Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Stephanie Zlatic"'
Publikováno v:
Neurobiology of Disease, Vol 81, Iss , Pp 154-161 (2015)
ATP7A mutations impair copper metabolism resulting in three distinct genetic disorders in humans. These diseases are characterized by neurological phenotypes ranging from intellectual disability to neurodegeneration. Severe ATP7A loss-of-function all
Externí odkaz:
https://doaj.org/article/0942e2c9bf204861b1f7dfa36e4b29a3
Autor:
Miranda Arnold, Rebecca Cross, Kaela S Singleton, Stephanie Zlatic, Ariana P Mullin, Christopher Chapleau, Isaiah Rolle, Carlene Moore, Anne Theibert, Lucas Pozzo-Miller, Victor Faundez, Jennifer Larimore
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 10 (2016)
AGAP1 is an Arf1 GTPase activating protein that interacts with the vesicle-associated protein complexes adaptor protein 3 (AP-3) and Biogenesis of Lysosome Related Organelles Complex-1 (BLOC-1). Overexpression of AGAP1 in non-neuronal cells results i
Externí odkaz:
https://doaj.org/article/008ce67f7a274e9ebac312cde6b3c1b4
Publikováno v:
AfCS-Nature Molecule Pages.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::472a733bc6048da7fd5bccdce002c197
https://doi.org/10.1038/mp.a002733.01
https://doi.org/10.1038/mp.a002733.01