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A Pizzuti

Showing results (71-80 of 117) with videos related to

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Neuroreport|May 28, 1998
Immunomagnetic isolation of human developing motor neuronsV Silani, A Brioschi, M Braga, et al.
Journal of Medical Genetics|February 4, 2005
Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factorsA Sarkozy, E Conti, C Neri, et al.
Journal of Endocrinological Investigation|November 30, 2000
Characterization of novel genes in AZF regionsL Stuppia, V Gatta, I Fogh, et al.
Minerva Cardioangiologica|April 1, 1981
[Indications for temporary electrostimulation in acute myocardial infarct]G Borello, E Bellone, G C Bulgarelli, et al.
Journal of the Neurological Sciences|January 7, 2010
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiencyM Luigetti, A Pizzuti, S Bartoletti, et al.
Biochemical and Biophysical Research Communications|January 5, 1995
Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5A Pizzuti, A Colosimo, A Ratti, et al.
American Journal of Medical Genetics|May 8, 1999
Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type IIP Mandich, E Bellone, E Di Maria, et al.
Human Mutation|January 1, 1996
Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locusF Capon, C Levato, E Bussaglia, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kbG Calabrese, L Telvi, F Capodiferro, et al.
Cytogenetics and Cell Genetics|July 4, 2001
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogasterA Ratti, F Amati, M Bozzali, et al.
Pageof 12

Showing results (71-80 of 117) with videos related to

Sort By:
Pageof 12
Neuroreport|May 28, 1998
Immunomagnetic isolation of human developing motor neuronsV Silani, A Brioschi, M Braga, et al.
Journal of Medical Genetics|February 4, 2005
Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factorsA Sarkozy, E Conti, C Neri, et al.
Journal of Endocrinological Investigation|November 30, 2000
Characterization of novel genes in AZF regionsL Stuppia, V Gatta, I Fogh, et al.
Minerva Cardioangiologica|April 1, 1981
[Indications for temporary electrostimulation in acute myocardial infarct]G Borello, E Bellone, G C Bulgarelli, et al.
Journal of the Neurological Sciences|January 7, 2010
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiencyM Luigetti, A Pizzuti, S Bartoletti, et al.
Biochemical and Biophysical Research Communications|January 5, 1995
Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5A Pizzuti, A Colosimo, A Ratti, et al.
American Journal of Medical Genetics|May 8, 1999
Exclusion of the ninjurin gene as a candidate for hereditary sensory neuropathies type I and type IIP Mandich, E Bellone, E Di Maria, et al.
Human Mutation|January 1, 1996
Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locusF Capon, C Levato, E Bussaglia, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kbG Calabrese, L Telvi, F Capodiferro, et al.
Cytogenetics and Cell Genetics|July 4, 2001
Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogasterA Ratti, F Amati, M Bozzali, et al.
Pageof 12