C24 GlcCer

C24 GlcCer is a lipid of Sphingolipids (SP) class. The related experimental models are Knock-out.

Cross Reference

Introduction

To understand associated biological information of C24 GlcCer, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with C24 GlcCer?

There are no associated biomedical information in the current reference collection.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with C24 GlcCer

MeSH term MeSH ID Detail
Leukodystrophy, Metachromatic D007966 4 associated lipids
Niemann-Pick Diseases D009542 25 associated lipids
Gaucher Disease D005776 13 associated lipids
Abetalipoproteinemia D000012 7 associated lipids
Lipidoses D008064 7 associated lipids
Fatigue D005221 10 associated lipids
Infarction D007238 3 associated lipids
Epilepsies, Myoclonic D004831 2 associated lipids
Venous Thrombosis D020246 11 associated lipids
Uveitis, Intermediate D015867 3 associated lipids
Per page 10 20 | Total 12

PubChem Associated disorders and diseases

What pathways are associated with C24 GlcCer

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with C24 GlcCer?

There are no associated biomedical information in the current reference collection.

What functions are associated with C24 GlcCer?

There are no associated biomedical information in the current reference collection.

What lipids are associated with C24 GlcCer?

There are no associated biomedical information in the current reference collection.

What genes are associated with C24 GlcCer?

There are no associated biomedical information in the current reference collection.

What common seen animal models are associated with C24 GlcCer?

Knock-out

Knock-out are used in the study 'Rho/ROCK pathway is essential to the expansion, differentiation, and morphological rearrangements of human neural stem/progenitor cells induced by lysophosphatidic acid.' (Frisca F et al., 2013).

Related references are published most in these journals:

Model Cross reference Weighted score Related literatures
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NCBI Entrez Crosslinks

All references with C24 GlcCer

Download all related citations
Per page 10 20 50 | Total 35
Authors Title Published Journal PubMed Link
Erickson JS and Radin NS N-hexyl-O-glucosyl sphingosine, an inhibitor of glucosyl ceramide -glucosidase. 1973 J. Lipid Res. pmid:4698260
Pilz H and Heipertz R [Differential diagnosis of congenital lipidoses by lipid analyses of body fluids, biopsy and autopsy tissue]. 1975 Fortschr Neurol Psychiatr Grenzgeb pmid:53174
Dawson G et al. Distribution of glycosphingolipids in the serum lipoproteins of normal human subjects and patients with hypo- and hyperlipidemias. 1976 J. Lipid Res. pmid:178813
Owada M et al. Neuropathic Gaucher's disease with normal 4-methylumbelliferyl-beta-glucosidase activity in the liver. 1977 Pediatr. Res. pmid:870871
Smith RL et al. Unusual cardiac, renal and pulmonary involvement in Gaucher's disease. Intersitial glucocerebroside accumulation, pulmonary hypertension and fatal bone marrow embolization. 1978 Am. J. Med. pmid:686020
Nishimura RN and Barranger JA Neurologic complications of Gaucher's disease, type 3. 1980 Arch. Neurol. pmid:6766716
Soffer D et al. Central nervous system involvement in adult-onset Gaucher's disease. 1980 Acta Neuropathol. pmid:7355669
Daniels LB et al. Brain glucocerebrosidase in Gaucher's disease. 1982 Arch. Neurol. pmid:6810854
Nilsson O and Svennerholm L Accumulation of glucosylceramide and glucosylsphingosine (psychosine) in cerebrum and cerebellum in infantile and juvenile Gaucher disease. 1982 J. Neurochem. pmid:7097276
Nilsson O et al. The occurrence of psychosine and other glycolipids in spleen and liver from the three major types of Gaucher's disease. 1982 Biochim. Biophys. Acta pmid:7126619