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Jeremy A Squire

Showing results (71-80 of 167) with videos related to

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Cancer Genetics and Cytogenetics|February 26, 2008
Complex rearrangement of chromosomes 19, 21, and 22 in Ewing sarcoma involving a novel reciprocal inversion-insertion mechanism of EWS-ERG fusion gene formation: a case analysis and literature reviewGeorges Maire, Christopher W Brown, Jane Bayani, et al.
Neoplasia (New York, N.Y.)|July 6, 2006
Three-color FISH analysis of TMPRSS2/ERG fusions in prostate cancer indicates that genomic microdeletion of chromosome 21 is associated with rearrangementMaisa Yoshimoto, Anthony M Joshua, Susan Chilton-Macneill, et al.
Molecular Syndromology|February 6, 2020
Partial Monosomy 4p and Trisomy 12q due to a t(4;12)(p16.3;q24.31) Familial Translocation in Two CousinsTatiana Mozer Joaquim, Carlos H Paiva Grangeiro, Flávia Gaona de Oliveira Gennaro, et al.
Genes, Chromosomes & Cancer|October 20, 2005
Concordant copy number and transcriptional activity of genes mapping to derivative chromosomes 8 during cellular immortalization in vitroLesa Begley, David Keeney, Ben Beheshti, et al.
Nature Reviews. Urology|February 21, 2018
Clinical implications of PTEN loss in prostate cancerTamara Jamaspishvili, David M Berman, Ashley E Ross, et al.
Human Molecular Genetics|August 18, 2009
The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann regionLouis Lefebvre, Lynn Mar, Aaron Bogutz, et al.
Journal of Clinical Pathology|July 2, 2010
FISH assay development for the detection of p16/CDKN2A deletion in malignant pleural mesotheliomaCatherine T-S Chung, Gilda Da Cunha Santos, David M Hwang, et al.
Genes, Chromosomes & Cancer|November 3, 2011
PTEN genomic deletions that characterize aggressive prostate cancer originate close to segmental duplicationsMaisa Yoshimoto, Olga Ludkovski, Dave DeGrace, et al.
The American Journal of Dermatopathology|November 7, 2014
Composite mantle cell and primary cutaneous anaplastic large cell lymphoma: case report and review of the literatureCharles Leduc, Ivan I P Blandino, Abdulmohsen Alhejaily, et al.
Molecular Oncology|August 31, 2010
Genomic instability and copy-number heterogeneity of chromosome 19q, including the kallikrein locus, in ovarian carcinomasJane Bayani, Paula Marrano, Cassandra Graham, et al.
Pageof 17

Showing results (71-80 of 167) with videos related to

Sort By:
Pageof 17
Cancer Genetics and Cytogenetics|February 26, 2008
Complex rearrangement of chromosomes 19, 21, and 22 in Ewing sarcoma involving a novel reciprocal inversion-insertion mechanism of EWS-ERG fusion gene formation: a case analysis and literature reviewGeorges Maire, Christopher W Brown, Jane Bayani, et al.
Neoplasia (New York, N.Y.)|July 6, 2006
Three-color FISH analysis of TMPRSS2/ERG fusions in prostate cancer indicates that genomic microdeletion of chromosome 21 is associated with rearrangementMaisa Yoshimoto, Anthony M Joshua, Susan Chilton-Macneill, et al.
Molecular Syndromology|February 6, 2020
Partial Monosomy 4p and Trisomy 12q due to a t(4;12)(p16.3;q24.31) Familial Translocation in Two CousinsTatiana Mozer Joaquim, Carlos H Paiva Grangeiro, Flávia Gaona de Oliveira Gennaro, et al.
Genes, Chromosomes & Cancer|October 20, 2005
Concordant copy number and transcriptional activity of genes mapping to derivative chromosomes 8 during cellular immortalization in vitroLesa Begley, David Keeney, Ben Beheshti, et al.
Nature Reviews. Urology|February 21, 2018
Clinical implications of PTEN loss in prostate cancerTamara Jamaspishvili, David M Berman, Ashley E Ross, et al.
Human Molecular Genetics|August 18, 2009
The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann regionLouis Lefebvre, Lynn Mar, Aaron Bogutz, et al.
Journal of Clinical Pathology|July 2, 2010
FISH assay development for the detection of p16/CDKN2A deletion in malignant pleural mesotheliomaCatherine T-S Chung, Gilda Da Cunha Santos, David M Hwang, et al.
Genes, Chromosomes & Cancer|November 3, 2011
PTEN genomic deletions that characterize aggressive prostate cancer originate close to segmental duplicationsMaisa Yoshimoto, Olga Ludkovski, Dave DeGrace, et al.
The American Journal of Dermatopathology|November 7, 2014
Composite mantle cell and primary cutaneous anaplastic large cell lymphoma: case report and review of the literatureCharles Leduc, Ivan I P Blandino, Abdulmohsen Alhejaily, et al.
Molecular Oncology|August 31, 2010
Genomic instability and copy-number heterogeneity of chromosome 19q, including the kallikrein locus, in ovarian carcinomasJane Bayani, Paula Marrano, Cassandra Graham, et al.
Pageof 17