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R A Sturm

Showing results (31-40 of 64) with videos related to

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American Journal of Human Genetics|November 5, 1997
Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 geneP Manga, J G Kromberg, N F Box, et al.
Journal of Molecular Evolution|May 1, 1994
The marsupial MHC: the tammar wallaby, Macropus eugenii, contains an expressed DNA-like gene on chromosome 1R W Slade, P T Hale, D I Francis, et al.
Human Molecular Genetics|September 25, 1997
Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hairN F Box, J R Wyeth, L E O'Gorman, et al.
The Journal of Investigative Dermatology|January 5, 2000
Inhibition of melanin synthesis by cystamine in human melanoma cellsL Qiu, M Zhang, R A Sturm, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 1, 1997
A gel mobility shift assay for probing the effect of drug-DNA adducts on DNA-binding proteinsS M Cutts, A Masta, C Panousis, et al.
Pigment Cell Research|August 1, 1994
Expression studies of pigmentation and POU-domain genes in human melanoma cellsR A Sturm, B J O'Sullivan, J A Thomson, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 16, 2011
Osteopontin expression in plasma of melanoma patients and in melanocytic tumoursT Maier, R P Laubender, R A Sturm, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 13, 2013
'Eruptive' amelanotic compound nevi in children with facial freckles and pale skin colour: more than an occasion?I Zalaudek, E Moscarella, R A Sturm, et al.
Oncogene|September 19, 1996
Inhibition of retinoblastoma protein translation by UVB in human melanocytic cells and reduced cell cycle arrest following repeated irradiationJ Pedley, E M Ablett, A Pettit, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 4, 2015
Lack of protection from development of multiple melanomas by an injected melanocortin analogue in a combined high-risk MC1R/CDKN2A genotype patientM Böhm, K Jagirdar, R A Sturm, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|November 5, 1997
Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 geneP Manga, J G Kromberg, N F Box, et al.
Journal of Molecular Evolution|May 1, 1994
The marsupial MHC: the tammar wallaby, Macropus eugenii, contains an expressed DNA-like gene on chromosome 1R W Slade, P T Hale, D I Francis, et al.
Human Molecular Genetics|September 25, 1997
Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hairN F Box, J R Wyeth, L E O'Gorman, et al.
The Journal of Investigative Dermatology|January 5, 2000
Inhibition of melanin synthesis by cystamine in human melanoma cellsL Qiu, M Zhang, R A Sturm, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 1, 1997
A gel mobility shift assay for probing the effect of drug-DNA adducts on DNA-binding proteinsS M Cutts, A Masta, C Panousis, et al.
Pigment Cell Research|August 1, 1994
Expression studies of pigmentation and POU-domain genes in human melanoma cellsR A Sturm, B J O'Sullivan, J A Thomson, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|August 16, 2011
Osteopontin expression in plasma of melanoma patients and in melanocytic tumoursT Maier, R P Laubender, R A Sturm, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 13, 2013
'Eruptive' amelanotic compound nevi in children with facial freckles and pale skin colour: more than an occasion?I Zalaudek, E Moscarella, R A Sturm, et al.
Oncogene|September 19, 1996
Inhibition of retinoblastoma protein translation by UVB in human melanocytic cells and reduced cell cycle arrest following repeated irradiationJ Pedley, E M Ablett, A Pettit, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 4, 2015
Lack of protection from development of multiple melanomas by an injected melanocortin analogue in a combined high-risk MC1R/CDKN2A genotype patientM Böhm, K Jagirdar, R A Sturm, et al.
Pageof 7