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Lance D. Miller

Researcher at Wake Forest University

Publications -  208
Citations -  16169

Lance D. Miller is an academic researcher from Wake Forest University. The author has contributed to research in topics: Cancer & Breast cancer. The author has an hindex of 58, co-authored 195 publications receiving 14459 citations. Previous affiliations of Lance D. Miller include University of Texas MD Anderson Cancer Center & East Carolina University.

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Journal ArticleDOI

Identification of White Spot Syndrome Virus Latency-Related Genes in Specific-Pathogen-Free Shrimps by Use of a Microarray

TL;DR: Viral sequences could be PCR amplified from genomic DNA of SPF shrimp, further supporting the suggestion that these shrimps are asymptomatic carriers of white spot syndrome virus.
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Neurotensin receptor 1 determines the outcome of non-small cell lung cancer.

TL;DR: NTSR1 expression was identified as a potential new prognostic biomarker for surgically resected stage I lung adenocarcinomas, as NTSR1 activation was shown to participate in lung cancer progression.
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JMJD6 is a driver of cellular proliferation and motility and a marker of poor prognosis in breast cancer

TL;DR: Jumonji Domain Containing 6 (JMJD6) protein was expressed at highest levels in tumors associated with worse outcomes, including ER- and basal-like, Claudin-low, Her2-enriched, and ER+ Luminal B tumors, suggesting that JMJD6 may affect similar pathways in primary breast cancer.
Journal ArticleDOI

Yin Yang 1 contains G-quadruplex structures in its promoter and 5′-UTR and its expression is modulated by G4 resolvase 1

TL;DR: Strong evidence is provided showing the presence of G4 structures in the promoter and the 5′-UTR of YY1, and the analysis of a gene array data consisting of the breast cancer samples of 258 patients indicates a significant, positive correlation between G4R1 and YY 1 expression.
Book ChapterDOI

Diversity in bacterial chemotactic responses and niche adaptation

TL;DR: The diversity of bacterial chemotaxis is explored and how gaining further insights into such diversity may potentially impact future drug and pesticides development and could inform bioremediation strategies is suggested.