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C Manson

Showing results (151-160 of 174) with videos related to

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Human Mutation|April 22, 2008
Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndromeMay Tassabehji, Zhi Ming Fang, Emma N Hilton, et al.
Journal of Cell Science|January 5, 2017
Sideroflexin 3 is an α-synuclein-dependent mitochondrial protein that regulates synaptic morphologyInês S Amorim, Laura C Graham, Roderick N Carter, et al.
American Journal of Human Genetics|June 2, 2009
The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1Dan Hanson, Philip G Murray, Amit Sud, et al.
Emerging Infectious Diseases|September 29, 2012
Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countriesAbigail B Diack, Diane Ritchie, Matthew Bishop, et al.
Cancer|June 3, 2015
Health-related quality-of-life results from PALETTE: A randomized, double-blind, phase 3 trial of pazopanib versus placebo in patients with soft tissue sarcoma whose disease has progressed during or after prior chemotherapy-a European Organization for research and treatment of cancer soft tissue and bone sarcoma group global network study (EORTC 62072)Corneel Coens, Winette T A van der Graaf, Jean-Yves Blay, et al.
Plos One|August 23, 2011
All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJDSandra McCutcheon, Anthony Richard Alejo Blanco, E Fiona Houston, et al.
Human Molecular Genetics|March 18, 2005
RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosminX Shu, A M Fry, B Tulloch, et al.
American Journal of Human Genetics|August 2, 2007
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosumElena Boland, Jill Clayton-Smith, Victoria G Woo, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2011
Childhood-onset autosomal recessive bestrophinopathyArundhati Dev Borman, Alice E Davidson, James O'Sullivan, et al.
Cell Death and Differentiation|July 12, 2008
Yes-associated protein (YAP) functions as a tumor suppressor in breastM Yuan, V Tomlinson, R Lara, et al.
Pageof 18

Showing results (151-160 of 174) with videos related to

Sort By:
Pageof 18
Human Mutation|April 22, 2008
Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndromeMay Tassabehji, Zhi Ming Fang, Emma N Hilton, et al.
Journal of Cell Science|January 5, 2017
Sideroflexin 3 is an α-synuclein-dependent mitochondrial protein that regulates synaptic morphologyInês S Amorim, Laura C Graham, Roderick N Carter, et al.
American Journal of Human Genetics|June 2, 2009
The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1Dan Hanson, Philip G Murray, Amit Sud, et al.
Emerging Infectious Diseases|September 29, 2012
Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countriesAbigail B Diack, Diane Ritchie, Matthew Bishop, et al.
Cancer|June 3, 2015
Health-related quality-of-life results from PALETTE: A randomized, double-blind, phase 3 trial of pazopanib versus placebo in patients with soft tissue sarcoma whose disease has progressed during or after prior chemotherapy-a European Organization for research and treatment of cancer soft tissue and bone sarcoma group global network study (EORTC 62072)Corneel Coens, Winette T A van der Graaf, Jean-Yves Blay, et al.
Plos One|August 23, 2011
All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJDSandra McCutcheon, Anthony Richard Alejo Blanco, E Fiona Houston, et al.
Human Molecular Genetics|March 18, 2005
RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosminX Shu, A M Fry, B Tulloch, et al.
American Journal of Human Genetics|August 2, 2007
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosumElena Boland, Jill Clayton-Smith, Victoria G Woo, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 10, 2011
Childhood-onset autosomal recessive bestrophinopathyArundhati Dev Borman, Alice E Davidson, James O'Sullivan, et al.
Cell Death and Differentiation|July 12, 2008
Yes-associated protein (YAP) functions as a tumor suppressor in breastM Yuan, V Tomlinson, R Lara, et al.
Pageof 18