نتایج جستجو برای: 26a

تعداد نتایج: 688  

2018
Sebastian Carballo Anna Pfenniger David Carballo Nicolas Garin Richard W James François Mach Dipen Shah Brenda R Kwak

Atrial fibrillation (AF) appears in the presence or absence of structural heart disease. The majority of foci causing AF are located near the ostia of pulmonary veins (PVs), where cardiomyocytes and vascular smooth muscle cells interdigitate. Connexins (Cx) form gap junction channels and participate in action potential propagation. Genetic variants in genes encoding Cx40 and Cx37 affect their e...

Journal: :The Journal of biological chemistry 1999
W J Wu B Vrhovski A S Weiss

Following cellular secretion into the extracellular matrix, tropoelastin is transported, deposited, and cross-linked to make elastin. Assembly by coacervation was examined for an isoform of tropoelastin that lacks the hydrophilic domain encoded by exon 26A. It is equivalent to a naturally secreted form of tropoelastin and shows similar coacervation performance to its partner containing 26A, the...

2015
Ying Zhu Jia-Lu Wang Zhi-Yi He Feng Jin Ling Tang Kandiah Jeyaseelan

BACKGROUND AND PURPOSE Perihematomal edema (PHE) contributes to secondary brain damage and aggravates patient outcomes after intracerebral hemorrhage (ICH). MicroRNAs (miRNAs) are stable in circulation, and their unique expression profiles have fundamental roles in modulating vascular disease. The objective of this study was to test the hypothesis that altered miRNA levels are associated with P...

2016
Wenhua Tao Xiaoyun Dong Guimei Kong Penghua Fang Xiaoli Huang Ping Bo

Background and Aims. Although the differential expression of microRNA (miRNA) genes has been identified in many diseases, little information exists concerning the miRNA expression profile in type 2 diabetes mellitus (T2DM) with diarrhea-predominant irritable bowel syndrome (D-IBS). Therefore, the specific expression of miRNAs in diabetes with D-IBS is identified in the study. Materials and Meth...

Journal: :Cancer research 2012
Bin Bao Shadan Ali Sanjeev Banerjee Zhiwei Wang Farah Logna Asfar S Azmi Dejuan Kong Aamir Ahmad Yiwei Li Subhash Padhye Fazlul H Sarkar

The histone methyltransferase EZH2 is a central epigenetic regulator of cell survival, proliferation, and cancer stem cell (CSC) function. EZH2 expression is increased in various human cancers, including highly aggressive pancreatic cancers, but the mechanisms underlying for its biologic effects are not yet well understood. In this study, we probed EZH2 function in pancreatic cancer using diflo...

2016
Giovanni Cochetti Giulia Poli Gabriella Guelfi Andrea Boni Maria Giulia Egidi Ettore Mearini

INTRODUCTION Diagnosis of prostate cancer (PCa) is based on prostate biopsy that is performed when prostate specific antigen (PSA) is persistently altered over time and/or abnormal digital rectal examination is found. Serum PSA levels increase in both PCa and benign prostatic hyperplasia, leading to an increased number of unnecessary biopsies. There is an urgent need to unravel PCa-specific mol...

2014
Milosz Jaguszewski Julia Osipova Jelena-Rima Ghadri Lars Christian Napp Christian Widera Jennifer Franke Marcin Fijalkowski Radoslaw Nowak Marta Fijalkowska Ingo Volkmann Hugo A. Katus Kai C. Wollert Johann Bauersachs Paul Erne Thomas F. Lüscher Thomas Thum Christian Templin

AIMS Takotsubo cardiomyopathy (TTC) remains a potentially life-threatening disease, which is clinically indistinguishable from acute myocardial infarction (MI). Today, no established biomarkers are available for the early diagnosis of TTC and differentiation from MI. MicroRNAs (miRNAs/miRs) emerge as promising sensitive and specific biomarkers for cardiovascular disease. Thus, we sought to iden...

Journal: :Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance 2016
Svetlana Becker Anca Florian Alexandru Patrascu Sabine Rösch Johannes Waltenberger Udo Sechtem Matthias Schwab Elke Schaeffeler Ali Yilmaz

BACKGROUND Duchenne and Becker muscular dystrophy (DMD and BMD) are X-chromosomal recessive neuromuscular disorders that are caused by mutations in the dystrophin gene and characterized by cardiac involvement. Circulating microRNAs (miRNAs) have been proposed as diagnostic biomarkers for various cardiovascular diseases. However, circulating miRNAs reflecting the presence and/or disease severity...

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