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Elizabeth Fitzpatrick

Showing results (51-60 of 56) with videos related to

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American Journal of Human Genetics|April 9, 2011
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesisPleasantine Mill, Paul J Lockhart, Elizabeth Fitzpatrick, et al.
Oncoimmunology|October 10, 2015
Progressive loss of anti-HER2 CD4<sup>+</sup> T-helper type 1 response in breast tumorigenesis and the potential for immune restorationJashodeep Datta, Cinthia Rosemblit, Erik Berk, et al.
Orphanet Journal of Rare Diseases|March 29, 2014
Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiencyJoe C H Sim, Susan M White, Elizabeth Fitzpatrick, et al.
Mabs|November 25, 2010
A fibronectin scaffold approach to bispecific inhibitors of epidermal growth factor receptor and insulin-like growth factor-I receptorStuart L Emanuel, Linda J Engle, Ginger Chao, et al.
Physiotherapy Canada. Physiotherapie Canada|February 21, 2022
Heather Flowers, Paulette Guitard, Judy King, et al.
American Journal of Human Genetics|December 1, 2014
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathologyGabrielle R Wilson, Joe C H Sim, Catriona McLean, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
American Journal of Human Genetics|April 9, 2011
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesisPleasantine Mill, Paul J Lockhart, Elizabeth Fitzpatrick, et al.
Oncoimmunology|October 10, 2015
Progressive loss of anti-HER2 CD4<sup>+</sup> T-helper type 1 response in breast tumorigenesis and the potential for immune restorationJashodeep Datta, Cinthia Rosemblit, Erik Berk, et al.
Orphanet Journal of Rare Diseases|March 29, 2014
Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiencyJoe C H Sim, Susan M White, Elizabeth Fitzpatrick, et al.
Mabs|November 25, 2010
A fibronectin scaffold approach to bispecific inhibitors of epidermal growth factor receptor and insulin-like growth factor-I receptorStuart L Emanuel, Linda J Engle, Ginger Chao, et al.
Physiotherapy Canada. Physiotherapie Canada|February 21, 2022
Heather Flowers, Paulette Guitard, Judy King, et al.
American Journal of Human Genetics|December 1, 2014
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathologyGabrielle R Wilson, Joe C H Sim, Catriona McLean, et al.
Pageof 6