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Kyle M Walsh

Showing results (111-120 of 154) with videos related to

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Science (New York, N.Y.)|May 16, 2015
Cancer. The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancerRobert J A Bell, H Tomas Rube, Alex Kreig, et al.
Aging Cell|June 6, 2022
Accelerated epigenetic aging in newborns with Down syndromeKeren Xu, Shaobo Li, Ivo S Muskens, et al.
Cancer Research|November 5, 2016
Mutant IDH1 Expression Drives TERT Promoter Reactivation as Part of the Cellular Transformation ProcessShigeo Ohba, Joydeep Mukherjee, Tor-Christian Johannessen, et al.
Neuro-Oncology|February 22, 2023
Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locusJon Foss-Skiftesvik, Shaobo Li, Adam Rosenbaum, et al.
Endocrine-Related Cancer|December 9, 2010
A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileumKyle M Walsh, Murim Choi, Kjell Oberg, et al.
Genes, Chromosomes & Cancer|May 19, 2019
Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in childrenAdam J de Smith, Geneviève Lavoie, Kyle M Walsh, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 15, 2023
The Enduring Effects of COVID for Cancer Care: Learning from Real-Life Clinical PracticeAlex Broom, Leah Williams Veazey, Katherine Kenny, et al.
Cancer Epidemiology|June 13, 2024
Genetic variation near GRB10 associated with bone growth and osteosarcoma risk in canine and human populationsSydney E Lucas, Tianzhong Yang, Courtney E Wimberly, et al.
Frontiers in Genetics|October 24, 2012
Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approachDaniel I Jacobs, Kyle M Walsh, Margaret Wrensch, et al.
Cancer Research|November 4, 2015
A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal EvolutionKyle M Walsh, Adam J de Smith, Helen M Hansen, et al.
Pageof 16

Showing results (111-120 of 154) with videos related to

Sort By:
Pageof 16
Science (New York, N.Y.)|May 16, 2015
Cancer. The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancerRobert J A Bell, H Tomas Rube, Alex Kreig, et al.
Aging Cell|June 6, 2022
Accelerated epigenetic aging in newborns with Down syndromeKeren Xu, Shaobo Li, Ivo S Muskens, et al.
Cancer Research|November 5, 2016
Mutant IDH1 Expression Drives TERT Promoter Reactivation as Part of the Cellular Transformation ProcessShigeo Ohba, Joydeep Mukherjee, Tor-Christian Johannessen, et al.
Neuro-Oncology|February 22, 2023
Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locusJon Foss-Skiftesvik, Shaobo Li, Adam Rosenbaum, et al.
Endocrine-Related Cancer|December 9, 2010
A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileumKyle M Walsh, Murim Choi, Kjell Oberg, et al.
Genes, Chromosomes & Cancer|May 19, 2019
Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in childrenAdam J de Smith, Geneviève Lavoie, Kyle M Walsh, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 15, 2023
The Enduring Effects of COVID for Cancer Care: Learning from Real-Life Clinical PracticeAlex Broom, Leah Williams Veazey, Katherine Kenny, et al.
Cancer Epidemiology|June 13, 2024
Genetic variation near GRB10 associated with bone growth and osteosarcoma risk in canine and human populationsSydney E Lucas, Tianzhong Yang, Courtney E Wimberly, et al.
Frontiers in Genetics|October 24, 2012
Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approachDaniel I Jacobs, Kyle M Walsh, Margaret Wrensch, et al.
Cancer Research|November 4, 2015
A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal EvolutionKyle M Walsh, Adam J de Smith, Helen M Hansen, et al.
Pageof 16