Dopamine D_1 Receptor Regulation of Phospholipase C
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概要
- 論文の詳細を見る
- 1995-06-01
著者
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FELDER Robin
Department of Pathology, University of Virginia Health Sciences Center
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JOSE Pedro
Department of Pediatrics, Center for Molecular Physiology Research, Children's National Medical Cent
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MOURADIAN M.
Genetic Pharmacology Unit, Experimental Therapeutics Branch, National Institute of Neurological Diso
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Jose Pedro
Department Of Pediatrics Center For Molecular Physiology Research Children's National Medical C
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Jose Pedro
Department Of Pediatrics Georgetown University Medical Center
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Mouradian M.
Genetic Pharmacology Unit Experimental Therapeutics Branch National Institute Of Neurological Disord
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Mouradian M.
Genetic Pharmacology Unit National Institute Of Neurological Disorders And Stroke
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Felder Robin
Department Of Pathology University Of Virginia School Of Medicine
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Felder Robin
Department Of Pathology The University Of Virginia Health Sciences Center
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Yu Pei-ying
Department Of Pediatrics Georgetown University Medical Center
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YAMAGUCHI Ikuyo
Department of Pathology, University of Virginia School of Medicine
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EISNER Gilbert
Department of Physiology and Biophysics, Georgetown University School of Medicine
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FELDER Christian
Laboratory of Cell Biology. National Institute of Mental Health
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Eisner Gilbert
Department Of Physiology And Biophysics Georgetown University School Of Medicine
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Yamaguchi Ikuyo
Department Of Pathology University Of Virginia School Of Medicine
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Yamaguchi Ikuyo
Department Of Pathology The University Of Virginia Health Sciences Center
関連論文
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- Effects of Decreased Renal Cortical Expression of G Protein-Coupled Receptor Kinase 4 and Angiotensin Type 1 Receptors in Rats
- Dopamine D_1 Receptor Regulation of Phospholipase C
- Studying the Dopaminergic System with Transfected Receptors
- Role of Gα_- and Gα_-protein subunit linkage of D_3 dopamine receptors in the natriuretic effect of D_3 dopamine receptor in kidney
- D_3 dopamine receptor regulation of D_5 receptor expression and function in renal proximal tubule cells
- Protection of nigral neurons by GDNF-engineered marrow cell transplantation