CDKL5 PROTEIN SUBSTITUTION THERAPY RESCUES NEUROLOGICAL PHENOTYPES OF A MOUSE MODEL OF CDKL5 DISORDER.

scientific article published on 20 February 2018

CDKL5 PROTEIN SUBSTITUTION THERAPY RESCUES NEUROLOGICAL PHENOTYPES OF A MOUSE MODEL OF CDKL5 DISORDER. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1093/HMG/DDY064
P8608Fatcat IDrelease_e2pkclevorgmfiy6jnfrd3x6ei
P698PubMed publication ID29474534

P50authorGiorgio MediciQ87860972
P2093author name stringElisabetta Ciani
Stefania Trazzi
Claudia Fuchs
Tommaso Pizzorusso
Giovanna Zoccoli
Stefano Bastianini
Viviana Lo Martire
Rocchina Viggiano
Roberto Rimondini
Renata Bartesaghi
Elisa Ren
Raffaele Mazziotti
Leonardo Lupori
Marianna De Franceschi
P2860cites workThe amyloid precursor protein (APP) triplicated gene impairs neuronal precursor differentiation and neurite development through two different domains in the Ts65Dn mouse model for Down syndromeQ37175063
P433issue9
P1104number of pages21
P304page(s)1572-1592
P577publication date2018-05-01
P1433published inHuman Molecular GeneticsQ2720965
P1476titleCDKL5 protein substitution therapy rescues neurological phenotypes of a mouse model of CDKL5 disorder
P478volume27

Reverse relations

cites work (P2860)
Q58094724A new consensus for evaluating CDKL5/STK9-dependent signalling mechanisms
Q64955844An electrochemiluminescence based assay for quantitative detection of endogenous and exogenously applied MeCP2 protein variants.
Q89805320CDKL5 Deficiency Disorder-A Complex Epileptic Encephalopathy
Q64939210Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review.
Q55436457Heterozygous CDKL5 Knockout Female Mice Are a Valuable Animal Model for CDKL5 Disorder.
Q89460115Increased DNA Damage and Apoptosis in CDKL5-Deficient Neurons
Q91678331Molecular and Synaptic Bases of CDKL5 Disorder
Q92160931Site-specific abnormalities in the visual system of a mouse model of CDKL5 deficiency disorder
Q89596064The green tea polyphenol epigallocatechin-3-gallate (EGCG) restores CDKL5-dependent synaptic defects in vitro and in vivo

Search more.