Blood

• t(4;14)-associated multiple myeloma
  2 January 2012

  References
  The MMSET histone methyl transferase switches global histone methylation and alters gene expression in t(4;14) multiple myeloma cells. Martinez-Garcia E, Popovic R, Min DJ, Sweet SM, Thomas PM, Zamdborg L, Heffner A, Will C, Lamy L, Staudt LM, Levens DL, Kelleher NL, Licht JD. Blood. 2011 Jan 6;117(1):211-20. PMID: #20974671#

• Howell-Jolly bodies
  20 December 2011

  Howell-Jolly inclusions; Howell-Jolly body
  Definition: Howell-Jolly bodies are histopathological findings of basophilic nuclear remnants (clusters of DNA) in circulating erythrocytes. It is named for William Henry Howell and Justin Marie Jolly.
  Images
  https://twitter.com/TeamCaptainJohn/status/731162965429395458
  See also
  Howell-Jolly body-like inclusions in neutrophils
  https://twitter.com/KyleBradleyMD/status/736893161159725056
  During maturation in the bone marrow erythrocytes (...)

• thrombophilia
  5 December 2011

  herethrombophilia ditary

• autoimmune cytopenia
  10 November 2010

  Etiology (Examples)
  hepatitis C virus infection (#12640185#)
  See also
  blood anomalies

• sicle cell-associated sudden death
  19 June 2010

  sicle cell anemia-associated sudden death; sicle cell hemoglobinopathy-associated sudden death

• megaloblastic anemia type 1
  2 October 2008

  MGA1, Imerslund-Grasbeck syndrome, Imerslund disease, enterocyte cobalamin malabsorption

• plasminogen deficiencies
  17 April 2008

  Plasminogen (plg) deficiency has been classified as (i) hypoplasminogenemia or ’true’ type I plasminogen deficiency (#16849641#), and (ii) dysplasminogenemia, also called type II plasminogen deficiency. Both forms, severe hypoplasminogenemia and dysplasminogenemia, are not causally linked to venous thrombosis.
  Type I plasminogen deficiency is caused by mutation in the gene encoding plasminogen (PLG) MIM.173350).
  Congenital plasminogen deficiency is a rare autosomal recessive disorder (...)

• plasminogen deficiency type 1
  17 April 2008

  Inherited plasminogen deficiency type I, congenital plasminogen deficiency type 1

• blood transcriptome
  10 January 2008

  References
  Mohr S, Liew CC. The peripheral-blood transcriptome: new insights into disease and risk assessment. Trends Mol Med. 2007 Oct;13(10):422-32. Epub 2007 Oct 4. PMID: #17919976#

• Blood
  12 September 2007

  Videos
  Blood smear (by Washington Deceit)
  See also
  hematologic system

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