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A Pierce

Showing results (781-790 of 808) with videos related to

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American Journal of Human Genetics|May 11, 2020
Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant CiliopathyBenjamin Cogné, Xenia Latypova, Lokuliyanage Dona Samudita Senaratne, et al.
Nature Genetics|July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosisMarni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, et al.
Nature Medicine|March 15, 2016
Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1Jean-Sébastien Joyal, Ye Sun, Marin L Gantner, et al.
Cell|July 1, 2017
Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct MechanismsVictor Rusu, Eitan Hoch, Josep M Mercader, et al.
American Journal of Hematology|December 2, 2020
Venetoclax with decitabine vs intensive chemotherapy in acute myeloid leukemia: A propensity score matched analysis stratified by risk of treatment-related mortalityAbhishek Maiti, Wei Qiao, Koji Sasaki, et al.
The New England Journal of Medicine|April 29, 2008
Safety and efficacy of gene transfer for Leber's congenital amaurosisAlbert M Maguire, Francesca Simonelli, Eric A Pierce, et al.
Cell|September 20, 2016
Inhibition of Dihydroorotate Dehydrogenase Overcomes Differentiation Blockade in Acute Myeloid LeukemiaDavid B Sykes, Youmna S Kfoury, François E Mercier, et al.
Lancet (London, England)|October 27, 2009
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trialAlbert M Maguire, Katherine A High, Alberto Auricchio, et al.
Development (Cambridge, England)|October 6, 2016
Mapping a multiplexed zoo of mRNA expressionHarry M T Choi, Colby R Calvert, Naeem Husain, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed casesSarah L Stenton, Kristen Laricchia, Nicole J Lake, et al.
Pageof 81

Showing results (781-790 of 808) with videos related to

Sort By:
Pageof 81
American Journal of Human Genetics|May 11, 2020
Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant CiliopathyBenjamin Cogné, Xenia Latypova, Lokuliyanage Dona Samudita Senaratne, et al.
Nature Genetics|July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosisMarni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, et al.
Nature Medicine|March 15, 2016
Retinal lipid and glucose metabolism dictates angiogenesis through the lipid sensor Ffar1Jean-Sébastien Joyal, Ye Sun, Marin L Gantner, et al.
Cell|July 1, 2017
Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct MechanismsVictor Rusu, Eitan Hoch, Josep M Mercader, et al.
American Journal of Hematology|December 2, 2020
Venetoclax with decitabine vs intensive chemotherapy in acute myeloid leukemia: A propensity score matched analysis stratified by risk of treatment-related mortalityAbhishek Maiti, Wei Qiao, Koji Sasaki, et al.
The New England Journal of Medicine|April 29, 2008
Safety and efficacy of gene transfer for Leber's congenital amaurosisAlbert M Maguire, Francesca Simonelli, Eric A Pierce, et al.
Cell|September 20, 2016
Inhibition of Dihydroorotate Dehydrogenase Overcomes Differentiation Blockade in Acute Myeloid LeukemiaDavid B Sykes, Youmna S Kfoury, François E Mercier, et al.
Lancet (London, England)|October 27, 2009
Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trialAlbert M Maguire, Katherine A High, Alberto Auricchio, et al.
Development (Cambridge, England)|October 6, 2016
Mapping a multiplexed zoo of mRNA expressionHarry M T Choi, Colby R Calvert, Naeem Husain, et al.
Medrxiv : the Preprint Server for Health Sciences|January 7, 2025
Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed casesSarah L Stenton, Kristen Laricchia, Nicole J Lake, et al.
Pageof 81