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TNRC6B
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A Set of Regulatory Genes Co-Expressed in Embryonic Human Brain Is Implicated in Disrupted Speech Development
Autism and Cancer Share Risk Genes, Pathways, and Drug Targets
HHS Public Access Author Manuscript
Molecular Architecture Underlying Fluid Absorption by the Developing Inner
Genomic Analysis of Follicular Dendritic Cell Sarcoma by Molecular
Evaluating the Gene Targets of Micrornas Associated with Parkinson's Disease
Transcriptional Regulators Are Upregulated in the Substantia Nigra
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
Exercise Alters Mouse Sperm Small Noncoding Rnas and Induces a Transgenerational Modification of Male Offspring Conditioned Fear and Anxiety
FOXP2 and Language Alterations in Psychiatric Pathology Salud Mental, Vol
The Role of 4E-T in Translational Regulation and Mrna Decay
Association of BET1L and TNRC6B with Uterine Leiomyoma Risk and Its
Noncoding RNA–Related Polymorphisms in Pediatric Acute Lymphoblastic Leukemia Susceptibility
CRM1 Mediates Nuclear-Cytoplasmic Shuttling of Mature Micrornas
Identifying an Lncrna-Related Cerna Network to Reveal Novel Targets for a Cutaneous Squamous Cell Carcinoma
Supplementary Information
Promoterless Transposon Mutagenesis Drives Solid Cancers Via Tumor Suppressor Inactivation
Top View
A Generalized Gene Set Data Mining Approach
Genome-Wide and Species-Wide in Silico Screening for Intragenic Micrornas in Human, Mouse and Chicken
TNRC6 Proteins Modulate Hepatitis C Virus Replication by Spatially Regulating the Binding of Mir-122/Ago2 Complexes to Viral RNA You Li 1,2,*, Li Wang2,3,Efra´In E
A New Locus on Chromosome 22Q13.31 Linked to Recessive Genetic Epilepsy with Febrile Seizures Plus
Rabbit Anti-Eif2c2/FITC Conjugated Antibody-SL12450R-FITC
GW182 Proteins Restrict Extracellular Vesicle Mediated Selective Export Of
Identification of Human Genes and Its Genomics Functions Via Mirnas of C
Mouse Tnrc6b Knockout Project (CRISPR/Cas9)
Alternative Splicing Regulates Vesicular Trafficking Genes in Cardiomyocytes
Neurodevelopmental Disease Genes Implicated by De Novo Mutation and CNV Morbidity
De Novo and Rare Inherited Mutations Implicate the Transcriptional
Molecular Characterization of Human Argonaute-Containing Ribonucleoprotein Complexes and Their Bound Target Mrnas
Spike Protein Amino Acid Variants Increased Mirna Binding and Hence Reduced Virulence of SARS-Cov-2 in Jordan, Middle East
RNA Structure Drives Interaction with Proteins
Systems Biology Analysis of Human Genomes Points to Key Pathways