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P Gasparini

Showing results (171-180 of 204) with videos related to

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Molecular Metabolism|May 2, 2021
Dopamine D2 receptor agonist, bromocriptine, remodels adipose tissue dopaminergic signalling and upregulates catabolic pathways, improving metabolic profile in type 2 diabetesG Tavares, D Marques, C Barra, et al.
Genomics|September 24, 1999
Recombinant families locate the gene for non-type I cystinuria between markers C13 and D19S587 on chromosome 19q13.1L Feliubadaló, L Bisceglia, M Font, et al.
Nature Genetics|September 2, 1999
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locusA Grifa, C A Wagner, L D'Ambrosio, et al.
International Journal of Molecular Medicine|July 30, 1999
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndromeM Seri, S Melchionda, S Dreyer, et al.
Amino Acids|November 2, 2013
The molecular basis of cystinuria: the role of the rBAT geneM Palacín, C Mora, J Chillarón, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia lociM R Piemontese, E Memeo, M Carella, et al.
Gastroenterology|May 30, 1998
Heterogeneity of hemochromatosis in ItalyA Piperno, M Sampietro, A Pietrangelo, et al.
American Journal of Human Genetics|July 27, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossS Melchionda, N Ahituv, L Bisceglia, et al.
Journal of Molecular Graphics & Modelling|March 4, 2023
Unveiling mutation effects on the structural dynamics of the main protease from SARS-CoV-2 with hybrid simulation methodsP Gasparini, E A Philot, S Q Pantaleão, et al.
Human Molecular Genetics|September 1, 1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansL Zelante, P Gasparini, X Estivill, et al.
Pageof 21

Showing results (171-180 of 204) with videos related to

Sort By:
Pageof 21
Molecular Metabolism|May 2, 2021
Dopamine D2 receptor agonist, bromocriptine, remodels adipose tissue dopaminergic signalling and upregulates catabolic pathways, improving metabolic profile in type 2 diabetesG Tavares, D Marques, C Barra, et al.
Genomics|September 24, 1999
Recombinant families locate the gene for non-type I cystinuria between markers C13 and D19S587 on chromosome 19q13.1L Feliubadaló, L Bisceglia, M Font, et al.
Nature Genetics|September 2, 1999
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locusA Grifa, C A Wagner, L D'Ambrosio, et al.
International Journal of Molecular Medicine|July 30, 1999
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndromeM Seri, S Melchionda, S Dreyer, et al.
Amino Acids|November 2, 2013
The molecular basis of cystinuria: the role of the rBAT geneM Palacín, C Mora, J Chillarón, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
A YAC contig spanning the blepharophimosis-ptosis-epicanthus inversus syndrome and propionic acidemia lociM R Piemontese, E Memeo, M Carella, et al.
Gastroenterology|May 30, 1998
Heterogeneity of hemochromatosis in ItalyA Piperno, M Sampietro, A Pietrangelo, et al.
American Journal of Human Genetics|July 27, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossS Melchionda, N Ahituv, L Bisceglia, et al.
Journal of Molecular Graphics & Modelling|March 4, 2023
Unveiling mutation effects on the structural dynamics of the main protease from SARS-CoV-2 with hybrid simulation methodsP Gasparini, E A Philot, S Q Pantaleão, et al.
Human Molecular Genetics|September 1, 1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansL Zelante, P Gasparini, X Estivill, et al.
Pageof 21