Defective membrane expression of human growth hormone (GH) receptor causes Laron-type GH insensitivity syndrome.

Ítems similars

• Recurrent nonsense mutations in the growth hormone receptor from patients with Laron dwarfism.
  per: Amselem, S, et al.
  Publicat: (1991)
• Alternatively spliced forms in the cytoplasmic domain of the human growth hormone (GH) receptor regulate its ability to generate a soluble GH-binding protein.
  per: Dastot, F, et al.
  Publicat: (1996)
• A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization.
  per: Duquesnoy, P, et al.
  Publicat: (1994)
• Primary growth hormone insensitivity (Laron syndrome) and acquired hypothyroidism: a case report
  per: Corneli Ginevra, et al.
  Publicat: (2011-07-01)
• Primary growth hormone insensitivity (Laron syndrome) and acquired hypothyroidism: a case report
  per: Cotta, Oana R, et al.
  Publicat: (2011)