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Victoria Alvarez

Showing results (121-130 of 181) with videos related to

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Progress in Neuro-Psychopharmacology & Biological Psychiatry|September 22, 2009
Genetic polymorphisms in the dopamine-2 receptor (DRD2), dopamine-3 receptor (DRD3), and dopamine transporter (SLC6A3) genes in schizophrenia: Data from an association studyPilar A Sáiz, M Paz García-Portilla, Celso Arango, et al.
Clinical Chemistry and Laboratory Medicine|April 13, 2011
Pharmacogenetics of tacrolimus after renal transplantation: analysis of polymorphisms in genes encoding 16 drug metabolizing enzymesBeatriz Tavira, Eliecer Coto, Eliecer Coto Garciá, et al.
Surgical Endoscopy|August 18, 2016
Can endoscopic papillectomy be curative for early ampullary adenocarcinoma of the ampulla of Vater?María-Victoria Alvarez-Sanchez, Inés Oria, Olivia B Luna, et al.
Journal of Translational Medicine|July 3, 2010
Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifierEliecer Coto, María Palacín, María Martín, et al.
Infection and Immunity|June 24, 2004
In vivo interleukin-6 protects neutrophils from apoptosis in osteomyelitisVíctor Asensi, Eulalia Valle, Alvaro Meana, et al.
Human Mutation|March 14, 2013
Do not trust the pedigree: reduced and sex-dependent penetrance at a novel mutation hotspot in ATL1 blurs autosomal dominant inheritance of spastic paraplegiaRita-Eva Varga, Rebecca Schüle, Hicham Fadel, et al.
Nitric Oxide : Biology and Chemistry|August 8, 2006
The NOS3 (27-bp repeat, intron 4) polymorphism is associated with susceptibility to osteomyelitisVictor Asensi, A Hugo Montes, Eulalia Valle, et al.
Molecular Neurobiology|December 8, 2016
The p. R151C Polymorphism in MC1R Gene Modifies the Age of Onset in Spanish Huntington's Disease PatientsGemma Tell-Marti, Joan Anton Puig-Butille, Pol Gimenez-Xavier, et al.
The Journal of Molecular Diagnostics : JMD|July 7, 2012
Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathyEliecer Coto, Julián R Reguero, María Palacín, et al.
United European Gastroenterology Journal|February 14, 2018
Effect of aspirin on the diagnostic accuracy of the faecal immunochemical test for colorectal advanced neoplasiaLuis Bujanda, Cristina Sarasqueta, Pablo Vega, et al.
Pageof 19

Showing results (121-130 of 181) with videos related to

Sort By:
Pageof 19
Progress in Neuro-Psychopharmacology & Biological Psychiatry|September 22, 2009
Genetic polymorphisms in the dopamine-2 receptor (DRD2), dopamine-3 receptor (DRD3), and dopamine transporter (SLC6A3) genes in schizophrenia: Data from an association studyPilar A Sáiz, M Paz García-Portilla, Celso Arango, et al.
Clinical Chemistry and Laboratory Medicine|April 13, 2011
Pharmacogenetics of tacrolimus after renal transplantation: analysis of polymorphisms in genes encoding 16 drug metabolizing enzymesBeatriz Tavira, Eliecer Coto, Eliecer Coto Garciá, et al.
Surgical Endoscopy|August 18, 2016
Can endoscopic papillectomy be curative for early ampullary adenocarcinoma of the ampulla of Vater?María-Victoria Alvarez-Sanchez, Inés Oria, Olivia B Luna, et al.
Journal of Translational Medicine|July 3, 2010
Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifierEliecer Coto, María Palacín, María Martín, et al.
Infection and Immunity|June 24, 2004
In vivo interleukin-6 protects neutrophils from apoptosis in osteomyelitisVíctor Asensi, Eulalia Valle, Alvaro Meana, et al.
Human Mutation|March 14, 2013
Do not trust the pedigree: reduced and sex-dependent penetrance at a novel mutation hotspot in ATL1 blurs autosomal dominant inheritance of spastic paraplegiaRita-Eva Varga, Rebecca Schüle, Hicham Fadel, et al.
Nitric Oxide : Biology and Chemistry|August 8, 2006
The NOS3 (27-bp repeat, intron 4) polymorphism is associated with susceptibility to osteomyelitisVictor Asensi, A Hugo Montes, Eulalia Valle, et al.
Molecular Neurobiology|December 8, 2016
The p. R151C Polymorphism in MC1R Gene Modifies the Age of Onset in Spanish Huntington's Disease PatientsGemma Tell-Marti, Joan Anton Puig-Butille, Pol Gimenez-Xavier, et al.
The Journal of Molecular Diagnostics : JMD|July 7, 2012
Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathyEliecer Coto, Julián R Reguero, María Palacín, et al.
United European Gastroenterology Journal|February 14, 2018
Effect of aspirin on the diagnostic accuracy of the faecal immunochemical test for colorectal advanced neoplasiaLuis Bujanda, Cristina Sarasqueta, Pablo Vega, et al.
Pageof 19