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 Seri

Showing results (51-60 of 73) with videos related to

Pageof 8
Sort By:
Neurogastroenterology and Motility|August 18, 2012
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathwaysC Evangelisti, F Bianco, L M Pradella, et al.
Human Mutation|September 12, 2000
MEFV mutations in Behçet's diseaseI Touitou, X Magne, N Molinari, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2C Lo Nigro, R Cusano, M Scaranari, et al.
International Journal of Molecular Medicine|July 30, 1999
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndromeM Seri, S Melchionda, S Dreyer, et al.
European Journal of Neurology|December 18, 2008
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneityT Pippucci, E Panza, E Pompilii, et al.
Human Immunology|April 21, 1998
Repertoire breadth of human CD4+ T cells specific for HIV gp120 and p66 (primary antigens) or for PPD and tetanus toxoid (secondary antigens)G Li Pira, L Oppezzi, M Seri, et al.
Clinical and Experimental Immunology|May 2, 2002
Preservation of clonal heterogeneity of the Pneumocystis carinii-specific CD4 T cell repertoire in HIV infected, asymptomatic individualsG Li Pira, D Fenoglio, L Bottone, et al.
European Journal of Neurology|December 8, 2009
A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutationsA Brussino, G Vaula, C Cagnoli, et al.
American Journal of Human Genetics|February 11, 1999
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophyM Seri, R Cusano, P Forabosco, et al.
Human Genetics|March 10, 1999
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopmentM Seri, G Martucciello, L Paleari, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Neurogastroenterology and Motility|August 18, 2012
Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathwaysC Evangelisti, F Bianco, L M Pradella, et al.
Human Mutation|September 12, 2000
MEFV mutations in Behçet's diseaseI Touitou, X Magne, N Molinari, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2C Lo Nigro, R Cusano, M Scaranari, et al.
International Journal of Molecular Medicine|July 30, 1999
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndromeM Seri, S Melchionda, S Dreyer, et al.
European Journal of Neurology|December 18, 2008
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneityT Pippucci, E Panza, E Pompilii, et al.
Human Immunology|April 21, 1998
Repertoire breadth of human CD4+ T cells specific for HIV gp120 and p66 (primary antigens) or for PPD and tetanus toxoid (secondary antigens)G Li Pira, L Oppezzi, M Seri, et al.
Clinical and Experimental Immunology|May 2, 2002
Preservation of clonal heterogeneity of the Pneumocystis carinii-specific CD4 T cell repertoire in HIV infected, asymptomatic individualsG Li Pira, D Fenoglio, L Bottone, et al.
European Journal of Neurology|December 8, 2009
A family with autosomal dominant leukodystrophy linked to 5q23.2-q23.3 without lamin B1 mutationsA Brussino, G Vaula, C Cagnoli, et al.
American Journal of Human Genetics|February 11, 1999
Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophyM Seri, R Cusano, P Forabosco, et al.
Human Genetics|March 10, 1999
Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopmentM Seri, G Martucciello, L Paleari, et al.
Pageof 8