Literature DB >> 10494825

The glycosphingolipidoses-from disease to basic principles of metabolism.

C G Schuette1, T Doering, T Kolter, K Sandhoff.   

Abstract

The glycosphingolipidoses are a set of diseases that are caused by defects in the lysosomal degradation of glycolipids derived from the plasma membrane. By investigating the molecular bases of the diseases, basic principles of storage disease pathology and of membrane digestion were discovered. The generation of mouse models has facilitated the development of new and promising therapeutic strategies for these diseases, most of which are not treatable at present. Lately, the discovery of the importance of glycosphingolipid metabolism for skin development has opened a new and interesting field.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10494825     DOI: 10.1515/BC.1999.096

Source DB:  PubMed          Journal:  Biol Chem        ISSN: 1431-6730            Impact factor:   3.915


  4 in total

Review 1.  My journey into the world of sphingolipids and sphingolipidoses.

Authors:  Konrad Sandhoff
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2012       Impact factor: 3.493

2.  Impaired selection of invariant natural killer T cells in diverse mouse models of glycosphingolipid lysosomal storage diseases.

Authors:  Stephan D Gadola; Jonathan D Silk; Aruna Jeans; Petr A Illarionov; Mariolina Salio; Gurdyal S Besra; Raymond Dwek; Terry D Butters; Frances M Platt; Vincenzo Cerundolo
Journal:  J Exp Med       Date:  2006-09-18       Impact factor: 14.307

Review 3.  Biological roles of glycans.

Authors:  Ajit Varki
Journal:  Glycobiology       Date:  2016-08-24       Impact factor: 4.313

Review 4.  Neurological Consequences of Sphingosine Phosphate Lyase Insufficiency.

Authors:  Krishan B Atreya; Julie D Saba
Journal:  Front Cell Neurosci       Date:  2022-09-14       Impact factor: 6.147

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.