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Carl Ernst

Showing results (71-80 of 89) with videos related to

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Nature Communications|February 19, 2021
Non-CG methylation and multiple histone profiles associate child abuse with immune and small GTPase dysregulationPierre-Eric Lutz, Marc-Aurèle Chay, Alain Pacis, et al.
Stem Cell Reports|June 26, 2018
Disruption of GRIN2B Impairs Differentiation in Human NeuronsScott Bell, Gilles Maussion, Malvin Jefri, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 26, 2018
A Dual Noradrenergic Mechanism for the Relief of Neuropathic Allodynia by the Antidepressant Drugs Duloxetine and AmitriptylineMélanie Kremer, Ipek Yalcin, Yannick Goumon, et al.
Human Genetics|January 29, 2013
Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palateAmelia M Lindgren, Tatiana Hoyos, Michael E Talkowski, et al.
Stem Cells Translational Medicine|March 11, 2020
Stimulation of L-type calcium channels increases tyrosine hydroxylase and dopamine in ventral midbrain cells induced from somatic cellsMalvin Jefri, Scott Bell, Huashan Peng, et al.
European Journal of Human Genetics : EJHG|January 17, 2013
Mosaic copy number variation in schizophreniaDouglas M Ruderfer, Kim Chambert, Jennifer Moran, et al.
Stem Cell Reports|July 2, 2021
Lesch-Nyhan disease causes impaired energy metabolism and reduced developmental potential in midbrain dopaminergic cellsScott Bell, Vincent McCarty, Huashan Peng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 16, 2019
Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayBettina E Mucha, Siddharth Banka, Norbert Fonya Ajeawung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayBettina E Mucha, Siddharth Banka, Norbert Fonya Ajeawung, et al.
The American Journal of Psychiatry|July 29, 2017
Association of a History of Child Abuse With Impaired Myelination in the Anterior Cingulate Cortex: Convergent Epigenetic, Transcriptional, and Morphological EvidencePierre-Eric Lutz, Arnaud Tanti, Alicja Gasecka, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Nature Communications|February 19, 2021
Non-CG methylation and multiple histone profiles associate child abuse with immune and small GTPase dysregulationPierre-Eric Lutz, Marc-Aurèle Chay, Alain Pacis, et al.
Stem Cell Reports|June 26, 2018
Disruption of GRIN2B Impairs Differentiation in Human NeuronsScott Bell, Gilles Maussion, Malvin Jefri, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 26, 2018
A Dual Noradrenergic Mechanism for the Relief of Neuropathic Allodynia by the Antidepressant Drugs Duloxetine and AmitriptylineMélanie Kremer, Ipek Yalcin, Yannick Goumon, et al.
Human Genetics|January 29, 2013
Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palateAmelia M Lindgren, Tatiana Hoyos, Michael E Talkowski, et al.
Stem Cells Translational Medicine|March 11, 2020
Stimulation of L-type calcium channels increases tyrosine hydroxylase and dopamine in ventral midbrain cells induced from somatic cellsMalvin Jefri, Scott Bell, Huashan Peng, et al.
European Journal of Human Genetics : EJHG|January 17, 2013
Mosaic copy number variation in schizophreniaDouglas M Ruderfer, Kim Chambert, Jennifer Moran, et al.
Stem Cell Reports|July 2, 2021
Lesch-Nyhan disease causes impaired energy metabolism and reduced developmental potential in midbrain dopaminergic cellsScott Bell, Vincent McCarty, Huashan Peng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 16, 2019
Correction: A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayBettina E Mucha, Siddharth Banka, Norbert Fonya Ajeawung, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 25, 2018
A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delayBettina E Mucha, Siddharth Banka, Norbert Fonya Ajeawung, et al.
The American Journal of Psychiatry|July 29, 2017
Association of a History of Child Abuse With Impaired Myelination in the Anterior Cingulate Cortex: Convergent Epigenetic, Transcriptional, and Morphological EvidencePierre-Eric Lutz, Arnaud Tanti, Alicja Gasecka, et al.
Pageof 9