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Jeffrey L Neul

Showing results (11-20 of 122) with videos related to

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Genes, Brain, and Behavior|May 4, 2021
Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndromeBridget E Collins, Jonathan K Merritt, Kirsty R Erickson, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 22, 2014
Low bone mineral mass is associated with decreased bone formation and diet in girls with Rett syndromeKathleen J Motil, Judy O Barrish, Jeffrey L Neul, et al.
Scientific Reports|August 24, 2017
Embryonic hindbrain patterning genes delineate distinct cardio-respiratory and metabolic homeostatic populations in the adultJenny J Sun, Teng-Wei Huang, Jeffrey L Neul, et al.
Journal of Neurodevelopmental Disorders|July 20, 2024
A clinical-translational review of sleep problems in neurodevelopmental disabilitiesSarika U Peters, Althea Robinson Shelton, Beth A Malow, et al.
Human Molecular Genetics|February 5, 2017
Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesisJosé A Herrera, Christopher S Ward, Xander H T Wehrens, et al.
Journal of Child Neurology|June 26, 2025
Sleep Problems and Clinical Severity in Rett SyndromeSarika U Peters, Cary Fu, Althea Robinson Shelton, et al.
Annals of the Child Neurology Society|August 29, 2025
Symptom Onset in Classic Rett Syndrome: Analysis of Initial Clinical Severity Scale EntriesAlan K Percy, Jeffrey L Neul, Amitha Ananth, et al.
Human Molecular Genetics|May 30, 2020
Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndromeJonathan K Merritt, Bridget E Collins, Kirsty R Erickson, et al.
Journal of Autism and Developmental Disorders|August 8, 2013
Brief report: MECP2 mutations in people without Rett syndromeBernhard Suter, Diane Treadwell-Deering, Huda Y Zoghbi, et al.
Translational Science of Rare Diseases|April 24, 2018
When Rett syndrome is due to genes other than <i>MECP2</i>Alan K Percy, Jane Lane, Fran Annese, et al.
Pageof 13

Showing results (11-20 of 122) with videos related to

Sort By:
Pageof 13
Genes, Brain, and Behavior|May 4, 2021
Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndromeBridget E Collins, Jonathan K Merritt, Kirsty R Erickson, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 22, 2014
Low bone mineral mass is associated with decreased bone formation and diet in girls with Rett syndromeKathleen J Motil, Judy O Barrish, Jeffrey L Neul, et al.
Scientific Reports|August 24, 2017
Embryonic hindbrain patterning genes delineate distinct cardio-respiratory and metabolic homeostatic populations in the adultJenny J Sun, Teng-Wei Huang, Jeffrey L Neul, et al.
Journal of Neurodevelopmental Disorders|July 20, 2024
A clinical-translational review of sleep problems in neurodevelopmental disabilitiesSarika U Peters, Althea Robinson Shelton, Beth A Malow, et al.
Human Molecular Genetics|February 5, 2017
Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesisJosé A Herrera, Christopher S Ward, Xander H T Wehrens, et al.
Journal of Child Neurology|June 26, 2025
Sleep Problems and Clinical Severity in Rett SyndromeSarika U Peters, Cary Fu, Althea Robinson Shelton, et al.
Annals of the Child Neurology Society|August 29, 2025
Symptom Onset in Classic Rett Syndrome: Analysis of Initial Clinical Severity Scale EntriesAlan K Percy, Jeffrey L Neul, Amitha Ananth, et al.
Human Molecular Genetics|May 30, 2020
Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndromeJonathan K Merritt, Bridget E Collins, Kirsty R Erickson, et al.
Journal of Autism and Developmental Disorders|August 8, 2013
Brief report: MECP2 mutations in people without Rett syndromeBernhard Suter, Diane Treadwell-Deering, Huda Y Zoghbi, et al.
Translational Science of Rare Diseases|April 24, 2018
When Rett syndrome is due to genes other than <i>MECP2</i>Alan K Percy, Jane Lane, Fran Annese, et al.
Pageof 13