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Sara Reynhout

Showing results (1-10 of 7) with videos related to

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Biochimica Et Biophysica Acta. Molecular Cell Research|July 22, 2018
Physiologic functions of PP2A: Lessons from genetically modified miceSara Reynhout, Veerle Janssens
Biochemical Society Transactions|July 9, 2021
Protein Phosphatase 2A (PP2A) mutations in brain function, development, and neurologic diseaseIris Verbinnen, Pieter Vaneynde, Sara Reynhout, et al.
Frontiers in Cell and Developmental Biology|December 19, 2022
Clinical and molecular characteristics of a novel rare <i>de novo</i> variant in <i>PPP2CA</i> in a patient with a developmental disorder, autism, and epilepsyIris Verbinnen, Sara S Procknow, Lisa Lenaerts, et al.
Journal of Medical Genetics|October 10, 2022
Clinical, neuroimaging and molecular characteristics of <i>PPP2R5D</i>-related neurodevelopmental disorders: an expanded series with functional characterisation and genotype-phenotype analysisNora Oyama, Pieter Vaneynde, Sara Reynhout, et al.
American Journal of Human Genetics|January 1, 2019
De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental DisordersSara Reynhout, Sandra Jansen, Dorien Haesen, et al.
American Journal of Human Genetics|February 9, 2019
De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental DisordersSara Reynhout, Sandra Jansen, Dorien Haesen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 27, 2020
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunctionLisa Lenaerts, Sara Reynhout, Iris Verbinnen, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Biochimica Et Biophysica Acta. Molecular Cell Research|July 22, 2018
Physiologic functions of PP2A: Lessons from genetically modified miceSara Reynhout, Veerle Janssens
Biochemical Society Transactions|July 9, 2021
Protein Phosphatase 2A (PP2A) mutations in brain function, development, and neurologic diseaseIris Verbinnen, Pieter Vaneynde, Sara Reynhout, et al.
Frontiers in Cell and Developmental Biology|December 19, 2022
Clinical and molecular characteristics of a novel rare <i>de novo</i> variant in <i>PPP2CA</i> in a patient with a developmental disorder, autism, and epilepsyIris Verbinnen, Sara S Procknow, Lisa Lenaerts, et al.
Journal of Medical Genetics|October 10, 2022
Clinical, neuroimaging and molecular characteristics of <i>PPP2R5D</i>-related neurodevelopmental disorders: an expanded series with functional characterisation and genotype-phenotype analysisNora Oyama, Pieter Vaneynde, Sara Reynhout, et al.
American Journal of Human Genetics|January 1, 2019
De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental DisordersSara Reynhout, Sandra Jansen, Dorien Haesen, et al.
American Journal of Human Genetics|February 9, 2019
De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental DisordersSara Reynhout, Sandra Jansen, Dorien Haesen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 27, 2020
The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunctionLisa Lenaerts, Sara Reynhout, Iris Verbinnen, et al.
Pageof 1