Brown heart

To date, no other studies related to the detection of deeply embedded defects such as vitreous melons, brown-hearted pears or frost-damaged citrus, have been... 

Scott, K.J. and Wills, R.B.H. (1974) Reduction of brown heart in pears by absorption of ethylene from the storage atmosphere. Australian J. Exp. Agricol. Animal Husbandry 14, 266-268. 

Brown heart of swedes Boron and turnips (Raan) deficiency... 

Tissue-Specific Expression. In the adult rodent, PPARy is expressed in brown and white adipose tissue, and at lower levels in intestine, retina, skeletal muscle, and lymphoid organs. In human, PPARy is most abundantly expressed in white adipose tissue and at lower levels in skeletal muscle, the heart, and liver, but not in lymphoid tissues, although PPARy has been identified in macrophages in human atheromas. 

The author thanks Alicia Brown for typing this article. He also acknowledges the financial support of DHEW (BRSG grant), the Research Corporation, and the South Carolina affiliate of the American Heart Association. 

Brown G. Acetaminophen-induced hypotension. Heart Lung 1996 25(2) 137-140. 

O Shaughnessy KM, Fu B, Dickerson C, Thurston D, Brown MJ. The gain-of-function G389R variant of the / -adrenoreceptor does not influence blood pressure or heart rate response to /1-blockade in hypertensive subjects. Clin Science 2000 99 233-238. 

ANOVA in these chapters also, back when it was still called Statistics in Spectroscopy [16-19] although, to be sure, our discussions were at a fairly elementary level. The experiment that Philip Brown did is eminently suitable for that type of computation. The experiment was formally a three-factor multilevel full-factorial design. Any nonlinearity in the data will show up in the analysis as what Statisticians call an interaction term, which can even be tested for statistical significance. He then used the wavelengths of maximum linearity to perform calibrations for the various sugars. We will discuss the results below, since they are at the heart of what makes this paper important. 

Grady D, Brown JS, Vittinghoff E, Applegate W, Varner E, Snyder T (2001) Postmenopausal hormones and incontinence the heart and estrogen/progestin replacement study. Obstet Gynecol 97 116-120... 

Lacerda, A.E., Kramer, J., Shen, K.Z., Thomas, D. and Brown, A.M. (2001) Comparison of block among cloned cardiac potassium channels by non-antiarrhythmic drugs. European Heart Journal Supplements, 3, K23-K30. 

Rampe, D., Wibble, B., Brown, A.M. and Dage, R.C. (1993) Effects of terfenadine and its metabolites on a delayed rectifier K+ channel doned from human heart. Molecular Pharmacology, 44, 1240-1245. 

Khat produces sympathomimetic effects, increasing heart rate and blood pressure. When khat is chewed, the increases are gradual, maximizing at about 2 hours and lasting for 4 hours. However, tolerance develops to blood pressure and heart rate effects in habitual users. Mydriasis and increases in respiration also occur. Cathinone induces thermogenesis in brown adipose tissue, which is mediated by jS-adrenergic receptors (Tariq et al. 1989). 

Atropine generally increases heart rate, but it may briefly and mildly decrease it initially, due to Ml receptors on postganglionic parasympathetic neurons. Larger doses of atropine produce greater tachycardia, due to M2 receptors on the sinoatrial node pacemaker cells. There are no changes in blood pressure, but arrhythmias may occur. Scopolamine produces more bradycardia and decreases arterial pressure, whereas atropine has little effect on blood pressure (Vesalainen et al. 1997 Brown and Taylor 1996). 

Hollow heart, brown core 4.7 se imaging, 1-D se imaging projections 92... 

Fig. 6. Spin-echo Image of diseased potato showing hollow heart (dark area) surrounded by brown tissue (bright area). Printed with permission, from Ref. 92.

Mager, D. E., Wan, R., Brown, M., Cheng, A., Wareski, P., Abernethy, D. R., and Mattson, M. P. (2006). Caloric restriction and intermittent fasting alter spectral measures of heart rate and blood pressure variability in rats. FASEB J. 20, 631-637. 

Simonson, S.G., Raza, A., Martin, P.D., Mitchell, P.D., Jarcho, J.A., Brown, C.D.A., Windass, A.S. and Schneck, D.W. (2004) Rosuvastatin pharmacokinetics in heart transplant recipients administered an antirejection regimen including cyclosporine. Clinical Pharmacology and Therapeutics (St. Louis), 76, 167-177. 

The jS-AR binding potency of 10 /n vitro was achieved using the corresponding nonradioactive fluorinated compound and ventricular membrane preparations from dilute brown agouti (DBA) mouse hearts. First preclinical evaluation studies in vivo using compound 10 that aim at the visualization of cardiac jS -AR receptors in small animals are planned. 

E. Erdman, K. Werdan, L. Brown (1985). Multiplicity of cardiac glycoside receptors in the heart. Trends Pharmacol. Sci. 6 293-295. 

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