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1 Ergebnisse
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KCNC3(R420H), a K(+) channel mutation causative in spinocer..:
Gallego-Iradi, Carolina
;
Bickford, Justin S
;
Khare, Swati
...
https://scholar.barrowneuro.org/neurobiology/1326. , 2014
Link:
https://scholar.barrowneuro.org/neurobiology/1326
RT Journal T1
KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking
UL https://suche.suub.uni-bremen.de/peid=base-ftbarrowneuroins:oai:scholar.barrowneuro.org:neurobiology-2337&Exemplar=1&LAN=DE A1 Gallego-Iradi, Carolina A1 Bickford, Justin S A1 Khare, Swati A1 Hall, Alexis A1 Nick, Jerelyn A A1 Salmasinia, Donya A1 Wawrowsky, Kolja A1 Bannykh, Serguei A1 Huynh, Duong P A1 Rincon-Limas, Diego E A1 Pulst, Stefan M A1 Nick, Harry S A1 Fernandez-Funez, Pedro A1 Waters, Michael F PB Barrow - St. Joseph's Scholarly Commons YR 2014 K1 Dominant inheritance K1 Golgi K1 KCNC3 K1 Protein trafficking K1 SCA13 K1 Spinocerebellar ataxia K1 Voltage-gated potassium channel K1 Animals K1 Genetically Modified K1 Arginine (genetics) K1 Biotinylation K1 COS Cells K1 Cadherins (metabolism) K1 Chlorocebus aethiops K1 Cytoplasm (genetics K1 metabolism) K1 Drosophila K1 Drosophila Proteins (genetics) K1 Endoplasmic Reticulum (metabolism) K1 Female K1 Histidine (genetics) K1 Humans K1 Intracellular Fluid (metabolism) K1 Male K1 Mutation (genetics) K1 Oocytes K1 Protein Processing K1 Post-Translational K1 Protein Transport K1 Shaw Potassium Channels (genetics) K1 Spinocerebellar Ataxias (congenital) K1 Spinocerebellar Degenerations (genetics K1 Transfection JF https://scholar.barrowneuro.org/neurobiology/1326 LK http://dx.doi.org/https://scholar.barrowneuro.org/neurobiology/1326 DO https://scholar.barrowneuro.org/neurobiology/1326 SF ELIB - SuUB Bremen
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