Literature DB >> 16584075

Methods for detection of carbohydrate-deficient glycoprotein syndromes.

John F O'Brien1.   

Abstract

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Year:  2005        PMID: 16584075     DOI: 10.1016/j.spen.2005.11.002

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


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  5 in total

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Journal:  Am J Hum Genet       Date:  2014-02-06       Impact factor: 11.025

Review 2.  The impact of mass spectrometry in the diagnosis of congenital disorders of glycosylation.

Authors:  Luisa Sturiale; Rita Barone; Domenico Garozzo
Journal:  J Inherit Metab Dis       Date:  2011-03-08       Impact factor: 4.982

3.  Employment of single-strand conformation polymorphism analysis in screening for α-1,3 glucosyltransferase gene mutation A333V in Croatian population.

Authors:  Sandra Supraha Goreta; Sanja Dabelic; Jerka Dumic
Journal:  J Clin Lab Anal       Date:  2011       Impact factor: 2.352

Review 4.  Laboratory diagnosis of congenital disorders of glycosylation type I by analysis of transferrin glycoforms.

Authors:  Dusica Babovic-Vuksanovic; John F O'Brien
Journal:  Mol Diagn Ther       Date:  2007       Impact factor: 4.074

5.  The effect of malnutrition on protein glycosylation in children.

Authors:  Oznur Bilen; Zekiye Altun; Nur Arslan; Banu Onvural; Pinar Akan; Canan Coker
Journal:  Iran J Pediatr       Date:  2014-06       Impact factor: 0.364

  5 in total

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