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IFT20
Role of Phytochemicals in Colon Cancer Prevention: a Nutrigenomics Approach
Cilia-Related Protein SPEF2 Regulates Osteoblast Differentiation
SPEF2 Functions in Microtubule-Mediated Transport in Elongating Spermatids to Ensure Proper Male Germ Cell Differentiation Mari S
Variation in Protein Coding Genes Identifies Information Flow
Investigating the Effect of Chronic Activation of AMP-Activated Protein
IFT20 (NM 001267774) Human Tagged ORF Clone Product Data
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Enrichment of in Vivo Transcription Data from Dietary Intervention
Leveraging Models of Cell Regulation and GWAS Data in Integrative Network-Based Association Studies
(NF1) As a Breast Cancer Driver
Genome-Wide Association Studies for Sperm Traits in Assaf Sheep Breed
Supplementary Figure 1 the Mutated Amino Acid Residues of SPEF2 and Their Conservativeness Across Species
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
New Class of Transcription Factors Controls Flagellar Assembly by Recruiting RNA Polymerase II
Downloaded from the Mouse Lysosome Gene Database, Mlgdb
IFT20 (3F3): Sc-517184
Genomic Analysis of the HER2/TOP2A Amplicon in Breast
Intraflagellar Transport Complex in Leishmania Spp. in Silico Genome
Top View
Mouse Ift20 Conditional Knockout Project (CRISPR/Cas9)
Downloaded from Placed in a Duplication Node More Closely Related to the the Gene Ontology’S Archive of MGI Gafs [52]
Use of Multivariate Discriminant Methodologies in the Analysis of Phenotypic and Genomic Data of Cattle
Cilia Interactome with Predicted Protein–Protein Interactions Reveals Connections to Alzheimer’S Disease, Aging and Other Neuropsychiatric Processes Kalyani B
Downloaded from the Cengen Website
Sixteen New Lung Function Signals Identified Through 1000 Genomes
Sperm Flagellar Protein 2 Expression in Mouse Tissues and Transfection in Mimcd3 Cells
Integrative Subcellular Proteomic Analysis Allows Accurate Prediction of Human Disease-Causing Genes
Genetic and Clinical Heterogeneity of Achondrogenesis Type 1A and Odontochondrodysplasia