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

M Vidaud

Showing results (101-110 of 135) with videos related to

Pageof 14
Sort By:
Cancer Research|September 1, 1995
Expression of human chorionic gonadotropin beta subunit genes in superficial and invasive bladder carcinomasV Lazar, S G Diez, A Laurent, et al.
Cancer Letters|November 2, 2001
ERBB2 status and benefit from adjuvant tamoxifen in ERalpha-positive postmenopausal breast carcinomaI Bièche, P Onody, F Lerebours, et al.
Human Genetics|September 1, 1990
Frequency of the cystic fibrosis delta F508 mutation in a large sample of the French populationM Vidaud, C Ferec, O Attree, et al.
Cancer Research|February 1, 1997
Malignant transformation of nontrophoblastic cells is associated with the expression of chorionic gonadotropin beta genes normally transcribed in trophoblastic cellsD Bellet, V Lazar, I Bièche, et al.
Blood|August 15, 2000
Somatic mosaicism and compound heterozygosity in female hemophilia BJ M Costa, D Vidaud, I Laurendeau, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX geneD Vidaud, M Vidaud, B R Bahnak, et al.
Human Mutation|January 1, 1992
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresisS Gandrille, M Vidaud, M Aiach, et al.
British Journal of Haematology|December 1, 1988
Identification of a CpG mutation in the coagulation factor-IX gene by analysis of amplified DNA sequencesV Siguret, S Amselem, M Vidaud, et al.
Leukemia|February 1, 1990
Frequent detection of minimal residual disease by use of the polymerase chain reaction in long-term survivors after bone marrow transplantation for chronic myeloid leukemiaJ M Pignon, T Henni, S Amselem, et al.
Hepatology (Baltimore, Md.)|October 5, 2001
High glucose and hyperinsulinemia stimulate connective tissue growth factor expression: a potential mechanism involved in progression to fibrosis in nonalcoholic steatohepatitisV Paradis, G Perlemuter, F Bonvoust, et al.
Pageof 14

Showing results (101-110 of 135) with videos related to

Sort By:
Pageof 14
Cancer Research|September 1, 1995
Expression of human chorionic gonadotropin beta subunit genes in superficial and invasive bladder carcinomasV Lazar, S G Diez, A Laurent, et al.
Cancer Letters|November 2, 2001
ERBB2 status and benefit from adjuvant tamoxifen in ERalpha-positive postmenopausal breast carcinomaI Bièche, P Onody, F Lerebours, et al.
Human Genetics|September 1, 1990
Frequency of the cystic fibrosis delta F508 mutation in a large sample of the French populationM Vidaud, C Ferec, O Attree, et al.
Cancer Research|February 1, 1997
Malignant transformation of nontrophoblastic cells is associated with the expression of chorionic gonadotropin beta genes normally transcribed in trophoblastic cellsD Bellet, V Lazar, I Bièche, et al.
Blood|August 15, 2000
Somatic mosaicism and compound heterozygosity in female hemophilia BJ M Costa, D Vidaud, I Laurendeau, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX geneD Vidaud, M Vidaud, B R Bahnak, et al.
Human Mutation|January 1, 1992
Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresisS Gandrille, M Vidaud, M Aiach, et al.
British Journal of Haematology|December 1, 1988
Identification of a CpG mutation in the coagulation factor-IX gene by analysis of amplified DNA sequencesV Siguret, S Amselem, M Vidaud, et al.
Leukemia|February 1, 1990
Frequent detection of minimal residual disease by use of the polymerase chain reaction in long-term survivors after bone marrow transplantation for chronic myeloid leukemiaJ M Pignon, T Henni, S Amselem, et al.
Hepatology (Baltimore, Md.)|October 5, 2001
High glucose and hyperinsulinemia stimulate connective tissue growth factor expression: a potential mechanism involved in progression to fibrosis in nonalcoholic steatohepatitisV Paradis, G Perlemuter, F Bonvoust, et al.
Pageof 14