Corvol, Pierre

An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels

Rigat, B., Hubert, C., Alhenc-Gelas, F., Cambien, F., Corvol, P., & Soubrier, F. (1990) · Journal of Clinical Investigation

Renin-Angiotensin System StudiesCoagulation, Bradykinin, Polyphosphates, and Angioedema

Cited by 3,767

The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway

Gimenez-Roqueplo, A.-P., Favier, J., Rustin, P., Mourad, J.-J., Plouin, P.-F., Corvol, P., Rötig, A., & Jeunemaitre, X. (2001) · The American Journal of Human Genetics

Adrenal and Paraganglionic TumorsNeurofibromatosis and Schwannoma Cases

Cited by 364

Effects of Induced Hyperthyroidism on Steroid Metabolism in Man

RUDER, H., CORVOL, P., MAHOUDEAU, J. A., ROSS, G. T., & LIPSETT, M. B. (1971) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsHormonal and reproductive studies

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The amino acid substitutions Ser288Gly and Val320Ala convert the cortisol producing enzyme, CYP11B1, into an aldosterone producing enzyme

Curnow, K. M., Mulatero, P., Emeric-Blanchouin, N., Aupetit-Faisant, B., Corvol, P., & Pascoe, L. (1997) · Nature Structural & Molecular Biology

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

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Recombinant CYP11B Genes Encode Enzymes that Can Catalyze Conversion of 11-Deoxycortisol to Cortisol, 18-Hydroxycortisol, and 18-Oxocortisol1

Mulatero, P., Curnow, K. M., Aupetit-Faisant, B., Foekling, M., Gomez-Sanchez, C., Veglio, F., Jeunemaitre, X., Corvol, P., & Pascoe, L. (1998) · The Journal of Clinical Endocrinology & Metabolism

Hormonal Regulation and HypertensionAdrenal Hormones and Disorders

Cited by 88

Self-Measurement and Self-Titration in HypertensionA Pilot Telemedicine Study

BOBRIE, G., POSTELVINAY, N., DELONCA, J., & CORVOL, P. (2007) · American Journal of Hypertension

Blood Pressure and Hypertension StudiesTelemedicine and Telehealth Implementation

Cited by 68

ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration

Hirose, T., Cabrera-Socorro, A., Chitayat, D., Lemonnier, T., Féraud, O., Cifuentes-Diaz, C., Gervasi, N., Mombereau, C., Ghosh, T., Stoica, L., et al. (2019) · Journal of Clinical Investigation

ATP Synthase and ATPases ResearchAutophagy in Disease and Therapy

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