Results 1 - 10 of 38 for vitamin k
  1. The VKORC1 gene provides instructions for making a vitamin K epoxide reductase enzyme. The VKORC1 enzyme is made ... Specifically, the VKORC1 enzyme converts one form of vitamin K into a different form of vitamin K that ...
  2. ... protein Sa PS21 PS22 PS23 PS24 PS25 PSA vitamin K-dependent plasma protein S Tests of PROS1 PubMed ...
  3. The F2 gene provides instructions for making a protein called prothrombin (also called coagulation factor II). Coagulation factors are a group of related ...
  4. ... believe it participates in a chemical pathway involving vitamin K. Evidence suggests that vitamin K normally plays a role in bone growth and ...
  5. ... Chylomicrons are needed to absorb fat-soluble vitamins (vitamins K, E, and D) and carry fats and cholesterol ...
  6. ... R, Oldenburg J, Asmis L. Congenital hypersensitivity to vitamin K antagonists due to FIX propeptide mutation at locus - ...
  7. ... S, Kaneko I, Tatsumi S, Segawa H, Miyamoto K. Vitamin D and type II sodium-dependent phosphate cotransporters. Contrib Nephrol. 2013;180:86-97. doi: 10.1159/000346786. Epub 2013 May 6. Review. ... Lapointe JY, Zelikovic I, Skorecki K. A loss-of-function mutation in NaPi-IIa ...
  8. ... absorption of certain fat-soluble vitamins, such as vitamins E, A, and K. In the liver, beta-lipoproteins include low-density lipoproteins (LDL) and very low-density lipoproteins (VLDL). These ... fat-soluble vitamins in the bloodstream to tissues throughout the body. ...
  9. ... A, Ito T, Sumi S, Yamada M, Ozawa K, Togari H. Vitamin B6-responsive ornithine aminotransferase deficiency with a novel mutation G237D. Tohoku J Exp Med. 2005 Apr;205(4):335-42. Citation on PubMed Peltola KE, Näntö-Salonen K, Heinonen OJ, Jääskeläinen S, Heinänen K, Simell O, ...
  10. ... Gene Dinour D, Beckerman P, Ganon L, Tordjman K, Eisenstein Z, Holtzman EJ. Loss-of-function mutations of CYP24A1, the vitamin D 24-hydroxylase gene, cause long-standing hypercalciuric ...
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