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pyridoxal phosphate and Thalassemia

pyridoxal phosphate has been researched along with Thalassemia in 6 studies

Pyridoxal Phosphate: This is the active form of VITAMIN B 6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (PYRIDOXAMINE).
pyridoxal 5'-phosphate : The monophosphate ester obtained by condensation of phosphoric acid with the primary hydroxy group of pyridoxal.

Thalassemia: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.

Research Excerpts

ExcerptRelevanceReference
"When G6PD deficiency occurs with heterozygous beta-thalassaemia, GR is usually saturated with FAD as in G6PD deficiency alone, unless there is an inherited, very slow red-cell metabolism of riboflavin to FMN."1.27Glutathione reductase activity and its relationship to pyridoxine phosphate activity in G6PD deficiency. ( Anderson, BB; Clements, JE; Perry, GM; Salsini, G; Studds, C; Vullo, C, 1987)

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19906 (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
Anderson, BB4
Perry, GM3
Modell, CB2
Child, JA2
Mollin, DL3
Clements, JE1
Studds, C1
Vullo, C1
Salsini, G1
Takaku, F1
Yano, Y1
Aoki, Y1
Nakao, K1
Wada, O1
Beutler, E1
Paniker, NV1
West, CJ1

Other Studies

6 other studies available for pyridoxal phosphate and Thalassemia

ArticleYear
Abnormal red-cell metabolism of pyridoxine associated with beta-thalassaemia.
    British journal of haematology, 1979, Volume: 41, Issue:4

    Topics: Adenosine Triphosphate; Adolescent; Adult; Aged; Child, Preschool; Erythrocytes; Female; Heterozygot

1979
Family studies of red-cell metabolism of pyridoxine in beta-thalassaemia.
    Biomedicine / [publiee pour l'A.A.I.C.I.G.], 1979, Volume: 30, Issue:1

    Topics: Erythrocytes; Humans; Pedigree; Pyridoxal Phosphate; Pyridoxine; Thalassemia

1979
Glutathione reductase activity and its relationship to pyridoxine phosphate activity in G6PD deficiency.
    European journal of haematology, 1987, Volume: 38, Issue:1

    Topics: Erythrocytes; Flavin Mononucleotide; Flavin-Adenine Dinucleotide; Flavoproteins; Glucosephosphate De

1987
-Aminolevulinic acid synthetase activity of human bone marrow erythroid cells in various hematological disorders.
    The Tohoku journal of experimental medicine, 1972, Volume: 107, Issue:3

    Topics: 5-Aminolevulinate Synthetase; Anemia, Hypochromic; Anemia, Sideroblastic; Bone Marrow; Bone Marrow C

1972
Red-cell metabolism of pyridoxine in sideroblastic anaemias and related anaemias.
    British journal of haematology, 1972, Volume: 23

    Topics: Adenosine Triphosphate; Adult; Aged; Anemia, Hypochromic; Anemia, Sideroblastic; Biological Assay; E

1972
Pyridoxine administration in sickle cell disease: an unsuccessful attempt to influence the properties of sickle hemoglobin.
    Biochemical medicine, 1972, Volume: 6, Issue:2

    Topics: Anemia, Sickle Cell; Aspartate Aminotransferases; Blood Viscosity; Chromium Isotopes; Erythrocytes;

1972