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Human Molecular Genetics|July 16, 2004
Differential expression of a novel ankyrin containing E3 ubiquitin-protein ligase, Hace1, in sporadic Wilms' tumor versus normal kidneyMichael S Anglesio, Valentina Evdokimova, Nataliya Melnyk, et al.
Open Biology|December 2, 2016
Tumour-suppressor microRNAs regulate ovarian cancer cell physical properties and invasive behaviourClara K Chan, Yinghong Pan, Kendra Nyberg, et al.
Scientific Reports|April 5, 2016
Tracking of Normal and Malignant Progenitor Cell Cycle Transit in a Defined NicheGabriel Pineda, Kathleen M Lennon, Nathaniel P Delos Santos, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 13, 2005
A high-resolution whole-genome cattle-human comparative map reveals details of mammalian chromosome evolutionAnnelie Everts-van der Wind, Denis M Larkin, Cheryl A Green, et al.
Research Square|July 1, 2024
A simple phylogenetic approach to analyze hypermutated HIV proviruses reveals insights into their dynamics and persistence during antiretroviral therapyAniqa Shahid, Bradley R Jones, Maggie C Duncan, et al.
Virus Evolution|January 13, 2025
A simple phylogenetic approach to analyze hypermutated HIV proviruses reveals insights into their dynamics and persistence during antiretroviral therapyAniqa Shahid, Bradley R Jones, Maggie C Duncan, et al.
Cell Genomics|October 15, 2024
Long-read sequencing of an advanced cancer cohort resolves rearrangements, unravels haplotypes, and reveals methylation landscapesKieran O'Neill, Erin Pleasance, Jeremy Fan, et al.
Cold Spring Harbor Molecular Case Studies|December 25, 2019
Fluorouracil sensitivity in a head and neck squamous cell carcinoma with a somatic <i>DPYD</i> structural variantElisa Majounie, Kathleen Wee, Laura M Williamson, et al.
Nucleic Acids Research|May 30, 2002
Systematic sequencing of cDNA clones using the transposon Tn5Yuriy Shevchenko, Gerard G Bouffard, Yaron S N Butterfield, et al.
Journal of Medical Genetics|January 16, 2007
Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14Björn Menten, Karen Buysse, Farah Zahir, et al.
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