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Timothy J Aitman

Showing results (41-50 of 103) with videos related to

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BMC Medical Genomics|April 8, 2020
Absolute measurement of the tissue origins of cell-free DNA in the healthy state and following paracetamol overdoseDanny Laurent, Fiona Semple, Philip J Starkey Lewis, et al.
Plos Genetics|October 24, 2006
Heritability and tissue specificity of expression quantitative trait lociEnrico Petretto, Jonathan Mangion, Nicholas J Dickens, et al.
Cell Reports|September 14, 2017
Changes in the Coding and Non-coding Transcriptome and DNA Methylome that Define the Schwann Cell Repair Phenotype after Nerve InjuryPeter J Arthur-Farraj, Claire C Morgan, Martyna Adamowicz, et al.
British Journal of Haematology|May 31, 2013
Target enrichment and high-throughput sequencing of 80 ribosomal protein genes to identify mutations associated with Diamond-Blackfan anaemiaGareth Gerrard, Mikel Valgañón, Hui En Foong, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 17, 2002
Radiation hybrid mapping of 70 rat genes from a data set of differentially expressed genesCaroline A Wallace, Saira Ali, Anne M Glazier, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemiaEllen R A Thomas, Santosh S Atanur, Penny J Norsworthy, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 18, 2013
The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemiaJana Vandrovcova, Ellen R A Thomas, Santosh S Atanur, et al.
The American Journal of Pathology|March 27, 2012
Genetic susceptibility to experimental autoimmune glomerulonephritis in the Wistar Kyoto ratJohn Reynolds, Paul R Cook, Jacques Behmoaras, et al.
Research Square|January 10, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:
Pageof 11
BMC Medical Genomics|April 8, 2020
Absolute measurement of the tissue origins of cell-free DNA in the healthy state and following paracetamol overdoseDanny Laurent, Fiona Semple, Philip J Starkey Lewis, et al.
Plos Genetics|October 24, 2006
Heritability and tissue specificity of expression quantitative trait lociEnrico Petretto, Jonathan Mangion, Nicholas J Dickens, et al.
Cell Reports|September 14, 2017
Changes in the Coding and Non-coding Transcriptome and DNA Methylome that Define the Schwann Cell Repair Phenotype after Nerve InjuryPeter J Arthur-Farraj, Claire C Morgan, Martyna Adamowicz, et al.
British Journal of Haematology|May 31, 2013
Target enrichment and high-throughput sequencing of 80 ribosomal protein genes to identify mutations associated with Diamond-Blackfan anaemiaGareth Gerrard, Mikel Valgañón, Hui En Foong, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|April 17, 2002
Radiation hybrid mapping of 70 rat genes from a data set of differentially expressed genesCaroline A Wallace, Saira Ali, Anne M Glazier, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemiaEllen R A Thomas, Santosh S Atanur, Penny J Norsworthy, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 18, 2013
The use of next-generation sequencing in clinical diagnosis of familial hypercholesterolemiaJana Vandrovcova, Ellen R A Thomas, Santosh S Atanur, et al.
The American Journal of Pathology|March 27, 2012
Genetic susceptibility to experimental autoimmune glomerulonephritis in the Wistar Kyoto ratJohn Reynolds, Paul R Cook, Jacques Behmoaras, et al.
Research Square|January 10, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
Pageof 11