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DCAF17
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Genomic Approaches to Reproductive Disorders
Hyperphosphorylation Repurposes the CRL4B E3 Ligase to Coordinate Mitotic Entry and Exit
Deletion of DDB1- and CUL4- Associated Factor-17 (Dcaf17) Gene
Supplementary Materials
Woodhouse-Sakati Syndrome: Clinical and Molecular Study on a Qatari Family with C2orf37 Gene Mutation
Oncoscore: a Novel, Internet-Based Tool to Assess the Oncogenic Potential of Genes
Bioinformatics Tools for the Analysis of Gene-Phenotype Relationships Coupled with a Next Generation Chip-Sequencing Data Processing Pipeline
The Emerging Role for Cullin 4 Family of E3 Ligases in Tumorigenesis T ⁎ ⁎ Ji Chenga,B,1, Jianping Guob,1, Brian J
Download 20190410); Fragmentation for 20 S
Dcaf17 (NM 001165982) Mouse Tagged ORF Clone – MG219128
Woodhouse-Sakati Syndrome: a Case Report from Indonesia
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Macaque Gene Symbols Were Mapped to Human Gene Symbols on June 2011
Gnomad Lof Supplement
Supplementary Figure S1 A
Expression Profiling of WD40 Family Genes Including DDB1- and CUL4
Mouse Mettl8 Conditional Knockout Project (CRISPR/Cas9)
Top View
Characterization of DCAF17 with Specific, Polyclonal Antibodies
In Silico Analysis of Coding Snps and 3
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Neurodegeneration with Brain Iron Accumulation Disorders: Valuable Models Aimed at Understanding the Pathogenesis of Iron Deposition
Transcriptomics Identified a Critical Role for Th2 Cell-Intrinsic Mir-155 In
The CUL4-DDB1 Ubiquitin Ligase Complex Controls Adult and Embryonic 2 Stem Cell Differentiation and Homeostasis 3 4 Jie Gao1,5, Shannon M
Brain Iron Accumulation Affects Myelin-Related Molecular Systems Implicated in a Rare Neurogenetic Disease Family with Neuropsychiatric Features
Identification and Characterization of Novel Genetic Causes of Dystonia
Autosomal Recessive Variants in Intellectual Disability and Autism Spectrum Disorder
Use of Multivariate Discriminant Methodologies in the Analysis of Phenotypic and Genomic Data of Cattle
Genes with High Penetrance for Syndromic and Non-Syndromic Autism Typically Function Within the Nucleus and Regulate Gene Expression Emily L
Crl2lrr1 Promotes Unloading of the Vertebrate Replisome from Chromatin During Replication Termination
UNIVERSITY of CALIFORNIA Los Angeles Identification of Genetic
Rare Gain-Of-Function KCND3 Variant Associated with Cerebellar Ataxia, Parkinsonism, Cognitive Dysfunction, and Brain Iron Accumulation
In Silico Analysis of Coding Snps and 3′-UTR Associated Mirnas In
DCAF17 Gene DDB1 and CUL4 Associated Factor 17
Supplementary Table 1. a Full List of Cancer Genes
PRODUCT SPECIFICATION Product Datasheet