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关键词:'544-40-1'
显示 1-6 共 6 条结果 关于 "544-40-1" 范围 论文
Feng Wang et al.
Oncology letters, 17(3), 2983-2992 (2019-03-12)
Anaplastic thyroid cancer (ATC), with a mean survival time of 6 months, was reported in 2012 to account for 1-2% of all thyroid tumor cases in the US. Understanding the molecular mechanisms underlying carcinogenesis and progression in ATC would contribute
Soo Mi Kim et al.
American journal of physiology. Renal physiology, 292(1), F415-F422 (2006-09-07)
In the current experiments, we determined the response of plasma renin concentration (PRC) to acute intraperitoneal administration of furosemide (40 mg/kg), hydralazine (2 mg/kg), isoproterenol (10 mg/kg), candesartan (50 microg), or quinaprilate (50 microg) in conscious wild-type (WT) and cyclooxygenase
Fei Lu et al.
Echocardiography (Mount Kisco, N.Y.), 27(5), 544-551 (2010-04-09)
The aim of this study was to evaluate enoximone echocardiography (EE) for the identification of residual myocardial viability in postinfarction patients. Findings obtained during EE were compared with those acquired by myocardial uptake of fluorine-18 fluorodeoxyglucose ((18)F-FDG) positron emission tomography
A Ritzhaupt et al.
The Journal of physiology, 513 ( Pt 3), 719-732 (1998-11-24)
1. Oligonucleotide primers based on the human heart monocarboxylate transporter (MCT1) cDNA sequence were used to isolate a 544 bp cDNA product from human colonic RNA by reverse transcription-polymerase chain reaction (RT-PCR). The sequence of the RT-PCR product was identical
Sungwook Lee et al.
Journal of virology, 83(23), 12368-12377 (2009-09-25)
B lymphocytes converted into lymphoblastoid cell lines (LCLs) by an Epstein-Barr virus that expresses a conditional EBNA3C require complementation with EBNA3C for growth under nonpermissive conditions. Complementation with relatively large EBNA3C deletion mutants identified amino acids (aa) 1 to 506
Imre Noth et al.
The Lancet. Respiratory medicine, 1(4), 309-317 (2014-01-17)
Idiopathic pulmonary fibrosis (IPF) is a devastating disease that probably involves several genetic loci. Several rare genetic variants and one common single nucleotide polymorphism (SNP) of MUC5B have been associated with the disease. Our aim was to identify additional common
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