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B4GALT7
The Skin in the Ehlers-Danlos Syndromes
Phenotype and Response to Growth Hormone Therapy in Siblings with B4GALT7 Deficiency T ⁎ Carla Sandler-Wilsona, Jennifer A
Pathophysiological Significance of Dermatan Sulfate Proteoglycans Revealed by Human Genetic Disorders
The Ehlers-Danlos Syndromes, Rare Types
Pathophysiological Significance of Dermatan
Chromatin Conformation Links Distal Target Genes to CKD Loci
Extracellular Matrix Deposition and Remodeling After Corneal Alkali Burn in Mice
Phenotype Informatics
Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers‒Danlos Syndromes
Expansion of B4GALT7 Linkeropathy Phenotype to Include Perinatal Lethal Skeletal Dysplasia
Absence of the Dermatan Sulfate Chain of Decorin Does Not Affect Mouse Development Pierre Moffatt1,2* , Yeqing Geng1, Lisa Lamplugh1, Antonio Nanci3 and Peter J
Cellular and Molecular Mechanisms in the Pathogenesis of Classical, Vascular, and Hypermobile Ehlers-Danlos Syndromes
Regulatory Region of the Cancer Associated Gene B4GALT1 and Its Comparison with the Gene Family
Galactosaminoglycan Function and Oligosaccharide Structure Determination
View Correction with a P Value,0.05
Genetic Disorders of the Extracellular Matrix
Genetic Testing for Connective Tissue Disorders AHS – M2144
Clinical Utility Gene Card For: B4GALT7-Defective Congenital Disorder of Glycosylation
Top View
B4GALT7 (NM 007255) Human Recombinant Protein Product Data
Defective Glycosylation of Decorin and Biglycan
Tick Galactosyltransferases Are Involved in Α-Gal Synthesis And
Ehlers Danlos 2016
1 SARS-Cov-2 Infection Depends on Cellular Heparan Sulfate and ACE2
Since January 2020 Elsevier Has Created a COVID-19 Resource Centre with Free Information in English and Mandarin on the Novel Coronavirus COVID- 19
Biglycan Modulation of Bone Morphogenetic Protein-2 Functions
A Homozygous B3GAT3 Mutation Causes a Severe Syndrome with Multiple Fractures, Expanding the Phenotype of Linkeropathy Syndromes Kelly L
Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome
A Novel Enhancer Near the Pitx1 Gene Influences Development And
Apcs Heparan Sulfates and Glycoprotein 96 In
Attachment of Chlamydia Trachomatis L2 to Host Cells Requires Sulfation
Dwarfism with Joint Laxity in Friesian Horses Is Associated with a Splice Site Mutation in B4GALT7
Expanding the Clinical Spectrum of B4GALT7 Deficiency: Homozygous
Severe Peripheral Joint Laxity Is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-B4GALT7 and Spondylodysplastic-EDS-B3GALT6
Extracellular Matrix in Development and Disease