Documents (356,316) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	20978009	Expression and the role of 3'-phosphoadenosine 5'-phosphosulfate transporters in human colorectal carcinoma. Sulfation represents an essential modification for various molecules and regulates many bio	1.33 KB	2019-05-30	56	12	-
PubMed	20040515	KSHV downregulation of galectin-3 in Kaposi's sarcoma. Galectins are a family of proteins that share an affinity for beta-galactoside containing glycoconjugates. In prostate, ovarian and breast cancer	1.76 KB	2019-05-30	56	18	-
PubMed	22611128	Mucin 21 in esophageal squamous epithelia and carcinomas: analysis with glycoform-specific monoclonal antibodies. Monoclonal antibodies (mAbs) against mucin 21 (MUC21), a human counterpart of mouse ep	1.57 KB	2019-05-30	56	6	-
PubMed	16371368	Effects of a leukemia-associated gain-of-function mutation of SHP-2 phosphatase on interleukin-3 signaling. Mutations in SHP-2 phosphatase that cause hyperactivation of its catalytic activity have bee	2.24 KB	2019-09-23	56	3	-
PubMed	20926598	DNA methylation and histone H3-K9 modifications contribute to MUC17 expression. MUC17 glycoprotein is a membrane-associated mucin that is mainly expressed in the digestive tract. It has been suggested	1.5 KB	2019-05-30	55	12	-
PubMed	12499404	Production in yeast of alpha-galactosidase A, a lysosomal enzyme applicable to enzyme replacement therapy for Fabry disease. A mammalian-like sugar moiety was created in glycoprotein by Saccharomyces	1.57 KB	2019-05-30	55	6	-
PubMed	16361247	Elimination of abnormal sialylglycoproteins in fibroblasts with sialidosis and galactosialidosis by normal gene transfer and enzyme replacement. Sialidosis and galactosialidosis are lysosomal storage	1.76 KB	2019-05-30	55	75	-
PubMed	11555618	Glycosidase active site mutations in human alpha-L-iduronidase. Mucopolysaccharidosis type I (MPS I; McKusick 25280) results from a deficiency in alpha-L-iduronidase activity. Using a bioinformatics a	1.75 KB	2019-05-30	55	3	-
PubMed	12626384	A biochemical and pharmacological comparison of enzyme replacement therapies for the glycolipid storage disorder Fabry disease. Fabry disease is a lysosomal storage disease arising from deficiency of	1.85 KB	2019-05-30	54	6	-
PubMed	15987957	Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy. Hereditary inclusion body myopathy (HI	1.7 KB	2018-03-09	54	6	-