Perspective: the importance of genetic defects in humans in elucidating the complexities of the hypothalamic-pituitary-gonadal axis

Endocrinology. 2001 Jun;142(6):2173-7. doi: 10.1210/endo.142.6.8261.
No abstract available

Publication types

  • Review

MeSH terms

  • Adrenal Insufficiency / congenital
  • Adrenal Insufficiency / genetics
  • Adrenal Insufficiency / physiopathology
  • Animals
  • DAX-1 Orphan Nuclear Receptor
  • DNA-Binding Proteins / genetics
  • Extracellular Matrix Proteins*
  • Female
  • Gonadotropins, Pituitary / genetics
  • Gonads / physiopathology*
  • Humans
  • Hypothalamus / physiopathology*
  • Kallmann Syndrome / genetics
  • Kallmann Syndrome / physiopathology
  • Male
  • Mutation*
  • Nerve Tissue Proteins / genetics
  • Pituitary Gland / physiopathology*
  • Receptors, Retinoic Acid / genetics
  • Repressor Proteins*
  • Transcription Factors / genetics

Substances

  • ANOS1 protein, human
  • DAX-1 Orphan Nuclear Receptor
  • DNA-Binding Proteins
  • Extracellular Matrix Proteins
  • Gonadotropins, Pituitary
  • NR0B1 protein, human
  • Nerve Tissue Proteins
  • Receptors, Retinoic Acid
  • Repressor Proteins
  • Transcription Factors