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S Caron

Showing results (81-90 of 423) with videos related to

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Genes, Brain, and Behavior|April 6, 2007
The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophreniaS C Bakker, M L C Hoogendoorn, J Hendriks, et al.
Cell|September 27, 2001
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and diseaseB G Bruneau, G Nemer, J P Schmitt, et al.
Brain : a Journal of Neurology|August 18, 2024
Exon 1-targeting miRNA reduces the pathogenic exon 1 HTT protein in Huntington's disease modelsMarina Sogorb-Gonzalez, Christian Landles, Nicholas S Caron, et al.
Human Genome Variation|April 15, 2022
Functional characterization of variants of unknown significance in a spinocerebellar ataxia patient using an unsupervised machine learning pipelineSiddharth Nath, Nicholas S Caron, Linda May, et al.
Oncogene|August 26, 1998
Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancerM G FitzGerald, D J Marsh, D Wahrer, et al.
Biomarker Research|April 21, 2025
Challenges and advances for huntingtin detection in cerebrospinal fluid: in support of relative quantificationRachel J Harding, Yuanyun Xie, Nicholas S Caron, et al.
Frontiers in Cellular Neuroscience|November 30, 2020
DAPK1 Promotes Extrasynaptic GluN2B Phosphorylation and Striatal Spine Instability in the YAC128 Mouse Model of Huntington DiseaseMandi E Schmidt, Nicholas S Caron, Amirah E Aly, et al.
Human Molecular Genetics|September 8, 2020
Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington diseaseGalen E B Wright, Nicholas S Caron, Bernard Ng, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Challenges and advances for huntingtin detection in cerebrospinal fluid: in support of relative quantificationRachel J Harding, Yuanyun Xie, Nicholas S Caron, et al.
Neurobiology of Disease|February 10, 2022
Cerebrospinal fluid mutant huntingtin is a biomarker for huntingtin lowering in the striatum of Huntington disease miceNicholas S Caron, Raul Banos, Amirah E Aly, et al.
Pageof 43

Showing results (81-90 of 423) with videos related to

Sort By:
Pageof 43
Genes, Brain, and Behavior|April 6, 2007
The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophreniaS C Bakker, M L C Hoogendoorn, J Hendriks, et al.
Cell|September 27, 2001
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and diseaseB G Bruneau, G Nemer, J P Schmitt, et al.
Brain : a Journal of Neurology|August 18, 2024
Exon 1-targeting miRNA reduces the pathogenic exon 1 HTT protein in Huntington's disease modelsMarina Sogorb-Gonzalez, Christian Landles, Nicholas S Caron, et al.
Human Genome Variation|April 15, 2022
Functional characterization of variants of unknown significance in a spinocerebellar ataxia patient using an unsupervised machine learning pipelineSiddharth Nath, Nicholas S Caron, Linda May, et al.
Oncogene|August 26, 1998
Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancerM G FitzGerald, D J Marsh, D Wahrer, et al.
Biomarker Research|April 21, 2025
Challenges and advances for huntingtin detection in cerebrospinal fluid: in support of relative quantificationRachel J Harding, Yuanyun Xie, Nicholas S Caron, et al.
Frontiers in Cellular Neuroscience|November 30, 2020
DAPK1 Promotes Extrasynaptic GluN2B Phosphorylation and Striatal Spine Instability in the YAC128 Mouse Model of Huntington DiseaseMandi E Schmidt, Nicholas S Caron, Amirah E Aly, et al.
Human Molecular Genetics|September 8, 2020
Gene expression profiles complement the analysis of genomic modifiers of the clinical onset of Huntington diseaseGalen E B Wright, Nicholas S Caron, Bernard Ng, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Challenges and advances for huntingtin detection in cerebrospinal fluid: in support of relative quantificationRachel J Harding, Yuanyun Xie, Nicholas S Caron, et al.
Neurobiology of Disease|February 10, 2022
Cerebrospinal fluid mutant huntingtin is a biomarker for huntingtin lowering in the striatum of Huntington disease miceNicholas S Caron, Raul Banos, Amirah E Aly, et al.
Pageof 43