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Annette Schenck

Showing results (61-70 of 83) with videos related to

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Brain : a Journal of Neurology|April 23, 2021
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxiaAdriana P Rebelo, Ilse Eidhof, Vivian P Cintra, et al.
Plos One|February 13, 2019
Conserved regulation of neurodevelopmental processes and behavior by FoxP in DrosophilaAnna Castells-Nobau, Ilse Eidhof, Michaela Fenckova, et al.
Human Molecular Genetics|September 18, 2015
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegenerationAline Dubos, Anna Castells-Nobau, Hamid Meziane, et al.
Human Molecular Genetics|April 2, 2009
SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathwaySimon T Cliffe, Jamie M Kramer, Khalid Hussain, et al.
Science Advances|June 5, 2021
The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defectsMireia Coll-Tané, Naihua N Gong, Samuel J Belfer, et al.
Plos Genetics|October 26, 2017
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorderTom S Koemans, Tjitske Kleefstra, Melissa C Chubak, et al.
Human Molecular Genetics|April 12, 2013
CEP89 is required for mitochondrial metabolism and neuronal function in man and flyBregje W M van Bon, Merel A W Oortveld, Leo G Nijtmans, et al.
Nature|June 5, 2014
Genome sequencing identifies major causes of severe intellectual disabilityChristian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, et al.
Human Molecular Genetics|February 8, 2013
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disordersZafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.
American Journal of Human Genetics|June 26, 2012
Disruption of an EHMT1-associated chromatin-modification module causes intellectual disabilityTjitske Kleefstra, Jamie M Kramer, Kornelia Neveling, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
Brain : a Journal of Neurology|April 23, 2021
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxiaAdriana P Rebelo, Ilse Eidhof, Vivian P Cintra, et al.
Plos One|February 13, 2019
Conserved regulation of neurodevelopmental processes and behavior by FoxP in DrosophilaAnna Castells-Nobau, Ilse Eidhof, Michaela Fenckova, et al.
Human Molecular Genetics|September 18, 2015
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegenerationAline Dubos, Anna Castells-Nobau, Hamid Meziane, et al.
Human Molecular Genetics|April 2, 2009
SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathwaySimon T Cliffe, Jamie M Kramer, Khalid Hussain, et al.
Science Advances|June 5, 2021
The CHD8/CHD7/Kismet family links blood-brain barrier glia and serotonin to ASD-associated sleep defectsMireia Coll-Tané, Naihua N Gong, Samuel J Belfer, et al.
Plos Genetics|October 26, 2017
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorderTom S Koemans, Tjitske Kleefstra, Melissa C Chubak, et al.
Human Molecular Genetics|April 12, 2013
CEP89 is required for mitochondrial metabolism and neuronal function in man and flyBregje W M van Bon, Merel A W Oortveld, Leo G Nijtmans, et al.
Nature|June 5, 2014
Genome sequencing identifies major causes of severe intellectual disabilityChristian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, et al.
Human Molecular Genetics|February 8, 2013
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disordersZafar Iqbal, Geert Vandeweyer, Monique van der Voet, et al.
American Journal of Human Genetics|June 26, 2012
Disruption of an EHMT1-associated chromatin-modification module causes intellectual disabilityTjitske Kleefstra, Jamie M Kramer, Kornelia Neveling, et al.
Pageof 9