(Q28289173)

English

Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production

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scholarly article

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Proteoglycan sulfation in cartilage and cell cultures from patients with sulfate transporter chondrodysplasias: relationship to clinical severity and indications on the role of intracellular sulfate production (English)

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4

object named as

D L Rimoin

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author name string

A Rossi

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I Kaitila

2

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W R Wilcox

3

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B Steinmann

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G Cetta

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A Superti-Furga

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language of work or name

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publication date

October 1998

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17

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361-9

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5

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A modified uronic acid carbazole reaction

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7 January 2021

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The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

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https://api.crossref.org/works/10.1016%2FS0945-053X%2898%2990088-9

7 January 2021

based on heuristic

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Sulphation by cultured cells. Cysteine, cysteinesulphinic acid and sulphite as sources for proteoglycan sulphate

1 reference

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7 January 2021

based on heuristic

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Measurement of contribution from intracellular cysteine to sulfate in phosphoadenosine phosphosulfate in rat ovarian granulosa cells

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based on heuristic

inferred from DOI database lookup

Amino acid sulfur as a source of sulfate for sulfated proteoglycans produced by Swiss mouse 3T3 cells

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Undersulfation of proteoglycans synthesized by chondrocytes from a patient with achondrogenesis type 1B homozygous for an L483P substitution in the diastrophic dysplasia sulfate transporter.

1 reference

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Undersulfation of cartilage proteoglycans ex vivo and increased contribution of amino acid sulfur to sulfation in vitro in McAlister dysplasia/atelosteogenesis type 2

1 reference

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based on heuristic

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Phenotypic and genotypic overlap between atelosteogenesis type 2 and diastrophic dysplasia

1 reference

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The structure and abundance of cartilage proteoglycans during early development of the human fetus

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Production of [3H]hexosamine-labeled proteoglycans by cultures of normal and diabetic skin fibroblasts: dilution of exogenous [3H]glucosamine by endogenous hexosamine from glucose and other sources

1 reference

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beta-D-xylosides and their analogues as artificial initiators of glycosaminoglycan chain synthesis. Aglycone-related variation in their effectiveness in vitro and in ovo

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2898%2990088-9

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based on heuristic

inferred from DOI database lookup

Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2898%2990088-9

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based on heuristic

inferred from DOI database lookup

Specific activity of radiolabeled hexosamines in metabolic labeling experiments

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2898%2990088-9

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based on heuristic

inferred from DOI database lookup

Analysis of unsaturated disaccharides from glycosaminoglycuronan by high-performance liquid chromatography

1 reference

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based on heuristic

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Identifiers

10.1016/S0945-053X(98)90088-9

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release_lit2ajp7vvh6dmbdhpnfzbp7k4

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