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Sarah J Fletcher

Showing results (11-20 of 15) with videos related to

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Oncotarget|July 16, 2014
USP17 is required for clathrin mediated endocytosis of epidermal growth factor receptorJakub Jaworski, Michelle de la Vega, Sarah J Fletcher, et al.
The Journal of Clinical Investigation|August 18, 2015
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defectsSarah J Fletcher, Ben Johnson, Gillian C Lowe, et al.
Frontiers in Microbiology|May 6, 2016
A Carotenoid-Deficient Mutant in Pantoea sp. YR343, a Bacteria Isolated from the Rhizosphere of Populus deltoides, Is Defective in Root ColonizationAmber N Bible, Sarah J Fletcher, Dale A Pelletier, et al.
Blood|May 29, 2016
Novel mutations in RASGRP2, which encodes CalDAG-GEFI, abrogate Rap1 activation, causing platelet dysfunctionMaría Luisa Lozano, Aaron Cook, José María Bastida, et al.
Haematologica|August 2, 2016
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsBen Johnson, Gillian C Lowe, Jane Futterer, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Oncotarget|July 16, 2014
USP17 is required for clathrin mediated endocytosis of epidermal growth factor receptorJakub Jaworski, Michelle de la Vega, Sarah J Fletcher, et al.
The Journal of Clinical Investigation|August 18, 2015
SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defectsSarah J Fletcher, Ben Johnson, Gillian C Lowe, et al.
Frontiers in Microbiology|May 6, 2016
A Carotenoid-Deficient Mutant in Pantoea sp. YR343, a Bacteria Isolated from the Rhizosphere of Populus deltoides, Is Defective in Root ColonizationAmber N Bible, Sarah J Fletcher, Dale A Pelletier, et al.
Blood|May 29, 2016
Novel mutations in RASGRP2, which encodes CalDAG-GEFI, abrogate Rap1 activation, causing platelet dysfunctionMaría Luisa Lozano, Aaron Cook, José María Bastida, et al.
Haematologica|August 2, 2016
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defectsBen Johnson, Gillian C Lowe, Jane Futterer, et al.
Pageof 2