The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
about
Cloning of human PEX cDNA. Expression, subcellular localization, and endopeptidase activityEffect of polyamine depletion on caspase activation: a study with spermine synthase-deficient cellsA Genetic Murine Model of Endolymphatic Hydrops: The Phex Mouse.Spermine synthase deficiency leads to deafness and a profound sensitivity to alpha-difluoromethylornithine.X-linked hypophosphatemia: the mutant gene is expressed in teeth as well as in kidneySpermine synthase.New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice.The molecular background to hypophosphataemic rickets.Normal regulation of calcitriol production in Gy mice. Evidence for biochemical heterogeneity in the X-linked hypophosphatemic diseases.X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome.Increased polyamine intake inhibits age-associated alteration in global DNA methylation and 1,2-dimethylhydrazine-induced tumorigenesisGenetically altered mouse models: the good, the bad, and the ugly.The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes.An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets.Animal disease models generated by genetic engineering of polyamine metabolism.Dosage effect of a Phex mutation in a murine model of X-linked hypophosphatemia.Mouse models to investigate the function of spermineTherapeutic management of hypophosphatemic rickets from infancy to adulthood.Vitamin D metabolism and rickets in domestic animals: a review.Polyamines, androgens, and skeletal muscle hypertrophy.Tooth dentin defects reflect genetic disorders affecting bone mineralization.Inflammation, carcinogenesis and neurodegeneration studies in transgenic animal models for polyamine research.Skin fibroblasts from spermine synthase-deficient hemizygous gyro male (Gy/Y) mice overproduce spermidine and exhibit increased resistance to oxidative stress but decreased resistance to UV irradiation.Functions of Polyamines in MammalsMutation watch: PEX PLUS? Gene(s) for X-linked hypophosphatemia and deafness.Effect of spermine synthase on the sensitivity of cells to anti-tumour agents.Effect of spermine synthase deficiency on polyamine biosynthesis and content in mice and embryonic fibroblasts, and the sensitivity of fibroblasts to 1,3-bis-(2-chloroethyl)-N-nitrosoureaSpermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome.Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.Spermine synthesis is required for normal viability, growth, and fertility in the mouse.Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets.Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia.Polyamines: Bio-Molecules with Diverse Functions in Plant and Human Health and Disease.Spermine synthase activity affects the content of decarboxylated S-adenosylmethionine.The genomic response of the mouse kidney to low-phosphate diet is altered in X-linked hypophosphatemia.Mitochondrial nicotinamide adenine dinucleotide reduced (NADH) oxidation links the tricarboxylic acid (TCA) cycle with methionine metabolism and nuclear DNA methylation.
P2860
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P2860
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
description
1986 nî lūn-bûn
@nan
1986 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
@ast
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
@en
type
label
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
@ast
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
@en
prefLabel
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
@ast
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
@en
P2093
P2860
P356
P1476
The Gy mutation: another cause of X-linked hypophosphatemia in mouse.
@en
P2093
P2860
P304
P356
10.1073/PNAS.83.13.4899
P407
P577
1986-07-01T00:00:00Z