J
Judith D. Brown
Researcher at University of Connecticut
Publications - 16
Citations - 592
Judith D. Brown is an academic researcher from University of Connecticut. The author has contributed to research in topics: Genome & Gene. The author has an hindex of 13, co-authored 16 publications receiving 536 citations.
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Journal ArticleDOI
Chromosomes, conflict, and epigenetics: chromosomal speciation revisited.
TL;DR: This review will examine both classical and current models of chromosomal speciation and describe the "evolving" theory of genetic conflict, epigenetics, and chromosomal Speciation.
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Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1
Noelle D. Germain,Pin-Fang Chen,Alex M. Plocik,Heather Glatt-Deeley,Judith D. Brown,James J Fink,Kaitlyn A. Bolduc,Tiwanna M. Robinson,Eric S. Levine,Lawrence T. Reiter,Brenton R. Graveley,Marc Lalande,Stormy J. Chamberlain +12 more
TL;DR: Genome-wide analyses suggest that common neuronal pathways may be disrupted in both the Angelman and Dup15q syndromes, and chromatin structure may influence gene expression across the 15q11-q13.1 region in neurons.
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Four core genotypes mouse model: localization of the Sry transgene and bioassay for testicular hormone levels.
Yuichiro Itoh,Ryan Mackie,Kathy Kampf,Shelly Domadia,Judith D. Brown,Rachel J. O’Neill,Arthur P. Arnold +6 more
TL;DR: The Sry transgene in FCG mice is present in multiple copies at one locus on chromosome 3, which does not interrupt known genes, suggesting that differences between XX and XY mice with the same type of gonad are not caused by difference in prenatal androgen levels.
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Making a long story short: noncoding RNAs and chromosome change.
TL;DR: Recent evidence that ncRNAs can facilitate chromosome change is summarized and mechanisms by which nc RNAs create DNA breaks are presented, which present hypotheses on how they may create novel karyotypes and thus affect chromosome evolution.
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Orthotopic transplantation of v-src-expressing glioma cell lines into immunocompetent mice: establishment of a new transplantable in vivo model for malignant glioma.
Henry M. Smilowitz,Jakob Weissenberger,Jakob Weissenberger,Joachim Weis,Joachim Weis,Judith D. Brown,Rachel J. O’Neill,Jean A. Laissue +7 more
TL;DR: The high rate of engraftment, the similarity to the high-grade malignant glioma of origin, and the rapid, locally invasive growth of these tumors should make this murine model useful in testing novel therapies for human malignantgliomas.