Literature DB >> 992027

Characterization of a mannose-containing glycoasparagine isolated from urine of a patient with aspartylglycosylaminuria (AGU).

M Akasaki, K Sugahara, I Funakoshi, P Aula, I Yamashina.   

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Year:  1976        PMID： 992027     DOI： 10.1016/0014-5793(76)80684-9

Source DB:  PubMed          Journal:  FEBS Lett        ISSN： 0014-5793            Impact factor:   4.124


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  3 in total

Review 1.  Aspartylglycosaminuria: an inborn error of glycoprotein catabolism.

Authors:  C P Maury
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

2.  The core-specific lysosomal alpha(1-6)-mannosidase activity depends on aspartamidohydrolase activity.

Authors:  J F Haeuw; T Grard; C Alonso; G Strecker; J C Michalski
Journal:  Biochem J       Date:  1994-02-01       Impact factor: 3.857

3.  Characterization of four monosialo and a novel disialo Asn N-glycosides from the urine of a patient with aspartylglycosaminuria.

Authors:  F Irie; H Murakoshi; T Suzuki; Y Suzuki; K Kon; S Ando; K Yoshida; Y Hirabayashi
Journal:  Glycoconj J       Date:  1995-06       Impact factor: 2.916
  3 in total

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