inosine-triphosphate has been researched along with Intellectual-Disability* in 2 studies
2 other study(ies) available for inosine-triphosphate and Intellectual-Disability
Article | Year |
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Partial trisomy 20 confirmed by gene dosage studies.
We describe a female infant with multiple congenital anomalies and mental retardation, pre- and postnatal growth failure, microcephaly, unusual facial appearance, and minor skeletal anomalies, all very suggestive of the partial trisomy 20(p) syndrome. Although she was born to karyotypically normal parents, she had an extra small metacentric chromosome. Analysis of metaphase and prometaphase chromosomes by GTG banding and Giemsa 11 staining showed that the extra chromosome was a number 20 with a deletion of the distal end of the long arm. Gene dose studies of adenosine deaminase (ADA) and inosine triphosphatase (ITP) supported the cytogenetic interpretation. Topics: Abnormalities, Multiple; Adenosine Deaminase; Chromosome Banding; Chromosome Mapping; Chromosomes, Human, 19-20; Female; Genes; Genetic Markers; Humans; Infant, Newborn; Inosine Triphosphatase; Inosine Triphosphate; Intellectual Disability; Psychomotor Disorders; Pyrophosphatases; Trisomy | 1979 |
Human inosine triphosphatase: catalytic properties and population studies.
Using a reliable 2-step colorimetric assay, some catalytic properties of human erythrocyte ITPase (inosine triphosphate pyrophosphohydrolase) (EC 3.6.1.19) were determined. The enzyme hydrolyses ITP, dITP (deoxyinosine triphosphate) and XTP (xanthine triphosphate) but not other nucleotides. IDP is a competitive inhibitor. Subcellular fractionation of cultured lymphoid-line cells showed ITPase activity to be in the cytosol. ATP and GTP hydrolysing activities were not enriched in the cytosol fraction. The range of activity was investigated in erythrocytes, peripheral leukocytes, amniotic fluid cells, skin fibroblasts, long term lymphoid lines and bone marrow fibroblasts. The mean ITPase activity was found to vary in different cell types from 4.9 to 294 units per mg protein. Fractionation of red blood cells by age revealed that the enzyme decays exponentially with erythrocyte age with a half-life of 35 days. The enzyme had a wide range of specific activity in erythrocytes from 150 normal randomly selected individuals (15--722 pmol/h/g Hb). Within the low range of erythrocyte specific activities (from 15 to 200) a correlation was found between an individual's erythrocyte activity and the activity in peripheral leukocytes. This correlation was not found at higher erythrocyte ITPase activities. Two individuals were detected who had erythrocyte ITPase activities which were close to the lowest ITPase activities of all samples tested. Thus, low or absent ITPase activity is an individual characteristic which may be expressed both in erythrocytes and in other cell types. Topics: Cell Line; Erythrocyte Aging; Erythrocytes; Fibroblasts; Humans; Inosine Triphosphatase; Inosine Triphosphate; Intellectual Disability; Leukocytes; Lymphoid Tissue; Pyrophosphatases; Schizophrenia; Subcellular Fractions | 1979 |