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CTDP1
Congenital Cataracts–Facial Dysmorphism–Neuropathy
Identification and Characterization of TPRKB Dependency in TP53 Deficient Cancers
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Triplet Repeat Length Bias and Variation in the Human Transcriptome
Common Variants in SOX-2 and Congenital Cataract Genes Contribute to Age-Related Nuclear Cataract
Supplementary Materials
Analysis of the Indacaterol-Regulated Transcriptome in Human Airway
Whole Exome Sequencing in Families at High Risk for Hodgkin Lymphoma: Identification of a Predisposing Mutation in the KDR Gene
Integrated Analysis of Human Influenza a (H1N1) Virus Infection
Investigating Trait Variability of Gene Co-Expression Network Architecture in Brain by Manipulating Genomic Signatures of Schizophrenia Risk
Deoxyribonucleic Acid Copy Number Aberrations in Vasospastic Angina Patients Using an Array Comparative Genomic Hybridization
Datasheet: VPA00440 Product Details
Chromosome 18 Gene Dosage Map 2.0
Supplementary Table 1: Genes Located on Chromosome 18P11-18Q23, an Area Significantly Linked to TMPRSS2-ERG Fusion
RPRD1A and RPRD1B Are Human RNA Polymerase II C-Terminal Domain Scaffolds for Ser5 Dephosphorylation
Controllability Analysis of the Directed Human Protein Interaction Network Identifies Disease Genes and Drug Targets
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
Gnomad Lof Supplement
Top View
Genetic Adaptation of the Human Circadian Clock to Day-Length
Identification of Novel Regulatory Genes in Acetaminophen
Structural Basis of Transcription Initiation by RNA Polymerase II
Pipeline for Efficient Splicing Events Calling Sokolov A1*, Mazur A1, Zhigalova N1, Prokhortchouk A1, Gruzdeva N2 and Prokhortchouk E1,2
Datasheet: VPA00440KT Product Details
Linking Uniprotkb/Swiss-Prot Proteins to Pathway Information
Useful 'Junk': Alu Rnas in the Human Transcriptome
Discovering Novel Snps That Are Correlated with Patient Outcome in A
When Cri Du Chat Syndrome Meets Edwards Syndrome
Gain of Chromosome Region 18Q21 Including the MALT1 Gene Is
1 Termination Control by an RNA
Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders from the South of Brazil
Breakpoints and Deleted Genes Identification of Ring Chromosome
Selective Inhibition of CDK7 Reveals High-Confidence Targets and New Models for TFIIH Function in Transcription
RPRD1A and RPRD1B Are Human RNA Polymerase II C-Terminal Domain Scaffolds for Ser5 Dephosphorylation
CTDP1 Regulates Breast Cancer Survival and DNA Repair Through
Regulation of Transcription Termination by FUS and TDP-43
A Knowledge-Based Machine Learning Approach to Gene Prioritisation in Amyotrophic Lateral Sclerosis