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Patrick May

Showing results (181-190 of 209) with videos related to

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Nature Communications|February 14, 2019
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafishAleksandra Siekierska, Hannah Stamberger, Tine Deconinck, et al.
Brain : a Journal of Neurology|October 21, 2017
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic featuresCristina Elena Niturad, Dorit Lev, Vera M Kalscheuer, et al.
Acta Neuropathologica|October 3, 2020
Patient-derived organoids and orthotopic xenografts of primary and recurrent gliomas represent relevant patient avatars for precision oncologyAnna Golebiewska, Ann-Christin Hau, Anaïs Oudin, et al.
Frontiers in Microbiology|March 11, 2021
Statistical and Machine Learning Techniques in Human Microbiome Studies: Contemporary Challenges and SolutionsIsabel Moreno-Indias, Leo Lahti, Miroslava Nedyalkova, et al.
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Dopamine pathway and Parkinson's risk variants are associated with levodopa-induced dyskinesiaYuri L Sosero, Sara Bandres-Ciga, Bart Ferwerda, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 12, 2024
Dopamine Pathway and Parkinson's Risk Variants Are Associated with Levodopa-Induced DyskinesiaYuri L Sosero, Sara Bandres-Ciga, Bart Ferwerda, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Neurology|March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
Brain : a Journal of Neurology|August 30, 2023
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysisArthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.
Nature Communications|December 16, 2021
Critical Assessment of MetaProteome Investigation (CAMPI): a multi-laboratory comparison of established workflowsTim Van Den Bossche, Benoit J Kunath, Kay Schallert, et al.
Pageof 21

Showing results (181-190 of 209) with videos related to

Sort By:
Pageof 21
Nature Communications|February 14, 2019
Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafishAleksandra Siekierska, Hannah Stamberger, Tine Deconinck, et al.
Brain : a Journal of Neurology|October 21, 2017
Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic featuresCristina Elena Niturad, Dorit Lev, Vera M Kalscheuer, et al.
Acta Neuropathologica|October 3, 2020
Patient-derived organoids and orthotopic xenografts of primary and recurrent gliomas represent relevant patient avatars for precision oncologyAnna Golebiewska, Ann-Christin Hau, Anaïs Oudin, et al.
Frontiers in Microbiology|March 11, 2021
Statistical and Machine Learning Techniques in Human Microbiome Studies: Contemporary Challenges and SolutionsIsabel Moreno-Indias, Leo Lahti, Miroslava Nedyalkova, et al.
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Dopamine pathway and Parkinson's risk variants are associated with levodopa-induced dyskinesiaYuri L Sosero, Sara Bandres-Ciga, Bart Ferwerda, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 12, 2024
Dopamine Pathway and Parkinson's Risk Variants Are Associated with Levodopa-Induced DyskinesiaYuri L Sosero, Sara Bandres-Ciga, Bart Ferwerda, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Neurology|March 22, 2022
Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With <i>KCNC2</i> Pathogenic VariantsNiklas Schwarz, Simone Seiffert, Manuela Pendziwiat, et al.
Brain : a Journal of Neurology|August 30, 2023
SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysisArthur Stefanski, Eduardo Pérez-Palma, Tobias Brünger, et al.
Nature Communications|December 16, 2021
Critical Assessment of MetaProteome Investigation (CAMPI): a multi-laboratory comparison of established workflowsTim Van Den Bossche, Benoit J Kunath, Kay Schallert, et al.
Pageof 21