Publications by authors named "Elizabeth D Hughes"

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Neuronal splicing of the unmethylated histone H3K4 reader, PHF21A, prevents excessive synaptogenesis.
Masayoshi Nagai, Robert S Porter, Maxwell Miyasato, Aijia Wang, Cecilia M Gavilan, Elizabeth D Hughes

J Biol Chem· November 2024

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Development of a C3 Humanized Rat as a New Model for Evaluating Novel C3 Inhibitors.
Jin Y Chen, Lingjun Zhang, Maojing Yang, Elizabeth D Hughes, Zachary T Freeman

J Innate Immun· February 2024

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Angiogenesis depends upon EPHB4-mediated export of collagen IV from vascular endothelial cells.
Di Chen, Elizabeth D Hughes, Thomas L Saunders, Jiangping Wu, Magda N Hernandez Vasquez

JCI Insight· February 2022

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Knock-In Rat Lines with Cre Recombinase at the Dopamine D1 and Adenosine 2a Receptor Loci.
Jeffrey R Pettibone, Jai Y Yu, Rifka C Derman, Thomas W Faust, Elizabeth D Hughes

eNeuro· March 2020

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Next Generation Transgenic Rat Model Production.
Wanda E Filipiak, Elizabeth D Hughes, Galina B Gavrilina, Anna K LaForest, Thomas L Saunders

Methods Mol Biol· November 2019

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The chemerin knockout rat reveals chemerin dependence in female, but not male, experimental hypertension.
Stephanie W Watts, Emma S Darios, Adam E Mullick, Hannah Garver, Thomas L Saunders, Elizabeth D Hughes

FASEB J· June 2018

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Hair Cell Loss, Spiral Ganglion Degeneration, and Progressive Sensorineural Hearing Loss in Mice with Targeted Deletion of Slc44a2/Ctl2.
Pavan Kommareddi, Thankam Nair, Bala Naveen Kakaraparthi, Maria M Galano, Danielle Miller, Elizabeth D Hughes

J Assoc Res Otolaryngol· December 2015

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Blood vascular abnormalities in Rasa1(R780Q) knockin mice: implications for the pathogenesis of capillary malformation-arteriovenous malformation.
Beth A Lubeck, Philip E Lapinski, Timothy J Bauler, Jennifer A Oliver, Elizabeth D Hughes

Am J Pathol· December 2014

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A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice.
Jessica A Lehoczky, Peedikayil E Thomas, Kevin M Patrie, Kailey M Owens, Lisa M Villarreal, Elizabeth D Hughes

PLoS Genet· August 2014

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An inactivating caspase 11 passenger mutation originating from the 129 murine strain in mice targeted for c-IAP1.
Niall S Kenneth, J Michael Younger, Elizabeth D Hughes, Danielle Marcotte, Philip A Barker

Biochem J· April 2012

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Mice hypomorphic for Atr have increased DNA damage and abnormal checkpoint response.
Ryan L Ragland, Martin F Arlt, Elizabeth D Hughes, Thomas L Saunders, Thomas W Glover

Mamm Genome· June 2009

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Genetic analysis of SH2D4A, a novel adapter protein related to T cell-specific adapter and adapter protein in lymphocytes of unknown function, reveals a redundant function in T cells.
Philip E Lapinski, Jennifer A Oliver, Lynn A Kamen, Elizabeth D Hughes, Thomas L Saunders

J Immunol· August 2008

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Generation of mice with a conditional allele of the p120 Ras GTPase-activating protein.
Philip E Lapinski, Timothy J Bauler, Eric J Brown, Elizabeth D Hughes, Thomas L Saunders

Genesis· December 2007

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Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line.
Elizabeth D Hughes, Yun Yan Qu, Suzanne J Genik, Robert H Lyons, Christopher D Pacheco

Mamm Genome· August 2007

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Normal TCR signal transduction in mice that lack catalytically active PTPN3 protein tyrosine phosphatase.
Timothy J Bauler, Elizabeth D Hughes, Yutaka Arimura, Tomas Mustelin, Thomas L Saunders

J Immunol· March 2007

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Beta-mannosidosis mice: a model for the human lysosomal storage disease.
Mei Zhu, Kathryn L Lovell, Jon S Patterson, Thomas L Saunders, Elizabeth D Hughes

Hum Mol Genet· February 2006

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Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.
Tamar Ben-Yosef, Inna A Belyantseva, Thomas L Saunders, Elizabeth D Hughes, Kohei Kawamoto

Hum Mol Genet· August 2003

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