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A Cabello

Showing results (221-230 of 239) with videos related to

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Neuromuscular Disorders : NMD|June 12, 2003
Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypesY Campos, A García, P del Hoyo, et al.
Antonie Van Leeuwenhoek|February 24, 2001
Screening of basidiomycetes for antimicrobial activitiesI Suay, F Arenal, F J Asensio, et al.
Annals of Neurology|September 18, 2001
Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II geneY Campos, A García-Redondo, M A Fernández-Moreno, et al.
Nature Genetics|April 27, 2005
Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathwaysMatias Simons, Joachim Gloy, Athina Ganner, et al.
Acta Tropica|September 21, 2016
Schistosoma mansoni infection and related knowledge among schoolchildren in an endemic area of Minas Gerais, Brazil, prior to educational actionsRocio Karina S A A Cabello, Lilian C N H Beck, Cristiano L Massara, et al.
Journal of Inherited Metabolic Disease|November 20, 2009
PDH E1β deficiency with novel mutations in two patients with Leigh syndromeE Quintana, J A Mayr, M T García Silva, et al.
The Journal of Antibiotics|November 20, 1998
Inhibition of fungal sphingolipid biosynthesis by rustmicin, galbonolide B and their new 21-hydroxy analogsG H Harris, A Shafiee, M A Cabello, et al.
The Surgeon : Journal of the Royal Colleges of Surgeons of Edinburgh and Ireland|September 6, 2021
Benefica chirurgia. A global surgery project focusing on hernia surgeryJ M Ramia, A Cabello, J Garijo, et al.
Annals of Neurology|November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.
Neurology|January 15, 2003
Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozilJ Arenas, M A Fernández-Moreno, J A Molina, et al.
Pageof 24

Showing results (221-230 of 239) with videos related to

Sort By:
Pageof 24
Neuromuscular Disorders : NMD|June 12, 2003
Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypesY Campos, A García, P del Hoyo, et al.
Antonie Van Leeuwenhoek|February 24, 2001
Screening of basidiomycetes for antimicrobial activitiesI Suay, F Arenal, F J Asensio, et al.
Annals of Neurology|September 18, 2001
Early-onset multisystem mitochondrial disorder caused by a nonsense mutation in the mitochondrial DNA cytochrome C oxidase II geneY Campos, A García-Redondo, M A Fernández-Moreno, et al.
Nature Genetics|April 27, 2005
Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathwaysMatias Simons, Joachim Gloy, Athina Ganner, et al.
Acta Tropica|September 21, 2016
Schistosoma mansoni infection and related knowledge among schoolchildren in an endemic area of Minas Gerais, Brazil, prior to educational actionsRocio Karina S A A Cabello, Lilian C N H Beck, Cristiano L Massara, et al.
Journal of Inherited Metabolic Disease|November 20, 2009
PDH E1β deficiency with novel mutations in two patients with Leigh syndromeE Quintana, J A Mayr, M T García Silva, et al.
The Journal of Antibiotics|November 20, 1998
Inhibition of fungal sphingolipid biosynthesis by rustmicin, galbonolide B and their new 21-hydroxy analogsG H Harris, A Shafiee, M A Cabello, et al.
The Surgeon : Journal of the Royal Colleges of Surgeons of Edinburgh and Ireland|September 6, 2021
Benefica chirurgia. A global surgery project focusing on hernia surgeryJ M Ramia, A Cabello, J Garijo, et al.
Annals of Neurology|November 18, 2000
Multi-minicore disease--searching for boundaries: phenotype analysis of 38 casesA Ferreiro, B Estournet, D Chateau, et al.
Neurology|January 15, 2003
Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozilJ Arenas, M A Fernández-Moreno, J A Molina, et al.
Pageof 24