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Quoted phrase not found in phrase index: "Increased level of N-acetylneuraminic acid in fibroblasts"
Page 1
Dominant inheritance of sialuria, an inborn error of feedback inhibition.
Am J Hum Genet. 2001 Jun;68(6):1419-27. doi: 10.1086/320598. Epub 2001 Apr 18.
Am J Hum Genet. 2001.
PMID: 11326336
Free PMC article.
"French type" sialuria, a presumably dominant disorder that, until now, had been documented in only five patients, manifests with mildly coarse facies, slight motor delay, and urinary excretion of large quantities (>1 g/d) of free N-acetylneuraminic acid ( …
"French type" sialuria, a presumably dominant disorder that, until now, had been documented in only five patients, manifests with mildly coa …
The effects of sialic acid on the gene expression of fibrillar collagens: different changes in normal and fibrotic scar derived fibroblasts.
Kössi J, Aalto J, Haataja S, Niinikoski J, Peltonen J, Laato M.
Kössi J, et al.
Ann Chir Gynaecol. 2001;90 Suppl 215:25-8.
Ann Chir Gynaecol. 2001.
PMID: 12041923
RESULTS: Fibroblast lines react dissimilarly under the influence of sialic acid. Granulation tissue fibroblasts showed decrease in the gene expression of type I and III collagen, while keloid fibroblasts contrastingly showed an increase. ...
RESULTS: Fibroblast lines react dissimilarly under the influence of sialic acid. Granulation tissue fibroblasts showed …
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Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder.
Spaapen LJ, Bakker JA, van der Meer SB, Sijstermans HJ, Steet RA, Wevers RA, Jaeken J.
Spaapen LJ, et al.
J Inherit Metab Dis. 2005;28(5):707-14. doi: 10.1007/s10545-005-0015-z.
J Inherit Metab Dis. 2005.
PMID: 16151902
We report on two dysmorphic siblings with severe liver disease who died at the age of a few weeks. Increased activities of lysosomal enzymes in plasma were found, though total sialic acid in plasma was strongly decreased. ...O-Glycosylation was investigated by isoel …
We report on two dysmorphic siblings with severe liver disease who died at the age of a few weeks. Increased activities of lysosomal …
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An sLex-deficient variant of HL60 cells exhibits high levels of adhesion to vascular selectins: further evidence that HECA-452 and CSLEX1 monoclonal antibody epitopes are not essential for high avidity binding to vascular selectins.
Wagers AJ, Stoolman LM, Craig R, Knibbs RN, Kansas GS.
Wagers AJ, et al.
J Immunol. 1998 May 15;160(10):5122-9.
J Immunol. 1998.
PMID: 9590264
Although the precise molecular basis for the sLex(-/low) phenotype of HL60var remains uncertain, flow cytometric analysis with the sialic acid-specific Limax flavus lectin revealed a sharp reduction in HL60var surface sialylation. Thus, the loss in mAb reactivity may resul …
Although the precise molecular basis for the sLex(-/low) phenotype of HL60var remains uncertain, flow cytometric analysis with the sialic …
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