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# Ann.
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| PubMed |
2211661 |
Deficient expression of the gene coding for decorin in a lethal form of Marfan syndrome.
The markedly decreased level of the messenger RNA of decorin, an abundant dermatan/chondroitin sulfate proteogl |
1.15 KB |
2015-11-26 |
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46 |
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3 |
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| PubMed |
16152606 |
Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies.
Nijmegen breakage syndrome (NBS) is a human autosomal recessive |
1.76 KB |
2015-11-19 |
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45 |
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42 |
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| PubMed |
20682662 |
Lack of association of C-C chemokine receptor 5 Δ32 deletion status with rheumatoid arthritis, systemic lupus erythematosus, lupus nephritis, and disease severity.
OBJECTIVE: C-C chemokine receptor 5 |
1.69 KB |
2015-11-25 |
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45 |
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6 |
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| PubMed |
23275522 |
Cyclooxygenase-2 enzyme induces the expression of the α-2,3-sialyltransferase-3 (ST3Gal-I) in breast cancer.
Aberrant glycosylation is a common feature of malignant change. Changes in mucin-type O-lin |
1.77 KB |
2015-11-27 |
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45 |
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54 |
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| PubMed |
16867246 |
Association of DRD2 polymorphisms and chlorpromazine-induced extrapyramidal syndrome in Chinese schizophrenic patients.
AIM: Extrapyramidal syndrome (EPS) is most commonly affected by typical antipsyc |
1.65 KB |
2025-10-02 |
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45 |
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18 |
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| PubMed |
14707127 |
Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles.
Distal myopathy with rimmed vacuoles is an autosomal reces |
1.28 KB |
2015-11-18 |
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45 |
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3 |
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| PubMed |
18385794 |
Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia.
PURPOSE: Mutations in the SOX2 and CHX10 genes have been reported in p |
2.22 KB |
2015-11-24 |
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45 |
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9 |
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| PubMed |
25124036 |
Human trefoil factor 2 is a lectin that binds α-GlcNAc-capped mucin glycans with antibiotic activity against Helicobacter pylori.
Helicobacter pylori infection is the major cause of gastric cancer and |
1.93 KB |
2018-12-27 |
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45 |
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3 |
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| PubMed |
17436081 |
Alpha1,3 Fucosyltransferase-VII modifies the susceptibility of apoptosis induced by ultraviolet and retinoic acid in human hepatocarcinoma cells.
The role of alpha1,3fucosyltransferase-VII (alpha1,3 F |
1.59 KB |
2019-08-21 |
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45 |
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3 |
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| PubMed |
23458625 |
Proteogenomic analysis of human colon carcinoma cell lines LIM1215, LIM1899, and LIM2405.
As part of the genome-wide and chromosome-centric human proteomic project (C-HPP), we have integrated shotgun |
1.46 KB |
2019-08-21 |
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44 |
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6 |
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