"Phosphoglycerate Kinase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An enzyme catalyzing the transfer of a phosphate group from 3-phospho-D-glycerate in the presence of ATP to yield 3-phospho-D-glyceroyl phosphate and ADP. EC 2.7.2.3.
| Descriptor ID |
D010735
|
| MeSH Number(s) |
D08.811.913.696.630.700
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Phosphoglycerate Kinase".
Below are MeSH descriptors whose meaning is more specific than "Phosphoglycerate Kinase".
This graph shows the total number of publications written about "Phosphoglycerate Kinase" by people in this website by year, and whether "Phosphoglycerate Kinase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 2 | 0 | 2 |
| 2007 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Phosphoglycerate Kinase" by people in Profiles.
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Level of residual enzyme activity modulates the phenotype in phosphoglycerate kinase deficiency. Neurology. 2018 09 11; 91(11):e1077-e1082.
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Spermatogenesis associated retrogenes are expressed in the human ovary and ovarian cancers. PLoS One. 2009; 4(3):e5064.
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Craniofacial, skeletal, and cardiac defects associated with altered embryonic murine Zic3 expression following targeted insertion of a PGK-NEO cassette. Front Biosci. 2007 Jan 01; 12:1680-90.
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The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA. Br J Haematol. 2006 Jul; 134(2):233-7.
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Two new phosphoglycerate kinase mutations associated with chronic haemolytic anaemia and neurological dysfunction in two patients from Spain. Br J Haematol. 2006 Feb; 132(4):523-9.
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Expression from second-generation feline immunodeficiency virus vectors is impaired in human hematopoietic cells. Mol Ther. 2002 Nov; 6(5):645-52.
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Ectopic expression of Fgf-4 in chimeric mouse embryos induces the expression of early markers of limb development in the lateral ridge. Dev Genet. 1996; 19(1):51-65.
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DNA repair rates mapped along the human PGK1 gene at nucleotide resolution. Science. 1994 Mar 11; 263(5152):1438-40.
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Patterns of X chromosome inactivation in the Rett syndrome. Brain Dev. 1990; 12(1):131-5.