Marie‐Françoise Arthus

Author

Also Known As

M F Arthus, M.-F. Arthus, M.F. Arthus, Marie-Francoise Arthus, Marie-Françoise Arthus, Marie-Françoise Arthus, Marie‐Françoise Arthus

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Université de Montréal Hôpital du Sacré-Cœur de Montréal McGill University Baylor College of Medicine University College London

About

Marie‐Françoise Arthus is an author at Université de Montréal specializing in medicine, physiology, and diabetes.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	23	2.6K
2	Natural Sciences	4	4	753
3	Biochemistry	4	4	216
4	Health Sciences	3	3	253
5	Public Health	2	2	162

Marie‐Françoise Arthus

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
Pharmacological chaperones rescue cell-surface expression and function of misfolded V2 vasopressin receptor mutants Jean-Pierre Morello, Ali Salahpour, André Laperrière, Journal of Clinical Investigation V2 Vasopressin ReceptorCellular PhysiologyMolecular PharmacologyCell SurfaceChaperones	2000	556
Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus Walter Rosenthal, Anita Seibold, Anaid Antaramián, Nature Genetic DeterminantDevelopmental BiologyGenetic DisorderGeneticsDiabetes	1992	331
An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex. S.M. Mulders, Daniel G. Bichet, J.P.L. Rijss, Journal of Clinical Investigation BiologyMolecular PhysiologySignal TransductionDominant InheritanceOsmotic Stress	1998	260
Hemodynamic and Coagulation Responses to 1-Desamino[8-D-Arginine] Vasopressin in Patients with Congenital Nephrogenic Diabetes Insipidus Daniel G. Bichet, Mohammad Hossein Razi, Michèle Lonergan, New England Journal of Medicine HypertensionCentral DiabetesBlood PressureAdrenal GlandRenal Function	1988	253
Functional Rescue of the Constitutively Internalized V2 Vasopressin Receptor Mutant R137H by the Pharmacological Chaperone Action of SR49059 Virginie Bernier, Monique Lagacé, Michèle Lonergan, Molecular Endocrinology	2004	151
X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis. Daniel G. Bichet, Marie‐Françoise Arthus, Michèle Lonergan, Journal of Clinical Investigation GeneticsGenetic EpidemiologyHuman PolymorphismPathologyMolecular Genetics	1993	151
Three Families with Autosomal Dominant Nephrogenic Diabetes Insipidus Caused by Aquaporin-2 Mutations in the C-Terminus Michio Kuwahara, Kazuyuki Iwai, Toru Ooeda, The American Journal of Human Genetics BiologyMedicineGeneticsDiabetesMolecular Genetics	2001	148
Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus Erik‐Jan Kamsteeg, Daniel G. Bichet, Irene B. M. Konings, The Journal of Cell Biology Polarized DeliveryMolecular BiologyDominant Nephrogenic DiabetesCellular PhysiologyRenal Function	2003	118
Functional studies of twelve mutant V2 vasopressin receptors related to nephrogenic diabetes insipidus Didier Morin, Bernard Mouillac, Nancy Sabatier, Journal of the American Society of Nephrology Functional StudiesInsulin SignalingMetabolic SyndromeHypothalamic PeptideCell Signaling	1998	114
Association of Calnexin with Wild Type and Mutant AVPR2 that Cause Nephrogenic Diabetes Insipidus Jean-Pierre Morello, Ali Salahpour, Ulla E. Petäjä‐Repo, Biochemistry V2 Vasopressin ReceptorGeneticsPathologyMutant Avpr2Insulin Signaling	2001	108

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