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David J Adams

Showing results (541-550 of 602) with videos related to

Pageof 61
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Nature Communications|May 19, 2025
Wnt/β-catenin activation by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary basal cell adenomaKim Wong, Justin A Bishop, Ilan Weinreb, et al.
The Journal of Clinical Investigation|October 15, 2021
Combined presentation and immunogenicity analysis reveals a recurrent RAS.Q61K neoantigen in melanomaAviyah Peri, Erez Greenstein, Michal Alon, et al.
Nature Communications|May 29, 2021
Publisher Correction: Accelerating functional gene discovery in osteoarthritisNatalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
Cell|July 30, 2013
Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory ratSantosh S Atanur, Ana Garcia Diaz, Klio Maratou, et al.
Nature Communications|January 21, 2021
Accelerating functional gene discovery in osteoarthritisNatalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
Nature|March 27, 2012
IFITM3 restricts the morbidity and mortality associated with influenzaAaron R Everitt, Simon Clare, Thomas Pertel, et al.
JAMA Dermatology|December 27, 2018
Association of the POT1 Germline Missense Variant p.I78T With Familial MelanomaKim Wong, Carla Daniela Robles-Espinoza, David Rodriguez, et al.
Medrxiv : the Preprint Server for Health Sciences|July 2, 2026
Large distant deletion disrupts CDKN2A enhancer and predisposes to melanomaPeter A Johansson, Kelly Brooks, Jane M Palmer, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Nature Genetics|April 2, 2014
POT1 loss-of-function variants predispose to familial melanomaCarla Daniela Robles-Espinoza, Mark Harland, Andrew J Ramsay, et al.
Pageof 61

Showing results (541-550 of 602) with videos related to

Sort By:
Pageof 61
Nature Communications|May 19, 2025
Wnt/β-catenin activation by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary basal cell adenomaKim Wong, Justin A Bishop, Ilan Weinreb, et al.
The Journal of Clinical Investigation|October 15, 2021
Combined presentation and immunogenicity analysis reveals a recurrent RAS.Q61K neoantigen in melanomaAviyah Peri, Erez Greenstein, Michal Alon, et al.
Nature Communications|May 29, 2021
Publisher Correction: Accelerating functional gene discovery in osteoarthritisNatalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
Cell|July 30, 2013
Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory ratSantosh S Atanur, Ana Garcia Diaz, Klio Maratou, et al.
Nature Communications|January 21, 2021
Accelerating functional gene discovery in osteoarthritisNatalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
Nature|March 27, 2012
IFITM3 restricts the morbidity and mortality associated with influenzaAaron R Everitt, Simon Clare, Thomas Pertel, et al.
JAMA Dermatology|December 27, 2018
Association of the POT1 Germline Missense Variant p.I78T With Familial MelanomaKim Wong, Carla Daniela Robles-Espinoza, David Rodriguez, et al.
Medrxiv : the Preprint Server for Health Sciences|July 2, 2026
Large distant deletion disrupts CDKN2A enhancer and predisposes to melanomaPeter A Johansson, Kelly Brooks, Jane M Palmer, et al.
Cell|July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genesJacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Nature Genetics|April 2, 2014
POT1 loss-of-function variants predispose to familial melanomaCarla Daniela Robles-Espinoza, Mark Harland, Andrew J Ramsay, et al.
Pageof 61