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Hugo Vega

Showing results (11-20 of 18) with videos related to

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Plos Genetics|February 4, 2017
ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13Yihan Zhang, Haigen Huang, Gexin Zhao, et al.
Nucleic Acids Research|May 8, 2010
Genome-wide DNA methylation analysis in cohesin mutant human cell linesJinglan Liu, Zhe Zhang, Masashige Bando, et al.
Frontiers in Digital Health|June 26, 2026
Ensemble based in transfer learning for cytological classification in pleural fluidFrida López-Córdova, Hugo Vega-Huerta, Gisella Luisa Elena Maquen-Niño, et al.
Frontiers in Digital Health|July 15, 2026
Transfer learning and vision transformer for the automatic diagnosis of cataracts in ophthalmological imagesHugo Vega-Huerta, Camila Isabela Cuba-Aquino, Gari Mario Suca-Mariño, et al.
American Journal of Medical Genetics. Part A|February 8, 2014
Cornelia de Lange syndrome: further delineation of phenotype, cohesin biology and educational focus, 5th Biennial Scientific and Educational Symposium abstractsAntonie D Kline, Anne L Calof, Cheri A Schaaf, et al.
Human Molecular Genetics|April 16, 2008
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activityMiriam Gordillo, Hugo Vega, Alison H Trainer, et al.
Molecular Genetics and Metabolism|May 28, 2014
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivityDavid R Adams, Hongjie Yuan, Todd Holyoak, et al.
The New England Journal of Medicine|April 11, 2014
Glycosylation, hypogammaglobulinemia, and resistance to viral infectionsMohammed A Sadat, Susan Moir, Tae-Wook Chun, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Plos Genetics|February 4, 2017
ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13Yihan Zhang, Haigen Huang, Gexin Zhao, et al.
Nucleic Acids Research|May 8, 2010
Genome-wide DNA methylation analysis in cohesin mutant human cell linesJinglan Liu, Zhe Zhang, Masashige Bando, et al.
Frontiers in Digital Health|June 26, 2026
Ensemble based in transfer learning for cytological classification in pleural fluidFrida López-Córdova, Hugo Vega-Huerta, Gisella Luisa Elena Maquen-Niño, et al.
Frontiers in Digital Health|July 15, 2026
Transfer learning and vision transformer for the automatic diagnosis of cataracts in ophthalmological imagesHugo Vega-Huerta, Camila Isabela Cuba-Aquino, Gari Mario Suca-Mariño, et al.
American Journal of Medical Genetics. Part A|February 8, 2014
Cornelia de Lange syndrome: further delineation of phenotype, cohesin biology and educational focus, 5th Biennial Scientific and Educational Symposium abstractsAntonie D Kline, Anne L Calof, Cheri A Schaaf, et al.
Human Molecular Genetics|April 16, 2008
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activityMiriam Gordillo, Hugo Vega, Alison H Trainer, et al.
Molecular Genetics and Metabolism|May 28, 2014
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivityDavid R Adams, Hongjie Yuan, Todd Holyoak, et al.
The New England Journal of Medicine|April 11, 2014
Glycosylation, hypogammaglobulinemia, and resistance to viral infectionsMohammed A Sadat, Susan Moir, Tae-Wook Chun, et al.
Pageof 2