Zobrazeno 1 - 10
of 2 422
pro vyhledávání: '"A L Goldin"'
Autor:
Gueye, Abdoulaye
The present volume is a collection of 16 essays dealing with the place, the boundaries and the significance of indigenous knowledge in the contemporary world. In addition to these articles are 1) a foreword signed by an eminent Indian philosophist an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=openedition_::9b07817b44fd239e0bef5a85ff51e34c
http://etudesafricaines.revues.org/1558
http://etudesafricaines.revues.org/1558
Autor:
Debbie Guerrero-Given, Seth L. Goldin, Connon I. Thomas, Skylar A. Anthony, Diego Jerez, Naomi Kamasawa
Publikováno v:
Frontiers in Neuroanatomy, Vol 16 (2022)
Integral membrane proteins such as ion channels, transporters, and receptors shape cell activity and mediate cell-to-cell communication in the brain. The distribution, quantity, and clustering arrangement of those proteins contribute to the physiolog
Externí odkaz:
https://doaj.org/article/6ed72b6026444fb09f0d4dfbade5e858
Autor:
Abdoulaye GUEYE
Publikováno v:
Cahiers d'études africaines. 43
Publikováno v:
IUPHAR/BPS Guide to Pharmacology CITE. 2023
Sodium channels are voltage-gated sodium-selective ion channels present in the membrane of most excitable cells. Sodium channels comprise of one pore-forming α subunit, which may be associated with either one or two β subunits [179]. α-Subunits co
Publikováno v:
IUPHAR/BPS Guide to Pharmacology CITE, vol 2019, iss 4
Sodium channels are voltage-gated sodium-selective ion channels present in the membrane of most excitable cells. Sodium channels comprise of one pore-forming α subunit, which may be associated with either one or two β subunits [176]. α-Subunits co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::136121f7dc4a1526b80816c62290a34b
https://escholarship.org/uc/item/4j34x48m
https://escholarship.org/uc/item/4j34x48m
Publikováno v:
Neurobiology of Disease, Vol 68, Iss , Pp 16-25 (2014)
SCN1A mutations are the main cause of the epilepsy disorders Dravet syndrome (DS) and genetic epilepsy with febrile seizures plus (GEFS+). Mutations that reduce the activity of the mouse Scn8a gene, in contrast, are found to confer seizure resistance
Externí odkaz:
https://doaj.org/article/0975c33e03394cf5b32da8c07f8940cb
Publikováno v:
Research in Autism Spectrum Disorders. 103:102121
Publikováno v:
Research in Autism Spectrum Disorders. 103:102119
Publikováno v:
Research in Autism Spectrum Disorders. 103:102112
Publikováno v:
Research in Autism Spectrum Disorders. 103:102115