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Showing results (221-230 of 226) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2015
A genome-wide identified risk variant for PTSD is a methylation quantitative trait locus and confers decreased cortical activation to fearful facesLynn M Almli, Jennifer S Stevens, Alicia K Smith, et al.
Metallomics : Integrated Biometal Science|June 14, 2016
Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX)Gonzalo Perez-Siles, Adrienne Grant, Melina Ellis, et al.
Scientific Reports|June 11, 2021
High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assayMarkus H Kainulainen, Eric Bergeron, Payel Chatterjee, et al.
Addiction Biology|October 31, 2017
Problematic alcohol use associates with sodium channel and clathrin linker 1 (SCLT1) in trauma-exposed populationsLynn M Almli, Adriana Lori, Jacquelyn L Meyers, et al.
American Journal of Human Genetics|February 23, 2010
Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathyMarina L Kennerson, Garth A Nicholson, Stephen G Kaler, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 6, 2014
Oral treatment with Cu(II)(atsm) increases mutant SOD1 in vivo but protects motor neurons and improves the phenotype of a transgenic mouse model of amyotrophic lateral sclerosisBlaine R Roberts, Nastasia K H Lim, Erin J McAllum, et al.
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Showing results (221-230 of 226) with videos related to

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You have reached the last page of results.This site can display upto 226 results.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 20, 2015
A genome-wide identified risk variant for PTSD is a methylation quantitative trait locus and confers decreased cortical activation to fearful facesLynn M Almli, Jennifer S Stevens, Alicia K Smith, et al.
Metallomics : Integrated Biometal Science|June 14, 2016
Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX)Gonzalo Perez-Siles, Adrienne Grant, Melina Ellis, et al.
Scientific Reports|June 11, 2021
High-throughput quantitation of SARS-CoV-2 antibodies in a single-dilution homogeneous assayMarkus H Kainulainen, Eric Bergeron, Payel Chatterjee, et al.
Addiction Biology|October 31, 2017
Problematic alcohol use associates with sodium channel and clathrin linker 1 (SCLT1) in trauma-exposed populationsLynn M Almli, Adriana Lori, Jacquelyn L Meyers, et al.
American Journal of Human Genetics|February 23, 2010
Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathyMarina L Kennerson, Garth A Nicholson, Stephen G Kaler, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 6, 2014
Oral treatment with Cu(II)(atsm) increases mutant SOD1 in vivo but protects motor neurons and improves the phenotype of a transgenic mouse model of amyotrophic lateral sclerosisBlaine R Roberts, Nastasia K H Lim, Erin J McAllum, et al.
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