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Hugo Vega

Showing results (1-10 of 18) with videos related to

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Biomedica : Revista Del Instituto Nacional De Salud|December 21, 2006
[Colombian haplotypes of the Gaucher disease-causing N370S mutation may originate from a possible common ancestral haplotype]Ricardo Wilches, Hugo Vega, Olga Echeverri, et al.
Advances in Experimental Medicine and Biology|September 10, 2014
Genetic variation and RNA binding proteins: tools and techniques to detect functional polymorphismsRachel Soemedi, Hugo Vega, Judson M Belmont, et al.
Revista Medica Del Instituto Mexicano Del Seguro Social|November 28, 2023
[Analysis of life quality on patients with thoracolumbar fractures]Marco Polo Malacón-Gutiérrez, Hugo Vega-Álvarez, Iván Cruz-Aceves, et al.
Neuron|June 26, 2012
Activity-dependent growth of new dendritic spines is regulated by the proteasomeAndrew M Hamilton, Won Chan Oh, Hugo Vega-Ramirez, et al.
Translational Lung Cancer Research|July 25, 2015
(18)F-FDG-PET/CT in the assessment of pulmonary solitary nodules: comparison of different analysis methods and risk variables in the prediction of malignancyOber van Gómez López, Ana María García Vicente, Antonio Francisco Honguero Martínez, et al.
Minerva Endocrinologica|January 14, 2015
Role of 99mTc-HYNIC-Tyr3-octreotide scintigraphy in neuroendocrine tumors based on localization of the primary tumorGerman A Jimenez Londoño, Ana María García Vicente, Angel M Soriano Castrejon, et al.
Nature Genetics|April 12, 2005
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesionHugo Vega, Quinten Waisfisz, Miriam Gordillo, et al.
Neuron|September 6, 2016
Modulating Neuronal Competition Dynamics in the Dentate Gyrus to Rejuvenate Aging Memory CircuitsKathleen M McAvoy, Kimberly N Scobie, Stefan Berger, et al.
Plos Biology|May 27, 2009
Transcriptional dysregulation in NIPBL and cohesin mutant human cellsJinglan Liu, Zhe Zhang, Masashige Bando, et al.
Plos Genetics|February 28, 2017
Correction: ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13Yihan Zhang, Haigen Huang, Gexin Zhao, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Biomedica : Revista Del Instituto Nacional De Salud|December 21, 2006
[Colombian haplotypes of the Gaucher disease-causing N370S mutation may originate from a possible common ancestral haplotype]Ricardo Wilches, Hugo Vega, Olga Echeverri, et al.
Advances in Experimental Medicine and Biology|September 10, 2014
Genetic variation and RNA binding proteins: tools and techniques to detect functional polymorphismsRachel Soemedi, Hugo Vega, Judson M Belmont, et al.
Revista Medica Del Instituto Mexicano Del Seguro Social|November 28, 2023
[Analysis of life quality on patients with thoracolumbar fractures]Marco Polo Malacón-Gutiérrez, Hugo Vega-Álvarez, Iván Cruz-Aceves, et al.
Neuron|June 26, 2012
Activity-dependent growth of new dendritic spines is regulated by the proteasomeAndrew M Hamilton, Won Chan Oh, Hugo Vega-Ramirez, et al.
Translational Lung Cancer Research|July 25, 2015
(18)F-FDG-PET/CT in the assessment of pulmonary solitary nodules: comparison of different analysis methods and risk variables in the prediction of malignancyOber van Gómez López, Ana María García Vicente, Antonio Francisco Honguero Martínez, et al.
Minerva Endocrinologica|January 14, 2015
Role of 99mTc-HYNIC-Tyr3-octreotide scintigraphy in neuroendocrine tumors based on localization of the primary tumorGerman A Jimenez Londoño, Ana María García Vicente, Angel M Soriano Castrejon, et al.
Nature Genetics|April 12, 2005
Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesionHugo Vega, Quinten Waisfisz, Miriam Gordillo, et al.
Neuron|September 6, 2016
Modulating Neuronal Competition Dynamics in the Dentate Gyrus to Rejuvenate Aging Memory CircuitsKathleen M McAvoy, Kimberly N Scobie, Stefan Berger, et al.
Plos Biology|May 27, 2009
Transcriptional dysregulation in NIPBL and cohesin mutant human cellsJinglan Liu, Zhe Zhang, Masashige Bando, et al.
Plos Genetics|February 28, 2017
Correction: ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13Yihan Zhang, Haigen Huang, Gexin Zhao, et al.
Pageof 2