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Lawrence T Reiter

Showing results (51-60 of 59) with videos related to

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Molecular Autism|July 18, 2019
Mechanisms underlying the EEG biomarker in Dup15q syndromeJoel Frohlich, Lawrence T Reiter, Vidya Saravanapandian, et al.
Nature Communications|March 1, 2023
Linoleic acid improves PIEZO2 dysfunction in a mouse model of Angelman SyndromeLuis O Romero, Rebeca Caires, A Kaitlyn Victor, et al.
JMIR Research Protocols|October 20, 2017
Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early UsesOluwaseun Jessica Ajayi, Ebony Jeannae Smith, Teeradache Viangteeravat, et al.
Molecular Autism|February 20, 2015
Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1Noelle D Germain, Pin-Fang Chen, Alex M Plocik, et al.
Epilepsia|February 8, 2014
A survey of seizures and current treatments in 15q duplication syndromeKerry D Conant, Brenda Finucane, Nicole Cleary, et al.
Human Molecular Genetics|October 11, 2017
Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndromeNycole A Copping, Sarah G B Christian, Dylan J Ritter, et al.
Human Molecular Genetics|January 5, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregressionCamilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
Human Molecular Genetics|February 16, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregressionCamilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
JCI Insight|September 4, 2020
Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide productionHelen Chen, A Kaitlyn Victor, Jonathon Klein, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Molecular Autism|July 18, 2019
Mechanisms underlying the EEG biomarker in Dup15q syndromeJoel Frohlich, Lawrence T Reiter, Vidya Saravanapandian, et al.
Nature Communications|March 1, 2023
Linoleic acid improves PIEZO2 dysfunction in a mouse model of Angelman SyndromeLuis O Romero, Rebeca Caires, A Kaitlyn Victor, et al.
JMIR Research Protocols|October 20, 2017
Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early UsesOluwaseun Jessica Ajayi, Ebony Jeannae Smith, Teeradache Viangteeravat, et al.
Molecular Autism|February 20, 2015
Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1Noelle D Germain, Pin-Fang Chen, Alex M Plocik, et al.
Epilepsia|February 8, 2014
A survey of seizures and current treatments in 15q duplication syndromeKerry D Conant, Brenda Finucane, Nicole Cleary, et al.
Human Molecular Genetics|October 11, 2017
Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndromeNycole A Copping, Sarah G B Christian, Dylan J Ritter, et al.
Human Molecular Genetics|January 5, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregressionCamilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
Human Molecular Genetics|February 16, 2018
A recurrent de novo missense mutation in UBTF causes developmental neuroregressionCamilo Toro, Roderick T Hori, May Christine V Malicdan, et al.
JCI Insight|September 4, 2020
Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide productionHelen Chen, A Kaitlyn Victor, Jonathon Klein, et al.
Pageof 6