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Beate Peter

Showing results (31-40 of 53) with videos related to

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American Journal of Medical Genetics. Part A|February 11, 2021
A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocationBeate Peter, Nancy Scherer, Winnie S Liang, et al.
Journal of Science and Medicine in Sport|May 3, 2016
Effect of intermittent normobaric hypoxia on aerobic capacity and cognitive function in older peopleLutz Schega, Beate Peter, Tanja Brigadski, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2024
Joint exome and metabolome analysis in individuals with dyslexia: Evidence for associated dysregulations of olfactory perception and autoimmune functionsRohit Nandakumar, Xiaojian Shi, Haiwei Gu, et al.
Behavior Genetics|April 6, 2019
Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex EffectsBeate Peter, Valentin Dinu, Li Liu, et al.
American Journal of Speech-Language Pathology|October 17, 2022
Feasibility of a Proactive Parent-Implemented Communication Intervention Delivered via Telepractice for Children With Classic GalactosemiaLizbeth H Finestack, Nancy Potter, Mark VanDam, et al.
Neurobiology of Aging|February 21, 2025
Normative aging results in degradation of gene networks in a zebra finch basal ganglia nucleus dedicated to vocal behaviorCharles M Higgins, Sri Harsha Vishwanath, Fiona M McCarthy, et al.
Biorxiv : the Preprint Server for Biology|March 13, 2023
A data-fusion approach to identifying developmental dyslexia from multi-omics datasetsJackson Carrion, Rohit Nandakumar, Xiaojian Shi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2008
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21Wendy H Raskind, Mark Matsushita, Beate Peter, et al.
Plos Pathogens|January 31, 2018
A new mechanism of interferon's antiviral action: Induction of autophagy, essential for paramyxovirus replication, is inhibited by the interferon stimulated gene, TDRD7Gayatri Subramanian, Teodora Kuzmanovic, Ying Zhang, et al.
Journal of Neurodevelopmental Disorders|April 13, 2011
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sampleBeate Peter, Wendy H Raskind, Mark Matsushita, et al.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part A|February 11, 2021
A phenotypically diverse family with an atypical 22q11.2 deletion due to an unbalanced 18q23;22q11.2 translocationBeate Peter, Nancy Scherer, Winnie S Liang, et al.
Journal of Science and Medicine in Sport|May 3, 2016
Effect of intermittent normobaric hypoxia on aerobic capacity and cognitive function in older peopleLutz Schega, Beate Peter, Tanja Brigadski, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2024
Joint exome and metabolome analysis in individuals with dyslexia: Evidence for associated dysregulations of olfactory perception and autoimmune functionsRohit Nandakumar, Xiaojian Shi, Haiwei Gu, et al.
Behavior Genetics|April 6, 2019
Exome Sequencing of Two Siblings with Sporadic Autism Spectrum Disorder and Severe Speech Sound Disorder Suggests Pleiotropic and Complex EffectsBeate Peter, Valentin Dinu, Li Liu, et al.
American Journal of Speech-Language Pathology|October 17, 2022
Feasibility of a Proactive Parent-Implemented Communication Intervention Delivered via Telepractice for Children With Classic GalactosemiaLizbeth H Finestack, Nancy Potter, Mark VanDam, et al.
Neurobiology of Aging|February 21, 2025
Normative aging results in degradation of gene networks in a zebra finch basal ganglia nucleus dedicated to vocal behaviorCharles M Higgins, Sri Harsha Vishwanath, Fiona M McCarthy, et al.
Biorxiv : the Preprint Server for Biology|March 13, 2023
A data-fusion approach to identifying developmental dyslexia from multi-omics datasetsJackson Carrion, Rohit Nandakumar, Xiaojian Shi, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2008
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21Wendy H Raskind, Mark Matsushita, Beate Peter, et al.
Plos Pathogens|January 31, 2018
A new mechanism of interferon's antiviral action: Induction of autophagy, essential for paramyxovirus replication, is inhibited by the interferon stimulated gene, TDRD7Gayatri Subramanian, Teodora Kuzmanovic, Ying Zhang, et al.
Journal of Neurodevelopmental Disorders|April 13, 2011
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sampleBeate Peter, Wendy H Raskind, Mark Matsushita, et al.
Pageof 6