Mutant G-protein-coupled receptors as a cause of human diseases

This publication has 476 references indexed in Scilit:

• Osteoporosis in MCHR1-deficient mice
  Biochemical and Biophysical Research Communications, 2004
• Identification of two AGTR2 mutations in male patients with non-syndromic mental retardation
  Human Genetics, 2004
• Transgenic studies of α1-adrenergic receptor subtype function
  Life Sciences, 2002
• A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures
  Annals of Neurology, 2002
• New insights into ocular albinism type 1 (OA1): Mutations and polymorphisms of the OA1 gene
  Human Mutation, 2002
• Evaluation of the α2C-adrenoceptor as a neuropsychiatric drug target: Studies in transgenic mouse models
  Life Sciences, 2001
• Neuropeptide Y Receptor Gene y6: Multiple Deaths or Resurrections?
  Biochemical and Biophysical Research Communications, 2000
• Patent Ductus Arteriosus and Neonatal Death in Prostaglandin Receptor EP4-Deficient Mice
  Biochemical and Biophysical Research Communications, 1998
• Constitutive Activation of the Thyrotropin Receptor by Deletion of a Portion of the Extracellular Domain
  Biochemical and Biophysical Research Communications, 1995
• Role of cysteine residues in the extracellular domain and exoplasmic loops of the transmembrane domain of the TSH receptor: Effect of mutation to serine on TSH receptor activity and response to thyroid stimulating autoantibodies
  Biochemical and Biophysical Research Communications, 1992