Alison Mcbride

Dr. Alison Mcbride

Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA
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Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 October 2016 in Nucleic Acids Research
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Journal Article
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KDKoenraad Van Doorslaer
Koenraad Van Doorslaer
ZLZhiwen Li
Zhiwen Li
SXSandhya Xirasagar
Sandhya Xirasagar
PMPiet Maes
Piet Maes
DKDavid Kaminsky
David Kaminsky
AMAlison Mcbride
Alison Mcbride
The Papillomavirus Episteme (PaVE) is a database of curated papillomavirus genomic sequences, accompanied by web-based sequence analysis tools. This update describes the addition of major new features. The papillomavirus genomes within PaVE have been further annotated, and now includes the major spliced mRNA transcripts. Viral genes and transcripts can be visualized on both linear and circular genome browsers. Evolutionary relationships among PaVE reference protein sequences can be analysed using multiple sequence alignments and phylogenetic trees. To assist in viral discovery, PaVE offers a typing tool; a simplified algorithm to determine whether a newly sequenced virus is novel. PaVE also now contains an image library containing gross clinical and histopathological images of papillomavirus infected lesions. Database URL: https://pave.niaid.nih.gov/.

1 October 2013 in Virology
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Journal Article
Closed access
AMAlison Mcbride
Alison Mcbride

1 May 2012 in The American Journal of Human Genetics
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Journal Article
Closed access
CJCatherine T. Jordan
Catherine T. Jordan
LCLi Cao
Li Cao
ERElisha D.O. Roberson
Elisha D.O. Roberson
KPKatherine C. Pierson
Katherine C. Pierson
CYChi-Fan Yang
Chi-Fan Yang
ABAnne Bowcock
Anne Bowcock

14 September 2021 in Nature Reviews Microbiology
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Journal Article
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AMAlison Mcbride
Alison Mcbride

6 April 2017 in PLOS Pathogens
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Journal Article
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AMAlison Mcbride
Alison Mcbride
AWAlix Warburton
Alix Warburton

1 July 2010 in Journal of Clinical Investigation
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Journal Article
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SCSandra Chapman
Sandra Chapman
XLXuefeng Liu
Xuefeng Liu
CMCraig Meyers
Craig Meyers
RSRichard Schlegel
Richard Schlegel
AMAlison Mcbride
Alison Mcbride
Primary human keratinocytes are useful for studying the pathogenesis of many different diseases of the cutaneous and mucosal epithelia. In addition, they can form organotypic tissue equivalents in culture that can be used as epidermal autografts for wound repair as well as for the delivery of gene therapy. However, primary keratinocytes have a finite lifespan in culture that limits their proliferative capacity and clinical use. Here, we report that treatment of primary keratinocytes (originating from 3 different anatomical sites) with Y-27632, a Rho kinase inhibitor, greatly increased their proliferative capacity and resulted in efficient immortalization without detectable cell crisis. More importantly, the immortalized cells displayed characteristics typical of primary keratinocytes; they had a normal karyotype and an intact DNA damage response and were able to differentiate into a stratified epithelium. This is the first example to our knowledge of a defined chemical compound mediating efficient cell immortalization, and this finding could have wide-ranging and profound investigational and medical applications.