Voluntary running improves behavioral and structural abnormalities in a mouse model of CDKL5 deficiency disorder
N Mottolese, B Uguagliati, M Tassinari, CB Cerchier… - Biomolecules, 2023 - mdpi.com
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a rare
neurodevelopmental disease caused by mutations in the X-linked CDKL5 gene. CDD is …
neurodevelopmental disease caused by mutations in the X-linked CDKL5 gene. CDD is …
Preclinical studies of gene replacement therapy for CDKL5 deficiency disorder
G Voronin, J Narasimhan, J Gittens, J Sheedy, P Lipari… - Molecular Therapy, 2024 - cell.com
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a rare
neurodevelopmental disorder caused by a mutation in the X-linked CDKL5 gene. CDKL5 is …
neurodevelopmental disorder caused by a mutation in the X-linked CDKL5 gene. CDKL5 is …
Characterisation of sleep apneas and respiratory circuitry in mice lacking CDKL5
G Matteoli, S Alvente, S Bastianini… - Journal of Sleep …, 2024 - Wiley Online Library
CDKL5 deficiency disorder is a rare genetic disease caused by mutations in the CDKL5
gene. Central apneas during wakefulness have been reported in patients with CDKL5 …
gene. Central apneas during wakefulness have been reported in patients with CDKL5 …
[HTML][HTML] Early-onset brain alterations during postnatal development in a mouse model of CDKL5 deficiency disorder
M Tassinari, B Uguagliati, S Trazzi, CB Cerchier… - Neurobiology of …, 2023 - Elsevier
Mutations in the CDKL5 gene are the cause of CDKL5 deficiency disorder (CDD), a rare and
severe neurodevelopmental condition characterized by early-onset epilepsy, motor …
severe neurodevelopmental condition characterized by early-onset epilepsy, motor …
Effects of a ciliary neurotrophic factor (CNTF) small-molecule peptide mimetic in an in vitro and in vivo model of CDKL5 deficiency disorder
Background Mutations in the X-linked CDKL5 gene underlie a severe epileptic
encephalopathy, CDKL5 deficiency disorder (CDD), characterized by gross motor …
encephalopathy, CDKL5 deficiency disorder (CDD), characterized by gross motor …
A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profiling
C Quadalti, M Sannia, NE Humphreys, VA Baldassarro… - Heliyon, 2024 - cell.com
CDKL5 deficiency disorder (CDD) is a rare neurodevelopmental syndrome caused by
mutations in the X-linked CDKL5 gene. Hundreds of pathogenic variants have been …
mutations in the X-linked CDKL5 gene. Hundreds of pathogenic variants have been …
Role of neuroinflammation in the pathophysiology of CDKL5 deficiency disorder
N Mottolese - 2024 - amsdottorato.unibo.it
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD), a rare
neurodevelopmental disease caused by mutations in the X-linked CDKL5 gene, is …
neurodevelopmental disease caused by mutations in the X-linked CDKL5 gene, is …
Protein Delivery and Mimicry
Ü Langel - CPP, Cell-Penetrating Peptides, 2023 - Springer
Protein Delivery and Mimicry | SpringerLink Skip to main content Advertisement SpringerLink
Account Menu Find a journal Publish with us Track your research Search Cart Book cover …
Account Menu Find a journal Publish with us Track your research Search Cart Book cover …