Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Tetsuro Noguchi

Showing results (11-20 of 21) with videos related to

Pageof 3
Sort By:
Investigative Ophthalmology & Visual Science|May 4, 2019
Nrf2 Activator RS9 Suppresses Pathological Ocular Angiogenesis and HyperpermeabilityShinsuke Nakamura, Tetsuro Noguchi, Yuki Inoue, et al.
International Journal of Oncology|October 9, 2002
Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cellsEmmanuelle Charafe-Jauffret, Jean-François Moulin, Christophe Ginestier, et al.
Journal of Medical Genetics|August 6, 2010
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAPArnaud Lagarde, Etienne Rouleau, Anthony Ferrari, et al.
Familial Cancer|February 3, 2016
Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosisRenaud Sabatier, Elise Lavit, Jessica Moretta, et al.
Plos One|August 22, 2014
Poly(ADP-ribose) polymerase 1 (PARP1) overexpression in human breast cancer stem cells and resistance to olaparibMarine Gilabert, Simon Launay, Christophe Ginestier, et al.
Inflammatory Bowel Diseases|August 17, 2013
Functional polymorphisms in the regulatory regions of the VNN1 gene are associated with susceptibility to inflammatory bowel diseasesThomas Gensollen, Christophe Bourges, Pascal Rihet, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|April 26, 2013
Prediction of BRCA1 germ-line mutation status in patients with breast cancer using histoprognosis grade, MS110, Lys27H3, vimentin, and KI67Mohamed Hassanein, Laetitia Huiart, Violaine Bourdon, et al.
Bulletin Du Cancer|June 18, 2021
Mutational analysis of apoptotic genes in familial aggregation of hematological malignanciesWalid Sabri Hamadou, Rahma Mani, Nouha Bouali, et al.
Genes, Chromosomes & Cancer|March 17, 2010
Molecular characterization by array comparative genomic hybridization and DNA sequencing of 194 desmoid tumorsSébastien Salas, Frederic Chibon, Tetsuro Noguchi, et al.
American Journal of Human Genetics|October 1, 2021
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approachSandrine M Caputo, Lisa Golmard, Mélanie Léone, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Investigative Ophthalmology & Visual Science|May 4, 2019
Nrf2 Activator RS9 Suppresses Pathological Ocular Angiogenesis and HyperpermeabilityShinsuke Nakamura, Tetsuro Noguchi, Yuki Inoue, et al.
International Journal of Oncology|October 9, 2002
Loss of heterozygosity at microsatellite markers from region p11-21 of chromosome 8 in microdissected breast tumor but not in peritumoral cellsEmmanuelle Charafe-Jauffret, Jean-François Moulin, Christophe Ginestier, et al.
Journal of Medical Genetics|August 6, 2010
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAPArnaud Lagarde, Etienne Rouleau, Anthony Ferrari, et al.
Familial Cancer|February 3, 2016
Ovarian cancer patients at high risk of BRCA mutation: the constitutional genetic characterization does not change prognosisRenaud Sabatier, Elise Lavit, Jessica Moretta, et al.
Plos One|August 22, 2014
Poly(ADP-ribose) polymerase 1 (PARP1) overexpression in human breast cancer stem cells and resistance to olaparibMarine Gilabert, Simon Launay, Christophe Ginestier, et al.
Inflammatory Bowel Diseases|August 17, 2013
Functional polymorphisms in the regulatory regions of the VNN1 gene are associated with susceptibility to inflammatory bowel diseasesThomas Gensollen, Christophe Bourges, Pascal Rihet, et al.
Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|April 26, 2013
Prediction of BRCA1 germ-line mutation status in patients with breast cancer using histoprognosis grade, MS110, Lys27H3, vimentin, and KI67Mohamed Hassanein, Laetitia Huiart, Violaine Bourdon, et al.
Bulletin Du Cancer|June 18, 2021
Mutational analysis of apoptotic genes in familial aggregation of hematological malignanciesWalid Sabri Hamadou, Rahma Mani, Nouha Bouali, et al.
Genes, Chromosomes & Cancer|March 17, 2010
Molecular characterization by array comparative genomic hybridization and DNA sequencing of 194 desmoid tumorsSébastien Salas, Frederic Chibon, Tetsuro Noguchi, et al.
American Journal of Human Genetics|October 1, 2021
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approachSandrine M Caputo, Lisa Golmard, Mélanie Léone, et al.
Pageof 3