Search Results - "Parrish, Julia E."

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  1. 1

    Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE by Parrish, Julia E, Oostra, Ben A, Verkerk, Annemieke J.M.H, Richards, C. Sue, Reynolds, James, Spikes, Aimee S, Shaffer, Lisa G, Nelson, David L

    Published in Nature genetics (01-11-1994)
    “…Three folate-sensitive fragile sites, termed FRAXA, FRAXE and FRAXF, have been identified on the distal end of chromosome Xq. The first two contain expanded,…”
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  2. 2

    Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophy by Wulff, Karin, Parrish, Julia E., Herrmann, Falko H., Wehnert, Manfred

    Published in Human mutation (1997)
    “…Mutations in the emerin gene, also referred to as the STA‐ or EMD‐gene, have been found to be the cause of X‐linked Emery‐Dreifuss muscular dystrophy (EMD)…”
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  3. 3

    MSG1(Melanocyte-Specific Gene 1): Mapping to Chromosome Xq13.1, Genomic Organization, and Promoter Analysis by Fenner, Martin H, Parrish, Julia E, Boyd, Yvonne, Reed, Vivienne, MacDonald, Marcy, Nelson, David L, Isselbacher, Kurt J, Shioda, Toshi

    Published in Genomics (San Diego, Calif.) (01-08-1998)
    “…MSG1(melanocyte-specific gene 1) is a recently isolated gene predominantly expressed in cultured normal melanocytes and pigmented melanoma cells.MSG1encodes a…”
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  4. 4

    Abstract 4245: BLZ-100 provides optical contrast in animal models of breast cancer by Hansen, Stacey, Fidel, Janean, Kennedy, Katie, Dernell, William, Fransson, Boel, Ramsay, Josh, Wiss, Valorie, Stroud, Mark, Parrish-Novak, Julia E.

    Published in Cancer research (Chicago, Ill.) (15-07-2016)
    “…Abstract Over 230,000 new breast cancer cases occur in the US annually. Complete surgical removal of tumor tissue is critical to reduce the risk of local…”
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  5. 5

    Abstract 4936: Tumor PaintTM technology detects naturally occurring solid tumors in dogs by Dernell, William S., Fidel, Janean, Kennedy, Katie, Hansen, Stacey, Wiss, Valorie, Stroud, Mark, Parrish-Novak, Julia E.

    Published in Cancer research (Chicago, Ill.) (01-10-2014)
    “…Abstract Tumor PaintTM technology is designed to provide real-time visualization of tumors during surgery at improved resolution over existing methods. BLZ-100…”
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  6. 6

    Selection Against Mutant Alleles in Blood Leukocytes is a Consistent Feature in Incontinentia Pigmenti Type 2 by Parrish, Julia E., Scheuerle, Angela E., Lewis, Richard A., Levy, Moise L., Nelson, David L.

    Published in Human molecular genetics (01-11-1996)
    “…Incontinentia Pigmenti 2 (IP2) is an X-linked dominant disorder with male lethality. Affected females display a characteristic skin eruption that evolves…”
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  7. 7
  8. 8

    A muscle-specific DNase I-like gene in human Xq28 by Parrish, J E, Ciccodicola, A, Wehhert, M, Cox, G F, Chen, E, Nelson, D L

    Published in Human molecular genetics (01-09-1995)
    “…A novel cDNA which maps to human Xq28 has been isolated and characterized. Sequence similarity to DNase I is high at the DNA and peptide sequence levels. The…”
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  9. 9

    The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney by Wilson, Angus C., Parrish, Julia E., Massa, Hillary F., Nelson, David L., Trask, Barbara J., Herr, Winship

    Published in Genomics (San Diego, Calif.) (20-01-1995)
    “…After herpes simplex virus (HSV) infection, the viral regulatory protein VP16 activates transcription of the HSV immediate-early promoters by directing complex…”
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  10. 10

    Regional assignment of 19 X-linked ESTs by Parrish, J E, Nelson, D L

    Published in Human molecular genetics (01-11-1993)
    “…Subchromosomal localizations for 19 X-linked expressed sequence tags (ESTs) have been determined. Two ESTs are located in Xq28, adding two novel genes to this…”
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  11. 11

    Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome by Parrish, J E, Wagner, M J, Hecht, J T, Scott, Jr, C I, Wells, D E

    Published in Genomics (San Diego, Calif.) (01-09-1991)
    “…We have obtained lymphoblastoid cell lines from three patients with Langer-Giedion syndrome who have overlapping deletions in 8q24.1. To isolate the deletion…”
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  12. 12

    Alignment of physical and genetic maps of human 8q23-qter using somatic cell hybrid mapping panel by PARRISH, J. E, YANG WANG, WAGNER, M. J, WELLS, D. E

    Published in Somatic cell and molecular genetics (01-03-1994)
    “…We describe a mapping panel for the 8q23-qter region composed of human-hamster hybrid cell lines carrying deletion and translocation derivatives of human…”
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  13. 13

    Methods for finding genes. A major rate-limiting step in positional cloning by Parrish, J E, Nelson, D L

    “…Identification of transcribed sequences from within genomic regions has been a major rate-limiting step in the pursuit of genes involved in many human genetic…”
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