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Maria Luisa Tenchini

Showing results (11-20 of 33) with videos related to

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Brain Research Bulletin|July 13, 2004
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsyRomina Combi, Leda Dalprà, Massimo Malcovati, et al.
Haematologica|May 4, 2006
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain geneLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Gene|February 18, 2005
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAsGiulia Soldà, Silvia Boi, Stefano Duga, et al.
European Journal of Human Genetics : EJHG|October 19, 2004
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain geneSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
EMBO Reports|March 4, 2008
Hedgehogs, humans and high-school science. The benefits of involving high-school students in university researchGiulio Pavesi, Antonio Siccardi, Giovanna Viale, et al.
Thrombosis and Haemostasis|March 30, 2007
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defectsLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Haematologica|August 6, 2002
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemiaRosanna Asselta, Silvia Spena, Stefano Duga, et al.
Biochimica Et Biophysica Acta|October 16, 2003
Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain geneSilvia Spena, Rosanna Asselta, Stefano Duga, et al.
Haematologica|April 5, 2008
Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient ItaliansGiorgia Zadra, Rosanna Asselta, Maria Luisa Tenchini, et al.
Blood Cells, Molecules & Diseases|August 5, 2008
Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretionManuela Platè, Rosanna Asselta, Silvia Spena, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Brain Research Bulletin|July 13, 2004
Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsyRomina Combi, Leda Dalprà, Massimo Malcovati, et al.
Haematologica|May 4, 2006
Fibrinogen Mumbai: intracellular retention due to a novel G434D mutation in the Bbeta-chain geneLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Gene|February 18, 2005
In vivo RNA-RNA duplexes from human alpha3 and alpha5 nicotinic receptor subunit mRNAsGiulia Soldà, Silvia Boi, Stefano Duga, et al.
European Journal of Human Genetics : EJHG|October 19, 2004
Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain geneSilvia Spena, Stefano Duga, Rosanna Asselta, et al.
EMBO Reports|March 4, 2008
Hedgehogs, humans and high-school science. The benefits of involving high-school students in university researchGiulio Pavesi, Antonio Siccardi, Giovanna Viale, et al.
Thrombosis and Haemostasis|March 30, 2007
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defectsLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
Haematologica|August 6, 2002
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemiaRosanna Asselta, Silvia Spena, Stefano Duga, et al.
Biochimica Et Biophysica Acta|October 16, 2003
Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bbeta-chain geneSilvia Spena, Rosanna Asselta, Stefano Duga, et al.
Haematologica|April 5, 2008
Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient ItaliansGiorgia Zadra, Rosanna Asselta, Maria Luisa Tenchini, et al.
Blood Cells, Molecules & Diseases|August 5, 2008
Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretionManuela Platè, Rosanna Asselta, Silvia Spena, et al.
Pageof 4