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The Journal of Molecular Diagnostics : JMD|August 24, 2018
Validation of a Long-Read PCR Assay for Sensitive Detection and Sizing of C9orf72 Hexanucleotide Repeat ExpansionsEunRan Suh, Kaitlyn Grando, Vivianna M Van Deerlin
American Journal of Physiology. Gastrointestinal and Liver Physiology|January 13, 2004
Putative intestine-specific enhancers located in 5' sequence of the CDX1 gene regulate CDX1 expression in the intestineErinn B Rankin, Wei Xu, Debra G Silberg, et al.
The Journal of Biological Chemistry|April 6, 2002
Cloning of the human claudin-2 5'-flanking region revealed a TATA-less promoter with conserved binding sites in mouse and human for caudal-related homeodomain proteins and hepatocyte nuclear factor-1alphaTakanori Sakaguchi, Xiubin Gu, Heidi M Golden, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|May 23, 2002
Analysis of human cellular retinol-binding protein II promoter during enterocyte differentiationLiang Zhang, Xueping E, Kathryn E Luker, et al.
Cancer Biology & Therapy|June 23, 2005
Intestinal metaplasia with a high salt diet induces epithelial proliferation and alters cell composition in the gastric mucosa of miceFang Xiao, Mary Ann S Crissey, John P Lynch, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|December 4, 2004
Regulation of RELM/FIZZ isoform expression by Cdx2 in response to innate and adaptive immune stimulation in the intestineMei-Lun Wang, Marcus E Shin, Pamela A Knight, et al.
Acta Neuropathologica|May 9, 2014
C9orf72 hypermethylation protects against repeat expansion-associated pathology in ALS/FTDElaine Y Liu, Jenny Russ, Kathryn Wu, et al.
Annals of Clinical and Translational Neurology|June 28, 2022
Genetic prediction of impulse control disorders in Parkinson's diseaseDaniel Weintraub, Marijan Posavi, Pierre Fontanillas, et al.
JAMA Neurology|October 2, 2013
Development and validation of pedigree classification criteria for frontotemporal lobar degenerationElisabeth M Wood, Dana Falcone, Eunran Suh, et al.
Molecular Neurodegeneration|February 7, 2025
Disparate and shared transcriptomic signatures associated with cortical atrophy in genetic behavioral variant frontotemporal degenerationTing Shen, Jacob W Vogel, Vivianna M Van Deerlin, et al.
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