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EPS8L3
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
S1 Supplemental Materials Supplemental Methods Supplemental Figure 1. Immune Phenotype of Mcd19 Targeted CAR T and Dose Titratio
Effects and Mechanisms of Eps8 on the Biological Behaviour of Malignant Tumours (Review)
Développement D'une Signature Moléculaire Dans La Maladie
Whole Exome Sequencing in Families at High Risk for Hodgkin Lymphoma: Identification of a Predisposing Mutation in the KDR Gene
Detecting Remote, Functional Conserved Domains in Entire Genomes by Combining Relaxed Sequence-Database Searches with Fold Recognition
Cytogenetic and Molecular Characterization of the Macro- And
WO 2016/040794 Al 17 March 2016 (17.03.2016) P O P C T
Jnsclcase20102 1..5
Global Bpgen Supplement Page 1 Eight Blood Pressure Loci Identified by Genome-Wide Association Study of 34,433 People Of
Genetic Analysis of the Trichuris Muris-Induced Model of Colitis
Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians
Whole-Transcriptome Sequencing Reveals Heightened Inflammation and Defective Host Defence Responses in Chronic Rhinosinusitis with Nasal Polyps
Whole-Transcriptome Analysis of Fully Viable Energy Efficient Glycolytic
Investigating the Roles of Neurogenin 3 in Human Pancreas and Intestine
"Mineração De Genes Em Regiões Genômicas Bovinas Associadas À Resistência Ao Carrapato Rhipicephalus (Boophilus) Microplus"
Luciano Abreu Brito Variantes Genéticas De Risco Às Fissuras
Abnormal Gene Expression in Regular and Aggregated Somatic Cell Nuclear Transfer Placentas Bo-Woong Sim1,2, Chae-Won Park1, Myung-Hwa Kang3 and Kwan-Sik Min1*
Top View
Identification of Key Genes Potentially Related to Triple Receptor Negative Breast Cancer by Microarray Analysis
Identification of Novel Loci and New Risk Variant in Known Loci for Colorectal Cancer Risk in East Asians
Exome Sequencing Identified a Missense Mutation of EPS8L3 In
Number 11 November 2011
EPS8, Encoding an Actin-Binding Protein of Cochlear Hair Cell
Genome-Wide Association Studies of Skeletal Phenotypes: What We Have Learned and Where We Are Headed
Intestine of Zebrafish: Regionalization, Characterization and Stem Cells
Eps8l3 Rabbit Pab Antibody
Identification De Variants Génétiques Rares Aux Loci 1P13 Et 8Q22 Dans La Maladie Osseuse De Paget Les Gènes CTHRC1 Et TM7SF4 Associés À La Maladie Osseuse De Paget
Clinical and Molecular Characterization of Human Hereditary Disorders of Ectodermal Appendages
Transcriptomics Identified a Critical Role for Th2 Cell-Intrinsic Mir-155 In
Primepcr™Assay Validation Report
This Electronic Thesis Or Dissertation Has Been Downloaded from the King’S Research Portal At
Downloaded from the ICGC Data Portal (Dcc.Icgc.Org, (Qiagen)