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CDKL5
1 Long-Read Genome Sequencing for the Diagnosis Of
Complete Loss of CASK Causes Severe Ataxia Through Cerebellar Degeneration
Nephrotoxicity of the BRAF-Kinase Inhibitor Vemurafenib Is Driven By
Cldn19 Clic2 Clmp Cln3
Disease/Syndrome Features: Mutations in CDKL5 Are Associated
(CDKL5) Deficiency Disorder: Clinical Review
Pharmacological Reactivation of Inactive X-Linked Mecp2 in Cerebral Cortical Neurons of Living Mice
Report Mutations in the X-Linked Cyclin-Dependent Kinase–Like 5
CDKL5 Variants Improving Our Understanding of a Rare Neurologic Disorder
FINAL Rare Epilepsy Landscape Analysis
A New Microdeletion Syndrome Involving TBC1D24, ATP6V0C and PDPK1 Causes Epilepsy, Microcephaly and Developmental Delay. Bettina
Enrichment of Mutations in Chromatin Regulators in People with Rett Syndrome Lacking Mutations in MECP2
AR-Dependent Phosphorylation and Phospho-Proteome Targets in Prostate Cancer
Autism Spectrum Disorder Sequencing Panel
Loss of CDKL5 Disrupts Kinome Profile and Event-Related Potentials
Review Article Cyclin-Dependent Kinase-Like 5 (CDKL5): Possible Cellular Signalling Targets and Involvement in CDKL5 Deficiency Disorder
CDKL5 Gene Cyclin Dependent Kinase Like 5
(CDKL5) Mutation Screening in Rett Syndrome and Related Disorders
Top View
Molecular Diagnostic Testing Requisition
Connective Tissue Disorders
AJMG CDKL5 Manuscript Resubmission
XLMR Genes: Update 2007
Genetic Testing
Kin-2787, Is Active in Class Ii and Class Iii Braf Mutant Models
High Frequency of Mosaic Pathogenic Variants in Genes Causing Epilepsy-Related Neurodevelopmental Disorders
Deficiency of Cyclin-Dependent Kinase-Like 5 Causes Spontaneous Epileptic Seizures in Neonatal Mice
The Use of Panel Testing in Familial Breast and Ovarian Cancer
Genomic Unity® Prenatal Analysis
UNIVERSITY of CALIFORNIA SAN DIEGO CDKL5 Ipsc-Derived
Overview of Genetic Causes for Epilepsy in Children
Mtor Inhibition Represses Transcription of Cholesterol Biosynthesis Genes and Alters Cholesterol Levels in Primary Neurons and in the Developing Brain
Newborndxtm Advanced Sequencing Evaluation Disorders List
CDKL5 Deficiency Disorder—A Complex Epileptic Encephalopathy
Evaluating the Pathogenic Potential of Genes with De Novo Variants in Epileptic Encephalopathies
List of Gene Panels Used for Epilepsy Diagnosis in Different Companies
PG0453 Germline Multi-Gene Panel Testing
Probe Set ID Gene Symbol Gene Name Refseq Transcript ID Chrom . Loc. 1007 S at DDR1 Discoidin Domain Receptor Family, Member
Molecular Services Brochure
CDKL5 Variants Improving Our Understanding of a Rare Neurologic Disorder
Enrichment of Mutations in Chromatin Regulators in People with Rett Syndrome Lacking Mutations in MECP2
An Introductory Guide History Diagnosis Symptoms Treatments and Therapies Resources …And More Foreword Introduction
Prevalence and Onset of Comorbidities in the CDKL5 Disorder Differ From
Scanmaxsm Kinase Assay Panel
Neuron-Type Specific Loss of CDKL5 Leads to Alterations in Mtor Signaling and Synaptic Markers
Nngv3n6-Issue-Text-Proof Final.Pdf
Supporting Information Materials and Methods
HHS Public Access Author Manuscript
Two Novel Variants Affecting CDKL5 Transcript Associated with Epileptic Encephalopathy
Epilepsynext Positive Sample Report
Altered Network and Rescue of Human Neurons Derived from Individuals with Early-Onset Genetic Epilepsy
Genetic Diagnostics Test(S)/Gene(S)/Panel(S)
Profiling Data