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Achille Iolascon

Showing results (91-100 of 290) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 16, 2002
Spina bifida and folate-related genes: a study of gene-gene interactionsRaffaella de Franchis, Lorenzo D Botto, Gianfranco Sebastio, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 8, 2022
Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma SusceptibilityAlessandro Testori, Zalman Vaksman, Sharon J Diskin, et al.
Clinical Case Reports|February 14, 2022
Novel <i>PKLR</i> missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred-PK deficiency masquerading as congenital dyserythropoietic anemiaNaglaa Fawaz, Ismail Beshlawi, Alauldeen Alqasim, et al.
Journal of Human Genetics|June 11, 2010
MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thicknessMario Capasso, Fabrizio Ayala, Rosa Anna Avvisati, et al.
Haematologica|January 24, 2016
The role of Matriptase-2 during the early postnatal development in humansLuigia De Falco, Mariasole Bruno, Ebru Yilmaz-Keskin, et al.
Gene|January 21, 2014
Loeys-Dietz syndrome type 4, caused by chromothripsis, involving the TGFB2 genePaolo Fontana, Rita Genesio, Alberto Casertano, et al.
American Journal of Hematology|August 11, 2019
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variantImmacolata Andolfo, Barbara Eleni Rosato, Roberta Marra, et al.
Cell Reports|January 19, 2016
NCOA4 Deficiency Impairs Systemic Iron HomeostasisRoberto Bellelli, Giorgia Federico, Alessandro Matte', et al.
International Journal of Molecular Sciences|February 15, 2022
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic CellsBarbara Eleni Rosato, Roberta Marra, Vanessa D'Onofrio, et al.
HGG Advances|November 25, 2022
<i>CFDP1</i> is a neuroblastoma susceptibility gene that regulates transcription factors of the noradrenergic cell identityDaniela Formicola, Vito Alessandro Lasorsa, Sueva Cantalupo, et al.
Pageof 29

Showing results (91-100 of 290) with videos related to

Sort By:
Pageof 29
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 16, 2002
Spina bifida and folate-related genes: a study of gene-gene interactionsRaffaella de Franchis, Lorenzo D Botto, Gianfranco Sebastio, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 8, 2022
Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma SusceptibilityAlessandro Testori, Zalman Vaksman, Sharon J Diskin, et al.
Clinical Case Reports|February 14, 2022
Novel <i>PKLR</i> missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred-PK deficiency masquerading as congenital dyserythropoietic anemiaNaglaa Fawaz, Ismail Beshlawi, Alauldeen Alqasim, et al.
Journal of Human Genetics|June 11, 2010
MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thicknessMario Capasso, Fabrizio Ayala, Rosa Anna Avvisati, et al.
Haematologica|January 24, 2016
The role of Matriptase-2 during the early postnatal development in humansLuigia De Falco, Mariasole Bruno, Ebru Yilmaz-Keskin, et al.
Gene|January 21, 2014
Loeys-Dietz syndrome type 4, caused by chromothripsis, involving the TGFB2 genePaolo Fontana, Rita Genesio, Alberto Casertano, et al.
American Journal of Hematology|August 11, 2019
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variantImmacolata Andolfo, Barbara Eleni Rosato, Roberta Marra, et al.
Cell Reports|January 19, 2016
NCOA4 Deficiency Impairs Systemic Iron HomeostasisRoberto Bellelli, Giorgia Federico, Alessandro Matte', et al.
International Journal of Molecular Sciences|February 15, 2022
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic CellsBarbara Eleni Rosato, Roberta Marra, Vanessa D'Onofrio, et al.
HGG Advances|November 25, 2022
<i>CFDP1</i> is a neuroblastoma susceptibility gene that regulates transcription factors of the noradrenergic cell identityDaniela Formicola, Vito Alessandro Lasorsa, Sueva Cantalupo, et al.
Pageof 29