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K Hayward

Showing results (61-70 of 394) with videos related to

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Human Genetics|June 1, 1988
Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndromeM H Little, D B Thomson, N K Hayward, et al.
Molecular Medicine (Cambridge, Mass.)|January 1, 1997
The CDKN2A (p16) gene and human cancerW D Foulkes, T Y Flanders, P M Pollock, et al.
Genetical Research|October 1, 1989
Origin of rare Ha-ras alleles: relationship of VTR length to a 5' polymorphic Xho I siteG D Baxter, N K Hayward, R J Collins, et al.
Melanoma Management|September 8, 2018
Advantages of whole-genome sequencing for identification of tumor etiology and clinically actionable genomic aberrations: lessons from the Australian Melanoma Genome ProjectJames S Wilmott, Nicholas K Hayward, Graham J Mann, et al.
Pigment Cell & Melanoma Research|November 29, 2014
Genetics of familial melanoma: 20 years after CDKN2ALauren G Aoude, Karin A W Wadt, Antonia L Pritchard, et al.
Oncogene|August 17, 1995
Evidence for u.v. induction of CDKN2 mutations in melanoma cell linesP M Pollock, F Yu, L Qiu, et al.
The Journal of Investigative Dermatology|July 3, 2009
The association between MC1R genotype and BRAF mutation status in cutaneous melanoma: findings from an Australian populationElke Hacker, Nicholas K Hayward, Troy Dumenil, et al.
Journal of the National Cancer Institute|November 5, 1997
Germline CDKN2A mutations in childhood melanomaD C Whiteman, A Milligan, J Welch, et al.
Pigment Cell & Melanoma Research|November 23, 2012
Prevalence of germline BAP1 mutation in a population-based sample of uveal melanoma casesLauren G Aoude, Claire M Vajdic, Anne Kricker, et al.
Human Genetics|November 1, 1989
TaqI polymorphism within the c-Ha-ras-1 VTR is associated with melanomaN K Hayward, D J Nancarrow, P G Parsons, et al.
Pageof 40

Showing results (61-70 of 394) with videos related to

Sort By:
Pageof 40
Human Genetics|June 1, 1988
Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndromeM H Little, D B Thomson, N K Hayward, et al.
Molecular Medicine (Cambridge, Mass.)|January 1, 1997
The CDKN2A (p16) gene and human cancerW D Foulkes, T Y Flanders, P M Pollock, et al.
Genetical Research|October 1, 1989
Origin of rare Ha-ras alleles: relationship of VTR length to a 5' polymorphic Xho I siteG D Baxter, N K Hayward, R J Collins, et al.
Melanoma Management|September 8, 2018
Advantages of whole-genome sequencing for identification of tumor etiology and clinically actionable genomic aberrations: lessons from the Australian Melanoma Genome ProjectJames S Wilmott, Nicholas K Hayward, Graham J Mann, et al.
Pigment Cell & Melanoma Research|November 29, 2014
Genetics of familial melanoma: 20 years after CDKN2ALauren G Aoude, Karin A W Wadt, Antonia L Pritchard, et al.
Oncogene|August 17, 1995
Evidence for u.v. induction of CDKN2 mutations in melanoma cell linesP M Pollock, F Yu, L Qiu, et al.
The Journal of Investigative Dermatology|July 3, 2009
The association between MC1R genotype and BRAF mutation status in cutaneous melanoma: findings from an Australian populationElke Hacker, Nicholas K Hayward, Troy Dumenil, et al.
Journal of the National Cancer Institute|November 5, 1997
Germline CDKN2A mutations in childhood melanomaD C Whiteman, A Milligan, J Welch, et al.
Pigment Cell & Melanoma Research|November 23, 2012
Prevalence of germline BAP1 mutation in a population-based sample of uveal melanoma casesLauren G Aoude, Claire M Vajdic, Anne Kricker, et al.
Human Genetics|November 1, 1989
TaqI polymorphism within the c-Ha-ras-1 VTR is associated with melanomaN K Hayward, D J Nancarrow, P G Parsons, et al.
Pageof 40