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Glycobiology
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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 lipopolysaccharide
John 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 transplantation
A 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 disorders
R 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 study
J 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 Cells
Hector 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 apoptosis
Eusondia 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.
Page
of 27
Search research articles
Search
Showing results (191-200 of 270) with videos related to
Sort By:
Page
of 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 lipopolysaccharide
John 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 transplantation
A 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 disorders
R 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 study
J 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 Cells
Hector 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 apoptosis
Eusondia 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.
Page
of 27