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Showing results (181-190 of 248) with videos related to

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Geophysical Research Letters|January 3, 2020
Mars Science Laboratory Observations of Chloride Salts in Gale Crater, MarsN H Thomas, B L Ehlmann, P-Y Meslin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 13, 2015
Phosphorylation of synaptic vesicle protein 2A at Thr84 by casein kinase 1 family kinases controls the specific retrieval of synaptotagmin-1Ning Zhang, Sarah L Gordon, Maximilian J Fritsch, et al.
American Journal of Clinical Pathology|January 23, 2010
Comparison of fluorescence in situ hybridization, p57 immunostaining, flow cytometry, and digital image analysis for diagnosing molar and nonmolar products of conceptionBenjamin R Kipp, Rhett P Ketterling, Trynda N Oberg, et al.
Journal of Neurochemistry|August 2, 2024
SV2A controls the surface nanoclustering and endocytic recruitment of Syt1 during synaptic vesicle recyclingChristopher Small, Callista Harper, Anmin Jiang, et al.
BMC Genomics|April 16, 2024
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic diseaseNumrah Fadra, Laura E Schultz-Rogers, Pritha Chanana, et al.
Plos One|October 3, 2019
A tailored approach to fusion transcript identification increases diagnosis of rare inherited diseaseGavin R Oliver, Xiaojia Tang, Laura E Schultz-Rogers, et al.
Cold Spring Harbor Molecular Case Studies|May 11, 2017
Novel de novo variant in <i>EBF3</i> is likely to impact DNA binding in a patient with a neurodevelopmental disorder and expanded phenotypes: patient report, in silico functional assessment, and review of published casesPatrick R Blackburn, Sarah S Barnett, Michael T Zimmermann, et al.
Molecular Genetics and Metabolism Reports|August 24, 2017
The prevalence of diseases caused by lysosome-related genes in a cohort of undiagnosed patientsFilippo Pinto Vairo, Nicole J Boczek, Margot A Cousin, et al.
BMC Medical Genetics|December 7, 2016
A novel ANO3 variant identified in a 53-year-old woman presenting with hyperkinetic dysarthria, blepharospasm, hyperkinesias, and complex motor ticsPatrick R Blackburn, Michael T Zimmermann, Jennifer M Gass, et al.
Nature Communications|December 18, 2014
A molecular toggle after exocytosis sequesters the presynaptic syntaxin1a molecules involved in prior vesicle fusionDeirdre M Kavanagh, Annya M Smyth, Kirsty J Martin, et al.
Pageof 25

Showing results (181-190 of 248) with videos related to

Sort By:
Pageof 25
Geophysical Research Letters|January 3, 2020
Mars Science Laboratory Observations of Chloride Salts in Gale Crater, MarsN H Thomas, B L Ehlmann, P-Y Meslin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 13, 2015
Phosphorylation of synaptic vesicle protein 2A at Thr84 by casein kinase 1 family kinases controls the specific retrieval of synaptotagmin-1Ning Zhang, Sarah L Gordon, Maximilian J Fritsch, et al.
American Journal of Clinical Pathology|January 23, 2010
Comparison of fluorescence in situ hybridization, p57 immunostaining, flow cytometry, and digital image analysis for diagnosing molar and nonmolar products of conceptionBenjamin R Kipp, Rhett P Ketterling, Trynda N Oberg, et al.
Journal of Neurochemistry|August 2, 2024
SV2A controls the surface nanoclustering and endocytic recruitment of Syt1 during synaptic vesicle recyclingChristopher Small, Callista Harper, Anmin Jiang, et al.
BMC Genomics|April 16, 2024
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic diseaseNumrah Fadra, Laura E Schultz-Rogers, Pritha Chanana, et al.
Plos One|October 3, 2019
A tailored approach to fusion transcript identification increases diagnosis of rare inherited diseaseGavin R Oliver, Xiaojia Tang, Laura E Schultz-Rogers, et al.
Cold Spring Harbor Molecular Case Studies|May 11, 2017
Novel de novo variant in <i>EBF3</i> is likely to impact DNA binding in a patient with a neurodevelopmental disorder and expanded phenotypes: patient report, in silico functional assessment, and review of published casesPatrick R Blackburn, Sarah S Barnett, Michael T Zimmermann, et al.
Molecular Genetics and Metabolism Reports|August 24, 2017
The prevalence of diseases caused by lysosome-related genes in a cohort of undiagnosed patientsFilippo Pinto Vairo, Nicole J Boczek, Margot A Cousin, et al.
BMC Medical Genetics|December 7, 2016
A novel ANO3 variant identified in a 53-year-old woman presenting with hyperkinetic dysarthria, blepharospasm, hyperkinesias, and complex motor ticsPatrick R Blackburn, Michael T Zimmermann, Jennifer M Gass, et al.
Nature Communications|December 18, 2014
A molecular toggle after exocytosis sequesters the presynaptic syntaxin1a molecules involved in prior vesicle fusionDeirdre M Kavanagh, Annya M Smyth, Kirsty J Martin, et al.
Pageof 25