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

R Toro

Showing results (71-80 of 98) with videos related to

Pageof 10
Sort By:
Journal of Medical Genetics|February 1, 2008
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reportsJ R Toro, M-H Wei, G M Glenn, et al.
The Review of Scientific Instruments|January 3, 2024
A versatile pressure-cell design for studying ultrafast molecular-dynamics in supercritical fluids using coherent multi-pulse x-ray scatteringPriyanka Muhunthan, Haoyuan Li, Guillaume Vignat, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 6, 2007
Family history and the risk of kidney cancer: a multicenter case-control study in Central EuropeRayjean J Hung, Lee Moore, Paolo Boffetta, et al.
Blood|March 14, 2007
Abnormal microRNA-16 locus with synteny to human 13q14 linked to CLL in NZB miceElizabeth S Raveche, Erica Salerno, Brian J Scaglione, et al.
American Journal of Respiratory and Critical Care Medicine|February 27, 2007
Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with Birt-Hogg-Dubé syndromeJorge R Toro, Stephen E Pautler, Laveta Stewart, et al.
Neuroimage|August 10, 2014
Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrificationD Germanaud, J Lefèvre, C Fischer, et al.
Journal of Medical Genetics|June 7, 2005
Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancerM-H Wei, O Toure, G M Glenn, et al.
Antimicrobial Agents and Chemotherapy|November 4, 2015
Analysis of the Structure and Function of FOX-4 CephamycinaseS T Lefurgy, V N Malashkevich, J T Aguilan, et al.
American Journal of Human Genetics|September 5, 2001
Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2L S Schmidt, M B Warren, M L Nickerson, et al.
American Journal of Human Genetics|April 27, 2005
Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndromeLaura S Schmidt, Michael L Nickerson, Michelle B Warren, et al.
Pageof 10

Showing results (71-80 of 98) with videos related to

Sort By:
Pageof 10
Journal of Medical Genetics|February 1, 2008
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reportsJ R Toro, M-H Wei, G M Glenn, et al.
The Review of Scientific Instruments|January 3, 2024
A versatile pressure-cell design for studying ultrafast molecular-dynamics in supercritical fluids using coherent multi-pulse x-ray scatteringPriyanka Muhunthan, Haoyuan Li, Guillaume Vignat, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 6, 2007
Family history and the risk of kidney cancer: a multicenter case-control study in Central EuropeRayjean J Hung, Lee Moore, Paolo Boffetta, et al.
Blood|March 14, 2007
Abnormal microRNA-16 locus with synteny to human 13q14 linked to CLL in NZB miceElizabeth S Raveche, Erica Salerno, Brian J Scaglione, et al.
American Journal of Respiratory and Critical Care Medicine|February 27, 2007
Lung cysts, spontaneous pneumothorax, and genetic associations in 89 families with Birt-Hogg-Dubé syndromeJorge R Toro, Stephen E Pautler, Laveta Stewart, et al.
Neuroimage|August 10, 2014
Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrificationD Germanaud, J Lefèvre, C Fischer, et al.
Journal of Medical Genetics|June 7, 2005
Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancerM-H Wei, O Toure, G M Glenn, et al.
Antimicrobial Agents and Chemotherapy|November 4, 2015
Analysis of the Structure and Function of FOX-4 CephamycinaseS T Lefurgy, V N Malashkevich, J T Aguilan, et al.
American Journal of Human Genetics|September 5, 2001
Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2L S Schmidt, M B Warren, M L Nickerson, et al.
American Journal of Human Genetics|April 27, 2005
Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndromeLaura S Schmidt, Michael L Nickerson, Michelle B Warren, et al.
Pageof 10