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Achille Iolascon

Showing results (191-200 of 251) with videos related to

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Human Mutation|March 17, 2010
Novel TMPRSS6 mutations associated with iron-refractory iron deficiency anemia (IRIDA)Luigia De Falco, Francesca Totaro, Antonella Nai, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathyGianluca Caridi, Francesca Lugani, Monica Dagnino, et al.
Plos Genetics|March 26, 2011
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility LociLe B Nguyen, Sharon J Diskin, Mario Capasso, et al.
Cell Cycle (Georgetown, Tex.)|January 21, 2012
The metallophosphodiesterase Mpped2 impairs tumorigenesis in neuroblastomaLucia Liguori, Immacolata Andolfo, Paqualino de Antonellis, et al.
Haematologica|April 21, 2022
Evidence of protective effects of recombinant ADAMTS13 in a humanized model of sickle cell diseasePaolo Rossato, Enrica Federti, Alessandro Matte, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision|January 31, 2025
On the label-free analysis of white blood cells by holographic quantitative phase imaging flow cytometryGiusy Giugliano, Daniele Pirone, Jaromir Behal, et al.
Nature Genetics|September 4, 2012
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastomaSharon J Diskin, Mario Capasso, Robert W Schnepp, et al.
Cancer Letters|June 10, 2011
Loss of 10q26.1-q26.3 in association with 7q34-q36.3 gain or 17q24.3-q25.3 gain predict poor outcome in pediatric medulloblastomaAnnalisa Pezzolo, Simona Coco, Alessandro Raso, et al.
Human Mutation|August 27, 2014
Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studiesLuigia De Falco, Laura Silvestri, Caroline Kannengiesser, et al.
Oncotarget|March 25, 2016
Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progressionVito Alessandro Lasorsa, Daniela Formicola, Piero Pignataro, et al.
Pageof 26

Showing results (191-200 of 251) with videos related to

Sort By:
Pageof 26
Human Mutation|March 17, 2010
Novel TMPRSS6 mutations associated with iron-refractory iron deficiency anemia (IRIDA)Luigia De Falco, Francesca Totaro, Antonella Nai, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathyGianluca Caridi, Francesca Lugani, Monica Dagnino, et al.
Plos Genetics|March 26, 2011
Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility LociLe B Nguyen, Sharon J Diskin, Mario Capasso, et al.
Cell Cycle (Georgetown, Tex.)|January 21, 2012
The metallophosphodiesterase Mpped2 impairs tumorigenesis in neuroblastomaLucia Liguori, Immacolata Andolfo, Paqualino de Antonellis, et al.
Haematologica|April 21, 2022
Evidence of protective effects of recombinant ADAMTS13 in a humanized model of sickle cell diseasePaolo Rossato, Enrica Federti, Alessandro Matte, et al.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision|January 31, 2025
On the label-free analysis of white blood cells by holographic quantitative phase imaging flow cytometryGiusy Giugliano, Daniele Pirone, Jaromir Behal, et al.
Nature Genetics|September 4, 2012
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastomaSharon J Diskin, Mario Capasso, Robert W Schnepp, et al.
Cancer Letters|June 10, 2011
Loss of 10q26.1-q26.3 in association with 7q34-q36.3 gain or 17q24.3-q25.3 gain predict poor outcome in pediatric medulloblastomaAnnalisa Pezzolo, Simona Coco, Alessandro Raso, et al.
Human Mutation|August 27, 2014
Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studiesLuigia De Falco, Laura Silvestri, Caroline Kannengiesser, et al.
Oncotarget|March 25, 2016
Exome and deep sequencing of clinically aggressive neuroblastoma reveal somatic mutations that affect key pathways involved in cancer progressionVito Alessandro Lasorsa, Daniela Formicola, Piero Pignataro, et al.
Pageof 26