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of 3
pro vyhledávání: '"Kalbinder K Gill"'
Autor:
Andrew D Powell, Pierre-Philippe Saintot, Kalbinder K Gill, Ashtami Bharathan, S Caroline Buck, Gareth Morris, Premysl Jiruska, John G R Jefferys
Publikováno v:
PLoS ONE, Vol 9, Iss 5, p e95871 (2014)
Intellectual disability affects 2-3% of the population; mutations of the X-chromosome are a major cause of moderate to severe cases. The link between the molecular consequences of the mutation and impaired cognitive function remains unclear. Loss of
Externí odkaz:
https://doaj.org/article/fabc3018c0c546918c6f45aef1968598
Autor:
Marisol Sampedro Castañeda, Suzanne Claxton, Noreen Eder, Helen R. Flynn, Ambrosius P. Snijders, Roger George, Kalbinder K Gill, Amy Lin, Sila K. Ultanir, Irene Matucci
Publikováno v:
Life Science Alliance
Novel GAK phosphorylation targets are identified using chemical genetic methods. One of the substrates is the α subunit of the Na+/K+-ATPase, phosphorylation of which is necessary for its surface trafficking from endosomes. Conserved functions of NA
Autor:
Andrew D, Powell, Kalbinder K, Gill, Pierre-Philippe, Saintot, Premysl, Jiruska, Jamel, Chelly, Pierre, Billuart, John G R, Jefferys
Intellectual disability affects 2-3% of the population: those due to mutations of the X-chromosome are a major cause of moderate to severe cases (1.8/1000 males). Established theories ascribe the cellular aetiology of intellectual disability to malfo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e8fe0d5cf3db578792f1c03163903a09
https://europepmc.org/articles/PMC3381309/
https://europepmc.org/articles/PMC3381309/