Growth Hormone (GH) Deficiency Type II: A Novel GH-1 Gene Mutation (GH-R178H) Affecting Secretion and Action

Ítems similars

• Butyrate Increases Intracellular Calcium Levels and Enhances Growth Hormone Release from Rat Anterior Pituitary Cells via the G-Protein-Coupled Receptors GPR41 and 43
  per: Miletta, Maria Consolata, et al.
  Publicat: (2014)
• Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn(2+) for Normal Growth and Development
  per: Miletta, Maria Consolata, et al.
  Publicat: (2013)
• MON-LB014 Autosomal Dominant Growth Hormone Deficiency Due to a Novel c.178g>A Mutation in the GH1 Gene Is Caused by Alternative Splicing to Produce a Small GH Isoform
  per: Miller, Bradley Scott, et al.
  Publicat: (2020)
• Retinoic acid receptor beta and angiopoietin-like protein 1 are involved in the regulation of human androgen biosynthesis
  per: Udhane, Sameer S., et al.
  Publicat: (2015)
• Sterol O-Acyltransferase 1 (SOAT1, ACAT) Is a Novel Target of Steroidogenic Factor-1 (SF-1, NR5A1, Ad4BP) in the Human Adrenal
  per: Ferraz-de-Souza, Bruno, et al.
  Publicat: (2011)