Search Results - "Herzing, Laura B K"

Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice by Viemari, Jean-Charles, Roux, Jean-Christophe, Tryba, Andrew K, Saywell, Veronique, Burnet, Henri, Pena, Fernando, Zanella, Sebastien, Bevengut, Michelle, Barthelemy-Requin, Magali, Herzing, Laura B. K, Moncla, Anne, Mancini, Josette, Ramirez, Jan-Marino, Villard, Laurent, Hilaire, Gerard

“…Rett syndrome is a severe X-linked neurological disorder in which most patients have mutations in the methyl-CpG binding protein 2 (MECP2) gene and suffer from…”
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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

“…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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Gene × environment effects of serotonin transporter, dopamine receptor D4, and monoamine oxidase A genes with contextual and parenting risk factors on symptoms of oppositional defiant disorder, anxiety, and depression in a community sample of 4-year-old children by Lavigne, John V, Herzing, Laura B K, Cook, Edwin H, Lebailly, Susan A, Gouze, Karen R, Hopkins, Joyce, Bryant, Fred B

“…Genetic factors can play a key role in the multiple level of analyses approach to understanding the development of child psychopathology. The present study…”
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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.

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

“…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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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

“…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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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.

“…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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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.

“…15q11– q13 contains many imprinted genes, and undergoes duplicon-mediated rearrangements, including deletions, duplications and triplications, and generation…”
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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.

“…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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Construction of specific cosmids from YACs by homologous recombination in yeast by Herzing, Laura B. K., Ashworth, Alan

“…Images…”
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