Fibrillin-1 Mutations Causing Weill-Marchesani Syndrome and Acromicric and Geleophysic Dysplasias Disrupt Heparan Sulfate Interactions

PLoS ONE - United States
doi 10.1371/journal.pone.0048634
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Public Library of Science (PLoS)

Related search

Síndrome De Weill-Marchesani

Revista Chilena de Pediatria
Child HealthPediatricsPerinatology
1986English

Structural Analysis of Heparan Sulfate and Heparan Sulfate Oligosaccharides.

Trends in Glycoscience and Glycotechnology
BiochemistryOrganic Chemistry
1998English

Classical and Neonatal Marfan Syndrome Mutations in Fibrillin-1 Cause Differential Protease Susceptibilities and Protein Function

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2011English

Myeloperoxidase-Derived Oxidants Selectively Disrupt the Protein Core of the Heparan Sulfate Proteoglycan Perlecan

Matrix Biology
Molecular Biology
2010English

Wingless, Hedgehog and Heparan Sulfate Proteoglycans

Development (Cambridge)
Developmental BiologyMolecular Biology
2004English

Heparan Sulfate Glycosaminoglycan (HSGAG)

Science-Business eXchange
2013English

Interactions of Signaling Proteins, Growth Factors and Other Proteins With Heparan Sulfate: Mechanisms and Mysteries

Connective Tissue Research
Sports MedicineCell BiologyMolecular BiologyBiochemistryRheumatologyOrthopedics
2015English

Heparan Sulfate Glycosaminoglycan (HSGAG)

Science-Business eXchange
2013English

Peters Plus Syndrome Mutations Disrupt a Noncanonical ER Quality-Control Mechanism

Current Biology
GeneticsMolecular BiologyBiochemistryBiological SciencesNeuroscienceAgricultural
2015English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy