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1 - 6 of 6 results found for PGK1. Did you mean: pgk

  1. Isolation and characterization of three microsatellite markers in the proximal long arm...

    Three microsatellites have been identified in cosmids from the human X chromosome. The cosmids have been assigned locus numbers DXS554, DXS559, and DXS566 and have been localized to Xq12-q13 (DXS554 and DXS559) and Xq13 (DXS566). In addition, they

    http://iris.ucl.ac.uk/iris/publication/157659/2

  2. Physical mapping in the region of human Xq12-21.1 using pulsed field gel electrophoresis.

    A number of human disease genes have been localised to Xq12-21.1. A genetic map of this region has previously been constructed using family linkage studies and has been complemented by physical mapping studies using hybrid and deletion cell lines.

    http://iris.ucl.ac.uk/iris/publication/226680/2

  3. X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies:...

    The X-chromosome activity states of 11 manifesting carriers of dystrophinopathies, all with normal karyotypes, were estimated by restriction fragment length polymorphism (RFLP)-methylation analysis with the probes M27β (DXS255), p2-19(DXS605) and

    http://iris.ucl.ac.uk/iris/publication/1766129/7

  4. Spatial distribution of cellular function: the partitioning of proteins between...

    Concurrent proteomics analysis of the nuclei and mitochondria of MCF7 breast cancer cells identified 985 proteins (40% of all detected proteins) present in both organelles. Numerous proteins from all five complexes involved in oxidative

    http://iris.ucl.ac.uk/iris/publication/824948/2

  5. Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an...

    During a systematic chromosomal survey of 167 unrelated boys with the X-linked recessive Menkes disease (MIM 309400), a unique rearrangement of the X chromosome was detected, involving an insertion of the long arm segment Xq13.3-q21.2 into the short

    http://iris.ucl.ac.uk/iris/publication/1824573/7

  6. Reference genes selection for transcriptional profiling in blood of HD patients and R6/2...

    BACKGROUND: Huntington's disease is a neurodegenerative disorder characterized by transcriptional alterations both in central and peripheral tissues. Therefore, the identification of a transcriptional signature in an accessible tissue can

    http://iris.ucl.ac.uk/iris/publication/967790/2

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