC-199E-4828-BEC4-7B435361F152Q35586963-2CAD2EBA-AD9B-4286-B60B-D69F237ED760Q35991521-E28FB9EA-1261-44AB-BDCD-8F6023A1593BQ36387934-7F2D4039-F12C-46DB-BE1F-894285DB9667Q36967497-C542D201-B17E-4149-8289-3B70954787C4Q37086565-45758599-2CEF-4429-9845-E77A2E236179Q37164126-63FCFA3D-0F7C-4889-B454-1428AF7C9FD9Q37502776-A053FCE6-631A-488C-A6C1-29C8FB7B7072Q37521327-0129F2EC-CAF9-4AEB-ABB0-FEDB3E6605F8Q37684995-52731C44-B06B-45AA-B3CF-7FB1D59B96F5Q38578808-92A6586E-D56C-44ED-B6CF-F50D8BB59C70Q38686593-A36F9753-0185-46A0-B1F1-3BDB1913F7B6Q39099673-7A42CCB6-F583-4CE7-B024-C69CCC69C470Q41630502-7E4CCC22-4BB5-429E-A581-6CCECB335ECBQ44300144-9C975F8D-1F60-408D-B47E-D4F2B2C6560FQ46586458-900A7CBD-8B2D-4B46-93A9-B9788272C686Q49022572-6914134A-D8BD-4A1F-9FAE-2EAF05DEDF1DQ52573890-FAC7BA69-949C-41E1-9BE1-DBEE54E5B1F0
P2860
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
description
1962 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1962 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1962
@ast
im September 1962 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1962/09/01)
@sk
vědecký článek publikovaný v roce 1962
@cs
wetenschappelijk artikel (gepubliceerd op 1962/09/01)
@nl
наукова стаття, опублікована у вересні 1962
@uk
مقالة علمية (نشرت في سبتمبر 1962)
@ar
name
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@ast
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@en
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@nl
type
label
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@ast
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@en
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@nl
prefLabel
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@ast
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@en
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@nl
P3181
P1433
P1476
Tottering--a neuromusclar mutation in the mouse. And its linkage with oligosyndacylism
@en
P2093
M. C. Green
R. L. Sidman
P304
P3181
P356
10.1093/OXFORDJOURNALS.JHERED.A107180
P577
1962-09-01T00:00:00Z