Related references
Note: Only part of the references are listed.Clinical and molecular features of 66 patients with musculocontractural Ehlers-Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)
Mari Minatogawa et al.
JOURNAL OF MEDICAL GENETICS (2022)
The Specific Role of Dermatan Sulfate as an Instructive Glycosaminoglycan in Tissue Development
Shuji Mizumoto et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2022)
Case report: Multiple gastrointestinal perforations in a rare musculocontractural Ehlers-Danlos syndrome with multiple organ dysfunction
Huitao Qian et al.
FRONTIERS IN GENETICS (2022)
Alterations in glycosaminoglycan biosynthesis associated with the Ehlers- Danlos syndromes
Delfien Syx et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2022)
A new mouse model of Ehlers-Danlos syndrome generated using CRISPR/Cas9-mediated genomic editing
Yuko Nitahara-Kasahara et al.
DISEASE MODELS & MECHANISMS (2021)
Myopathy Associated With Dermatan Sulfate-Deficient Decorin and Myostatin in Musculocontractural Ehlers-Danlos Syndrome: A Mouse Model Investigation
Yuko Nitahara-Kasahara et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2021)
Systematic investigation of the skin in Chst14-/- mice: A model for skin fragility in musculocontractural Ehlers-Danlos syndrome caused by CHST14 variants (mcEDS-CHST14)
Takuya Hirose et al.
GLYCOBIOLOGY (2021)
DSE associated musculocontractural EDS, a milder phenotype or phenotypic variability
Schaida Schirwani et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2020)
Recent Advances in the Pathophysiology of Musculocontractural Ehlers-Danlos Syndrome
Tomoki Kosho et al.
GENES (2020)
The Ehlers-Danlos syndromes
Fransiska Malfait et al.
NATURE REVIEWS DISEASE PRIMERS (2020)
Backcrossing to an appropriate genetic background improves the birth rate of carbohydrate sulfotransferase 14 gene-deleted mice
Shin Shimada et al.
EXPERIMENTAL ANIMALS (2020)
Impaired Cognitive Function and Altered Hippocampal Synaptic Plasticity in Mice Lacking Dermatan Sulfotransferase Chst14/D4st1
Qifa Li et al.
FRONTIERS IN MOLECULAR NEUROSCIENCE (2019)
Vascular abnormalities in the placenta of Chst14-/- fetuses: implications in the pathophysiology of perinatal lethality of the murine model and vascular lesions in human CHST14/D4ST1 deficiency
Takahiro Yoshizawa et al.
GLYCOBIOLOGY (2018)
Dendritic Cell Migration to Skin-Draining Lymph Nodes Is Controlled by Dermatan Sulfate and Determines Adaptive Immunity Magnitude
Reza Nadafi et al.
FRONTIERS IN IMMUNOLOGY (2018)
Defect in dermatan sulfate in urine of patients with Ehlers-Danlos syndrome caused by a CHST14/D4ST1 deficiency
Shuji Mizumoto et al.
CLINICAL BIOCHEMISTRY (2017)
The Ehlers-Danlos Syndromes, Rare Types
Angela F. Brady et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2017)
The 2017 International Classification of the Ehlers-Danlos Syndromes
Fransiska Malfait et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2017)
The Phenotype of the Musculocontractural Type of Ehlers-Danlos Syndrome due to CHST14 Mutations
Andreas R. Janecke et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2016)
GERMLINE ABLATION OF DERMATAN-4O-SULFOTRANSFERASE1 REDUCES REGENERATION AFTER MOUSE SPINAL CORD INJURY
S. Rost et al.
NEUROSCIENCE (2016)
CHST14/D4ST1 deficiency: New form of Ehlers-Danlos syndrome
Tomoki Kosho
PEDIATRICS INTERNATIONAL (2016)
Fibroblast growth factor signaling in skeletal development and disease
David M. Ornitz et al.
GENES & DEVELOPMENT (2015)
Dermatan Sulfate-Free Mice Display Embryological Defects and Are Neonatal Lethal Despite Normal Lymphoid and Non-Lymphoid Organogenesis
Xanthi N. Stachtea et al.
PLOS ONE (2015)
Dermatan Sulfate Epimerase 1 Deficient Mice as a Model for Human Abdominal Wall Defects
Renata Gustafsson et al.
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY (2014)
Dermatan 4-O-sulfotransferase1 ablation accelerates peripheral nerve regeneration
Nuray Akyuez et al.
EXPERIMENTAL NEUROLOGY (2013)
Biological functions of iduronic acid in chondroitin/dermatan sulfate
Martin A. Thelin et al.
FEBS JOURNAL (2013)
Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural EhlersDanlos syndrome
Thomas Mueller et al.
HUMAN MOLECULAR GENETICS (2013)
Mouse development is not obviously affected by the absence of dermatan sulfate epimerase 2 in spite of a modified brain dermatan sulfate composition
Barbara Bartolini et al.
GLYCOBIOLOGY (2012)
Sugar-Coating Wound Repair: A Review of FGF-10 and Dermatan Sulfate in Wound Healing and Their Potential Application in Burn Wounds
Jennifer K. Plichta et al.
JOURNAL OF BURN CARE & RESEARCH (2012)
Delineation of Dermatan 4-O-sulfotransferase 1 Deficient Ehlers-Danlos Syndrome: Observation of Two Additional Patients and Comprehensive Review of 20 Reported Patients
Kenji Shimizu et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
Dermatan sulfate epimerase 2 is the predominant isozyme in the formation of the chondroitin sulfate/dermatan sulfate hybrid structure in postnatal developing mouse brain
Chizuru Akatsu et al.
GLYCOBIOLOGY (2011)
Dermatan sulfotransferase Chst14/D4st1, but not chondroitin sulfotransferase Chst11/C4st1, regulates proliferation and neurogenesis of neural progenitor cells
Shan Bian et al.
JOURNAL OF CELL SCIENCE (2011)
Extracellular matrix and cell signalling: the dynamic cooperation of integrin, proteoglycan and growth factor receptor
Soo-Hyun Kim et al.
JOURNAL OF ENDOCRINOLOGY (2011)
Musculocontractural Ehlers-Danlos Syndrome (Former EDS Type VIB) and Adducted Thumb Clubfoot Syndrome (ATCS) Represent a Single Clinical Entity Caused by Mutations in the Dermatan-4-sulfotransferase 1 Encoding CHST14 Gene
Fransiska Malfait et al.
HUMAN MUTATION (2010)
Loss-of-Function Mutations of CHST14 in a New Type of Ehlers-Danlos Syndrome
Noriko Miyake et al.
HUMAN MUTATION (2010)
A mouse knockout library for secreted and transmembrane proteins
Tracy Tang et al.
NATURE BIOTECHNOLOGY (2010)
Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome
Munis Duendar et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Two Dermatan Sulfate Epimerases Form Iduronic Acid Domains in Dermatan Sulfate
Benny Pacheco et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Dermatan Sulfate Epimerase 1-Deficient Mice Have Reduced Content and Changed Distribution of Iduronic Acids in Dermatan Sulfate and an Altered Collagen Structure in Skin
Marco Maccarana et al.
MOLECULAR AND CELLULAR BIOLOGY (2009)
Biosynthesis of dermatan sulfate -: Chondroitin-glucuronate C5-epimerase is identical to SART2
M Maccarana et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Specificities of three distinct human chondroitin/dermatan N-acetylgalactosamine 4-O-sulfotransferases demonstrated using partially desulfated dermatan sulfate as an acceptor -: Implication of differential roles in dermatan sulfate biosynthesis
T Mikami et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Molecular interaction of recombinant decorin and biglycan with type I collagen influences crystal growth
RV Sugars et al.
CONNECTIVE TISSUE RESEARCH (2003)
A novel CpG-associated brain-expressed candidate gene for chromosome 18q-linked bipolar disorder
D Goossens et al.
MOLECULAR PSYCHIATRY (2003)
Dermatan sulfate: new functions from an old glycosaminoglycan
JM Trowbridge et al.
GLYCOBIOLOGY (2002)
Biosynthesis of the linkage region of glycosaminoglycans -: Cloning and activity of galactosyltransferase II, the sixth member of the β1,3-galactosyltransferase family (β3GalT6)
XM Bai et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Molecular cloning and characterization of a dermatan-specific N-acetylgalactosamine 4-O-sulfotransferase
MR Evers et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Molecular cloning and expression of human UDP-D-xylose:proteoglycan core protein β-D-xylosyltransferase and its first isoform XT-II
C Götting et al.
JOURNAL OF MOLECULAR BIOLOGY (2000)
Share Paper
