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RBBP6
Autism Multiplex Family with 16P11.2P12.2 Microduplication Syndrome in Monozygotic Twins and Distal 16P11.2 Deletion in Their Brother
Chronic Exposure of Humans to High Level Natural Background Radiation Leads to Robust Expression of Protective Stress Response Proteins S
Structural Characterisation of the Interaction Between RBBP6 and The
Itraq‑Based Proteomics Analysis of the Therapeutic Effects of Combined Anticancer Bioactive Peptides and Oxaliplatin on Gastric Cancer Cells
Downloaded with Ma- Disease D D
Investigation of the Intra-Cellular Localisation of Retinoblastoma Binding Protein 6 Using Immunofluorescence Microscopy
Mechanisms of Action of Coxiella Burnetii Effectors Inferred from Host-Pathogen Protein Interactions
Anti-RBBP6 Antibody (ARG41302)
Sample Report for Solid Tumor Profile Plus (Lung Cancer)
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
Transcriptional Regulators Are Upregulated in the Substantia Nigra
The C. Elegans Homolog of RBBP6 (RBPL-1) Regulates Fertility Through Controlling Cell Proliferation in the Germline and Nutrient Synthesis in the Intestine
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
Product Datasheet RBBP6 Antibody NBP1-49542V
Functional Analysis of the Mouse RBBP6 Gene Using Interference RNA
Genetic Circuitry of Survival Motor Neuron, the Gene Underlying Spinal
The Genetics of Deafness in Domestic Animals
Product Datasheet
Top View
A Gene-Set Enrichment and Protein–Protein Interaction Network-Based
Primepcr™Assay Validation Report
Truncating Prolactin Receptor Mutations Promote Tumor Growth in Murine Estrogen Receptor-Alpha Mammary Carcinomas
IPA Assigned GO Annotation for the CIP2A Interactome
A Low-Density SNP Array for Analyzing Differential
Supporting Information
Modifiers of Beta-Amyloid Metabolism and Deposition in Mouse Models of Alzheimer’S Disease
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Identification and Characterisation of a Novel Gene, DWNN, Isolated From
A Novel Nicastrin Mutation in a Three‐Generation Dutch Family With
Gene Expression in the Mouse Eye: an Online Resource for Genetics Using 103 Strains of Mice
MRNA Transcription, Translation, and Defects in Developmental Cognitive and Behavioral Disorders
Charmy Starnod Twala, Master of Science in Biochemistry and Bioinformatics
(12) United States Patent (10) Patent No.: US 9,163,078 B2 Rao Et Al
The Drosophila Retinoblastoma Binding Protein 6 Family Member Has Two Isoforms and Is Potentially Involved in Embryonic Patterning
Genome-Wide and Functional Annotation of Human E3 Ubiquitin Ligases Identifies MULAN, a Mitochondrial E3 That Regulates the Orga
Causal Dynamical Modelling Predicts Novel Regulatory Genes of FOXP3 in Human Regulatory T Cells
A SARS-Cov-2-Human Protein-Protein Interaction Map Reveals Drug Targets and Potential Drug- Repurposing