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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Uniparental Disomy and TP53[original query]
Detailed analysis of p53 pathway defects in fludarabine-refractory chronic lymphocytic leukemia (CLL): dissecting the contribution of 17p deletion, TP53 mutation, p53-p21 dysfunction, and miR34a in a prospective clinical trial.
Blood 2009 Sep 114 (13): 2589-97.
Zenz Thorsten, Häbe Sonja, Denzel Tina, Mohr Julia, Winkler Dirk, Bühler Andreas, Sarno Antonio, Groner Silja, Mertens Daniel, Busch Raymonde, Hallek Michael, Döhner Hartmut, Stilgenbauer Steph
Molecular characterization of choroid plexus tumors reveals novel clinically relevant subgroups.
Clinical cancer research : an official journal of the American Association for Cancer Research 2015 Jan 21 (1): 184-92.
Merino Diana M, Shlien Adam, Villani Anita, Pienkowska Malgorzata, Mack Stephen, Ramaswamy Vijay, Shih David, Tatevossian Ruth, Novokmet Ana, Choufani Sanaa, Dvir Rina, Ben-Arush Myran, Harris Brent T, Hwang Eugene I, Lulla Rishi, Pfister Stefan M, Achatz Maria Isabel, Jabado Nada, Finlay Jonathan L, Weksberg Rosanna, Bouffet Eric, Hawkins Cynthia, Taylor Michael D, Tabori Uri, Ellison David W, Gilbertson Richard J, Malkin Dav
Mutational profiling of acute myeloid leukemia with normal cytogenetics in Brazilian patients: the value of next-generation sequencing for genomic classification.
Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2017 9 65 (8): 1155-1158.
de Noronha Thiago Rodrigo, Mitne-Neto Miguel, Chauffaille Maria de Lourd
Genome-Wide Analysis of Head and Neck Squamous Cell Carcinomas Reveals HPV, TP53, Smoking and Alcohol-Related Allele-Based Acquired Uniparental Disomy Genomic Alterations.
Neoplasia (New York, N.Y.) 2019 1 21 (2): 197-205.
Tuna Musaffe, Amos Christopher I, Mills Gordon
Germline Variants in Phosphodiesterase Genes and Genetic Predisposition to Pediatric Adrenocortical Tumors.
Cancers 2020 2 12 (2): .
Pinto Emilia Modolo, Faucz Fabio R, Paza Luana Z, Wu Gang, Fernandes Elizabeth S, Bertherat Jerome, Stratakis Constantine A, Lalli Enzo, Ribeiro Raul C, Rodriguez-Galindo Carlos, Figueiredo Bonald C, Zambetti Gerard
The prognostic significance of single-nucleotide polymorphism array-based whole-genome analysis and uniparental disomy in myelodysplastic syndrome.
International journal of laboratory hematology 2021 3 43 (5): 1062-1069.
Ou Yang, Yang Yan, Yu Hongbin, Zhang Xin, Liu Min, Wu
Whole-chromosome arm acquired uniparental disomy in cancer development is a consequence of isochromosome formation.
Neoplasia (New York, N.Y.) 2022 1 25 9-17.
Tuna Musaffe, Amos Christopher I, Mills Gordon
Genetic Profiling of Sebaceous Carcinoma Arising from an Ovarian Mature Teratoma: A Case Report.
International journal of molecular sciences 2024 6 25 (12): .
Sumika Zaitsu, Yoko Aoyagi, Haruto Nishida, Kohei Nakamura, Mitsutake Yano, Eiji Kobayas
Pediatric-type high-grade gliomas with PDGFRA amplification in adult patients with Li-Fraumeni syndrome: clinical and molecular characterization of three cases.
Acta neuropathologica communications 2024 4 12 (1): 57.
Yuji Kibe, Fumiharu Ohka, Kosuke Aoki, Junya Yamaguchi, Kazuya Motomura, Eiji Ito, Kazuhito Takeuchi, Yuichi Nagata, Satoshi Ito, Nobuhiko Mizutani, Yoshiki Shiba, Sachi Maeda, Tomohide Nishikawa, Hiroki Shimizu, Ryuta Sai
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