Cyclin-dependent kinase-like 5 deficiency disorder: clinical review

HE Olson, ST Demarest, EM Pestana-Knight… - Pediatric …, 2019 - Elsevier
Abstract Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a
developmental encephalopathy caused by pathogenic variants in the gene CDKL5. This …

Molecular and synaptic bases of CDKL5 disorder

YC Zhu, ZQ Xiong - Developmental Neurobiology, 2019 - Wiley Online Library
The X‐linked gene cyclin‐dependent kinase‐like 5 (CDKL5) encodes a serine/threonine
kinase abundantly expressed in the brain. Mutations in CDKL5 have been associated with …

CDKL5 deficiency disorder: molecular insights and mechanisms of pathogenicity to fast-track therapeutic development

NJ Van Bergen, S Massey, A Quigley… - Biochemical Society …, 2022 - portlandpress.com
CDKL5 deficiency disorder (CDD) is an X-linked brain disorder of young children and is
caused by pathogenic variants in the cyclin-dependent kinase-like 5 (CDKL5) gene …

Exercise improves cardiac function and glucose metabolism in mice with experimental myocardial infarction through inhibiting HDAC4 and upregulating GLUT1 …

H Jiang, D Jia, B Zhang, W Yang, Z Dong… - Basic Research in …, 2020 - Springer
This study aims to determine the effect of exercise on the cardiac function, metabolic profiles
and related molecular mechanisms in mice with ischemic-induced heart failure (HF). HF was …

Loss of CDKL5 in glutamatergic neurons disrupts hippocampal microcircuitry and leads to memory impairment in mice

S Tang, ITJ Wang, C Yue, H Takano… - Journal of …, 2017 - Soc Neuroscience
Cyclin-dependent kinase-like 5 (CDKL5) deficiency is a neurodevelopmental disorder
characterized by epileptic seizures, severe intellectual disability, and autistic features. Mice …

Luteolin treatment ameliorates brain development and behavioral performance in a mouse model of CDKL5 deficiency disorder

M Tassinari, N Mottolese, G Galvani, D Ferrara… - International Journal of …, 2022 - mdpi.com
CDKL5 deficiency disorder (CDD), a rare and severe neurodevelopmental disease caused
by mutations in the X-linked CDKL 5 gene, is characterized by early-onset epilepsy …

Chemical genetic identification of CDKL 5 substrates reveals its role in neuronal microtubule dynamics

LL Baltussen, PD Negraes, M Silvestre… - The EMBO …, 2018 - embopress.org
Loss‐of‐function mutations in CDKL 5 kinase cause severe neurodevelopmental delay and
early‐onset seizures. Identification of CDKL 5 substrates is key to understanding its function …

Butyrate, but not propionate, reverses maternal diet-induced neurocognitive deficits in offspring

L Yu, X Zhong, Y He, Y Shi - Pharmacological research, 2020 - Elsevier
Background Maternal diet plays a beneficial role in the health, including the
neurodevelopment, of offspring. Insufficient fibre consumption among the general population …

Inhibition of microglia overactivation restores neuronal survival in a mouse model of CDKL5 deficiency disorder

G Galvani, N Mottolese, L Gennaccaro, M Loi… - Journal of …, 2021 - Springer
Background CDKL5 deficiency disorder (CDD), a severe neurodevelopmental disorder
characterized by early onset epilepsy, intellectual disability, and autistic features, is caused …

Comprehensive behavioral analysis of the Cdkl5 knockout mice revealed significant enhancement in anxiety- and fear-related behaviors and impairment in both …

K Okuda, K Takao, A Watanabe, T Miyakawa… - PloS one, 2018 - journals.plos.org
Mutations in the Cyclin-dependent kinase-like 5 (CDKL5) gene cause severe
neurodevelopmental disorders. Recently we have generated Cdkl5 KO mice by targeting …