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M Ferrone

Showing results (1-10 of 19) with videos related to

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Clinical Genetics|December 1, 1992
Analysis of CA/GT microsatellite polymorphism in IVS8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a study of Italian CF familiesG Restagno, S Garnerone, C Gennaro, et al.
The Journal of Physical Chemistry. B|September 18, 2018
Water, Ions, and Hemoglobin: Effects on Allostery and PolymerizationMaria A Rotter, Jie Jiang, Stephanie M Ferrone, et al.
Contributions to Nephrology|November 2, 2001
Molecular genetic analysis of von Hippel-Lindau disease by denaturing high-performance liquid chromatographyE Menegatti, M Ferrone, S Gallone, et al.
Prenatal Diagnosis|July 1, 1995
Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected childG Restagno, M Ferrone, C Doriguzzi, et al.
Journal of Neurology|May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
Human Heredity|January 1, 1992
Mapping of human hexokinase 1 gene to 10q11----qterA Daniele, F Altruda, M Ferrone, et al.
The Journal of Experimental Medicine|November 1, 1995
Intercellular adhesion molecule-1 dimerization and its consequences for adhesion mediated by lymphocyte function associated-1J Miller, R Knorr, M Ferrone, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 29, 2001
The tumor autocrine motility factor receptor, gp78, is a ubiquitin protein ligase implicated in degradation from the endoplasmic reticulumS Fang, M Ferrone, C Yang, et al.
Human Molecular Genetics|February 1, 1993
A large deletion at the 3' end of the rhodopsin gene in an Italian family with a diffuse form of autosomal dominant retinitis pigmentosaG Restagno, M Maghtheh, S Bhattacharya, et al.
Clinical Genetics|June 18, 1998
Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR geneC Arduino, M Ferrone, A Brusco, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Clinical Genetics|December 1, 1992
Analysis of CA/GT microsatellite polymorphism in IVS8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a study of Italian CF familiesG Restagno, S Garnerone, C Gennaro, et al.
The Journal of Physical Chemistry. B|September 18, 2018
Water, Ions, and Hemoglobin: Effects on Allostery and PolymerizationMaria A Rotter, Jie Jiang, Stephanie M Ferrone, et al.
Contributions to Nephrology|November 2, 2001
Molecular genetic analysis of von Hippel-Lindau disease by denaturing high-performance liquid chromatographyE Menegatti, M Ferrone, S Gallone, et al.
Prenatal Diagnosis|July 1, 1995
Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected childG Restagno, M Ferrone, C Doriguzzi, et al.
Journal of Neurology|May 1, 1993
Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophyC Doriguzzi, L Palmucci, T Mongini, et al.
Human Heredity|January 1, 1992
Mapping of human hexokinase 1 gene to 10q11----qterA Daniele, F Altruda, M Ferrone, et al.
The Journal of Experimental Medicine|November 1, 1995
Intercellular adhesion molecule-1 dimerization and its consequences for adhesion mediated by lymphocyte function associated-1J Miller, R Knorr, M Ferrone, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 29, 2001
The tumor autocrine motility factor receptor, gp78, is a ubiquitin protein ligase implicated in degradation from the endoplasmic reticulumS Fang, M Ferrone, C Yang, et al.
Human Molecular Genetics|February 1, 1993
A large deletion at the 3' end of the rhodopsin gene in an Italian family with a diffuse form of autosomal dominant retinitis pigmentosaG Restagno, M Maghtheh, S Bhattacharya, et al.
Clinical Genetics|June 18, 1998
Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR geneC Arduino, M Ferrone, A Brusco, et al.
Pageof 2