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Laura Cremonesi

Showing results (51-60 of 65) with videos related to

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Blood|November 7, 2007
Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disordersDaniela Pietra, Sai Li, Angela Brisci, et al.
Human Mutation|January 6, 2006
Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolismFrancesca Ferrari, Barbara Foglieni, Paolo Arosio, et al.
Haematologica|January 14, 2011
Deep sequencing reveals double mutations in cis of MPL exon 10 in myeloproliferative neoplasmsDaniela Pietra, Angela Brisci, Elisa Rumi, et al.
Clinical Chemistry|June 12, 2004
Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variationsStefania Stenirri, Isabella Fermo, Stefania Battistella, et al.
Journal of Medical Genetics|February 26, 2016
COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasmaSilvia Galbiati, Alessandra Monguzzi, Francesco Damin, et al.
British Journal of Haematology|April 3, 2003
Scanning mutations of the 5'UTR regulatory sequence of L-ferritin by denaturing high-performance liquid chromatography: identification of new mutationsLaura Cremonesi, Rita Paroni, Barbara Foglieni, et al.
Journal of Hepatology|August 21, 2008
Clinical, pathological, and molecular correlates in ferroportin disease: a study of two novel mutationsDomenico Girelli, Ivana De Domenico, Claudia Bozzini, et al.
Annals of the New York Academy of Sciences|November 17, 2006
Different approaches for noninvasive prenatal diagnosis of genetic diseases based on PNA-mediated enriched PCRSilvia Galbiati, Gabriella Restagno, Barbara Foglieni, et al.
Clinical Chemistry and Laboratory Medicine|April 9, 2010
Evaluation of a panel of circulating DNA, RNA and protein potential markers for pathologies of pregnancySilvia Galbiati, Vincenza Causarano, Pamela Pinzani, et al.
BMC Genomics|October 10, 2008
Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel PyrosequencerRoberta Bordoni, Raoul Bonnal, Ermanno Rizzi, et al.
Pageof 7

Showing results (51-60 of 65) with videos related to

Sort By:
Pageof 7
Blood|November 7, 2007
Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disordersDaniela Pietra, Sai Li, Angela Brisci, et al.
Human Mutation|January 6, 2006
Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolismFrancesca Ferrari, Barbara Foglieni, Paolo Arosio, et al.
Haematologica|January 14, 2011
Deep sequencing reveals double mutations in cis of MPL exon 10 in myeloproliferative neoplasmsDaniela Pietra, Angela Brisci, Elisa Rumi, et al.
Clinical Chemistry|June 12, 2004
Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variationsStefania Stenirri, Isabella Fermo, Stefania Battistella, et al.
Journal of Medical Genetics|February 26, 2016
COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasmaSilvia Galbiati, Alessandra Monguzzi, Francesco Damin, et al.
British Journal of Haematology|April 3, 2003
Scanning mutations of the 5'UTR regulatory sequence of L-ferritin by denaturing high-performance liquid chromatography: identification of new mutationsLaura Cremonesi, Rita Paroni, Barbara Foglieni, et al.
Journal of Hepatology|August 21, 2008
Clinical, pathological, and molecular correlates in ferroportin disease: a study of two novel mutationsDomenico Girelli, Ivana De Domenico, Claudia Bozzini, et al.
Annals of the New York Academy of Sciences|November 17, 2006
Different approaches for noninvasive prenatal diagnosis of genetic diseases based on PNA-mediated enriched PCRSilvia Galbiati, Gabriella Restagno, Barbara Foglieni, et al.
Clinical Chemistry and Laboratory Medicine|April 9, 2010
Evaluation of a panel of circulating DNA, RNA and protein potential markers for pathologies of pregnancySilvia Galbiati, Vincenza Causarano, Pamela Pinzani, et al.
BMC Genomics|October 10, 2008
Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel PyrosequencerRoberta Bordoni, Raoul Bonnal, Ermanno Rizzi, et al.
Pageof 7