|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | The impact of ATP-sensitive K channel subtype selectivity of insulin secretagogues for the coronary vasculature and the myocardium显示文摘 | Quast U Stephan D Bieger S | 2004 | Diabetes2004，53，： | 1 |
| 2 | Glibenclamide binding to sulphonylurea receptor subtypes:dependence on adenine nucleotides 显示文摘 | Hambrock A Loffler-Walz C Quast U | 2002 | Br J Pharmacol2002，136，： | 1 |
| 3 | KCO912:a potent and selective opener of ATP - dependent potassium( K(ATP) )channels which suppresses airways hyperreactivity at doses devoid of cardiovascular effects 显示文摘 | Buchheit KH Manley PW Quast U | 2002 | Naunyn Schmiedebergs Arch Pharmacol2002，365，3： | 1 |
| 4 | The impacet of ATP-sensitive K channel subtype selectivity of insulin secretagogues for the coronary vasculature and the myocardium显示文摘 | Quast U Stephan D Bieger S | 2004 | Diabetes2004，53，3： | 1 |
| 5 | The impact of ATP-sensitive K channel subtype selectivity of insulin secretagogues for the coronary vasculature and the myocardium显示文摘 | Quast U Stephan D Bieger S | 2004 | Diabetes2004，53，3： | 1 |
| 6 | Chromanol 293B, a blocker of the slow delayed rectifier K+ current (ⅠKs), inhibits the CFTR Cl-current显示文摘 | Bachmann A Quast U Russ U | 2001 | Naunyn Schmiedebergs Arch Pharmacol2001，363，6： | 1 |
| 7 | Cellular pharmacology of potassium channel openers in vascular smooth muscle显示文摘 | Quast U Guillon JM Cavero I | 1994 | Cardiovasc Res1994，28，： | 1 |
| 8 | Mandibular iIffection as a possible aetiolo- gical factor in taurodontism显示文摘 | Reicbart P Quast U | 1975 | J Dent1975，3，5： | 1 |
| 9 | Physical treatment planning of total body irradiation 显示文摘 | Quast U | 2001 | Medizinische Physik2001，12，： | 1 |
| 10 | Ba2+ differentially inhibits the Rb + effiux promoting and the vasorelaxant effects of leveromakalim and minoxidil sulfate in rat isolated aorta 显示文摘 | Quast u Baumlin Y Loffier C | 1995 | Naunyn Schmiedebergs Arch Pharmacol1995，353，1： | 1 |
| 11 | Moving together: K+ channel openers and ATP sensitive K+ channels显示文摘 | QUAST U COOK NS | 1989 | Trends Pharmacol Sci1989，10，11： | 1 |
| 12 | Glibenclamide binding to sulphonylurea receptor subtypes:dependence on adenine nucleotides显示文摘 | Hambrock A Loffler-Walz C Quast U | 2002 | Br J Pharmacol2002，136，： | 1 |
| 13 | Structure-activity studies of potassium channel opening in pinacidil-type cyanoguanidines,nitroethenediamines,thioureas,and ureas显示文摘 | Manley PM Quast U | 1992 | J Med Chem1992，35，12： | 1 |
| 14 | Theoretical and ex- perimental investigations of advantageous refrigerant mix- ture applications 显示文摘 | Kruse H Kuever M Quast U | 1985 | ASHRAE Trans1985，97，1： | 1 |
| 15 | Glibenclamide binding to sulphonylurea receptor subtypes:dependence on adenine nucleotides显示文摘 | Hambrock A Loffler-Walz C Quast U | 2002 | Br J Pharmacol2002，136，： | 1 |
| 16 | ATP-sensitive K+ channels in the kidney显示文摘 | | 1996 | Naunyn Schmiedebergs Arch Pharmacol1996，354，3： | 1 |
| 17 | Sulphonylurea binding in rat isolated glomeruli: pharmacological characterization and dependence on cell metabolism and cytoskeleton显示文摘 | Loffler C Quast U | 1997 | Naunyn Schmiedebergs Arch Pharmacol1997，355，2： | 1 |
| 18 | Structure-activity studies of potassium channel opening in pinacidil-type cyanoguanidines, nitroethenediamines, thioureas, and ureas 显示文摘 | MANLEY P W QUAST U | 1992 | J Med Chem1992，35，： | 1 |
| 19 | Structure-activity studies of potassium channel opening in pinacidil-type cyanoguanidines, nitroethenediamines, thioureas, and ureas显示文摘 | Manley P W Quast U | 1992 | J Med Chem1992，35，12： | 1 |
| 20 | Binding and effects of P1075,an opener of ATP-sensitive K+ channels ,in the aorta from streptozotocintreated diabetic rats显示文摘 | Glocker -S Quast -U | 1997 | Naunyn schmiedebergs Arch Pharmacol1997，356，2： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员