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ARMC9
Supplementary Data
Análise Integrativa De Perfis Transcricionais De Pacientes Com
(A) Co-IP of HA Tagged ARMC9 with Flag Tagged Interactors
A CRISPR-Based Screen for Hedgehog Signaling Provides Insights Into Ciliary Function and Ciliopathies
Identification of Genetic Factors Underpinning Phenotypic Heterogeneity in Huntington’S Disease and Other Neurodegenerative Disorders
Gibco, 11995-065) Supplemented with 10%
A Comprehensive Portrait of Cilia and Ciliopathies from a CRISPR-Based Screen for Hedgehog Signaling
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Supplementary Table 1 Double Treatment Vs Single Treatment
Potential of Data Integration to Identify Regulatory Snps in Late-Onset Alzheimer’S Disease GWAS Findings
Detection of H3k4me3 Identifies Neurohiv Signatures, Genomic
Coexpression Networks Based on Natural Variation in Human Gene Expression at Baseline and Under Stress
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Deleterious Genetic Variants in Ciliopathy Genes Increase Risk Of
Genome and Single-Cell RNA-Sequencing of the Earthworm Eisenia Andrei Identifies Cellular Mechanisms Underlying Regeneration
2.04.107 Carrier Screening for Genetic Diseases Original Policy Date: February 1, 2017 Effective Date: January 1, 2020 Section: 2.0 Medicine Page: Page 1 of 24
Table S1. Global Proteomic Profile of Rats' Cerebellum Exposed Or Not To
A Germline Mutation of CDKN2A and a Novel RPLP1-C19MC Fusion Detected in a Rare Melanotic Neuroectodermal Tumor of Infancy: a Case Report David J
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Conditional Deletion of ELL2 Induces Murine Prostate Intraepithelial Neoplasia
HBV DNA Integration and Clonal Hepatocyte Expansion in Chronic Hepatitis B Patients Considered Immune Tolerant
Supplementary Methods
Identification of a New QTL Region on Mouse Chromosome 1
A CRISPR-Based Screen for Hedgehog Signaling Provides Insights Into Ciliary Function and Ciliopathies
Conformation and Dynamics of the Mammalian Chromosome
Detecting Gene Modules Differentially Expressed in Multiple Human Brain
Genetic Alterations of SUGP1 Mimic Mutant-SF3B1 Splice Pattern in Lung Adenocarcinoma and Other Cancers
Genome-Wide Association Study for Carcass Traits in an Experimental Nelore Cattle Population
Subclonal Architecture, Evolutionary Trajectories and Patterns of Inheritance of Germline
Whole Exome Sequencing Identified Sixty-Five Coding Mutations in Four
ARMC9 and TOGARAM1 Define a Joubert Syndrome-Associated Protein Module That Regulates
Conditional Deletion of ELL2 Induces Murine Prostate Intraepithelial Neoplasia
Cancer-Associated SF3B1 Mutations Affect Alternative Splicing by Promoting Alternative Branchpoint Usage S Alsafadi, a Houy, a Battistella, T Popova, M
Transcriptomic and Proteomic Profiling Provides Insight Into
Report 81584
Whole Exome Sequencing Reveals a Mutation in ARMC9 As a Cause of Mental Retardation, Ptosis and Polydactyly
BMC Research Notes Biomed Central