Search Results - "Herzing, Laura B.K."

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  1. 1

    Intergenerational and parent of origin effects of maternal calorie restriction on Igf2 expression in the adult rat hippocampus by Harper, Kathryn M, Tunc-Ozcan, Elif, Graf, Evan N, Herzing, Laura B.K, Redei, Eva E

    Published in Psychoneuroendocrinology (01-07-2014)
    “…Summary Insulin-like growth factor 2 ( Igf2 ) regulates development, memory and adult neurogenesis in the hippocampus. Calorie restriction (CR) is known to…”
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  2. 2

    Imprinting and expression of Dio3os mirrors Dio3 in rat by Dietz, William H, Masterson, Kevin, Sittig, Laura J, Redei, Eva E, Herzing, Laura B K

    Published in Frontiers in genetics (2012)
    “…Genomic imprinting, the preferential expression of maternal or paternal alleles of imprinted genes, is often maintained through expression of imprinted long…”
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  3. 3

    Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11– q13 duplications by Herzing, Laura B.K., Cook, Jr, Edwin H., Ledbetter, David H.

    Published in Human molecular genetics (15-07-2002)
    “…15q11– q13 contains many imprinted genes, and undergoes duplicon-mediated rearrangements, including deletions, duplications and triplications, and generation…”
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    Strain‐specific vulnerability to alcohol exposure in utero via hippocampal parent‐of‐origin expression of deiodinase‐III by Sittig, Laura J., Shukla, Pradeep K., Herzing, Laura B. K., Redei, Eva E.

    Published in The FASEB journal (01-07-2011)
    “…ABSTRACT Prenatal exposure to alcohol is thought to be the most prevalent nongenetic cause of a wide range of neurodevelopmental deficits. Insufficient thyroid…”
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  7. 7

    Xist has properties of the X-chromosome inactivation centre by Herzing, Laura B. K, Romer, Justyna T, Horn, Jacqueline M, Ashworth, Alan

    Published in Nature (London) (20-03-1997)
    “…X-chromosome inactivation is the process by which female mammals (with two X chromosomes) achieve expression of X-chromosomal genes equivalent to that of males…”
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  8. 8

    The Human Aminophospholipid-Transporting ATPase Gene ATP10C Maps Adjacent to UBE3A and Exhibits Similar Imprinted Expression by Herzing, Laura B.K., Kim, Soo-Jeong, Cook, Edwin H., Ledbetter, David H.

    Published in American journal of human genetics (01-06-2001)
    “…Maternal duplications of the imprinted 15q11-13 domain result in an estimated 1%–2% of autism-spectrum disorders, and linkage to autism has been identified…”
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  9. 9

    Mutation screening and transmission disequilibrium study of ATP10C in autism by Kim, Soo-Jeong, Herzing, Laura B.K., Veenstra-VanderWeele, Jeremy, Lord, Catherine, Courchesne, Rachel, Leventhal, Bennett L., Ledbetter, David H., Courchesne, Eric, Cook Jr, Edwin H.

    Published in American journal of medical genetics (08-03-2002)
    “…Autism is a complex genetic disorder. Chromosome 15 is of particular interest in this disorder, because of previous reports of individuals with autism with…”
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  10. 10

    Expression cloning of multiple human cDNAs that complement the phenotypic defects of ataxia-telangiectasia group D fibroblasts by STEPHEN MEYN, M, LU-KUO, J. M, HERZING, L. B. K

    Published in American journal of human genetics (01-12-1993)
    “…Ataxia-telangiectasia (A-T) is an inherited human disease of unknown etiology associated with neurologic degeneration, immune dysfunction, cancer risk, and…”
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    Novel lacZ-based recombination vectors for mammalian cells by Herzing, L B, Meyn, M S

    Published in Gene (31-12-1993)
    “…We have constructed two sets of Escherichia coli lacZ-based vectors for use in studies of general mitotic recombination, both in somatic mammalian cells grown…”
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