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[Alcohol dehydrogenase--polymorphism, properties and role in ethanol metabolism].

Postepy higieny i medycyny doswiadczalnej

Chrostek L, Szmitkowski M.
PMID: 1293588
Postepy Hig Med Dosw. 1992;46(4):403-15.

The paper presents the molecular and kinetics aspects of alcohol dehydrogenase polymorphism. The role of this enzyme in ethanol metabolism are too discussed.

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Chrostek L, Szmitkowski M. Dehydrogenaza alkoholowa--polimorfizm, właściwości oraz udział w metabolizmie etanolu. [Alcohol dehydrogenase--polymorphism, properties and role in ethanol metabolism]. Postepy Hig Med Dosw. 1992;46(4):403-15
Chrostek, L., & Szmitkowski, M. (1992). Dehydrogenaza alkoholowa--polimorfizm, właściwości oraz udział w metabolizmie etanolu. [Alcohol dehydrogenase--polymorphism, properties and role in ethanol metabolism]. Postepy higieny i medycyny doswiadczalnej, 46(4), 403-15.
Chrostek, L, and Szmitkowski, M. "Dehydrogenaza alkoholowa--polimorfizm, właściwości oraz udział w metabolizmie etanolu." [Alcohol dehydrogenase--polymorphism, properties and role in ethanol metabolism]. Postepy higieny i medycyny doswiadczalnej vol. 46,4 (1992): 403-15.
Chrostek L, Szmitkowski M. Dehydrogenaza alkoholowa--polimorfizm, właściwości oraz udział w metabolizmie etanolu. [Alcohol dehydrogenase--polymorphism, properties and role in ethanol metabolism]. Postepy Hig Med Dosw. 1992;46(4):403-15. Polish. PMID: 1293588.
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Binding and functional effects of atrial natriuretic factor in isolated rat kidney.

The American journal of physiology

Suzuki M, Almeida FA, Nussenzveig DR, Sawyer D, Maack T.
PMID: 2961276
Am J Physiol. 1987 Nov;253(5):F917-28. doi: 10.1152/ajprenal.1987.253.5.F917.

A new methodological approach was developed to study the relationship between specific binding and dose-response curves of the renal effects of atrial natriuretic factor (ANF) in isolated perfused rat kidneys (IK). IK were perfused with 125I-labeled and unlabeled ANF...

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Suzuki M, Almeida FA, Nussenzveig DR, et al. Binding and functional effects of atrial natriuretic factor in isolated rat kidney. Am J Physiol. 1987;253(5):F917-28doi: 10.1152/ajprenal.1987.253.5.F917.
Suzuki, M., Almeida, F. A., Nussenzveig, D. R., Sawyer, D., & Maack, T. (1987). Binding and functional effects of atrial natriuretic factor in isolated rat kidney. The American journal of physiology, 253(5), F917-28. https://doi.org/10.1152/ajprenal.1987.253.5.F917
Suzuki, M, et al. "Binding and functional effects of atrial natriuretic factor in isolated rat kidney." The American journal of physiology vol. 253,5 (1987): F917-28. doi: https://doi.org/10.1152/ajprenal.1987.253.5.F917
Suzuki M, Almeida FA, Nussenzveig DR, Sawyer D, Maack T. Binding and functional effects of atrial natriuretic factor in isolated rat kidney. Am J Physiol. 1987 Nov;253(5):F917-28. doi: 10.1152/ajprenal.1987.253.5.F917. PMID: 2961276.
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Pharmacokinetic considerations on Orgaran (Org 10172) therapy.

Haemostasis

Danhof M, de Boer A, Magnani HN, Stiekema JC.
PMID: 1379967
Haemostasis. 1992;22(2):73-84. doi: 10.1159/000216298.

Pharmacokinetic investigations on Orgaran (Org 10172) have been conducted by monitoring the following biological effects: plasma anti-Xa, anti-IIa and IIa-generation-inhibiting (IIaGI) activities. In addition, a limited number of studies were conducted on the basis of concentrations of the No-affinity...

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Danhof M, de Boer A, Magnani HN, et al. Pharmacokinetic considerations on Orgaran (Org 10172) therapy. Haemostasis. 1992;22(2):73-84doi: 10.1159/000216298.
Danhof, M., de Boer, A., Magnani, H. N., & Stiekema, J. C. (1992). Pharmacokinetic considerations on Orgaran (Org 10172) therapy. Haemostasis, 22(2), 73-84. https://doi.org/10.1159/000216298
Danhof, M, et al. "Pharmacokinetic considerations on Orgaran (Org 10172) therapy." Haemostasis vol. 22,2 (1992): 73-84. doi: https://doi.org/10.1159/000216298
Danhof M, de Boer A, Magnani HN, Stiekema JC. Pharmacokinetic considerations on Orgaran (Org 10172) therapy. Haemostasis. 1992;22(2):73-84. doi: 10.1159/000216298. PMID: 1379967.
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The consequences of doxorubicin quinone reduction in vivo in tumour tissue.

Biochemical pharmacology

Cummings J, Willmott N, Hoey BM, Marley ES, Smyth JF.
PMID: 1472081
Biochem Pharmacol. 1992 Dec 01;44(11):2165-74. doi: 10.1016/0006-2952(92)90343-h.

A clear role for quinone reduction in the mechanism of action of doxorubicin has still to be established. There are three possible outcomes of this form of doxorubicin metabolism: (1) drug free radical formation, redox cycling and generation of...

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Cummings J, Willmott N, Hoey BM, et al. The consequences of doxorubicin quinone reduction in vivo in tumour tissue. Biochem Pharmacol. 1992;44(11):2165-74doi: 10.1016/0006-2952(92)90343-h.
Cummings, J., Willmott, N., Hoey, B. M., Marley, E. S., & Smyth, J. F. (1992). The consequences of doxorubicin quinone reduction in vivo in tumour tissue. Biochemical pharmacology, 44(11), 2165-74. https://doi.org/10.1016/0006-2952(92)90343-h
Cummings, J, et al. "The consequences of doxorubicin quinone reduction in vivo in tumour tissue." Biochemical pharmacology vol. 44,11 (1992): 2165-74. doi: https://doi.org/10.1016/0006-2952(92)90343-h
Cummings J, Willmott N, Hoey BM, Marley ES, Smyth JF. The consequences of doxorubicin quinone reduction in vivo in tumour tissue. Biochem Pharmacol. 1992 Dec 01;44(11):2165-74. doi: 10.1016/0006-2952(92)90343-h. PMID: 1472081.
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Effect of PEG 400, ethanol and laurocapram (Azone) on the transport of testosterone through rat skin.

Die Pharmazie

Singh J, Satyanarayana S, Singh S.
PMID: 1293619
Pharmazie. 1992 Dec;47(12):948-9.

No abstract available.

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Singh J, Satyanarayana S, Singh S. Effect of PEG 400, ethanol and laurocapram (Azone) on the transport of testosterone through rat skin. Pharmazie. 1992;47(12):948-9
Singh, J., Satyanarayana, S., & Singh, S. (1992). Effect of PEG 400, ethanol and laurocapram (Azone) on the transport of testosterone through rat skin. Die Pharmazie, 47(12), 948-9.
Singh, J, et al. "Effect of PEG 400, ethanol and laurocapram (Azone) on the transport of testosterone through rat skin." Die Pharmazie vol. 47,12 (1992): 948-9.
Singh J, Satyanarayana S, Singh S. Effect of PEG 400, ethanol and laurocapram (Azone) on the transport of testosterone through rat skin. Pharmazie. 1992 Dec;47(12):948-9. PMID: 1293619.
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Impact of imipenem/cilastatin on cyclosporine metabolism and excretion.

Transplantation proceedings

Mraz W, Modic PK, Hammer C.
PMID: 1412804
Transplant Proc. 1992 Oct;24(5):1704-8.

No abstract available.

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Mraz W, Modic PK, Hammer C. Impact of imipenem/cilastatin on cyclosporine metabolism and excretion. Transplant Proc. 1992;24(5):1704-8
Mraz, W., Modic, P. K., & Hammer, C. (1992). Impact of imipenem/cilastatin on cyclosporine metabolism and excretion. Transplantation proceedings, 24(5), 1704-8.
Mraz, W, et al. "Impact of imipenem/cilastatin on cyclosporine metabolism and excretion." Transplantation proceedings vol. 24,5 (1992): 1704-8.
Mraz W, Modic PK, Hammer C. Impact of imipenem/cilastatin on cyclosporine metabolism and excretion. Transplant Proc. 1992 Oct;24(5):1704-8. PMID: 1412804.
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Cyclosporine dosage according to pharmacokinetic profiles leads to better graft and patient survival rates and a decrease in cyclosporine consumption.

Transplantation proceedings

Masri MA, Dhawan VS, Hayes K, Karim T, Pingle A.
PMID: 1412808
Transplant Proc. 1992 Oct;24(5):1718-20.

No abstract available.

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Masri MA, Dhawan VS, Hayes K, et al. Cyclosporine dosage according to pharmacokinetic profiles leads to better graft and patient survival rates and a decrease in cyclosporine consumption. Transplant Proc. 1992;24(5):1718-20
Masri, M. A., Dhawan, V. S., Hayes, K., Karim, T., & Pingle, A. (1992). Cyclosporine dosage according to pharmacokinetic profiles leads to better graft and patient survival rates and a decrease in cyclosporine consumption. Transplantation proceedings, 24(5), 1718-20.
Masri, M A, et al. "Cyclosporine dosage according to pharmacokinetic profiles leads to better graft and patient survival rates and a decrease in cyclosporine consumption." Transplantation proceedings vol. 24,5 (1992): 1718-20.
Masri MA, Dhawan VS, Hayes K, Karim T, Pingle A. Cyclosporine dosage according to pharmacokinetic profiles leads to better graft and patient survival rates and a decrease in cyclosporine consumption. Transplant Proc. 1992 Oct;24(5):1718-20. PMID: 1412808.
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[Experimental chronic phenylmercuric chloride poisoning in pigs].

Veterinarni medicina

Raszyk J, Docekalová H, Rubes J, Navrátil S, Masek J, Rodák L.
PMID: 1413400
Vet Med (Praha). 1992 Jul;37(7):379-91.

Four gilts, sisters from one litter, aged 70 days and weighing 20-24 kg, were used for a trial. Two experimental gilts (P) were administered an experimental feed mixture containing phenylmercury chloride (40 mg/kg). Two control gilts (K) were fed...

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Raszyk J, Docekalová H, Rubes J, et al. Experimentální chronická intoxikace prasat fenylmerkurichloridem. [Experimental chronic phenylmercuric chloride poisoning in pigs]. Vet Med (Praha). 1992;37(7):379-91
Raszyk, J., Docekalová, H., Rubes, J., Navrátil, S., Masek, J., & Rodák, L. (1992). Experimentální chronická intoxikace prasat fenylmerkurichloridem. [Experimental chronic phenylmercuric chloride poisoning in pigs]. Veterinarni medicina, 37(7), 379-91.
Raszyk, J, et al. "Experimentální chronická intoxikace prasat fenylmerkurichloridem." [Experimental chronic phenylmercuric chloride poisoning in pigs]. Veterinarni medicina vol. 37,7 (1992): 379-91.
Raszyk J, Docekalová H, Rubes J, Navrátil S, Masek J, Rodák L. Experimentální chronická intoxikace prasat fenylmerkurichloridem. [Experimental chronic phenylmercuric chloride poisoning in pigs]. Vet Med (Praha). 1992 Jul;37(7):379-91. Czech. PMID: 1413400.
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Organic cation transport by rat liver plasma membrane vesicles: studies with tetraethylammonium.

The American journal of physiology

Moseley RH, Jarose SM, Permoad P.
PMID: 1443152
Am J Physiol. 1992 Nov;263(5):G775-85. doi: 10.1152/ajpgi.1992.263.5.G775.

Recently, an organic cation:H+ antiport was selectively identified on the sinusoidal domain of rat liver with the use of the endogenous organic cation N1-methylnicotinamide (NMN). Absence of NMN+:H+ exchange on canalicular membrane suggested that this transport process was primarily...

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Moseley RH, Jarose SM, Permoad P. Organic cation transport by rat liver plasma membrane vesicles: studies with tetraethylammonium. Am J Physiol. 1992;263(5):G775-85doi: 10.1152/ajpgi.1992.263.5.G775.
Moseley, R. H., Jarose, S. M., & Permoad, P. (1992). Organic cation transport by rat liver plasma membrane vesicles: studies with tetraethylammonium. The American journal of physiology, 263(5), G775-85. https://doi.org/10.1152/ajpgi.1992.263.5.G775
Moseley, R H, et al. "Organic cation transport by rat liver plasma membrane vesicles: studies with tetraethylammonium." The American journal of physiology vol. 263,5 (1992): G775-85. doi: https://doi.org/10.1152/ajpgi.1992.263.5.G775
Moseley RH, Jarose SM, Permoad P. Organic cation transport by rat liver plasma membrane vesicles: studies with tetraethylammonium. Am J Physiol. 1992 Nov;263(5):G775-85. doi: 10.1152/ajpgi.1992.263.5.G775. PMID: 1443152.
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Pharmacokinetics following a single intravenous administration and a dosage regimen for sulfadoxine in buffalo calves (Bubalus bubalis).

Veterinary research communications

Srivastava AK, Chaudhary RK, Bal MS.
PMID: 1413482
Vet Res Commun. 1992;16(3):215-9. doi: 10.1007/BF01839158.

No abstract available.

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Srivastava AK, Chaudhary RK, Bal MS. Pharmacokinetics following a single intravenous administration and a dosage regimen for sulfadoxine in buffalo calves (Bubalus bubalis). Vet Res Commun. 1992;16(3):215-9doi: 10.1007/BF01839158.
Srivastava, A. K., Chaudhary, R. K., & Bal, M. S. (1992). Pharmacokinetics following a single intravenous administration and a dosage regimen for sulfadoxine in buffalo calves (Bubalus bubalis). Veterinary research communications, 16(3), 215-9. https://doi.org/10.1007/BF01839158
Srivastava, A K, et al. "Pharmacokinetics following a single intravenous administration and a dosage regimen for sulfadoxine in buffalo calves (Bubalus bubalis)." Veterinary research communications vol. 16,3 (1992): 215-9. doi: https://doi.org/10.1007/BF01839158
Srivastava AK, Chaudhary RK, Bal MS. Pharmacokinetics following a single intravenous administration and a dosage regimen for sulfadoxine in buffalo calves (Bubalus bubalis). Vet Res Commun. 1992;16(3):215-9. doi: 10.1007/BF01839158. PMID: 1413482.
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Synthesis and biodistribution of an 123I labelled flunitrazepam derivative: a potential in vivo tracer for benzodiazepine receptors.

International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes

Zecca L, Ferrario P.
PMID: 2838440
Int J Rad Appl Instrum A. 1988;39(4):353-6. doi: 10.1016/0883-2889(88)90029-9.

A method for the synthesis of no-carrier-added of 7-[123I]iodo-1,3-dihydro-5-(2-fluorophenyl)-1-methyl-2H-1,4- benzodiazepine-2-one with a radiochemical yield of 25-30% has been developed. This benzodiazepine was prepared by reaction of [123I]iodide with the corresponding piperidyltriazene in acid medium and the reaction has been...

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Zecca L, Ferrario P. Synthesis and biodistribution of an 123I labelled flunitrazepam derivative: a potential in vivo tracer for benzodiazepine receptors. Int J Rad Appl Instrum A. 1988;39(4):353-6doi: 10.1016/0883-2889(88)90029-9.
Zecca, L., & Ferrario, P. (1988). Synthesis and biodistribution of an 123I labelled flunitrazepam derivative: a potential in vivo tracer for benzodiazepine receptors. International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 39(4), 353-6. https://doi.org/10.1016/0883-2889(88)90029-9
Zecca, L, and Ferrario, P. "Synthesis and biodistribution of an 123I labelled flunitrazepam derivative: a potential in vivo tracer for benzodiazepine receptors." International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes vol. 39,4 (1988): 353-6. doi: https://doi.org/10.1016/0883-2889(88)90029-9
Zecca L, Ferrario P. Synthesis and biodistribution of an 123I labelled flunitrazepam derivative: a potential in vivo tracer for benzodiazepine receptors. Int J Rad Appl Instrum A. 1988;39(4):353-6. doi: 10.1016/0883-2889(88)90029-9. PMID: 2838440.
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Beta-adrenergic blockade for the treatment of hyperthyroidism.

The American journal of medicine

Geffner DL, Hershman JM.
PMID: 1352658
Am J Med. 1992 Jul;93(1):61-8. doi: 10.1016/0002-9343(92)90681-z.

PURPOSE: To review the clinical and biochemical effects of beta-adrenergic blocking drugs on hyperthyroidism.MATERIALS AND METHODS: Studies published since 1972 were identified through a computerized search of MEDLINE and extensive searching of the bibliographies of the articles identified. Based...

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Geffner DL, Hershman JM. Beta-adrenergic blockade for the treatment of hyperthyroidism. Am J Med. 1992;93(1):61-8doi: 10.1016/0002-9343(92)90681-z.
Geffner, D. L., & Hershman, J. M. (1992). Beta-adrenergic blockade for the treatment of hyperthyroidism. The American journal of medicine, 93(1), 61-8. https://doi.org/10.1016/0002-9343(92)90681-z
Geffner, D L, and Hershman, J M. "Beta-adrenergic blockade for the treatment of hyperthyroidism." The American journal of medicine vol. 93,1 (1992): 61-8. doi: https://doi.org/10.1016/0002-9343(92)90681-z
Geffner DL, Hershman JM. Beta-adrenergic blockade for the treatment of hyperthyroidism. Am J Med. 1992 Jul;93(1):61-8. doi: 10.1016/0002-9343(92)90681-z. PMID: 1352658.
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Showing 1 to 12 of 302067 entries