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2,3-diphosphoglycerate and Elliptocytosis, Hereditary

2,3-diphosphoglycerate has been researched along with Elliptocytosis, Hereditary in 1 studies

2,3-Diphosphoglycerate: A highly anionic organic phosphate which is present in human red blood cells at about the same molar ratio as hemoglobin. It binds to deoxyhemoglobin but not the oxygenated form, therefore diminishing the oxygen affinity of hemoglobin. This is essential in enabling hemoglobin to unload oxygen in tissue capillaries. It is also an intermediate in the conversion of 3-phosphoglycerate to 2-phosphoglycerate by phosphoglycerate mutase (EC 5.4.2.1). (From Stryer Biochemistry, 4th ed, p160; Enzyme Nomenclature, 1992, p508)
2,3-bisphosphoglyceric acid : A bisphosphoglyceric acid that is glyceric acid carrying two phospho substituents at positions 2 and 3.

Elliptocytosis, Hereditary: An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mentzer, WC1
Iarocci, TA1
Mohandas, N1
Lane, PA1
Smith, B1
Lazerson, J1
Hays, T1

Other Studies

1 other study available for 2,3-diphosphoglycerate and Elliptocytosis, Hereditary

ArticleYear
Modulation of erythrocyte membrane mechanical stability by 2,3-diphosphoglycerate in the neonatal poikilocytosis/elliptocytosis syndrome.
    The Journal of clinical investigation, 1987, Volume: 79, Issue:3

    Topics: 2,3-Diphosphoglycerate; Diphosphoglyceric Acids; Elliptocytosis, Hereditary; Erythrocyte Deformabili

1987