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Achille Iolascon

Showing results (131-140 of 290) with videos related to

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Human Mutation|February 16, 2005
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlationVeronica Servedio, Maria d'Apolito, Nunzia Maiorano, et al.
BMC Medical Genetics|February 28, 2019
HIF-1 transcription activity: HIF1A driven response in normoxia and in hypoxiaFlora Cimmino, Marianna Avitabile, Vito Alessandro Lasorsa, et al.
Contrast Media & Molecular Imaging|April 28, 2012
Mn-loaded apoferritin: a highly sensitive MRI imaging probe for the detection and characterization of hepatocarcinoma lesions in a transgenic mouse modelSimonetta Geninatti Crich, Juan Carlos Cutrin, Stefania Lanzardo, et al.
Molecular Medicine (Cambridge, Mass.)|March 5, 2010
Galectin-1 and its involvement in hepatocellular carcinoma aggressivenessDaniela Spano, Roberta Russo, Vittorio Di Maso, et al.
American Journal of Hematology|October 14, 2010
Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B geneRoberta Russo, Maria Rosaria Esposito, Roberta Asci, et al.
Light, Science & Applications|September 1, 2018
Tomographic flow cytometry by digital holographyFrancesco Merola, Pasquale Memmolo, Lisa Miccio, et al.
Journal of Nephrology|December 24, 2002
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approachMaddalena Gigante, Fausta Monno, Roberta Roberto, et al.
Blood|March 6, 2002
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibitionSilverio Perrotta, Bruno Nobili, Francesca Rossi, et al.
Analytical Chemistry|May 25, 2018
Label-Free Optical Marker for Red-Blood-Cell Phenotyping of Inherited AnemiasMartina Mugnano, Pasquale Memmolo, Lisa Miccio, et al.
Frontiers in Genetics|November 28, 2022
Clinical exome-based panel testing for medically actionable secondary findings in a cohort of 383 Italian participantsStefania Martone, Autilia Tommasina Buonagura, Roberta Marra, et al.
Pageof 29

Showing results (131-140 of 290) with videos related to

Sort By:
Pageof 29
Human Mutation|February 16, 2005
Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlationVeronica Servedio, Maria d'Apolito, Nunzia Maiorano, et al.
BMC Medical Genetics|February 28, 2019
HIF-1 transcription activity: HIF1A driven response in normoxia and in hypoxiaFlora Cimmino, Marianna Avitabile, Vito Alessandro Lasorsa, et al.
Contrast Media & Molecular Imaging|April 28, 2012
Mn-loaded apoferritin: a highly sensitive MRI imaging probe for the detection and characterization of hepatocarcinoma lesions in a transgenic mouse modelSimonetta Geninatti Crich, Juan Carlos Cutrin, Stefania Lanzardo, et al.
Molecular Medicine (Cambridge, Mass.)|March 5, 2010
Galectin-1 and its involvement in hepatocellular carcinoma aggressivenessDaniela Spano, Roberta Russo, Vittorio Di Maso, et al.
American Journal of Hematology|October 14, 2010
Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B geneRoberta Russo, Maria Rosaria Esposito, Roberta Asci, et al.
Light, Science & Applications|September 1, 2018
Tomographic flow cytometry by digital holographyFrancesco Merola, Pasquale Memmolo, Lisa Miccio, et al.
Journal of Nephrology|December 24, 2002
Congenital nephrotic syndrome of the Finnish type in Italy: a molecular approachMaddalena Gigante, Fausta Monno, Roberta Roberto, et al.
Blood|March 6, 2002
Infant hypervitaminosis A causes severe anemia and thrombocytopenia: evidence of a retinol-dependent bone marrow cell growth inhibitionSilverio Perrotta, Bruno Nobili, Francesca Rossi, et al.
Analytical Chemistry|May 25, 2018
Label-Free Optical Marker for Red-Blood-Cell Phenotyping of Inherited AnemiasMartina Mugnano, Pasquale Memmolo, Lisa Miccio, et al.
Frontiers in Genetics|November 28, 2022
Clinical exome-based panel testing for medically actionable secondary findings in a cohort of 383 Italian participantsStefania Martone, Autilia Tommasina Buonagura, Roberta Marra, et al.
Pageof 29