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Jeffrey L Neul

Showing results (91-100 of 122) with videos related to

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Elife|June 22, 2016
Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disordersXiangling Meng, Wei Wang, Hui Lu, et al.
Journal of Medical Genetics|January 9, 2014
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndromeVishnu Anand Cuddapah, Rajesh B Pillai, Kiran V Shekar, et al.
American Journal of Medical Genetics. Part A|September 28, 2023
Parental age effects and Rett syndromeXiaolan Fang, Lauren M Baggett, Raymond C Caylor, et al.
The Journal of Pediatrics|January 22, 2022
Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett SyndromeKathleen J Motil, Suzanne Geerts, Fran Annese, et al.
Human Molecular Genetics|August 13, 2024
Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoformsLadan Kalani, Bo-Hyun Kim, Alberto Ruiz de Chavez, et al.
Journal of Neurodevelopmental Disorders|March 4, 2023
Comparison of evoked potentials across four related developmental encephalopathiesJoni N Saby, Sarika U Peters, Timothy A Benke, et al.
American Journal of Medical Genetics. Part A|November 10, 2020
Phenotypic features in MECP2 duplication syndrome: Effects of ageSarika U Peters, Cary Fu, Eric D Marsh, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2009
Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalitiesRodney C Samaco, Caleigh Mandel-Brehm, Hsiao-Tuan Chao, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 12, 2018
The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2Jeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.
Human Molecular Genetics|September 15, 2024
Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levelsSameer S Bajikar, Yehezkel Sztainberg, Alexander J Trostle, et al.
Pageof 13

Showing results (91-100 of 122) with videos related to

Sort By:
Pageof 13
Elife|June 22, 2016
Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disordersXiangling Meng, Wei Wang, Hui Lu, et al.
Journal of Medical Genetics|January 9, 2014
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndromeVishnu Anand Cuddapah, Rajesh B Pillai, Kiran V Shekar, et al.
American Journal of Medical Genetics. Part A|September 28, 2023
Parental age effects and Rett syndromeXiaolan Fang, Lauren M Baggett, Raymond C Caylor, et al.
The Journal of Pediatrics|January 22, 2022
Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett SyndromeKathleen J Motil, Suzanne Geerts, Fran Annese, et al.
Human Molecular Genetics|August 13, 2024
Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoformsLadan Kalani, Bo-Hyun Kim, Alberto Ruiz de Chavez, et al.
Journal of Neurodevelopmental Disorders|March 4, 2023
Comparison of evoked potentials across four related developmental encephalopathiesJoni N Saby, Sarika U Peters, Timothy A Benke, et al.
American Journal of Medical Genetics. Part A|November 10, 2020
Phenotypic features in MECP2 duplication syndrome: Effects of ageSarika U Peters, Cary Fu, Eric D Marsh, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2009
Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalitiesRodney C Samaco, Caleigh Mandel-Brehm, Hsiao-Tuan Chao, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 12, 2018
The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2Jeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.
Human Molecular Genetics|September 15, 2024
Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levelsSameer S Bajikar, Yehezkel Sztainberg, Alexander J Trostle, et al.
Pageof 13