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 Pieretti

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

Pageof 3
Sort By:
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|November 9, 2010
Development of a questionnaire to measure quality of life in adolescents with food allergy: the FAQL-teenElena S Resnick, Mariah M Pieretti, Jennifer Maloney, et al.
Human Pathology|April 1, 1995
Hypermethylation at a chromosome 17 "hot spot" is a common event in ovarian cancerM Pieretti, D E Powell, H H Gallion, et al.
Human Pathology|April 1, 1995
Genetic alterations on chromosome 17 distinguish different types of epithelial ovarian tumorsM Pieretti, D E Powell, H H Gallion, et al.
Human Molecular Genetics|September 1, 1992
DNA methylation represses FMR-1 transcription in fragile X syndromeJ S Sutcliffe, D L Nelson, F Zhang, et al.
American Journal of Obstetrics and Gynecology|April 1, 1996
Evidence for a unifocal origin in familial ovarian cancerH H Gallion, A Guarino, P D DePriest, et al.
Cell|August 23, 1991
Absence of expression of the FMR-1 gene in fragile X syndromeM Pieretti, F P Zhang, Y H Fu, et al.
Cell|May 31, 1991
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeA J Verkerk, M Pieretti, J S Sutcliffe, et al.
Gynecologic Oncology|November 11, 1992
Molecular genetic changes in human epithelial ovarian malignanciesH H Gallion, D E Powell, J K Morrow, et al.
Cell|December 30, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradoxY H Fu, D P Kuhl, A Pizzuti, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1991
Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locusD L Nelson, A Ballabio, M F Victoria, et al.
Pageof 3

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

Sort By:
Pageof 3
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|November 9, 2010
Development of a questionnaire to measure quality of life in adolescents with food allergy: the FAQL-teenElena S Resnick, Mariah M Pieretti, Jennifer Maloney, et al.
Human Pathology|April 1, 1995
Hypermethylation at a chromosome 17 "hot spot" is a common event in ovarian cancerM Pieretti, D E Powell, H H Gallion, et al.
Human Pathology|April 1, 1995
Genetic alterations on chromosome 17 distinguish different types of epithelial ovarian tumorsM Pieretti, D E Powell, H H Gallion, et al.
Human Molecular Genetics|September 1, 1992
DNA methylation represses FMR-1 transcription in fragile X syndromeJ S Sutcliffe, D L Nelson, F Zhang, et al.
American Journal of Obstetrics and Gynecology|April 1, 1996
Evidence for a unifocal origin in familial ovarian cancerH H Gallion, A Guarino, P D DePriest, et al.
Cell|August 23, 1991
Absence of expression of the FMR-1 gene in fragile X syndromeM Pieretti, F P Zhang, Y H Fu, et al.
Cell|May 31, 1991
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeA J Verkerk, M Pieretti, J S Sutcliffe, et al.
Gynecologic Oncology|November 11, 1992
Molecular genetic changes in human epithelial ovarian malignanciesH H Gallion, D E Powell, J K Morrow, et al.
Cell|December 30, 1991
Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradoxY H Fu, D P Kuhl, A Pizzuti, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1991
Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locusD L Nelson, A Ballabio, M F Victoria, et al.
Pageof 3