Absence of PRSS1 mutations and association of SPINK1 trypsin inhibitor mutations in hereditary and non-hereditary chronic pancreatitis

Podobne zapisy

• Mutations in the pancreatic secretory trypsin inhibitor gene (PSTI/SPINK1) rather than the cationic trypsinogen gene (PRSS1) are significantly associated with tropical calcific pancreatitis
  od: Chandak, G, i wsp.
  Wydane: (2002)
• Missense mutations in pancreatic secretory trypsin inhibitor (SPINK1) cause intracellular retention and degradation
  od: Király, Orsolya, i wsp.
  Wydane: (2007)
• PRSS1 and SPINK1 mutations in idiopathic chronic and recurrent acute pancreatitis
  od: Pelaez-Luna, Mario, i wsp.
  Wydane: (2014)
• The Histopathology of PRSS1 Hereditary Pancreatitis
  od: Singhi, Aatur D., i wsp.
  Wydane: (2014)
• Mutations in anionic trypsinogen gene are not associated with tropical calcific pancreatitis
  od: Idris, M M, i wsp.
  Wydane: (2005)