Azupedia

Items without sitelinks

Showing below up to 50 results in range #661 to #710.

View ( | ) (20 | 50 | 100 | 250 | 500)

  1. pyridoxal biosynthetic process (Q21891)
  2. pyridoxal metabolic process (Q21890)
  3. pyridoxal import across plasma membrane (Q21889)
  4. pyridoxal transmembrane transport (Q21888)
  5. pyridoxal transmembrane transporter activity (Q21887)
  6. pyridoxal transport (Q21886)
  7. pyridoxal binding (Q21885)
  8. nicotinamide mononucleotide transmembrane transporter activity (Q21882)
  9. nicotinamide mononucleotide transport (Q21881)
  10. nicotinamide mononucleotide transmembrane transport (Q21880)
  11. oxidoreductase activity, acting on diphenols and related substances as donors (Q21878)
  12. dihydronicotinamide riboside quinone reductase activity (Q21877)
  13. nicotinamide riboside transport (Q21876)
  14. nicotinamide riboside transmembrane transporter activity (Q21875)
  15. pyridine nucleoside biosynthetic process (Q21874)
  16. nicotinamide riboside biosynthetic process (Q21873)
  17. nicotinamide riboside metabolic process (Q21872)
  18. pyridine nucleoside metabolic process (Q21871)
  19. pyridine nucleoside catabolic process (Q21870)
  20. nicotinamide riboside catabolic process (Q21869)
  21. constitutional dyserythropoietic anemia (Q21865)
  22. neoplastic syndrome (Q21864)
  23. hematologic cancer (Q21863)
  24. soft tissue disorder (Q21862)
  25. connective and soft tissue neoplasms (Q21861)
  26. musculoskeletal neoplasm (Q21860)
  27. musculoskeletal system cancer (Q21859)
  28. connective tissue neoplasm (Q21858)
  29. rare neoplastic disease (Q21857)
  30. rare tumor (Q21856)
  31. tumor of hematopoietic and lymphoid tissues (Q21855)
  32. myeloproliferative disorders (Q21854)
  33. myelodysplastic syndrome (Q21853)
  34. bone marrow impairment (Q21852)
  35. bone marrow disease (Q21851)
  36. bone marrow failure (Q21850)
  37. aplastic anemia (Q21849)
  38. sideroblastic anaemia P (Q21848)
  39. dyserythropoiesis (Q21847)
  40. ineffective erythropoiesis (Q21846)
  41. congenital hemolytic anemia (Q21845)
  42. congenital dyserythropoietic anemia (Q21844)
  43. genetic hematologic disease (Q21843)
  44. neonatal anemia (Q21842)
  45. congenital anemia (Q21841)
  46. constitutional deficiency anemia (Q21840)
  47. vitamin B12- and folate-independent constitutional megaloblastic anemia (Q21839)
  48. inborn errors of purine–pyrimidine metabolism (Q21838)
  49. pyrimidine metabolic disorder (Q21837)
  50. orotic aciduria (Q21836)

View ( | ) (20 | 50 | 100 | 250 | 500)

Retrieved from "https://wiki.tiffa.net/wiki/Special:ItemsWithoutSitelinks"