The clinical chemistry of inorganic sulfate

Critical Reviews in Clinical Laboratory Sciences

Volumn 37, Issue 4, 2000, Pages 299-344

  Cole, David E C ^a,b   Evrovski, Jovan ^c  

^a UNIVERSITY OF TORONTO   (Canada)

^b TORONTO GENERAL HOSPITAL   (Canada)

^c Departments of Laboratory Medicine and Pathobiology

Author keywords

Biological fluids; Clinical chemistry; Inorganic sulfate; Serum; Urine

Indexed keywords

SULFATE;

AMINO ACID METABOLISM; ANION TRANSPORT; CLINICAL CHEMISTRY; HUMAN; INORGANIC CHEMISTRY; NEPHELOMETRY; NONHUMAN; OXIDATION; PRECIPITATION; PRIORITY JOURNAL; REVIEW; URINARY EXCRETION;

EID: 0033811616     PISSN: 10408363     EISSN: None     Source Type: Journal    
DOI: 10.1080/10408360091174231     Document Type: Review

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219. 2- concentration
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276. 2- transport protein NaSi-1
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278. Functional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycans
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281. Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): Evidence for a phenotypic series involving three chondrodysplasias
282. The Down regulated in Adenoma (dra) gene encodes an intestine-specific membrane sulfate transport protein