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Dodelson

Showing results (81-90 of 95) with videos related to

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Scientific Reports|September 19, 2014
A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDGM A Delgado, G Martinez-Domenech, P Sarrión, et al.
Journal of Inherited Metabolic Disease|June 16, 2010
The molecular landscape of propionic acidemia and methylmalonic aciduria in Latin AmericaBelén Pérez, Celia Angaroni, Rocio Sánchez-Alcudia, et al.
Molecular Cancer Therapeutics|May 13, 2020
Blockade of Cell Volume Regulatory Protein NKCC1 Increases TMZ-Induced Glioma Apoptosis and Reduces AstrogliosisLanxin Luo, Xiudong Guan, Gulnaz Begum, et al.
Gene|December 26, 2012
Neuronal ceroid lipofuscinosis type CLN2: a new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South AmericaRomina Kohan, María Noelia Carabelos, Winnie Xin, et al.
Plos One|August 1, 2012
Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff disease: functional characterization of 9 novel sequence variantsStefania Zampieri, Silvia Cattarossi, Ana Maria Oller Ramirez, et al.
The Journal of Comparative Neurology|September 2, 2020
Putative dendritic correlates of chronic traumatic encephalopathy: A preliminary quantitative Golgi explorationAllysa Warling, Riri Uchida, Hyunsoo Shin, et al.
Resuscitation|February 12, 2022
Severe cerebral edema in substance-related cardiac arrest patientsAnnelise M Kulpanowski, William A Copen, Brandon L Hancock, et al.
Resuscitation|May 25, 2025
Automated detection of severe cerebral edema using explainable deep transfer learning after hypoxic ischemic brain injuryZihao Wang, Annelise M Kulpanowski, William A Copen, et al.
Journal of Human Genetics|February 16, 2006
The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South AmericaRoser Urreizti, Carla Asteggiano, Marta Bermudez, et al.
Journal of Human Genetics|February 9, 2020
Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South AmericaRoser Urreizti, Carla Asteggiano, Marta Bermudez, et al.
Pageof 10

Showing results (81-90 of 95) with videos related to

Sort By:
Pageof 10
Scientific Reports|September 19, 2014
A broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDGM A Delgado, G Martinez-Domenech, P Sarrión, et al.
Journal of Inherited Metabolic Disease|June 16, 2010
The molecular landscape of propionic acidemia and methylmalonic aciduria in Latin AmericaBelén Pérez, Celia Angaroni, Rocio Sánchez-Alcudia, et al.
Molecular Cancer Therapeutics|May 13, 2020
Blockade of Cell Volume Regulatory Protein NKCC1 Increases TMZ-Induced Glioma Apoptosis and Reduces AstrogliosisLanxin Luo, Xiudong Guan, Gulnaz Begum, et al.
Gene|December 26, 2012
Neuronal ceroid lipofuscinosis type CLN2: a new rationale for the construction of phenotypic subgroups based on a survey of 25 cases in South AmericaRomina Kohan, María Noelia Carabelos, Winnie Xin, et al.
Plos One|August 1, 2012
Sequence and copy number analyses of HEXB gene in patients affected by Sandhoff disease: functional characterization of 9 novel sequence variantsStefania Zampieri, Silvia Cattarossi, Ana Maria Oller Ramirez, et al.
The Journal of Comparative Neurology|September 2, 2020
Putative dendritic correlates of chronic traumatic encephalopathy: A preliminary quantitative Golgi explorationAllysa Warling, Riri Uchida, Hyunsoo Shin, et al.
Resuscitation|February 12, 2022
Severe cerebral edema in substance-related cardiac arrest patientsAnnelise M Kulpanowski, William A Copen, Brandon L Hancock, et al.
Resuscitation|May 25, 2025
Automated detection of severe cerebral edema using explainable deep transfer learning after hypoxic ischemic brain injuryZihao Wang, Annelise M Kulpanowski, William A Copen, et al.
Journal of Human Genetics|February 16, 2006
The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South AmericaRoser Urreizti, Carla Asteggiano, Marta Bermudez, et al.
Journal of Human Genetics|February 9, 2020
Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South AmericaRoser Urreizti, Carla Asteggiano, Marta Bermudez, et al.
Pageof 10