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Frontiers in Molecular Neuroscience, ISSN 1662-5099, 02/2019, Volume 12, p. 26
Chondroitin sulfate (CS) and dermatan sulfate (DS) proteoglycans (PGs) are major extracellular matrix (ECM) components of the central nervous system (CNS). A... 
Learning and memory | LTP | Chst14/D4st1 | Dermatan sulfate | Synaptic plasticity | CHONDROITIN SULFATE/DERMATAN SULFATE | PROLIFERATION | HYBRID CHAINS | RADIAL GLIA | NEUROSCIENCES | ETHYLMALEIMIDE-SENSITIVE FACTOR | dermatan sulfate | learning and memory | MEMORY | IDURONIC ACID | B-50 GAP-43 | synaptic plasticity | LONG-TERM POTENTIATION | RECEPTORS | Sulfates
Journal Article
Human Mutation, ISSN 1059-7794, 05/2015, Volume 36, Issue 5, pp. 535 - 547
Bi-allelic variants in CHST14, encoding dermatan 4-O-sulfotransferase-1 (D4ST1), cause musculocontractural Ehlers-Danlos syndrome (MC-EDS), a recessive... 
Ehlers–Danlos syndrome | dermatan 4 | dermatan sulfate epimerase‐1 | EDS | sulfotransferase‐1 | DSE | CHST14 | Ehlers-Danlos syndrome | Dermatan sulfate epimerase-1 | Dermatan 4-O-sulfotransferase-1 | PROTEIN | ADDUCTED THUMB | CONTRACTURES | dermatan sulfate epimerase-1 | DERMATAN-4-SULFOTRANSFERASE | FOOT SYNDROME | CHST14 GENE | IDURONIC ACID | THUMB-CLUBFOOT SYNDROME | GENETICS & HEREDITY | dermatan 4-O-sulfotransferase-1 | CHONDROITIN/DERMATAN SULFATE | MUTATIONS | Exons | Humans | Extracellular Matrix - metabolism | Molecular Sequence Data | Dermatan Sulfate - biosynthesis | Male | Neoplasm Proteins - metabolism | RNA, Messenger - metabolism | DNA-Binding Proteins - metabolism | Young Adult | Ehlers-Danlos Syndrome - genetics | Facies | Antigens, Neoplasm - metabolism | Adult | Female | Sulfotransferases - metabolism | Neoplasm Proteins - genetics | Child | Skin - pathology | Sulfotransferases - genetics | Amino Acid Sequence | Antigens, Neoplasm - genetics | RNA, Messenger - genetics | DNA-Binding Proteins - genetics | Fibronectins - metabolism | Genetic Heterogeneity | Collagen - metabolism | Phenotype | Sequence Alignment | Ehlers-Danlos Syndrome - metabolism | Biopsy | Pedigree | Adolescent | Skin - ultrastructure | Ehlers-Danlos Syndrome - diagnosis | Mutation | Sulfotransferases - chemistry | Fibronectins | Glycosaminoglycans | Collagen | Physiological aspects | Genetic research | Family | Biosynthesis | Sulfates | Cell differentiation | Genetic disorders | Cell adhesion & migration
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 201 - 216
Journal Article
Human Mutation, ISSN 1059-7794, 08/2010, Volume 31, Issue 8, pp. 966 - 974
Journal Article
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 08/2011, Volume 155, Issue 8, pp. 1949 - 1958
Loss‐of‐function mutations in CHST14 , dermatan 4‐ O ‐sulfotransferase 1 (D4ST1) deficiency, have recently been found to cause adducted thumb‐clubfoot syndrome... 
malformations | congenital contractures | dermatan 4 | progressive multisystem fragility‐related manifestations | musculocontractural Ehlers–Danlos syndrome | adducted thumb‐clubfoot syndrome | Ehlers–Danlos syndrome Kosho type | sulfotransferase 1 deficiency | Malformations | Musculocontractural Ehlers-Danlos syndrome | Congenital contractures | Adducted thumb-clubfoot syndrome | Ehlers-Danlos syndrome Kosho type | Dermatan 4-O-sulfotransferase 1 deficiency | Progressive multisystem fragility-related manifestations | dermatan 4-O-sulfotransferase 1 deficiency | ADDUCTED THUMB | CONTRACTURES | musculocontractural Ehlers-Danlos syndrome | DERMATAN-4-SULFOTRANSFERASE | adducted thumb-clubfoot syndrome | VIB | GENE | GENETICS & HEREDITY | CLUB FOOT SYNDROME | progressive multisystem fragility-related manifestations | MUTATIONS | CHST14 | JOINT | Sulfotransferases - genetics | Genetic Association Studies | Humans | Child, Preschool | Male | Developmental Disabilities - genetics | Sulfotransferases - deficiency | Ehlers-Danlos Syndrome - genetics | Phenotype | DNA Mutational Analysis | Clubfoot - surgery | Child | Cryptorchidism - genetics | Ehlers-Danlos Syndrome - enzymology | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Heart | Ehlers-Danlos syndrome | Congenital defects | Central nervous system | Birth | Procollagen-lysine 5-dioxygenase | Kidney | Dislocation | Fibrillogenesis | Collagen | Hematoma | Skin | Children | Mutation | Joints | Age
Journal Article
Journal Article