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Satu-Leena Sallinen

Showing results (1-10 of 9) with videos related to

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Journal of Neuro-Oncology|August 4, 2005
CHEK2 mutations in primary glioblastomasSatu-Leena Sallinen, Tarja Ikonen, Hannu Haapasalo, et al.
Breast Cancer Research : BCR|March 2, 2011
Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individualsKirsi M Kuusisto, Aleksandra Bebel, Mauno Vihinen, et al.
Cancer Genetics and Cytogenetics|June 18, 2003
Arm-specific multicolor fluorescence in situ hybridization reveals widespread chromosomal instability in glioma cell linesSatu-Leena Sallinen, Pauli Sallinen, Minna Ahlstedt-Soini, et al.
Journal of Neuro-Oncology|May 9, 2009
Detection of human herpesvirus-6 in adult central nervous system tumors: predominance of early and late viral antigens in glial tumorsJohn R Crawford, Maria Rita Santi, Robbie Cornelison, et al.
International Journal of Cancer|July 9, 2004
Absence of KLF6 gene mutations in human astrocytic tumors and cell linesPasi A Koivisto, Xiaohui Zhang, Satu-Leena Sallinen, et al.
International Journal of Cancer|January 29, 2009
Large genomic rearrangements and germline epimutations in Lynch syndromeAnnette Gylling, Maaret Ridanpää, Outi Vierimaa, et al.
Familial Cancer|January 22, 2010
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndromePia Vahteristo, Taru A Koski, Laura Näätsaari, et al.
Brain : a Journal of Neurology|August 16, 2011
Genetic spectrum of hereditary neuropathies with onset in the first year of lifeJonathan Baets, Tine Deconinck, Els De Vriendt, et al.
Human Mutation|November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesisOlivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Journal of Neuro-Oncology|August 4, 2005
CHEK2 mutations in primary glioblastomasSatu-Leena Sallinen, Tarja Ikonen, Hannu Haapasalo, et al.
Breast Cancer Research : BCR|March 2, 2011
Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individualsKirsi M Kuusisto, Aleksandra Bebel, Mauno Vihinen, et al.
Cancer Genetics and Cytogenetics|June 18, 2003
Arm-specific multicolor fluorescence in situ hybridization reveals widespread chromosomal instability in glioma cell linesSatu-Leena Sallinen, Pauli Sallinen, Minna Ahlstedt-Soini, et al.
Journal of Neuro-Oncology|May 9, 2009
Detection of human herpesvirus-6 in adult central nervous system tumors: predominance of early and late viral antigens in glial tumorsJohn R Crawford, Maria Rita Santi, Robbie Cornelison, et al.
International Journal of Cancer|July 9, 2004
Absence of KLF6 gene mutations in human astrocytic tumors and cell linesPasi A Koivisto, Xiaohui Zhang, Satu-Leena Sallinen, et al.
International Journal of Cancer|January 29, 2009
Large genomic rearrangements and germline epimutations in Lynch syndromeAnnette Gylling, Maaret Ridanpää, Outi Vierimaa, et al.
Familial Cancer|January 22, 2010
No evidence for a genetic modifier for renal cell cancer risk in HLRCC syndromePia Vahteristo, Taru A Koski, Laura Näätsaari, et al.
Brain : a Journal of Neurology|August 16, 2011
Genetic spectrum of hereditary neuropathies with onset in the first year of lifeJonathan Baets, Tine Deconinck, Els De Vriendt, et al.
Human Mutation|November 19, 2011
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesisOlivier Gribouval, Vincent Morinière, Audrey Pawtowski, et al.
Pageof 1