548-80-1

应用筛选条件

关键词:'548-80-1'

显示 1-4 共 4 条结果关于 "548-80-1" 范围论文

H-point standard addition method for the selective simultaneous determination of nickel and copper using 1-(2-pyridylazo)-2-naphthol in Tween 80 micellar media.

Habibollah Eskandari et al.

Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 20(7), 1095-1098 (2004-08-06)

The H-point standard addition method (HPSAM) has been applied for the simultaneous determination of nickel and copper in trace levels, using 1-(2-pyridylazo)-2-naphthol (PAN) as a chromogenic reagent in aqueous Tween 80 micellar media. Under the optimum condition, the simultaneous determinations

Disruption of the circadian clock within the cardiomyocyte influences myocardial contractile function, metabolism, and gene expression.

Molly S Bray et al.

American journal of physiology. Heart and circulatory physiology, 294(2), H1036-H1047 (2007-12-25)

Virtually every mammalian cell, including cardiomyocytes, possesses an intrinsic circadian clock. The role of this transcriptionally based molecular mechanism in cardiovascular biology is poorly understood. We hypothesized that the circadian clock within the cardiomyocyte influences diurnal variations in myocardial biology.

Molecular diagnosis in LGMD2A: mutation analysis or protein testing?

M Fanin et al.

Human mutation, 24(1), 52-62 (2004-06-29)

Limb girdle muscular dystrophy (LGMD) type 2A (LGMD2A) is caused by mutations in the CAPN3 gene encoding for calpain-3, a muscle specific protease. While a large number of CAPN3 gene mutations have already been described in calpainopathy patients, the diagnosis

Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.

Christopher Newton-Cheh et al.

BMC medical genetics, 8 Suppl 1, S7-S7 (2007-10-16)

Heritable electrocardiographic (ECG) and heart rate variability (HRV) measures, reflecting pacemaking, conduction, repolarization and autonomic function in the heart have been associated with risks for cardiac arrhythmias. Whereas several rare monogenic conditions with extreme phenotypes have been noted, few common

1/1