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P Gasparini

Showing results (151-160 of 204) with videos related to

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Molecular and Cellular Probes|June 1, 1997
Hereditary hemochromatosis: a HpaI polymorphism within the HLA-H geneA Totaro, A Grifa, M Carella, et al.
American Journal of Human Genetics|August 27, 1998
Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter)M Carella, G Stewart, J F Ajetunmobi, et al.
American Journal of Human Genetics|April 1, 1997
Mutation analysis of the HLA-H gene in Italian hemochromatosis patientsM Carella, L D'Ambrosio, A Totaro, et al.
Genomics|February 1, 1996
Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I regionA Totaro, J M Rommens, A Grifa, et al.
Neuroscience|September 29, 2011
D184E mutation in aquaporin-4 gene impairs water permeability and links to deafnessG P Nicchia, R Ficarella, A Rossi, et al.
Neurology|January 14, 2004
A novel mutation in SACS gene in a family from southern ItalyC Criscuolo, S Banfi, M Orio, et al.
Ecancermedicalscience|January 26, 2012
Chromosomal rearrangements in acute myeloid leukemia (AML)E Belloni, M Trubia, P Gasparini, et al.
Metabolism: Clinical and Experimental|August 23, 2000
Plasma nitric oxide concentrations are elevated in insulin-resistant healthy subjectsI Zavaroni, P M Platti, L D Monti, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2000
Myocilin Gln368stop mutation and advanced age as risk factors for late-onset primary open-angle glaucomaA Angius, P Spinelli, G Ghilotti, et al.
Lancet (London, England)|March 3, 1998
Connexin-26 mutations in sporadic and inherited sensorineural deafnessX Estivill, P Fortina, S Surrey, et al.
Pageof 21

Showing results (151-160 of 204) with videos related to

Sort By:
Pageof 21
Molecular and Cellular Probes|June 1, 1997
Hereditary hemochromatosis: a HpaI polymorphism within the HLA-H geneA Totaro, A Grifa, M Carella, et al.
American Journal of Human Genetics|August 27, 1998
Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter)M Carella, G Stewart, J F Ajetunmobi, et al.
American Journal of Human Genetics|April 1, 1997
Mutation analysis of the HLA-H gene in Italian hemochromatosis patientsM Carella, L D'Ambrosio, A Totaro, et al.
Genomics|February 1, 1996
Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I regionA Totaro, J M Rommens, A Grifa, et al.
Neuroscience|September 29, 2011
D184E mutation in aquaporin-4 gene impairs water permeability and links to deafnessG P Nicchia, R Ficarella, A Rossi, et al.
Neurology|January 14, 2004
A novel mutation in SACS gene in a family from southern ItalyC Criscuolo, S Banfi, M Orio, et al.
Ecancermedicalscience|January 26, 2012
Chromosomal rearrangements in acute myeloid leukemia (AML)E Belloni, M Trubia, P Gasparini, et al.
Metabolism: Clinical and Experimental|August 23, 2000
Plasma nitric oxide concentrations are elevated in insulin-resistant healthy subjectsI Zavaroni, P M Platti, L D Monti, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2000
Myocilin Gln368stop mutation and advanced age as risk factors for late-onset primary open-angle glaucomaA Angius, P Spinelli, G Ghilotti, et al.
Lancet (London, England)|March 3, 1998
Connexin-26 mutations in sporadic and inherited sensorineural deafnessX Estivill, P Fortina, S Surrey, et al.
Pageof 21