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Florence Demenais

Showing results (71-80 of 97) with videos related to

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Nature Communications|June 3, 2020
Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanomaJiyeon Choi, Tongwu Zhang, Andrew Vu, et al.
Genome Biology|March 12, 2017
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenomeWarren A Cheung, Xiaojian Shao, Andréanne Morin, et al.
Genome Biology|May 9, 2019
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenomeWarren A Cheung, Xiaojian Shao, Andréanne Morin, et al.
The Journal of Allergy and Clinical Immunology|March 20, 2012
Genome-wide association study of lung function decline in adults with and without asthmaMedea Imboden, Emmanuelle Bouzigon, Ivan Curjuric, et al.
Journal of Medical Genetics|August 15, 2006
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continentsAlisa M Goldstein, May Chan, Mark Harland, et al.
Nature Genetics|May 20, 2008
Common sequence variants on 20q11.22 confer melanoma susceptibilityKevin M Brown, Stuart Macgregor, Grant W Montgomery, et al.
Journal of the American Academy of Dermatology|February 8, 2019
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICTNicholas J Taylor, Nandita Mitra, Lu Qian, et al.
Cancer Research|October 19, 2006
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMELAlisa M Goldstein, May Chan, Mark Harland, et al.
International Journal of Cancer|August 1, 2014
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regionsJennifer H Barrett, John C Taylor, Chloe Bright, et al.
The Journal of Investigative Dermatology|August 24, 2017
Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma FamiliesNicholas J Taylor, Nandita Mitra, Alisa M Goldstein, et al.
Pageof 10

Showing results (71-80 of 97) with videos related to

Sort By:
Pageof 10
Nature Communications|June 3, 2020
Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanomaJiyeon Choi, Tongwu Zhang, Andrew Vu, et al.
Genome Biology|March 12, 2017
Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenomeWarren A Cheung, Xiaojian Shao, Andréanne Morin, et al.
Genome Biology|May 9, 2019
Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenomeWarren A Cheung, Xiaojian Shao, Andréanne Morin, et al.
The Journal of Allergy and Clinical Immunology|March 20, 2012
Genome-wide association study of lung function decline in adults with and without asthmaMedea Imboden, Emmanuelle Bouzigon, Ivan Curjuric, et al.
Journal of Medical Genetics|August 15, 2006
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continentsAlisa M Goldstein, May Chan, Mark Harland, et al.
Nature Genetics|May 20, 2008
Common sequence variants on 20q11.22 confer melanoma susceptibilityKevin M Brown, Stuart Macgregor, Grant W Montgomery, et al.
Journal of the American Academy of Dermatology|February 8, 2019
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICTNicholas J Taylor, Nandita Mitra, Lu Qian, et al.
Cancer Research|October 19, 2006
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMELAlisa M Goldstein, May Chan, Mark Harland, et al.
International Journal of Cancer|August 1, 2014
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regionsJennifer H Barrett, John C Taylor, Chloe Bright, et al.
The Journal of Investigative Dermatology|August 24, 2017
Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma FamiliesNicholas J Taylor, Nandita Mitra, Alisa M Goldstein, et al.
Pageof 10