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C Wallace

Showing results (1151-1160 of 1,458) with videos related to

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Nutrients|August 23, 2020
PHAGE-2 Study: Supplemental Bacteriophages Extend <i>Bifidobacterium animalis</i> subsp. <i>lactis</i> BL04 Benefits on Gut Health and Microbiota in Healthy AdultsDiana S Grubb, Scott D Wrigley, Kimberley E Freedman, et al.
Surgical Neurology International|May 12, 2025
Presentation of extranodal NK/T-cell lymphoma as a pituitary mass: A case report and review of the literatureMolly Butler, Christopher Carr, Mehul Mehra, et al.
Oncogene|May 8, 2012
Mitochondrial genome instability resulting from SUV3 haploinsufficiency leads to tumorigenesis and shortened lifespanP-L Chen, C-F Chen, Y Chen, et al.
American Journal of Medical Genetics|June 1, 1994
Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorderJ L Van Hove, S Shanske, F Ciacci, et al.
Annals of Neurology|November 1, 1995
Apolipoprotein E genotype in patients with Alzheimer's disease: implications for the risk of dementia among relativesL A Farrer, L A Cupples, C M van Duijn, et al.
Cell|January 16, 2007
Manipulating the mouse genome to engineer precise functional syntenic replacements with human sequenceHelen A C Wallace, Fatima Marques-Kranc, Melville Richardson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 1999
Sequence-tagged connectors: a sequence approach to mapping and scanning the human genomeG G Mahairas, J C Wallace, K Smith, et al.
Clinical and Translational Science|October 17, 2013
Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndromePuya G Yazdi, Hailing Su, Svetlana Ghimbovschi, et al.
Neurochemical Research|January 10, 2012
Drug resistance in glioblastoma: a mini reviewCatherine P Haar, Preetha Hebbar, Gerald C Wallace, et al.
American Journal of Human Genetics|March 1, 1990
Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineagesT G Schurr, S W Ballinger, Y Y Gan, et al.
Pageof 146

Showing results (1151-1160 of 1,458) with videos related to

Sort By:
Pageof 146
Nutrients|August 23, 2020
PHAGE-2 Study: Supplemental Bacteriophages Extend <i>Bifidobacterium animalis</i> subsp. <i>lactis</i> BL04 Benefits on Gut Health and Microbiota in Healthy AdultsDiana S Grubb, Scott D Wrigley, Kimberley E Freedman, et al.
Surgical Neurology International|May 12, 2025
Presentation of extranodal NK/T-cell lymphoma as a pituitary mass: A case report and review of the literatureMolly Butler, Christopher Carr, Mehul Mehra, et al.
Oncogene|May 8, 2012
Mitochondrial genome instability resulting from SUV3 haploinsufficiency leads to tumorigenesis and shortened lifespanP-L Chen, C-F Chen, Y Chen, et al.
American Journal of Medical Genetics|June 1, 1994
Mitochondrial myopathy with anemia, cardiomyopathy, and lactic acidosis: a distinct late onset mitochondrial disorderJ L Van Hove, S Shanske, F Ciacci, et al.
Annals of Neurology|November 1, 1995
Apolipoprotein E genotype in patients with Alzheimer's disease: implications for the risk of dementia among relativesL A Farrer, L A Cupples, C M van Duijn, et al.
Cell|January 16, 2007
Manipulating the mouse genome to engineer precise functional syntenic replacements with human sequenceHelen A C Wallace, Fatima Marques-Kranc, Melville Richardson, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 1999
Sequence-tagged connectors: a sequence approach to mapping and scanning the human genomeG G Mahairas, J C Wallace, K Smith, et al.
Clinical and Translational Science|October 17, 2013
Differential gene expression reveals mitochondrial dysfunction in an imprinting center deletion mouse model of Prader-Willi syndromePuya G Yazdi, Hailing Su, Svetlana Ghimbovschi, et al.
Neurochemical Research|January 10, 2012
Drug resistance in glioblastoma: a mini reviewCatherine P Haar, Preetha Hebbar, Gerald C Wallace, et al.
American Journal of Human Genetics|March 1, 1990
Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineagesT G Schurr, S W Ballinger, Y Y Gan, et al.
Pageof 146