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

Maria Luisa Tenchini

Showing results (1-10 of 33) with videos related to

Pageof 4
Sort By:
RNA (New York, N.Y.)|April 14, 2006
Cryptic splice site usage in exon 7 of the human fibrinogen Bbeta-chain gene is regulated by a naturally silent SF2/ASF binding site within this exonSilvia Spena, Maria Luisa Tenchini, Emanuele Buratti
The International Journal of Biochemistry & Cell Biology|May 19, 2004
Coagulation factor VStefano Duga, Rosanna Asselta, Maria Luisa Tenchini
Journal of Sleep Research|October 11, 2008
Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsyRomina Combi, Luigi Ferini-Strambi, Maria Luisa Tenchini
Sleep Medicine|January 30, 2008
CHRNA2 mutations are rare in the NFLE population: evaluation of a large cohort of Italian patientsRomina Combi, Luigi Ferini-Strambi, Maria Luisa Tenchini
Journal of Neurology|August 19, 2004
Autosomal dominant nocturnal frontal lobe epilepsy--a critical overviewRomina Combi, Leda Dalprà, Maria Luisa Tenchini, et al.
Biochimica Et Biophysica Acta|May 29, 2007
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patientManuela Platé, Rosanna Asselta, Flora Peyvandi, et al.
British Journal of Haematology|September 15, 2007
Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemiaSilvia Spena, Rosanna Asselta, Manuela Platé, et al.
Haematologica|December 7, 2005
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiencyGiulia Soldà, Rosanna Asselta, Rossella Ghiotto, et al.
Blood|October 24, 2002
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sitesSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
Haematologica|December 6, 2006
Coagulation factor V gene analysis in five Indian patients: identification of three novel small deletionsRosanna Asselta, Claudia Dall'Osso, Stefano Duga, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
RNA (New York, N.Y.)|April 14, 2006
Cryptic splice site usage in exon 7 of the human fibrinogen Bbeta-chain gene is regulated by a naturally silent SF2/ASF binding site within this exonSilvia Spena, Maria Luisa Tenchini, Emanuele Buratti
The International Journal of Biochemistry & Cell Biology|May 19, 2004
Coagulation factor VStefano Duga, Rosanna Asselta, Maria Luisa Tenchini
Journal of Sleep Research|October 11, 2008
Compound heterozygosity with dominance in the Corticotropin Releasing Hormone (CRH) promoter in a case of nocturnal frontal lobe epilepsyRomina Combi, Luigi Ferini-Strambi, Maria Luisa Tenchini
Sleep Medicine|January 30, 2008
CHRNA2 mutations are rare in the NFLE population: evaluation of a large cohort of Italian patientsRomina Combi, Luigi Ferini-Strambi, Maria Luisa Tenchini
Journal of Neurology|August 19, 2004
Autosomal dominant nocturnal frontal lobe epilepsy--a critical overviewRomina Combi, Leda Dalprà, Maria Luisa Tenchini, et al.
Biochimica Et Biophysica Acta|May 29, 2007
Molecular characterization of the first missense mutation in the fibrinogen Aalpha-chain gene identified in a compound heterozygous afibrinogenemic patientManuela Platé, Rosanna Asselta, Flora Peyvandi, et al.
British Journal of Haematology|September 15, 2007
Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen gamma-chain gene as a novel mechanism for congenital afibrinogenaemiaSilvia Spena, Rosanna Asselta, Manuela Platé, et al.
Haematologica|December 7, 2005
A type II mutation (Glu117stop), induction of allele-specific mRNA degradation and factor XI deficiencyGiulia Soldà, Rosanna Asselta, Rossella Ghiotto, et al.
Blood|October 24, 2002
Congenital afibrinogenemia: first identification of splicing mutations in the fibrinogen Bbeta-chain gene causing activation of cryptic splice sitesSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
Haematologica|December 6, 2006
Coagulation factor V gene analysis in five Indian patients: identification of three novel small deletionsRosanna Asselta, Claudia Dall'Osso, Stefano Duga, et al.
Pageof 4