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ELP4
Analysis of Gene Expression Data for Gene Ontology
Exploring the Relationship Between Gut Microbiota and Major Depressive Disorders
A Yeast Phenomic Model for the Influence of Warburg Metabolism on Genetic Buffering of Doxorubicin Sean M
Preferentially Paternal Origin of De Novo 11P13 Chromosome Deletions Revealed in Patients with Congenital Aniridia and WAGR Syndrome
Integrative Framework for Identification of Key Cell Identity Genes Uncovers
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Title: a Yeast Phenomic Model for the Influence of Warburg Metabolism on Genetic
Identification of New Risk Factors for Rolandic Epilepsy: CNV at Xp22.31
ELP-Dependent Expression of MCL1 Promotes Resistance to EGFR Inhibition in Triple-Negative Breast Cancer Cells
A Graph Diffusion Kernel for Predicting Novel Genetic Interactions and Co-Complex Membership from Yeast Genetic Interactions
Structural Variations in the Human Genome M
216141 2 En Bookbackmatter 461..490
Centrotemporal Sharp Wave EEG Trait in Rolandic Epilepsy Maps to Elongator Protein Complex 4 (ELP4)
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental
Synthetic Dosage Lethality Screen with Actin Cytoskeleton in Yeast
Thesis for Final Submission3
A Genetic Epidemiologic Study of Candidate Genes Involved in the Optic Nerve Head Morphology
Genetic Approaches to Study Transcriptional Activation and Tumor Suppression: a Dissertation
Top View
PAX6 Genotypic and Retinal Phenotypic Characterization in Congenital Aniridia
Analysis of Pax6 Contiguous Gene Deletions in the Mouse
Elp2 Mutations Perturb the Epitranscriptome and Lead to a Complex Neurodevelopmental Phenotype
Supplementary Information for Friedman and Perrimon, “A Functional Genomic Rnai Screen for Novel Regulators of RTK and ERK Signaling,” 2006
A Genetic Epidemiologic Study of Candidate Genes Involved in The
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THE GENETICS of EPILEPSY These Genes in the Population, the Disease Will Only Manifest Itself When Both Genes Searching for Disease-Causing Genes Is No Simple Task
Loss of Critical Developmental and Human Disease-Causing Genes In
A Functional Analysis of the Rna Polymerase Ii Large Subunit Carboxy-Terminal Domain
A Large Novel Deletion Downstream Ofpax6 Gene in a Chinese Family with Ocular Coloboma