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L Bisceglia

Showing results (21-30 of 79) with videos related to

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Clinical Genetics|July 1, 1997
Detection of dystrophin deletion carriers using FISH analysisS Calvano, E Memeo, M R Piemontese, et al.
Blood|December 1, 1995
Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation")D Girelli, R Corrocher, L Bisceglia, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Phenotype characterization and prevalence of rBAT M467T mutation in Italian cystinuric patientsL de Sanctis, M Bruno, G Bonetti, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|March 29, 2011
[Source apportionment of benzo(a)pyrene in Taranto and carcinogenic risk estimate in general population]L Bisceglia, R Giua, A Morabito, et al.
Indian Journal of Nephrology|March 9, 2018
Cystinuria in a 13-month-old Girl with Absence of Mutations in the SLC3A1 and SLC7A9 GenesS Krishnamurthy, C Pavani, P M Kurup, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|February 15, 2013
[Environmental and biological monitoring of exposure to PAHs in Taranto coke-oven workers and in two groups of the general population from Apulia]L Campo, L Vimercati, A Carrus, et al.
American Journal of Medical Genetics|February 15, 2001
C677T variant form at the MTHFR gene and CL/P: a risk factor for mothers?M Martinelli, L Scapoli, F Pezzetti, et al.
Clinical Nephrology|January 5, 2002
Cystinuria phenotyping by oral lysine and arginine loadingL de Sanctis, G Bonetti, M Bruno, et al.
Nucleic Acids Research|October 25, 1995
Stability and functional effectiveness of phosphorothioate modified duplex DNA and synthetic 'mini-genes'S A Ciafrè, M Rinaldi, P Gasparini, et al.
Molecular and Cellular Probes|September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome geneL Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Pageof 8

Showing results (21-30 of 79) with videos related to

Sort By:
Pageof 8
Clinical Genetics|July 1, 1997
Detection of dystrophin deletion carriers using FISH analysisS Calvano, E Memeo, M R Piemontese, et al.
Blood|December 1, 1995
Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the "Verona mutation")D Girelli, R Corrocher, L Bisceglia, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Phenotype characterization and prevalence of rBAT M467T mutation in Italian cystinuric patientsL de Sanctis, M Bruno, G Bonetti, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|March 29, 2011
[Source apportionment of benzo(a)pyrene in Taranto and carcinogenic risk estimate in general population]L Bisceglia, R Giua, A Morabito, et al.
Indian Journal of Nephrology|March 9, 2018
Cystinuria in a 13-month-old Girl with Absence of Mutations in the SLC3A1 and SLC7A9 GenesS Krishnamurthy, C Pavani, P M Kurup, et al.
Giornale Italiano Di Medicina Del Lavoro Ed Ergonomia|February 15, 2013
[Environmental and biological monitoring of exposure to PAHs in Taranto coke-oven workers and in two groups of the general population from Apulia]L Campo, L Vimercati, A Carrus, et al.
American Journal of Medical Genetics|February 15, 2001
C677T variant form at the MTHFR gene and CL/P: a risk factor for mothers?M Martinelli, L Scapoli, F Pezzetti, et al.
Clinical Nephrology|January 5, 2002
Cystinuria phenotyping by oral lysine and arginine loadingL de Sanctis, G Bonetti, M Bruno, et al.
Nucleic Acids Research|October 25, 1995
Stability and functional effectiveness of phosphorothioate modified duplex DNA and synthetic 'mini-genes'S A Ciafrè, M Rinaldi, P Gasparini, et al.
Molecular and Cellular Probes|September 4, 1998
Cellular Retinol Binding Protein 1 (RBP1): a frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome geneL Bisceglia, L d'Ambrosio, M R Piemontese, et al.
Pageof 8