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CHST15 gene
Known as:
N-ACETYLGALACTOSAMINE 4-SULFATE 6-O-SULFOTRANSFERASE
, CARBOHYDRATE SULFOTRANSFERASE 15
, KIAA0598
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This gene is involved in chondroitin sulfate metabolism.
National Institutes of Health
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Related topics
Related topics
3 relations
CHST15 protein, human
Carbohydrate Metabolism
protein metabolism
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Increased CHST15 follows decline in arylsulfatase B (ARSB) and disinhibition of non-canonical WNT signaling: potential impact on epithelial and mesenchymal identity
S. Bhattacharyya
,
L. Feferman
,
+4 authors
J. Tobacman
OncoTarget
2020
Corpus ID: 220056559
Expression of CHST15 (carbohydrate sulfotransferase 15; chondroitin 4-sulfate-6-sulfotransferase; BRAG), the sulfotransferase…
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2016
2016
Mice deficient in N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase exhibit enhanced liver fibrosis and delayed recovery from fibrosis in carbon tetrachloride-treated mice
H. Habuchi
,
T. Ushida
,
O. Habuchi
Heliyon
2016
Corpus ID: 14148228
2016
2016
EPIDEMICS, EPISTEMOPHILIA, AND RACISM: ECOLOGICAL LITERARY CRITICISM AND "THE RAG DOLL PLAGUES"
María Herrera-Sobek
2016
Corpus ID: 140436229
Ecology: the body of knowledge concerning the economy of nature?the inves tigation of the total relations of the animal both to…
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2015
2015
[Material Composition Research on Tibetan Medicine "Brag-zhun"].
Yun Cao
,
Rui Gu
,
Yu-ying Ma
,
Shi-hong Zhong
,
R. Zeng
,
Xue-feng Lu
Zhong yao cai = Zhongyaocai = Journal of Chinese…
2015
Corpus ID: 22789623
OBJECTIVE To study the material composition of Tibetan medicine "Brag-zhun", and to provide the basis for interpretation of its…
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2011
2011
Substantial Dissociation Energies for the Recently Synthesized NC-Ag-NH3 and Br-Ag-NH3 Molecules and Their Isovalent Family Members M(CN)XY3 and M(Br)XY3 (M = Cu, Ag, Au; X = N, P; Y = H, F).
Q. Luo
,
Qian-shu Li
,
Yaoming Xie
,
R. King
,
H. Schaefer
Journal of Chemical Theory and Computation
2011
Corpus ID: 206905479
Chippindale et al. have recently synthesized the unique molecules (NC)Ag(NH3) and BrAg(NH3) and shown the heavy atom skeletal…
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2010
2010
Mice Deficient in N-Acetylgalactosamine 4-Sulfate 6-O-Sulfotransferase Are Unable to Synthesize Chondroitin/Dermatan Sulfate containing N-Acetylgalactosamine 4,6-Bissulfate Residues and Exhibit…
Shiori Ohtake-Niimi
,
Sachiko Kondo
,
+5 authors
O. Habuchi
Journal of Biological Chemistry
2010
Corpus ID: 20276108
Chondroitin sulfate (CS) and dermatan sulfate (DS) containing N-acetylgalactosamine 4,6-bissulfate (GalNAc(4,6-SO4)) show various…
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2010
2010
Inhibition of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase by ß-D-4-O-sulfo-N-acetylgalactosaminides bearing various hydrophobic aglycons
Hiroko Nozaki
,
Yuri Tomoyama
,
+9 authors
O. Habuchi
Glycoconjugate Journal
2010
Corpus ID: 8687356
N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) transfers sulfate to position 6 of GalNAc(4SO4) residues of…
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2007
2007
Molecular cloning of squid N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase and synthesis of a unique chondroitin sulfate containing E-D hybrid tetrasaccharide structure by the recombinant enzyme…
Teruyoshi Yamaguchi
,
Shiori Ohtake
,
K. Kimata
,
O. Habuchi
Glycobiology
2007
Corpus ID: 20479680
N-Acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) transfers sulfate to position 6 of GalNAc(4SO(4)) residues in…
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2005
2005
Synthesis of sulfated phenyl 2-acetamido-2-deoxy-D-galactopyranosides. 4-O-Sulfated phenyl 2-acetamido-2-deoxy-beta-D-galactopyranoside is a competitive acceptor that decreases sulfation of…
Toshihiko Sawada
,
Sonoko Fujii
,
H. Nakano
,
Shiori Ohtake
,
K. Kimata
,
O. Habuchi
Carbohydrate Research
2005
Corpus ID: 36553773
1988
1988
Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria via enzyme activity measurements in chorionic villi, chorionic villous fibroblasts or amniocytes using a simple spectrophotometric method
R. Wanders
,
R. Schutgens
,
B. H. M. Zoeters
Journal of Inherited Metabolic Disease
1988
Corpus ID: 32294170
3-Hydroxy-3-methylglutaric aciduria is an autosomal recessive disorder of leucine degradation caused by a deficiency of the…
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