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Showing results (451-460 of 480) with videos related to

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Molecular Oncology|April 23, 2009
Gene expression signature associated with BRAF mutations in human primary cutaneous melanomasCaroline Kannengiesser, Alain Spatz, Stefan Michiels, et al.
Archives of Disease in Childhood|January 24, 2006
Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assaysL Pasquier, V Laugel, L Lazaro, et al.
Scientific Reports|January 30, 2020
Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase ηLeticia K Lerner, Thuy V Nguyen, Ligia P Castro, et al.
Human Mutation|December 21, 2012
Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stressDaniela T Soltys, Clarissa R R Rocha, Letícia K Lerner, et al.
DNA Repair|June 27, 2006
Adenovirus mediated transduction of the human DNA polymerase eta cDNAKeronninn Moreno Lima-Bessa, Vanessa Chiganças, Anne Stary, et al.
Lab on a Chip|September 25, 2008
A microarray to measure repair of damaged plasmids by cell lysatesJ-F Millau, A-L Raffin, S Caillat, et al.
Human Mutation|March 5, 2009
Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patientsCaroline Kannengiesser, Sharon Brookes, Anna Gutierrez del Arroyo, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1996
[Xeroderma pigmentosum. A study in 40 Algerian patients]B Bouadjar, F Aït-Belkacem, L Daya-Grosjean, et al.
The Journal of Investigative Dermatology|January 8, 2010
A prevalent mutation with founder effect in xeroderma pigmentosum group C from north AfricaNadem Soufir, Cecile Ged, Agnes Bourillon, et al.
Pigment Cell & Melanoma Research|May 1, 2012
A prognostic signature of defective p53-dependent G1 checkpoint function in melanoma cell linesCraig Carson, Bernard Omolo, Haitao Chu, et al.
Pageof 48

Showing results (451-460 of 480) with videos related to

Sort By:
Pageof 48
Molecular Oncology|April 23, 2009
Gene expression signature associated with BRAF mutations in human primary cutaneous melanomasCaroline Kannengiesser, Alain Spatz, Stefan Michiels, et al.
Archives of Disease in Childhood|January 24, 2006
Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assaysL Pasquier, V Laugel, L Lazaro, et al.
Scientific Reports|January 30, 2020
Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase ηLeticia K Lerner, Thuy V Nguyen, Ligia P Castro, et al.
Human Mutation|December 21, 2012
Novel XPG (ERCC5) mutations affect DNA repair and cell survival after ultraviolet but not oxidative stressDaniela T Soltys, Clarissa R R Rocha, Letícia K Lerner, et al.
DNA Repair|June 27, 2006
Adenovirus mediated transduction of the human DNA polymerase eta cDNAKeronninn Moreno Lima-Bessa, Vanessa Chiganças, Anne Stary, et al.
Lab on a Chip|September 25, 2008
A microarray to measure repair of damaged plasmids by cell lysatesJ-F Millau, A-L Raffin, S Caillat, et al.
Human Mutation|March 5, 2009
Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patientsCaroline Kannengiesser, Sharon Brookes, Anna Gutierrez del Arroyo, et al.
Annales De Dermatologie Et De Venereologie|January 1, 1996
[Xeroderma pigmentosum. A study in 40 Algerian patients]B Bouadjar, F Aït-Belkacem, L Daya-Grosjean, et al.
The Journal of Investigative Dermatology|January 8, 2010
A prevalent mutation with founder effect in xeroderma pigmentosum group C from north AfricaNadem Soufir, Cecile Ged, Agnes Bourillon, et al.
Pigment Cell & Melanoma Research|May 1, 2012
A prognostic signature of defective p53-dependent G1 checkpoint function in melanoma cell linesCraig Carson, Bernard Omolo, Haitao Chu, et al.
Pageof 48