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Miguel Mitne-Neto

Showing results (21-30 of 29) with videos related to

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Human Molecular Genetics|April 14, 2020
Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegenerationDanyllo Oliveira, David A Morales-Vicente, Murilo S Amaral, et al.
Diagnostics (Basel, Switzerland)|August 27, 2021
A Novel Saliva RT-LAMP Workflow for Rapid Identification of COVID-19 Cases and Restraining Viral SpreadGerson Shigeru Kobayashi, Luciano Abreu Brito, Danielle de Paula Moreira, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 16, 2021
Frequency of carriers for rare recessive Mendelian diseases in a Brazilian cohort of 320 patientsCaio Robledo D'Angioli Costa Quaio, Christine Hsiaoyun Chung, Sandro Felix Perazzio, et al.
Open Biology|February 1, 2022
Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pairMateus V de Castro, Keity S Santos, Juliana S Apostolico, et al.
Frontiers in Immunology|October 15, 2021
MHC Variants Associated With Symptomatic <i>Versus</i> Asymptomatic SARS-CoV-2 Infection in Highly Exposed IndividualsErick C Castelli, Mateus V de Castro, Michel S Naslavsky, et al.
Genetics and Molecular Biology|October 5, 2021
Exome sequencing and targeted gene panels: a simulated comparison of diagnostic yield using data from 158 patients with rare diseasesCaio Robledo D'Angioli Costa Quaio, María José Rivadeneira Obando, Sandro Felix Perazzio, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 1, 2020
Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseasesCaio Robledo D'Angioli Costa Quaio, Caroline Monaco Moreira, Gil Monteiro Novo-Filho, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
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Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Human Molecular Genetics|April 14, 2020
Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegenerationDanyllo Oliveira, David A Morales-Vicente, Murilo S Amaral, et al.
Diagnostics (Basel, Switzerland)|August 27, 2021
A Novel Saliva RT-LAMP Workflow for Rapid Identification of COVID-19 Cases and Restraining Viral SpreadGerson Shigeru Kobayashi, Luciano Abreu Brito, Danielle de Paula Moreira, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 16, 2021
Frequency of carriers for rare recessive Mendelian diseases in a Brazilian cohort of 320 patientsCaio Robledo D'Angioli Costa Quaio, Christine Hsiaoyun Chung, Sandro Felix Perazzio, et al.
Open Biology|February 1, 2022
Recurrence of COVID-19 associated with reduced T-cell responses in a monozygotic twin pairMateus V de Castro, Keity S Santos, Juliana S Apostolico, et al.
Frontiers in Immunology|October 15, 2021
MHC Variants Associated With Symptomatic <i>Versus</i> Asymptomatic SARS-CoV-2 Infection in Highly Exposed IndividualsErick C Castelli, Mateus V de Castro, Michel S Naslavsky, et al.
Genetics and Molecular Biology|October 5, 2021
Exome sequencing and targeted gene panels: a simulated comparison of diagnostic yield using data from 158 patients with rare diseasesCaio Robledo D'Angioli Costa Quaio, María José Rivadeneira Obando, Sandro Felix Perazzio, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 1, 2020
Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseasesCaio Robledo D'Angioli Costa Quaio, Caroline Monaco Moreira, Gil Monteiro Novo-Filho, et al.
Science Translational Medicine|February 23, 2022
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALSPaul J Hop, Ramona A J Zwamborn, Eilis Hannon, et al.
Nature Genetics|December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biologyWouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
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