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M Genuardi

Showing results (51-60 of 101) with videos related to

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Annals of Oncology : Official Journal of the European Society for Medical Oncology|August 4, 2001
Familial microsatellite-stable non-polyposis colorectal cancer: incidence and characteristics in a clinic-based populationV Rovella, S Carrara, S C Crucitti, et al.
Clinical Genetics|February 1, 2005
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancerE Lucci-Cordisco, M Zollino, S Baglioni, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studiesM Genuardi, C Tozzi, M G Pomponi, et al.
Clinical Genetics|January 1, 1995
Dicentric chromosome Y associated with Leydig cell agenesis and sex reversalM Genuardi, B Bardoni, G Floridia, et al.
American Journal of Medical Genetics|February 13, 1995
Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defectG Sorge, S Ardito, M Genuardi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1A Bellacosa, L Cicchillitti, F Schepis, et al.
The Journal of Biological Chemistry|August 10, 2000
Biphasic kinetics of the human DNA repair protein MED1 (MBD4), a mismatch-specific DNA N-glycosylaseF Petronzelli, A Riccio, G D Markham, et al.
ESMO Open|November 10, 2022
Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral centerL Poliani, L Greco, M Barile, et al.
ESMO Open|June 4, 2023
Corrigendum to "Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral center": [ESMO Open 7 (2022) 100607]L Poliani, L Greco, M Barile, et al.
Journal of Cellular Physiology|October 31, 2000
Investigation of the substrate spectrum of the human mismatch-specific DNA N-glycosylase MED1 (MBD4): fundamental role of the catalytic domainF Petronzelli, A Riccio, G D Markham, et al.
Pageof 11

Showing results (51-60 of 101) with videos related to

Sort By:
Pageof 11
Annals of Oncology : Official Journal of the European Society for Medical Oncology|August 4, 2001
Familial microsatellite-stable non-polyposis colorectal cancer: incidence and characteristics in a clinic-based populationV Rovella, S Carrara, S C Crucitti, et al.
Clinical Genetics|February 1, 2005
A novel microdeletion syndrome with loss of the MSH2 locus and hereditary non-polyposis colorectal cancerE Lucci-Cordisco, M Zollino, S Baglioni, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studiesM Genuardi, C Tozzi, M G Pomponi, et al.
Clinical Genetics|January 1, 1995
Dicentric chromosome Y associated with Leydig cell agenesis and sex reversalM Genuardi, B Bardoni, G Floridia, et al.
American Journal of Medical Genetics|February 13, 1995
Proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H): a model of a developmental field defectG Sorge, S Ardito, M Genuardi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1A Bellacosa, L Cicchillitti, F Schepis, et al.
The Journal of Biological Chemistry|August 10, 2000
Biphasic kinetics of the human DNA repair protein MED1 (MBD4), a mismatch-specific DNA N-glycosylaseF Petronzelli, A Riccio, G D Markham, et al.
ESMO Open|November 10, 2022
Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral centerL Poliani, L Greco, M Barile, et al.
ESMO Open|June 4, 2023
Corrigendum to "Canonical and uncanonical pathogenic germline variants in colorectal cancer patients by next-generation sequencing in a European referral center": [ESMO Open 7 (2022) 100607]L Poliani, L Greco, M Barile, et al.
Journal of Cellular Physiology|October 31, 2000
Investigation of the substrate spectrum of the human mismatch-specific DNA N-glycosylase MED1 (MBD4): fundamental role of the catalytic domainF Petronzelli, A Riccio, G D Markham, et al.
Pageof 11