Jean-Pierre Morello, Ph.D.

Affiliations: 
2001 Université de Montréal, Montréal, Canada 
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"Jean-Pierre Morello"
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Michel Bouvier grad student 2001 Université de Montréal
 (Mutations leading to misfolding and endoplasmic reticulum retention of the V2 vasopressin receptor: Assessing pharmacologically-assisted folding and targeting.)
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Publications

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Ndong C, Pradhan A, Puma C, et al. (2009) Role of rat sensory neuron-specific receptor (rSNSR1) in inflammatory pain: contribution of TRPV1 to SNSR signaling in the pain pathway. Pain. 143: 130-7
Bernier V, Morello JP, Zarruk A, et al. (2006) Pharmacologic chaperones as a potential treatment for X-linked nephrogenic diabetes insipidus. Journal of the American Society of Nephrology : Jasn. 17: 232-43
Gervais FG, Morello JP, Beaulieu C, et al. (2005) Identification of a potent and selective synthetic agonist at the CRTH2 receptor. Molecular Pharmacology. 67: 1834-9
Petäjä-Repo UE, Hogue M, Bhalla S, et al. (2002) Ligands act as pharmacological chaperones and increase the efficiency of delta opioid receptor maturation. The Embo Journal. 21: 1628-37
Morello JP, Salahpour A, Petäjä-Repo UE, et al. (2001) Association of calnexin with wild type and mutant AVPR2 that causes nephrogenic diabetes insipidus. Biochemistry. 40: 6766-75
Morello JP, Bichet DG. (2001) Nephrogenic diabetes insipidus. Annual Review of Physiology. 63: 607-30
Morello JP, Petäjä-Repo UE, Bichet DG, et al. (2000) Pharmacological chaperones: a new twist on receptor folding. Trends in Pharmacological Sciences. 21: 466-9
Morello JP, Salahpour A, Laperrière A, et al. (2000) Pharmacological chaperones rescue cell-surface expression and function of misfolded V2 vasopressin receptor mutants. The Journal of Clinical Investigation. 105: 887-95
Morello JP, Bouvier M. (1996) Palmitoylation: a post-translational modification that regulates signalling from G-protein coupled receptors. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 74: 449-57
Hebert TE, Moffett S, Morello JP, et al. (1996) A peptide derived from a beta2-adrenergic receptor transmembrane domain inhibits both receptor dimerization and activation. The Journal of Biological Chemistry. 271: 16384-92
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