Zhi-Liang Lu

发表

Diversity of actions of GnRHs mediated by ligand-induced selective signaling

Adam J Pawson, K. Morgan, R. Millar, 2008, Frontiers in Neuroendocrinology.

Impaired P2X signalling pathways in renal microvascular myocytes in genetic hypertension.

D. Gordienko, O. Povstyan, M. Harhun, 2015, Cardiovascular research.

A Network of Conserved Intramolecular Contacts Defines the Off-state of the Transmembrane Switch Mechanism in a Seven-transmembrane Receptor*

E. Hulme, Zhi-Liang Lu, 2000, The Journal of Biological Chemistry.

A Crucial Role for G (cid:1) q/11 , But Not G (cid:1) i/o or G (cid:1) s , in Gonadotropin-Releasing Hormone Receptor-Mediated Cell Growth Inhibition

K. Morgan, R. Millar, Colin D. White, 2008 .

Gonadotropin-releasing hormone analog structural determinants of selectivity for inhibition of cell growth: support for the concept of ligand-induced selective signaling.

Adam J Pawson, S. Langdon, Stuart Maudsley, 2008, Molecular endocrinology.

Bovine and ovine gonadotropin-releasing hormone (GnRH)-II ligand precursors and type II GnRH receptor genes are functionally inactivated.

Adam J Pawson, K. Morgan, R. Millar, 2006, Endocrinology.

Evolution of Constrained Gonadotropin-releasing Hormone Ligand Conformation and Receptor Selectivity*

Adam J Pawson, P. Barran, M. Bowers, 2005, Journal of Biological Chemistry.

Mammalian type I gonadotropin-releasing hormone receptors undergo slow, constitutive, agonist-independent internalization.

Adam J Pawson, E. Faccenda, Stuart Maudsley, 2008, Endocrinology.

Gonadotropin-releasing hormone receptors.

Adam J Pawson, Kevin Morgan, Stuart Maudsley, 2004, Endocrine reviews.

Antiproliferative Effects of GnRH Agonists: Prospects and Problems for Cancer Therapy

K. Morgan, R. Millar, A. Stewart, 2008, Neuroendocrinology.

Molecular Genetic Analysis of Normosmic Hypogonadotropic Hypogonadism in a Turkish Population: Identification and Detailed Functional Characterization of a Novel Mutation in the Gonadotropin-Releasing Hormone Receptor Gene

S. O’Rahilly, I. Farooqi, A. Topaloğlu, 2007, Neuroendocrinology.

Identification of a Novel Ligand Binding Residue Arg 38(1.35) in the Human GnRH Receptor

R. Millar, A. Stewart, Zhi-Liang Lu, 2007 .

Seven-transmembrane receptors: crystals clarify.

J. Saldanha, E. Hulme, Edward C Hulme, 2002, Trends in pharmacological sciences.

Helix 8 of the M1 Muscarinic Acetylcholine Receptor: Scanning Mutagenesis Delineates a G Protein Recognition Site

J. Saldanha, E. Hulme, Edward C Hulme, 2011, Molecular Pharmacology.

Mutations Remote from the Human Gonadotropin-releasing Hormone (GnRH) Receptor-binding Sites Specifically Increase Binding Affinity for GnRH II but Not GnRH I

R. Millar, Zhi-Liang Lu, Ryan Gallagher, 2005, Journal of Biological Chemistry.

Conserved amino acid residues that are important for ligand binding in the type I gonadotropin-releasing hormone (GnRH) receptor are required for high potency of GnRH II at the type II GnRH receptor.

R. Millar, A. Katz, C. Flanagan, 2007, Molecular endocrinology.

Title: Conserved Amino acid residues that are important for ligand binding in the type I GnRH receptor are required for high potency of GnRH II at the type II GnRH receptor

R. Millar, C. Flanagan, Zhi-Liang Lu, 2006 .

Structural Determinants for Ligand-Receptor Conformational Selection in a Peptide G Protein-coupled Receptor*

R. Millar, Colin D. White, Zhi-Liang Lu, 2007, Journal of Biological Chemistry.

GnRH analog structural determinants of selectivity for inhibition of cell growth: support for the concept of ligand- induced-selective-signalling

Adam J Pawson, S. Langdon, K. Morgan, 2008 .

The multifunctional poly(A)-binding protein (PABP) 1 is subject to extensive dynamic post-translational modification, which molecular modelling suggests plays an important role in co-ordinating its activities

N. Gray, J. Reddington, N. Morrice, 2011, The Biochemical journal.

Transmembrane Domains 4 and 7 of the M1Muscarinic Acetylcholine Receptor Are Critical for Ligand Binding and the Receptor Activation Switch*

J W Saldanha, E C Hulme, J. Saldanha, 2001, The Journal of Biological Chemistry.

Scanning mutagenesis of transmembrane domain 3 of the m1 muscarinic acetylcholine receptor

E. Hulme, Zhi-Liang Lu, 1998, Journal of Physiology-Paris.

The Functional Topography of Transmembrane Domain 3 of the M1 Muscarinic Acetylcholine Receptor, Revealed by Scanning Mutagenesis*

E C Hulme, E. Hulme, Z L Lu, 1999, The Journal of Biological Chemistry.

The role of the aspartate-arginine-tyrosine triad in the m1 muscarinic receptor: mutations of aspartate 122 and tyrosine 124 decrease receptor expression but do not abolish signaling.

E. Hulme, J. Pavia, Z. L. Lu, 1997, Molecular pharmacology.

Effects of micromolar concentrations of Mn, Mo, and Si on α1adrenoceptor-mediated contraction in porcine coronary artery

Ming Yan, Xiaojun Du, Zhi-Liang Lu, 1998, Biological Trace Element Research.

A crucial role for Galphaq/11, but not Galphai/o or Galphas, in gonadotropin-releasing hormone receptor-mediated cell growth inhibition.

K. Morgan, R. Millar, Colin D. White, 2008, Molecular endocrinology.

Identification of a Novel Ligand Binding Residue Arg38(1.35) in the Human Gonadotropin-Releasing Hormone Receptor

R. Millar, Zhi-Liang Lu, R. Sellar, 2008, Molecular Pharmacology.

Human GnRH Receptor

R. Millar, Zhi-Liang Lu, R. Sellar, 2007 .