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EXTL3
Aneuploidy: Using Genetic Instability to Preserve a Haploid Genome?
Specific Functions of Exostosin-Like 3 (EXTL3) Gene Products Shuhei Yamada
Gene Silencing of EXTL2 and EXTL3 As a Substrate Deprivation Therapy for Heparan Sulphate Storing Mucopolysaccharidoses
A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita
The Tissue-Specific Transcriptomic Landscape of the Mid-Gestational Mouse Embryo Martin Werber1, Lars Wittler1, Bernd Timmermann2, Phillip Grote1,* and Bernhard G
Variation in Protein Coding Genes Identifies Information Flow
A Network of Clinically and Functionally Relevant Genes Is Involved in The
The Pathogenic Roles of Heparan Sulfate Deficiency in Hereditary Multiple Exostoses
EXTL3 Mutations Cause Skeletal Dysplasia, Immune Deficiency, and Developmental Delay
UC San Diego Electronic Theses and Dissertations
Peripheral Nerve Single-Cell Analysis Identifies Mesenchymal Ligands That Promote Axonal Growth
The Link Between Heparan Sulfate and Hereditary Bone Disease: Finding a Function for the EXT Family of Putative Tumor Suppressor Proteins
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
A Statistical Framework for Cross-Tissue Transcriptome-Wide
Deep Sequencing of a Recurrent Oligodendroglioma and the Derived
Molecular and Clinical Examination of an Italian DEFECT11 Family
IMPLICATIONS for PERSONALIZED MEDICINE and CANCER BIOLOGY Bulent¨ Arman Aksoy, Ph.D
Prediction of Individualized Therapeutic Vulnerabilities in Cancer
Top View
Hereditary Multiple Exostoses, Macrocephaly, Congenital Heart
Gene Ontology Analysis of Arthrogryposis (Multiple Congenital Contractures)
A Novel 8 Mb Interstitial Deletion of Chromosome 8P12-P21.2
Chromosome 8P As a Potential Hub for Developmental Neuropsychiatric
Downloaded CRISPR Screen Gene Summary Data Corrected (Fraser & Plotkin, 2007)
A Novel Deletion Mutation of the EXT2 Gene in a Large Chinese Pedigree with Hereditary Multiple Exostosis
Investigating the Influence of Perinatal Nicotine and Alcohol Exposure On
Atlas Journal
Unraveling the Molecular Mechanism Underlying ALS-Linked Astrocyte
Table 10: H. Sapiens Recon 1 Network Confidence Scores and Citations
1 Mutations in EXTL3 Cause Neuro-Immuno-Skeletal
A Statistical Framework for Cross-Tissue Transcriptome-Wide Association Analysis
The Extostosin Family: Proteins with Many Functions☆
EXTL3 Mutations Cause Skeletal Dysplasia, Immune Deficiency, and Developmental Delay
Supplementary Table 1. a Full List of Cancer Genes