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J Montoya

Showing results (191-200 of 270) with videos related to

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Glycobiology|December 31, 2004
The wbbD gene of E. coli strain VW187 (O7:K1) encodes a UDP-Gal: GlcNAc{alpha}-pyrophosphate-R {beta}1,3-galactosyltransferase involved in the biosynthesis of O7-specific lipopolysaccharideJohn G Riley, Mohammed Menggad, Pedro J Montoya-Peleaz, et al.
Anales De Medicina Interna (Madrid, Spain : 1984)|April 1, 1989
[Effect of an oral calcium supplement in the treatment of slight-to- moderate essential arterial hypertension]J Oliván Martínez, R Pérez Cano, M J Miranda García, et al.
Revista De Neurologia|July 23, 2002
[Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)]A Playán, A Solano-Palacios, J B González de la Rosa, et al.
Transplantation Proceedings|May 2, 2006
Ancillary hospital personnel faced with organ donation and transplantationA Ríos, C Conesa, P Ramírez, et al.
Biofactors (Oxford, England)|July 29, 2006
Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disordersR Montero, R Artuch, P Briones, et al.
Annals of the Rheumatic Diseases|October 14, 2015
Patients with ankylosing spondylitis have been breast fed less often than healthy controls: a case-control retrospective studyJ Montoya, N B Matta, P Suchon, et al.
Journal of Visualized Experiments : Jove|June 19, 2018
Adaptation of Hybridization Capture of Chromatin-associated Proteins for Proteomics to Mammalian CellsHector Guillen-Ahlers, Prahlad K Rao, Danu S Perumalla, et al.
Plos Pathogens|June 22, 2018
PPARγ is critical for Mycobacterium tuberculosis induction of Mcl-1 and limitation of human macrophage apoptosisEusondia Arnett, Ashlee M Weaver, Kiersten C Woodyard, et al.
Revista De Neurologia|December 31, 2004
[A patient with bilateral lesion in the striatum and slowly progressive dystonia secondary to T14487C mutation in the ND6 gene of complex I of the mitochondrial respiratory chain]M Raspall-Chaure, A Solano, E Vázquez, et al.
Revista De Neurologia|January 3, 2007
[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2]R Delgado-Sánchez, A Zárate-Moysen, A Monsalvo-Reyes, et al.
Pageof 27

Showing results (191-200 of 270) with videos related to

Sort By:
Pageof 27
Glycobiology|December 31, 2004
The wbbD gene of E. coli strain VW187 (O7:K1) encodes a UDP-Gal: GlcNAc{alpha}-pyrophosphate-R {beta}1,3-galactosyltransferase involved in the biosynthesis of O7-specific lipopolysaccharideJohn G Riley, Mohammed Menggad, Pedro J Montoya-Peleaz, et al.
Anales De Medicina Interna (Madrid, Spain : 1984)|April 1, 1989
[Effect of an oral calcium supplement in the treatment of slight-to- moderate essential arterial hypertension]J Oliván Martínez, R Pérez Cano, M J Miranda García, et al.
Revista De Neurologia|July 23, 2002
[Leigh syndrome resulting from a de novo mitochondrial DNA mutation (T8993G)]A Playán, A Solano-Palacios, J B González de la Rosa, et al.
Transplantation Proceedings|May 2, 2006
Ancillary hospital personnel faced with organ donation and transplantationA Ríos, C Conesa, P Ramírez, et al.
Biofactors (Oxford, England)|July 29, 2006
Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disordersR Montero, R Artuch, P Briones, et al.
Annals of the Rheumatic Diseases|October 14, 2015
Patients with ankylosing spondylitis have been breast fed less often than healthy controls: a case-control retrospective studyJ Montoya, N B Matta, P Suchon, et al.
Journal of Visualized Experiments : Jove|June 19, 2018
Adaptation of Hybridization Capture of Chromatin-associated Proteins for Proteomics to Mammalian CellsHector Guillen-Ahlers, Prahlad K Rao, Danu S Perumalla, et al.
Plos Pathogens|June 22, 2018
PPARγ is critical for Mycobacterium tuberculosis induction of Mcl-1 and limitation of human macrophage apoptosisEusondia Arnett, Ashlee M Weaver, Kiersten C Woodyard, et al.
Revista De Neurologia|December 31, 2004
[A patient with bilateral lesion in the striatum and slowly progressive dystonia secondary to T14487C mutation in the ND6 gene of complex I of the mitochondrial respiratory chain]M Raspall-Chaure, A Solano, E Vázquez, et al.
Revista De Neurologia|January 3, 2007
[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2]R Delgado-Sánchez, A Zárate-Moysen, A Monsalvo-Reyes, et al.
Pageof 27