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Matthew E. Roth

Researcher at Baylor College of Medicine

Publications -  30
Citations -  4523

Matthew E. Roth is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Gene & Gene expression. The author has an hindex of 21, co-authored 27 publications receiving 4117 citations. Previous affiliations of Matthew E. Roth include Yale University & University of Illinois at Urbana–Champaign.

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A Regulatory Cascade of the Nuclear Receptors FXR, SHP-1, and LRH-1 Represses Bile Acid Biosynthesis

TL;DR: A potent, nonsteroidal FXR ligand is used to show that FXR induces expression of small heterodimer partner 1 (SHP-1), an atypical member of the nuclear receptor family that lacks a DNA-binding domain that provides a molecular basis for the coordinate suppression of CYP7A1 and other genes involved in bile acid biosynthesis.
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Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis.

TL;DR: Mice heterozygous for the GATA3 mutation are fertile and appear in all respects to be normal, whereas homozygous mutant embryos die between days 11 and 12 postcoitum (p.c.) and display massive internal bleeding, marked growth retardation, severe deformities of the brain and spinal cord, and gross aberrations in fetal liver haematopoiesis.
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Down-Regulation of Rad51 and Decreased Homologous Recombination in Hypoxic Cancer Cells

TL;DR: It is reported that hypoxia specifically down-regulates the expression of RAD51, a key mediator of homologous recombination in mammalian cells, and a novel mechanism of genetic instability in the tumor microenvironment mediated by hypoxIA-induced suppression of the homologously recombination pathway in cancer cells is proposed.
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Embryonic expression and cloning of the murine GATA-3 gene

TL;DR: In situ hybridization shows that mGATA-3 mRNA accumulation is temporally and spatially regulated during early development, and at least two regulatory elements appear to be required for appropriate tissue-restricted regulation after transfection of mGata-3-directed reporter genes into cells that naturally express GATA- 3 (T lymphocytes and neuroblastoma cells).
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Gene expression analysis by transcript profiling coupled to a gene database query.

TL;DR: An mRNA profiling technique for determining differential gene expression that utilizes, but does not require, prior knowledge of gene sequences is described, which permits high-throughput reproducible detection of most expressed sequences with a sensitivity of greater than 1 part in 100,000.