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標(biāo)題: Titlebook: Anti-Inflammatory Drugs; John R. Vane,Sergio H. Ferreira Book 1979 Springer-Verlag Berlin Heidelberg 1979 Antiphlogistikum.Drugs [打印本頁(yè)]

作者: 變更    時(shí)間: 2025-3-21 16:46
書目名稱Anti-Inflammatory Drugs影響因子(影響力)




書目名稱Anti-Inflammatory Drugs影響因子(影響力)學(xué)科排名




書目名稱Anti-Inflammatory Drugs網(wǎng)絡(luò)公開度




書目名稱Anti-Inflammatory Drugs網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Anti-Inflammatory Drugs被引頻次




書目名稱Anti-Inflammatory Drugs被引頻次學(xué)科排名




書目名稱Anti-Inflammatory Drugs年度引用




書目名稱Anti-Inflammatory Drugs年度引用學(xué)科排名




書目名稱Anti-Inflammatory Drugs讀者反饋




書目名稱Anti-Inflammatory Drugs讀者反饋學(xué)科排名





作者: Lethargic    時(shí)間: 2025-3-21 22:00
Einführung in die Kryptographie959; . and ., 1963). The development and availability of thermometers capable of recording skin temperature accurately and rapidly have led to the use of this parameter by some investigators to evaluate inflammatory and anti-inflammatory effects.
作者: obligation    時(shí)間: 2025-3-22 01:17

作者: 駭人    時(shí)間: 2025-3-22 06:53

作者: Gerontology    時(shí)間: 2025-3-22 12:30
Einführung in die Kultur- und Kunst?konomiehe earlier antihistamines were first reported only in 1972 by Black and colleagues. They are referred to as antagonists at H. receptors, in distinction from the earlier antihistamines whose inhibitory effects at low concentrations characterised a histamine receptor for which Ash and Schild in 1966 h
作者: cogitate    時(shí)間: 2025-3-22 14:26

作者: Aura231    時(shí)間: 2025-3-22 18:44

作者: Filibuster    時(shí)間: 2025-3-22 23:27
Inhibition of Erythema and Local Hyperthermia959; . and ., 1963). The development and availability of thermometers capable of recording skin temperature accurately and rapidly have led to the use of this parameter by some investigators to evaluate inflammatory and anti-inflammatory effects.
作者: Malcontent    時(shí)間: 2025-3-23 03:16

作者: enterprise    時(shí)間: 2025-3-23 06:46

作者: nonsensical    時(shí)間: 2025-3-23 09:53
Antagonists of Histamine, 5-Hydroxytryptamine and SRS-Ahe earlier antihistamines were first reported only in 1972 by Black and colleagues. They are referred to as antagonists at H. receptors, in distinction from the earlier antihistamines whose inhibitory effects at low concentrations characterised a histamine receptor for which Ash and Schild in 1966 h
作者: 推測(cè)    時(shí)間: 2025-3-23 15:47
Inhibitors of the Release of Anaphylactic Mediatorsor antigen. This has been confirmed by . et al. (1970 a) in studies using double sensitization with two antigenically distinct rat reagins. Furthermore, since the compound is effective in passively sensitized tissues, and in clinical usage does not reduce serum IgE levels (. and ., 1971), it does no
作者: 心神不寧    時(shí)間: 2025-3-23 20:18
,Der AES-Verschlüsslungsalgorithmus,ctory. . et al. (1973) stated bluntly: “All of these in vitro methods are virtually useless for a predictive assessment of drugs in vivo. They are useful only after drugs are discovered in other systems.” The above statement was justified when in vitro methods relied entirely on non-specific interac
作者: 雜色    時(shí)間: 2025-3-24 01:21

作者: 效果    時(shí)間: 2025-3-24 05:52

作者: Invigorate    時(shí)間: 2025-3-24 07:43
Kongruenzen und Restklassenringe,1). MSU needles can be seen by ordinary light microscopy, but the strongly negative birefringence with axial extinction by compensated polarized light microscopy is a much more sensitive test that is quite specific. . (b. 1633) was the first to describe urate crystals, having obtained them from a dr
作者: 撫育    時(shí)間: 2025-3-24 12:27
Kongruenzen und Restklassenringe, . alluded to “the temptation to select the present, inadequate drugs, design tests that give positive results and then with the aid of these tests to search for further compounds giving positive results. Such methodology may lead only to ‘old’ antiinflammatory agents instead of ‘new’.” More recentl
作者: fulmination    時(shí)間: 2025-3-24 17:40

作者: accessory    時(shí)間: 2025-3-24 21:33

作者: 織物    時(shí)間: 2025-3-24 23:49

作者: 摸索    時(shí)間: 2025-3-25 04:53
Einführung in die Kryptographiels and their accumulation in inflamed or injured tissues. The early morphological event is the movement of leucocytes from the center to the periphery of the bloodstream, followed by the adhesion of the cells to the luminal surface of the vascular endothelium, especially of the postcapillary venules
作者: infatuation    時(shí)間: 2025-3-25 10:14
https://doi.org/10.1007/978-3-642-39775-2people in the United States suffering from arthritis (., 1975). About half of this population is under medical care and the other half is self-treated; of those under medical care, one-third require chronic drug administration, and the remainder, intermittent administration. Arthritis is a prevalent
作者: CYT    時(shí)間: 2025-3-25 11:50
Von Geheimschriften zu Kryptosystemen, human acute and chronic inflammation which have the common property of inhibiting fatty acid oxidative cyclization, in particular the formation of prostaglandins (PGs) and throm-boxanes. We have retained for this group of substances the term PG synthetase inhibitors because thromboxane synthetase c
作者: 粗語(yǔ)    時(shí)間: 2025-3-25 18:12
https://doi.org/10.1007/978-3-8348-2269-7lammation. This approach has made little impact in rheumatoid arthritis (RA), a disease which appears to be more appropriately treated with specific drugs like D-penicillamine. Drugs of this type are not only more effective than anti-inflammatory drugs in RA but, with long-term therapy, they may alt
作者: oncologist    時(shí)間: 2025-3-25 21:45

作者: Coterminous    時(shí)間: 2025-3-26 00:10
,Einführung: Was ist Kultur?konomie?,indings which are outside the scope of this chapter have been reviewed by Pepys (1973) and Brogden et al. (1974). Laboratory studies revealed that this compound was neither a bronchodilator nor an antagonist of histamine, 5-hydroxytryptamine (5-HT) nor slow reacting substance of anaphylaxis (SRS-A),
作者: instulate    時(shí)間: 2025-3-26 05:03

作者: 動(dòng)脈    時(shí)間: 2025-3-26 10:54
Antagonism of Bradykinin Bronchoconstriction by Anti-Inflammatory Drugst-lys-bradykinin and gly-arg-met-lys-bradykinin. Bk is thought to be an inflammatory mediator; kallidin and met-lys-bradykinin also occur in mammalian tissues. In general, there are only qualitative differences between the activities of this group of substances (. and ., 1972).
作者: corporate    時(shí)間: 2025-3-26 14:01
Inhibition of Cell Migration in vivo and Granuloma Formationls and their accumulation in inflamed or injured tissues. The early morphological event is the movement of leucocytes from the center to the periphery of the bloodstream, followed by the adhesion of the cells to the luminal surface of the vascular endothelium, especially of the postcapillary venules.
作者: 不能強(qiáng)迫我    時(shí)間: 2025-3-26 18:30
Penicillamine and Drugs With a Specific Action in Rheumatoid Arthritislammation. This approach has made little impact in rheumatoid arthritis (RA), a disease which appears to be more appropriately treated with specific drugs like D-penicillamine. Drugs of this type are not only more effective than anti-inflammatory drugs in RA but, with long-term therapy, they may alter the eventual outcome of the disease.
作者: Adjourn    時(shí)間: 2025-3-27 00:31
Anti-Inflammatory Drugs978-3-642-66891-3Series ISSN 0171-2004 Series E-ISSN 1865-0325
作者: engrave    時(shí)間: 2025-3-27 01:52

作者: 言行自由    時(shí)間: 2025-3-27 05:27
Kryptographische Hashfunktionen,t-lys-bradykinin and gly-arg-met-lys-bradykinin. Bk is thought to be an inflammatory mediator; kallidin and met-lys-bradykinin also occur in mammalian tissues. In general, there are only qualitative differences between the activities of this group of substances (. and ., 1972).
作者: 拖網(wǎng)    時(shí)間: 2025-3-27 13:01

作者: Frenetic    時(shí)間: 2025-3-27 16:02

作者: 做作    時(shí)間: 2025-3-27 21:07

作者: lattice    時(shí)間: 2025-3-28 01:35

作者: Prognosis    時(shí)間: 2025-3-28 02:39

作者: Mnemonics    時(shí)間: 2025-3-28 08:38
Prostaglandin Synthetase Inhibitors IThe prostaglandins (PGs) are a group of lipid-soluble C.-carboxylic acids containing an oxygenated five-membered ring and two parallel aliphatic side-chains. Chemically they are named as substituted prostenoic (1) or prostadienoic (2) acids.
作者: 初次登臺(tái)    時(shí)間: 2025-3-28 13:39

作者: conservative    時(shí)間: 2025-3-28 17:55

作者: 發(fā)電機(jī)    時(shí)間: 2025-3-28 19:34

作者: Fecundity    時(shí)間: 2025-3-29 02:04
Screening and Assessment of the Potency of Anti-Inflammatory Drugs in vitroctory. . et al. (1973) stated bluntly: “All of these in vitro methods are virtually useless for a predictive assessment of drugs in vivo. They are useful only after drugs are discovered in other systems.” The above statement was justified when in vitro methods relied entirely on non-specific interac
作者: EWE    時(shí)間: 2025-3-29 06:36

作者: 陶醉    時(shí)間: 2025-3-29 08:59

作者: mercenary    時(shí)間: 2025-3-29 13:06

作者: Lipoprotein(A)    時(shí)間: 2025-3-29 16:18
Experimental Models of Arthritis in Animals as Screening Tests for Drugs to Treat Arthritis in Man . alluded to “the temptation to select the present, inadequate drugs, design tests that give positive results and then with the aid of these tests to search for further compounds giving positive results. Such methodology may lead only to ‘old’ antiinflammatory agents instead of ‘new’.” More recentl
作者: escalate    時(shí)間: 2025-3-29 21:27

作者: OTHER    時(shí)間: 2025-3-30 03:18

作者: Dedication    時(shí)間: 2025-3-30 07:53

作者: 打擊    時(shí)間: 2025-3-30 09:38

作者: PRE    時(shí)間: 2025-3-30 13:04
Evaluation of the Toxicity of Anti-Inflammatory Drugspeople in the United States suffering from arthritis (., 1975). About half of this population is under medical care and the other half is self-treated; of those under medical care, one-third require chronic drug administration, and the remainder, intermittent administration. Arthritis is a prevalent
作者: 鍵琴    時(shí)間: 2025-3-30 20:14
Mode of Action of Anti-Inflammatory Agents Which are Prostaglandin Synthetase Inhibitors human acute and chronic inflammation which have the common property of inhibiting fatty acid oxidative cyclization, in particular the formation of prostaglandins (PGs) and throm-boxanes. We have retained for this group of substances the term PG synthetase inhibitors because thromboxane synthetase c
作者: mitral-valve    時(shí)間: 2025-3-30 22:53

作者: 虛情假意    時(shí)間: 2025-3-31 01:47

作者: mighty    時(shí)間: 2025-3-31 07:22

作者: 血友病    時(shí)間: 2025-3-31 10:51
Cytostats with Effects in Chronic Inflammationinic have a tolerable therapeutic index. The acceptability of some of these toxic drugs may be due to any one or more of the following reasons: (1) they have a reversible effect on cell populations that turn over slowly; (2) they mainly delete cells from populations with a high rate of generation; (
作者: ARBOR    時(shí)間: 2025-3-31 14:16
Oedema and Increased Vascular Permeabilitys by the membrane resistance of isolated cells; and anti-epileptic drugs by antagonism of electroshock-induced convulsions. Practically, it does not matter whether one measures a . in an assay rather than the . effect, so long as these vary together in a known manner.
作者: Cupping    時(shí)間: 2025-3-31 18:08





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