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PubMed 11032626 Does APO epsilon4 correlate with MRI changes in Alzheimer's disease? OBJECTIVE: To assess the relation between APO E genotype and MRI white matter changes in Alzheimer's disease. The APO epsilon4 alle 1.57 KB 2015-11-21 3 3
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PubMed 12675842 Uremic toxins of organic anions up-regulate PAI-1 expression by induction of NF-kappaB and free radical in proximal tubular cells. BACKGROUND: Uremic toxins have been suggested to promote progression 2.1 KB 2015-11-22 2 7
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PubMed 20065295 Neogenin inhibits HJV secretion and regulates BMP-induced hepcidin expression and iron homeostasis. Neogenin, a deleted in colorectal cancer (DCC) family member, has been identified as a receptor for 1.34 KB 2015-11-25 4 3
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PubMed 20074440 The relationship between a common catechol-O-methyltransferase (COMT) polymorphism val(158) met and fibromyalgia. OBJECTIVES: Fibromyalgia syndrome (FM) is an idiopathic chronic pain syndrome characte 1.67 KB 2015-11-25 4 3
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PubMed 11170080 Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG. Long QT syndrome is a congenital disorder that presents with a defective cardiac ion channel 1.53 KB 2015-11-17 5 3
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PubMed 22977194 FoxM1 inhibition sensitizes resistant glioblastoma cells to temozolomide by downregulating the expression of DNA-repair gene Rad51. PURPOSE: Recurrent glioblastoma multiforme (GBM) is characterized by 1.65 KB 2015-11-26 4 8
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PubMed 23378578 EpCAM modulates NF-κB signaling and interleukin-8 expression in breast cancer. The epithelial cell adhesion molecule (EpCAM) is a 40-kD type I transmembrane protein that is overexpressed in human epit 1.75 KB 2015-11-27 4 31
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PubMed 23470247 Molecular and functional analysis of the large 5' promoter region of CFTR gene revealed pathogenic mutations in CF and CFTR-related disorders. Patients with cystic fibrosis (CF) manifest a multisystem 1.44 KB 2015-11-27 3 11
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PubMed 18382768 Endothelin receptor antagonism prevents hypoxia-induced mortality and morbidity in a mouse model of sickle-cell disease. Patients with sickle-cell disease (SCD) suffer from tissue damage and life-thre 1.29 KB 2018-11-29 3 3
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PubMed 23401156 Spectrum of mutations that cause distal arthrogryposis types 1 and 2B. The distal arthrogryposis (DA) syndromes are a group of disorders characterized by non-progressive congenital contractures of the 1.21 KB 2016-01-11 3 9
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