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WDR45
Alzheimer Disease
Clinician's Guide to Genes Associated with Rett‐Like Phenotypes
RNA-Seq Transcriptome Reveals Different Molecular Responses
Whole Genome Sequencing Report
WDR45 Mutations May Cause a MECP2 Mutation-Negative Rett Syndrome Phenotype
Anti-WDR45 Antibody (ARG23721)
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
BPAN), in Brain Development
Enrichment of Mutations in Chromatin Regulators in People with Rett Syndrome Lacking Mutations in MECP2
WIPI-4 (G-12): Sc-398272
Genetic Circuitry of Survival Motor Neuron, the Gene Underlying Spinal
Epileptic Spasms: a Previously Unreported Manifestation of WDR45 Gene Mutation*
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Lessons from a Pair of Siblings with BPAN
Atypical Cerebral Palsy: Genomics Analysis Enables Precision Medicine
S00335-021-09875-3.Pdf
From Novel Disease Genes to New Mouse Models - a Complementary Approach
WDR45 (NM 007075) Human Tagged ORF Clone – RC209654L3
Top View
Wasin Vol. 9 N. 4 2558.Pmd
Inhibition of the Pim1 Oncogene Results in Diminished Visual Function
Beta-Propeller Protein-Associated Neurodegeneration (BPAN) Detected in a Child with Epileptic Spasms
WDR45 Antibody Catalog # ASM10526
WDR45 Contributes to Neurodegeneration Through Regulation of ER
Accepted Article
Autophagy Research: Current Status and Future Perspectives Dr
WDR45 Antibody (N-Term) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap13313a
Detecting Gene Modules Differentially Expressed in Multiple Human Brain
A Case of Beta-Propeller Protein-Associated Neurodegeneration Due to a Heterozygous Deletion of WDR45
Early-Onset Epileptic Encephalopathy As the Initial Clinical Presentation Of
Neurodegeneration with Brain Iron Accumulation Disorders: Valuable Models Aimed at Understanding the Pathogenesis of Iron Deposition
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force
WIPI Proteins: Essential Ptdins3p Effectors at the Nascent
Enrichment of Mutations in Chromatin Regulators in People with Rett Syndrome Lacking Mutations in MECP2
Molecular Mechanisms and Biological Functions of Autophagy for Genetics of Hearing Impairment
Novel De Novo Mutation in the Autophagy Gene WDR45 Causes
Functional Mrna Analysis Reveals Aberrant Splicing Caused by Novel Intronic Mutation in WDR45 in NBIA Patient