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Distallation

Figure Bl.2.11. Biologically active centre in myoglobin or one of the subunits of haemoglobin. The bound CO molecule as well as the proximal and distal histidines are shown m addition to the protohaeme unit. From Rousseau D L and Friedman J M 1988 Biological Applications of Raman Spectroscopy vol 3, ed T G Spiro (New York Wiley). Reprinted by pennission of John Wiley and Sons Inc. Figure Bl.2.11. Biologically active centre in myoglobin or one of the subunits of haemoglobin. The bound CO molecule as well as the proximal and distal histidines are shown m addition to the protohaeme unit. From Rousseau D L and Friedman J M 1988 Biological Applications of Raman Spectroscopy vol 3, ed T G Spiro (New York Wiley). Reprinted by pennission of John Wiley and Sons Inc.
Cortisol-Cortisone Conversion. Under normal conditions, this equilibrium slightly favors the oxidized compound. Similarly, the conversion of corticosterone to 11-deoxycorticosterone is also mediated by the liP-hydroxysteroid dehydrogenase enzyme system and requites NAD(P) /NAD(P)H. This conversion is especially important both in the protection of the human fetus from excessive glucocorticoid exposure, and in the protection of distal nephron mineral ocorticoid receptors from glucocorticoid exposure (14). The impairment of this conversion is thought to result in hypertension associated with renal insufficiency (15). [Pg.97]

Spironolactone is the most clinically usehil steroidal aldosterone antagonist, and unlike GR antagonists, this compound is utilized much more frequendy than aldosterone agonists. Interfering with reabsorption and secretion in the late distal segment, this compound is predominantiy used with other diuretics. Canrenone, an olefinic metaboHte of spironolactone, and potassium canrenoate, in which the C-17 lactone has been hydrolyzed open, are also potent mineralocorticoid antagonists. [Pg.109]

The largest use of endoscopic techniques is in the examination of the gastrointestinal tract. Upper intestinal endoscopy is the examination of the esophagus, stomach, and proximal duodenum. Colonoscopy is the examination of the colon, large intestine, and in some cases the distal parts of the small intestine. Cholangiopancreatography is the examination of the biUary tree and pancreas. [Pg.49]

A useful specialized type of analytical iastmmentation is the fibei-optic sensoi oi optiode (253,254), ia which an optical tiansducei monitois some chemically selective change. These aie often based on the fluorescence of a leagent immobilized at the distal end of the ftbei (255). [Pg.320]

Absorption, Transport, and Excretion. The vitamin is absorbed through the mouth, the stomach, and predominantly through the distal portion of the small intestine, and hence, penetrates into the bloodstream. Ascorbic acid is widely distributed to the cells of the body and is mainly present in the white blood cells (leukocytes). The ascorbic acid concentration in these cells is about 150 times its concentration in the plasma (150,151). Dehydroascorbic acid is the main form in the red blood cells (erythrocytes). White blood cells are involved in the destmction of bacteria. [Pg.22]

Potassium-Sparing Diuretics. Potassium-sparing diuretics act on the aldosterone-sensitive portion of cortical collecting tubules, and partially in the distal convoluted tubules of the nephron. The commonly used potassium-sparing diuretics are triamterene, amiloride, and spironolactone (Table 3). Spironolactone is a competitive aldosterone receptor antagonist, whereas triamterene and amiloride are not (44,45). [Pg.207]

Spironolactone antagonizes the effects of aldosterone by binding at the aldosterone receptor in the cytosol of the late distal tubules and renal collecting ducts. Side effects of spironolactone are gynecomastia, decreased Hbido, and impotency. [Pg.208]

The DNA part of each control module can be divided into three main regions, the core or basal promoter elements, the promoter proximal elements and the distal enhancer elements (Figure 9.1). The best characterized core promoter element is the TATA box, a DNA sequence that is rich in A-T base pairs and located 25 base pairs upstream of the transcription start site. The TATA box is recognized by one of the basal transcription factors, the TATA box-binding protein, TBP, which is part of a multisubunit complex called TFIID. This complex in combination with RNA polymerase 11 and other basal transcription factors such as TFIIA and TFIIB form a preinitiation complex for transcription. [Pg.151]

Figure 9.1 The transcriptional elements of a eucaryotic structural gene extend over a large region of DNA. The regulatory sequences can be divided into three main regions (1) the basal promoter elements such as the TATA box, (2) the promoter proximal elements close to the initiation site, and (3) distal enhancer elements far from the initiation site. Figure 9.1 The transcriptional elements of a eucaryotic structural gene extend over a large region of DNA. The regulatory sequences can be divided into three main regions (1) the basal promoter elements such as the TATA box, (2) the promoter proximal elements close to the initiation site, and (3) distal enhancer elements far from the initiation site.
Airway cross-sections have the nominal anatomy shown in Fig. 5.16. Airway surface liquid (AST), primarily composed of mucus gel and water, surrounds the airway lumen with a thickness thought to vary from 5 to 10 mm. AST lies on the apical surface of airway epithelial cells (mostly columnar ciliated epithelium). This layer of cells, roughly two to three cells thick in proximal airways and eventually thinning to a single cell thickness in distal airways, rests along a basement membrane on its basal surface. Connective tissue (collagen fibers, basement membranes, elastin, and water) lies between the basement membrane and airway smooth muscle. Edema occurs when the volume of water within the connective tissue increases considerably. Interspersed within the smooth muscle are respiratory supply vessels (capillaries, arteriovenous anastomoses), nerves, and lymphatic vessels. [Pg.200]


See other pages where Distallation is mentioned: [Pg.521]    [Pg.448]    [Pg.465]    [Pg.213]    [Pg.481]    [Pg.48]    [Pg.381]    [Pg.255]    [Pg.189]    [Pg.189]    [Pg.50]    [Pg.423]    [Pg.133]    [Pg.142]    [Pg.142]    [Pg.202]    [Pg.203]    [Pg.203]    [Pg.203]    [Pg.203]    [Pg.205]    [Pg.207]    [Pg.208]    [Pg.210]    [Pg.211]    [Pg.214]    [Pg.214]    [Pg.126]    [Pg.94]    [Pg.151]    [Pg.152]    [Pg.295]    [Pg.317]    [Pg.196]    [Pg.196]    [Pg.196]    [Pg.198]    [Pg.199]    [Pg.199]   
See also in sourсe #XX -- [ Pg.53 , Pg.70 , Pg.71 , Pg.298 , Pg.299 , Pg.350 , Pg.462 ]




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1.3- Distal derivatives

Airways distal respiratory

Biceps Brachii Distal Tendon

Biceps Femoris Distal Tendon

Branch formation, distal

Convoluted tubules distal, diuretics acting

Distal

Distal Branching of i-Type Polylactosamine Backbones

Distal Ganglia

Distal Interphalangeal Joint

Distal Osteoarthritis

Distal Radio-Ulnar Joint

Distal Rheumatoid Arthritis

Distal Synovitis

Distal Triceps Tendon

Distal alveolar spaces

Distal arginine

Distal arteriovenous fistula

Distal axonal degeneration

Distal bronchial epithelium

Distal cleavage

Distal colon

Distal convoluted tubule

Distal convoluted tubule, transport

Distal convoluted tubule, transport mechanisms

Distal cytoplasm

Distal deposition

Distal duodenum

Distal effects

Distal enhancer

Distal histidine

Distal histidine residue

Distal internal maxillary artery

Distal intestinal obstruction syndrome

Distal ligand

Distal myopathy with rimmed vacuoles

Distal nephron

Distal nephron injury

Distal polar effect

Distal rectosigmoid colon

Distal region

Distal region pocket

Distal renal tubular acidosis

Distal side effects

Distal small bowel obstruction

Distal symmetric polyneuropathy

Distal symmetric sensorimotor polyneuropathy

Distal tip cell

Distal trachea

Distal tubular acidosis

Distal tubule

Distal tubule water reabsorption

Distal-side steric effects

Distal/proximal ratio

Distally-bridged

Dynamic distallation

Enhancer elements, distal

Fibrosis distal

Hemoglobin distal histidine

Hemoglobin distal, proximal histidine

Incomplete distal renal tubular acidosis

Kidney distal convoluted tubule

Kidneys distal tubule

Ligand distal atom

Myoglobin distal histidine

Neuropathy distal sensory peripheral

Nickel distal

Organ distal

Perichaetial module distal

Peroxidase distal histidine

Primary module distal reiteration

Proximal and Distal Determinants of Task Difficulty

Reiteration distal

Tubular transport distal tubule

Vessel distal

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