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R Osborne

Showing results (551-560 of 560) with videos related to

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Development (Cambridge, England)|September 13, 2005
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasiaAnn M Flenniken, Lucy R Osborne, Nicole Anderson, et al.
The Medical Journal of Australia|December 14, 2020
Beyond the black stump: rapid reviews of health research issues affecting regional, rural and remote AustraliaSonya R Osborne, Laura V Alston, Kristy A Bolton, et al.
AJNR. American Journal of Neuroradiology|December 1, 2025
Clinical Utility of [F18]-Fluciclovine PET/MRI for Differentiating True Progression from Treatment-Related Changes in Patients with GlioblastomaJana Ivanidze, Kellen Vo Vu, Rongwei Fu, et al.
Nature|November 7, 2008
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genomeTimothy J Ley, Elaine R Mardis, Li Ding, et al.
The New England Journal of Medicine|November 12, 2010
DNMT3A mutations in acute myeloid leukemiaTimothy J Ley, Li Ding, Matthew J Walter, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
Nature|November 6, 2007
Characterizing the cancer genome in lung adenocarcinomaBarbara A Weir, Michele S Woo, Gad Getz, et al.
Nature|October 25, 2008
Somatic mutations affect key pathways in lung adenocarcinomaLi Ding, Gad Getz, David A Wheeler, et al.
Science (New York, N.Y.)|April 12, 2003
Human chromosome 7: DNA sequence and biologyStephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, et al.
Biorxiv : the Preprint Server for Biology|June 26, 2025
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental DisordersJacob Ellegood, Antoine Beauchamp, Yohan Yee, et al.
Pageof 56

Showing results (551-560 of 560) with videos related to

Sort By:
Pageof 56
You have reached the last page of results.This site can display upto 560 results.
Development (Cambridge, England)|September 13, 2005
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasiaAnn M Flenniken, Lucy R Osborne, Nicole Anderson, et al.
The Medical Journal of Australia|December 14, 2020
Beyond the black stump: rapid reviews of health research issues affecting regional, rural and remote AustraliaSonya R Osborne, Laura V Alston, Kristy A Bolton, et al.
AJNR. American Journal of Neuroradiology|December 1, 2025
Clinical Utility of [F18]-Fluciclovine PET/MRI for Differentiating True Progression from Treatment-Related Changes in Patients with GlioblastomaJana Ivanidze, Kellen Vo Vu, Rongwei Fu, et al.
Nature|November 7, 2008
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genomeTimothy J Ley, Elaine R Mardis, Li Ding, et al.
The New England Journal of Medicine|November 12, 2010
DNMT3A mutations in acute myeloid leukemiaTimothy J Ley, Li Ding, Matthew J Walter, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
Nature|November 6, 2007
Characterizing the cancer genome in lung adenocarcinomaBarbara A Weir, Michele S Woo, Gad Getz, et al.
Nature|October 25, 2008
Somatic mutations affect key pathways in lung adenocarcinomaLi Ding, Gad Getz, David A Wheeler, et al.
Science (New York, N.Y.)|April 12, 2003
Human chromosome 7: DNA sequence and biologyStephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, et al.
Biorxiv : the Preprint Server for Biology|June 26, 2025
Assigning Targetable Molecular Pathways to Transdiagnostic Subgroups Across Autism and Related Neurodevelopmental DisordersJacob Ellegood, Antoine Beauchamp, Yohan Yee, et al.
Pageof 56