Amy A. Larson
University of California, San Diego
5 Papers
209 Citations
Amy A. Larson is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Loss of heterozygosity & Tumor progression. The author has an hindex of 5, co-authored 5 publications.
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Papers
Genetic Alterations Accumulate During Cervical Tumorigenesis and Indicate a Common Origin for Multifocal Lesions
TL;DR: In this article, loss of heterozygosity (LOH) analyses of invasive cervical carcinomas have identified several chromosomal arms likely to harbor tumor suppressor genes, of which regions on 3p,4p, 4q, and 11q have been validated extensively.
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•Journal Article
Genetic Alterations Accumulate during Cervical Tumorigenesis and Indicate a Common Origin for Multifocal Lesions
TL;DR: In this paper, loss of heterozygosity (LOH) analyses of invasive cervical carcinomas have identified several chromosomal arms likely to harbor tumor suppressor genes, of which regions on 3p,4p, 4q, and 11q have been validated extensively.
•Journal Article
A Defined Region of Loss of Heterozygosity at 11q23 in Cutaneous Malignant Melanoma
Rudolf A. Herbst,Amy A. Larson,Jürgen Weiss,Webster K. Cavenee,Garret M. Hampton,Karen C. Arden +5 more
TL;DR: The findings indicate that a tumor suppressor gene that plays a role in malignant melanoma is located on the long arm of chromosome 11, likely within a 51 cM region at 11q23.
68
•Journal Article
High resolution analysis of chromosome 3p alterations in cervical carcinoma
Amy A. Larson,Suzanne G. Kern,Shannon Curtiss,Robert Gordon,Webster K. Cavenee,Garret M. Hampton +5 more
TL;DR: This is the first report of HDs encompassing the FHIT gene region in primary tumor samples and underscores the usefulness of high resolution genetic analysis of tumor genomes in determining the chromosomal aberrations underlying the malignant progression of CC.
•Journal Article
Analysis of Replication Error (RER+) Phenotypes in Cervical Carcinoma
Amy A. Larson,Suzanne G. Kern,Robin L. Sommers,Jun Yokota,Webster K. Cavenee,Garret M. Hampton +5 more
TL;DR: The findings suggest that defects in DNA repair-associated genes are rarely acquired and do not supersede allelic loss during cervical carcinogenesis, and the semiautomated multiplex approach has proven unequivocal in the detection and interpretation of MI.