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Achille Iolascon

Showing results (151-160 of 290) with videos related to

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American Journal of Hematology|August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian populationRoberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
Haematologica|September 21, 2004
Genes transcriptionally modulated by interferon alpha2a correlate with the cytokine activityAchille Iolascon, Stefano Volinia, Adriana Borriello, et al.
Blood|May 17, 2003
The "stomatin" gene and protein in overhydrated hereditary stomatocytosisBritta Fricke, Annette C Argent, Margaret C Chetty, et al.
Genes|October 27, 2022
Different Mechanisms Cause Hypomethylation of Both <i>H19</i> and <i>KCNQ1OT1</i> Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome SpectrumFrancesco Passaretti, Laura Pignata, Giuseppina Vitiello, et al.
Haematologica|December 2, 2017
PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosisImmacolata Andolfo, Francesco Manna, Gianluca De Rosa, et al.
Computational and Structural Biotechnology Journal|September 2, 2022
Single-cell transcriptomics of neuroblastoma identifies chemoresistance-associated genes and pathwaysMarianna Avitabile, Ferdinando Bonfiglio, Vincenzo Aievola, et al.
Clinical Chemistry and Laboratory Medicine|June 13, 2019
Molecular diagnosis of MODY3 permitted to reveal a de novo 12q24.31 deletion and to explain a complex phenotype in a young diabetic patientFernanda Iafusco, Paola De Sanctis, Daniele Pirozzi, et al.
Journal of Translational Medicine|May 19, 2016
An 18 gene expression-based score classifier predicts the clinical outcome in stage 4 neuroblastomaDaniela Formicola, Giuseppe Petrosino, Vito Alessandro Lasorsa, et al.
Haematologica|April 27, 2023
One gene, two opposite phenotypes: a case report of hereditary anemia due to a loss-of-function variant in the <i>EPAS1</i> geneBarbara Eleni Rosato, Roberta Marra, Federica Del Giudice, et al.
Journal of Proteome Research|September 7, 2016
Proteomic Alterations in Response to Hypoxia Inducible Factor 2α in Normoxic Neuroblastoma CellsFlora Cimmino, Lucia Pezone, Marianna Avitabile, et al.
Pageof 29

Showing results (151-160 of 290) with videos related to

Sort By:
Pageof 29
American Journal of Hematology|August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian populationRoberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
Haematologica|September 21, 2004
Genes transcriptionally modulated by interferon alpha2a correlate with the cytokine activityAchille Iolascon, Stefano Volinia, Adriana Borriello, et al.
Blood|May 17, 2003
The "stomatin" gene and protein in overhydrated hereditary stomatocytosisBritta Fricke, Annette C Argent, Margaret C Chetty, et al.
Genes|October 27, 2022
Different Mechanisms Cause Hypomethylation of Both <i>H19</i> and <i>KCNQ1OT1</i> Imprinted Differentially Methylated Regions in Two Cases of Silver-Russell Syndrome SpectrumFrancesco Passaretti, Laura Pignata, Giuseppina Vitiello, et al.
Haematologica|December 2, 2017
PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosisImmacolata Andolfo, Francesco Manna, Gianluca De Rosa, et al.
Computational and Structural Biotechnology Journal|September 2, 2022
Single-cell transcriptomics of neuroblastoma identifies chemoresistance-associated genes and pathwaysMarianna Avitabile, Ferdinando Bonfiglio, Vincenzo Aievola, et al.
Clinical Chemistry and Laboratory Medicine|June 13, 2019
Molecular diagnosis of MODY3 permitted to reveal a de novo 12q24.31 deletion and to explain a complex phenotype in a young diabetic patientFernanda Iafusco, Paola De Sanctis, Daniele Pirozzi, et al.
Journal of Translational Medicine|May 19, 2016
An 18 gene expression-based score classifier predicts the clinical outcome in stage 4 neuroblastomaDaniela Formicola, Giuseppe Petrosino, Vito Alessandro Lasorsa, et al.
Haematologica|April 27, 2023
One gene, two opposite phenotypes: a case report of hereditary anemia due to a loss-of-function variant in the <i>EPAS1</i> geneBarbara Eleni Rosato, Roberta Marra, Federica Del Giudice, et al.
Journal of Proteome Research|September 7, 2016
Proteomic Alterations in Response to Hypoxia Inducible Factor 2α in Normoxic Neuroblastoma CellsFlora Cimmino, Lucia Pezone, Marianna Avitabile, et al.
Pageof 29