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EXT1
Familial Nephropathy and Multiple Exostoses with Exostosin-1 (EXT1) Gene Mutation
CRISPR Screening of Porcine Sgrna Library Identifies Host Factors
Selectin Ligand Sialyl-Lewis X Antigen Drives Metastasis of Hormone-Dependent Breast Cancers
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
ZNF263 Is a Transcriptional Regulator of Heparin and Heparan Sulfate Biosynthesis
Viruses Like Sugars: How to Assess Glycan Involvement in Viral Attachment
Drosophila and Human Transcriptomic Data Mining Provides Evidence for Therapeutic
Drug Metabolism Determines Resistance of Colorectal Cancer to Resorcinol-Based HSP90 Inhibitors
Hereditary Multiple Osteochondromas
A Mouse Model of Chondrocyte-Specific Somatic
MDA-MB-231 Breast Cancer Cell Viability, Motility and Matrix
SSIEM Classification of Inborn Errors of Metabolism 2011
Multiplexed Surrogate Analysis of Glycotransferase Activity in Whole Biospecimens † † ‡ Chad R
Heparan Sulfate Proteoglycans Undergo Differential Expression
Supplemental Figures 04 12 2017
Hereditary Multiple Osteochondromas in Jordanian Patients: Mutational and Immunohistochemical Analysis of EXT1 and EXT2 Genes
The Link Between Heparan Sulfate and Hereditary Bone Disease: Finding a Function for the EXT Family of Putative Tumor Suppressor Proteins
Downloaded from The
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A Combined Growth Factor-Deleted and Thymidine Kinase-Deleted Vaccinia Virus Vector
MOL #82305 TITLE PAGE Title: Induced CYP3A4 Expression In
Bone & Soft Tissue
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
And Lymphocyte Homing Heparan
Supplementary Tables
The Genetic Landscape of Renal Complications in Type 1 Diabetes
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism Istanbul, Turkey, 31 August– 3 September 2010
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Handbook of Glycosyltransferases and Related Genes
Integration of Cistromic and Transcriptomic Analyses Identifies Nphs2, Mafb, and Magi2 As Wilms' Tumor 1 Target Genes in Podoc
Inborn Metabolic Diseases, DOI 10.1007/978-3-662-49771-5 , © Springer-Verlag Berlin Heidelberg 2016 644 Subject Index
Genes That Are Preferentially Expressed in Type I Cells Figure 4A
Review Article J Med Genet: First Published As 10.1136/Jmg.31.4.265 on 1 April 1994
A Radiation Hybrid Map of 40 Loci for the Distal Long Arm of Human Chromosome 8 Tracey B
Biosynthesis of Heparan Sulfate
Diseases of Glycosylation Beyond Classical Congenital Disorders of Glycosylation
A Novel Deletion Mutation of the EXT2 Gene in a Large Chinese Pedigree with Hereditary Multiple Exostosis
Metabolske Sykdommer V02
Supplemmental Table S4
Responsive Nuclear Proteins in Collecting Duct Cells
Association of Somatic Mutations of ADAMTS Genes with Improved Chemotherapy Sensitivity and Survival in High-Grade Serous Ovarian Carcinoma
CRISPR Screening of Porcine Sgrna Library Identified Host Factors Essential for Japanese Encephalitis Virus Replication
Table 10: H. Sapiens Recon 1 Network Confidence Scores and Citations
The Contribution of Hereditary Cancer-Related Germline Mutations to Lung Cancer Susceptibility
Glycosyltransferase Genes That Cause Monogenic Congenital
Supplementary Data
Physician's Guide to the Diagnosis, Treatment, and Follow-Up Of
Individual Genome Sequence Gene List (By Disease)
1 Selectin Ligand Sialyl-Lewis X Antigen Drives Metastasis Of
Vulnerability to Shear Stress Caused by Altered Peri-Endothelial Matrix Is A
Tiling Resolution Array-CGH Shows That Somatic Mosaic Deletion of The
Rapid Mendelian Sequencing Gene List December 2018
Supplementary Table S1 . 939 Differentially Expressed Genes in Invasive Cells with EGFR Over-Expression and P53 Mutation
EXT1 Gene Exostosin Glycosyltransferase 1
Supporting Information
Alterations in the Glycome After HDAC Inhibition Impact Oncogenic Potential in Epigenetically Plastic SW13 Cells Mckale R
<Supplementary Materials>
Differential Expression of Glycosyltransferases Identified Through Comprehensive Pan-Cancer Analysis
Cross-Comparison of the Genome Sequences from Human