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Nature Communications
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May 19, 2025
Wnt/β-catenin activation by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary basal cell adenoma
Kim 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 melanoma
Aviyah Peri, Erez Greenstein, Michal Alon, et al.
Nature Communications
|
May 29, 2021
Publisher Correction: Accelerating functional gene discovery in osteoarthritis
Natalie 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 rat
Santosh S Atanur, Ana Garcia Diaz, Klio Maratou, et al.
Nature Communications
|
January 21, 2021
Accelerating functional gene discovery in osteoarthritis
Natalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
Nature
|
March 27, 2012
IFITM3 restricts the morbidity and mortality associated with influenza
Aaron R Everitt, Simon Clare, Thomas Pertel, et al.
JAMA Dermatology
|
December 27, 2018
Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma
Kim 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 melanoma
Peter 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 genes
Jacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Nature Genetics
|
April 2, 2014
POT1 loss-of-function variants predispose to familial melanoma
Carla Daniela Robles-Espinoza, Mark Harland, Andrew J Ramsay, et al.
Page
of 61
Search research articles
Search
Showing results (541-550 of 602) with videos related to
Sort By:
Page
of 61
Nature Communications
|
May 19, 2025
Wnt/β-catenin activation by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary basal cell adenoma
Kim 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 melanoma
Aviyah Peri, Erez Greenstein, Michal Alon, et al.
Nature Communications
|
May 29, 2021
Publisher Correction: Accelerating functional gene discovery in osteoarthritis
Natalie 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 rat
Santosh S Atanur, Ana Garcia Diaz, Klio Maratou, et al.
Nature Communications
|
January 21, 2021
Accelerating functional gene discovery in osteoarthritis
Natalie C Butterfield, Katherine F Curry, Julia Steinberg, et al.
Nature
|
March 27, 2012
IFITM3 restricts the morbidity and mortality associated with influenza
Aaron R Everitt, Simon Clare, Thomas Pertel, et al.
JAMA Dermatology
|
December 27, 2018
Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma
Kim 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 melanoma
Peter 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 genes
Jacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Nature Genetics
|
April 2, 2014
POT1 loss-of-function variants predispose to familial melanoma
Carla Daniela Robles-Espinoza, Mark Harland, Andrew J Ramsay, et al.
Page
of 61