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Sean D Mooney

Showing results (81-90 of 131) with videos related to

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Molecular Biology of the Cell|October 26, 2012
Tor1 regulates protein solubility in Saccharomyces cerevisiaeTheodore W Peters, Matthew J Rardin, Gregg Czerwieniec, et al.
Bioinformatics (Oxford, England)|September 9, 2017
When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variantsKymberleigh A Pagel, Vikas Pejaver, Guan Ning Lin, et al.
NPJ Digital Medicine|August 14, 2025
Transformer patient embedding using electronic health records enables patient stratification and progression analysisSu Xian, Monika E Grabowska, Iftikhar J Kullo, et al.
Aging Cell|November 23, 2011
Proteomic analysis of age-dependent changes in protein solubility identifies genes that modulate lifespanPedro Reis-Rodrigues, Gregg Czerwieniec, Theodore W Peters, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2013
Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathwaysMatthew J Rardin, John C Newman, Jason M Held, et al.
BMC Pulmonary Medicine|August 9, 2023
Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approachNeha A Sathe, Su Xian, F Linzee Mabrey, et al.
Stem Cell Reports|December 15, 2015
Genomic Analysis Reveals Disruption of Striatal Neuronal Development and Therapeutic Targets in Human Huntington's Disease Neural Stem CellsKaren L Ring, Mahru C An, Ningzhe Zhang, et al.
Stem Cells (Dayton, Ohio)|May 8, 2025
Cerulenin Partially Corrects the Disrupted Developmental Transcriptomic Signature in Huntington's Disease Striatal Medium Spiny NeuronsCarlos Galicia Aguirre, Kizito-Tshitoko Tshilenge, Elena Battistoni, et al.
Nature Communications|November 21, 2020
Inferring the molecular and phenotypic impact of amino acid variants with MutPred2Vikas Pejaver, Jorge Urresti, Jose Lugo-Martinez, et al.
Thescientificworldjournal|December 3, 2013
Medium-chain acyl-CoA deficiency: outlines from newborn screening, in silico predictions, and molecular studiesSerena Catarzi, Anna Caciotti, Janita Thusberg, et al.
Pageof 14

Showing results (81-90 of 131) with videos related to

Sort By:
Pageof 14
Molecular Biology of the Cell|October 26, 2012
Tor1 regulates protein solubility in Saccharomyces cerevisiaeTheodore W Peters, Matthew J Rardin, Gregg Czerwieniec, et al.
Bioinformatics (Oxford, England)|September 9, 2017
When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variantsKymberleigh A Pagel, Vikas Pejaver, Guan Ning Lin, et al.
NPJ Digital Medicine|August 14, 2025
Transformer patient embedding using electronic health records enables patient stratification and progression analysisSu Xian, Monika E Grabowska, Iftikhar J Kullo, et al.
Aging Cell|November 23, 2011
Proteomic analysis of age-dependent changes in protein solubility identifies genes that modulate lifespanPedro Reis-Rodrigues, Gregg Czerwieniec, Theodore W Peters, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2013
Label-free quantitative proteomics of the lysine acetylome in mitochondria identifies substrates of SIRT3 in metabolic pathwaysMatthew J Rardin, John C Newman, Jason M Held, et al.
BMC Pulmonary Medicine|August 9, 2023
Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approachNeha A Sathe, Su Xian, F Linzee Mabrey, et al.
Stem Cell Reports|December 15, 2015
Genomic Analysis Reveals Disruption of Striatal Neuronal Development and Therapeutic Targets in Human Huntington's Disease Neural Stem CellsKaren L Ring, Mahru C An, Ningzhe Zhang, et al.
Stem Cells (Dayton, Ohio)|May 8, 2025
Cerulenin Partially Corrects the Disrupted Developmental Transcriptomic Signature in Huntington's Disease Striatal Medium Spiny NeuronsCarlos Galicia Aguirre, Kizito-Tshitoko Tshilenge, Elena Battistoni, et al.
Nature Communications|November 21, 2020
Inferring the molecular and phenotypic impact of amino acid variants with MutPred2Vikas Pejaver, Jorge Urresti, Jose Lugo-Martinez, et al.
Thescientificworldjournal|December 3, 2013
Medium-chain acyl-CoA deficiency: outlines from newborn screening, in silico predictions, and molecular studiesSerena Catarzi, Anna Caciotti, Janita Thusberg, et al.
Pageof 14