The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21 (Q24323031)

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J J Mallee

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H M Kwon

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J S Rim

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W R Mulla

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M Muenke

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N B Spinner

Use of whole cosmid cloned genomic sequences for chromosomal localization by non-radioactive in situ hybridization

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language of work or name

English

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publication date

20 January 1995

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published in

Genomics

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volume

25

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issue

2

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page(s)

507-13

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cites work

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Measurement of myo-inositol in single cells and defined areas of the nervous system by selected ion monitoring

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Myoinositol uptake by four cultured mammalian cell lines

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Active transport of myo-inositol and its relation to the sugar transport system in hamster small intestine

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Free and total lipid myo-inositol concentrations decrease with age in human brain.

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Inositol uptake by cultured isolated rat Schwann cells

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Myo-inositol transport into endothelial cells derived from nervous system microvessels.

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Inositol and inositol 1,4,5-trisphosphate content of Down syndrome fibroblasts exhibiting enhanced inositol uptake

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Kinetic evidence for compartmentalization of myo-inositol in hepatocytes

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Gas chromatographic analysis of myo-inositol in microgram samples of brain

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Myo inositol levels in the cerebrospinal fluid of infants

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Expression cloning and cDNA sequencing of the Na+/glucose co-transporter

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The molecular heterogeneity of protein kinase C and its implications for cellular regulation

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Inositol phosphates and cell signalling

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The distribution of free mesoinositol in mammalian tissues, including some observations on the lactating rat.

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Studies on the metabolic role of myo-inositol. Distribution of radioactive myo-inositol in the male rat.

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Down's syndrome fibroblasts exhibit enhanced inositol uptake

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myo-inositol transport and metabolism in fetal-bovine aortic endothelial cells

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Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

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Structure and evolution of four POU domain genes expressed in mouse brain

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Down syndrome phenotypes: the consequences of chromosomal imbalance

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Inositol accumulation by brain slices in vitro.

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Distribution of myo-inositol in the cat cochlear nucleus.

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Immunohistochemical staining and enzyme activity measurements show myo-inositol-1-phosphate synthase to be localized in the vasculature of brain

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Polyols in the cerebrospinal fluid and plasma of neurological, diabetic and uraemic patients

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The free myo-inositol concentration of adult and fetal tissues of several species

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The inositol content of foetal blood and foetal fluids

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Control of brain volume during hyperosmolar and hypoosmolar conditions

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Metabolism and function of myo-inositol and inositol phospholipids

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Upregulation of inositol transport mediates inositol accumulation in hyperosmolar brain cells

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Osmoregulation of Na(+)-inositol cotransporter activity and mRNA levels in brain glial cells

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Regulation of renal cell organic osmolyte transport by tonicity

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Myo-inositol transport in the central nervous system

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Renal medullary organic osmolytes

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Molecular mapping of twenty-four features of Down syndrome on chromosome 21.

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Concentration of myo-inositol in skeletal muscle of the rat occurs without active transport

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Sodium- and energy-dependent uptake of myo-inositol by rabbit peripheral nerve. Competitive inhibition by glucose and lack of an insulin effect

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myo-inositol: a newly identified nonnitrogenous osmoregulatory molecule in mammalian brain

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Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

1091799

1091799

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

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