MeSH term | MeSH ID | Detail |
---|---|---|
Body Weight | D001835 | 333 associated lipids |
Kidney Neoplasms | D007680 | 29 associated lipids |
Spinocerebellar Ataxias | D020754 | 4 associated lipids |
Dl-serine is a lipid of Fatty Acyls (FA) class. Dl-serine is associated with abnormalities such as Spastic syndrome, Machado-Joseph Disease, Huntington Disease, Infection and Gram positive septicemia. The involved functions are known as Lipid Binding, Proteolysis, Protein Processing, Post-Translational, Cytokinesis and Phosphorylation. Dl-serine often locates in Anatomic Site, Membrane, Cytoplasmic Domain, Extracellular and Blood. The associated genes with Dl-serine are polyserine, lipovitellin, Polypeptides, CSNK2A1 wt Allele and Spider Proteins. The related experimental models are Mouse Model.
To understand associated biological information of Dl-serine, 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.
Dl-serine is suspected in Huntington Disease, Infection, Spastic syndrome, Machado-Joseph Disease, Gram positive septicemia and other diseases in descending order of the highest number of associated sentences.
Disease | Cross reference | Weighted score | Related literature |
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We collected disease MeSH terms mapped to the references associated with Dl-serine
MeSH term | MeSH ID | Detail |
---|---|---|
Body Weight | D001835 | 333 associated lipids |
Kidney Neoplasms | D007680 | 29 associated lipids |
Spinocerebellar Ataxias | D020754 | 4 associated lipids |
There are no associated biomedical information in the current reference collection.
Associated locations are in red color. Not associated locations are in black.
Location | Cross reference | Weighted score | Related literatures |
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Function | Cross reference | Weighted score | Related literatures |
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There are no associated biomedical information in the current reference collection.
Gene | Cross reference | Weighted score | Related literatures |
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Mouse Model are used in the study 'Polyalanine and polyserine frameshift products in Huntington's disease.' (Davies JE and Rubinsztein DC, 2006).
Model | Cross reference | Weighted score | Related literatures |
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Authors | Title | Published | Journal | PubMed Link |
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Lefebvre-Lavoie J et al. | Profiling of differentially expressed genes in wound margin biopsies of horses using suppression subtractive hybridization. | 2005 | Physiol. Genomics | pmid:15870397 |
Nagata H et al. | Structural scaffold of 18-crown-6 tetracarboxylic Acid for optical resolution of chiral amino acid: x-ray crystal analyses of complexes of D- and L-isomers of serine and glutamic acid. | 2006 | Chem. Pharm. Bull. | pmid:16595944 |
Li C | Voltammetric determination of tyrosine based on an L-serine polymer film electrode. | 2006 | Colloids Surf B Biointerfaces | pmid:16797945 |
Davies JE and Rubinsztein DC | Polyalanine and polyserine frameshift products in Huntington's disease. | 2006 | J. Med. Genet. | pmid:16801344 |
Mizejewski GJ et al. | Anticancer versus antigrowth activities of three analogs of the growth-inhibitory peptide: relevance to physicochemical properties. | 2006 Jul-Aug | Anticancer Res. | pmid:16886636 |
Ali S et al. | High performance microbiological transformation of L-tyrosine to L-dopa by Yarrowia lipolytica NRRL-143. | 2007 | BMC Biotechnol. | pmid:17705832 |
Kim TS et al. | Nonsurgical and surgical periodontal therapy in single-rooted teeth. | 2007 | Clin Oral Investig | pmid:17690922 |
Lobsiger CS et al. | Toxicity from different SOD1 mutants dysregulates the complement system and the neuronal regenerative response in ALS motor neurons. | 2007 | Proc. Natl. Acad. Sci. U.S.A. | pmid:17463094 |
Santi I et al. | Functional characterization of a newly identified group B Streptococcus pullulanase eliciting antibodies able to prevent alpha-glucans degradation. | 2008 | PLoS ONE | pmid:19023424 |
Takeda K et al. | Clinicopathological significance of expression of p-c-Jun, TCF4 and beta-Catenin in colorectal tumors. | 2008 | BMC Cancer | pmid:18992165 |