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A Meloni

Showing results (41-50 of 130) with videos related to

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Journal of Endocrinological Investigation|May 1, 1997
A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfismM Putzolu, A Meloni, S Loche, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|January 31, 1983
[Electron microscopic features of neoplastic cells (SGS-3A) cultivated in agar]M A Meloni, P Pippia, M Morf-Valluchi, et al.
Biochemical Pharmacology|November 1, 1984
Antiviral properties of psoralen derivatives: a biological and physico-chemical investigationG Palù, M Palumbo, R Cusinato, et al.
Biochemical and Biophysical Research Communications|May 29, 1987
DAPI-pUC8 complex: a tool to investigate biological effects of nucleic acid-drug interactionG Palu, S Valisena, M L Barcellona, et al.
Cancer Genetics and Cytogenetics|April 1, 1996
Analysis of 3p allelic loss in papillary and nonpapillary renal cell carcinomas. Correlation with tumor karyotypesM D Hughson, A Meloni, S Dougherty, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|October 1, 1990
[Effect of dimethyladipimidate and dimethylsuberimidate on cell-cell adhesion in rat fibroblasts]P Pippia, A Cogoli, L Sciola, et al.
Prenatal Diagnosis|November 1, 1992
A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletionsV Faà, M C Rosatelli, R Sardu, et al.
Human Mutation|January 1, 1994
A novel beta-thalassemia mutation: frameshift at codon 59 detected in an Italian carrierA Meloni, M Demurtas, L Moi, et al.
Molecular Genetics & Genomic Medicine|October 2, 2019
Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literatureFernanda T Bellucco, Claudia B de Mello, Vera A Meloni, et al.
Human Mutation|February 16, 2005
Two novel mutations of the AIRE protein affecting its homodimerization propertiesA Meloni, E Fiorillo, D Corda, et al.
Pageof 13

Showing results (41-50 of 130) with videos related to

Sort By:
Pageof 13
Journal of Endocrinological Investigation|May 1, 1997
A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfismM Putzolu, A Meloni, S Loche, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|January 31, 1983
[Electron microscopic features of neoplastic cells (SGS-3A) cultivated in agar]M A Meloni, P Pippia, M Morf-Valluchi, et al.
Biochemical Pharmacology|November 1, 1984
Antiviral properties of psoralen derivatives: a biological and physico-chemical investigationG Palù, M Palumbo, R Cusinato, et al.
Biochemical and Biophysical Research Communications|May 29, 1987
DAPI-pUC8 complex: a tool to investigate biological effects of nucleic acid-drug interactionG Palu, S Valisena, M L Barcellona, et al.
Cancer Genetics and Cytogenetics|April 1, 1996
Analysis of 3p allelic loss in papillary and nonpapillary renal cell carcinomas. Correlation with tumor karyotypesM D Hughson, A Meloni, S Dougherty, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|October 1, 1990
[Effect of dimethyladipimidate and dimethylsuberimidate on cell-cell adhesion in rat fibroblasts]P Pippia, A Cogoli, L Sciola, et al.
Prenatal Diagnosis|November 1, 1992
A simple electrophoretic procedure for fetal diagnosis of beta-thalassaemia due to short deletionsV Faà, M C Rosatelli, R Sardu, et al.
Human Mutation|January 1, 1994
A novel beta-thalassemia mutation: frameshift at codon 59 detected in an Italian carrierA Meloni, M Demurtas, L Moi, et al.
Molecular Genetics & Genomic Medicine|October 2, 2019
Malan syndrome in a patient with 19p13.2p13.12 deletion encompassing NFIX and CACNA1A genes: Case report and review of the literatureFernanda T Bellucco, Claudia B de Mello, Vera A Meloni, et al.
Human Mutation|February 16, 2005
Two novel mutations of the AIRE protein affecting its homodimerization propertiesA Meloni, E Fiorillo, D Corda, et al.
Pageof 13