CDKN2C Homozygous Loss Identifies a Distinct Subtype of TP53/RB1-wildtype Leiomyosarcoma With Frequent CIC Genomic Alterations and 1p/19q-Codeletion

doi 10.1101/2020.03.02.973305
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Cold Spring Harbor Laboratory

Related search

Neuroimaging-Based Classification Algorithm for Predicting 1p/19q-Codeletion Status in IDH-Mutant Lower Grade Gliomas

American Journal of Neuroradiology
MedicineNuclear MedicineNeurologyImagingRadiology
2019English

Targeted Genomic Profiling Identifies Frequent Deleterious Mutations in FAT4 and TP53 Genes in HBV-associated Hepatocellular Carcinoma

BMC Cancer
Cancer ResearchOncologyGenetics
2019English

Mass Spectrometry-Based Assay for the Molecular Diagnosis of Glioma: Concomitant Detection of Chromosome 1p/19q Codeletion, and IDH1, IDH2, and TERT Mutation Status

Oncotarget
Oncology
2017English

ACGH Detects Distinct Genomic Alterations of Primary Intrahepatic Cholangiocarcinomas and Matched Lymph Node Metastases and Identifies a Poor Prognosis Subclass

Scientific Reports
Multidisciplinary
2018English

Genomic Profiling Identifies Recurrent Genetic Alterations in SCLC

Cancer Discovery
Oncology
2015English

RB1 and TP53 Pathways in Radiation-Induced Sarcomas

Oncogene
Cancer ResearchGeneticsMolecular Biology
2007English

Age-Related Differences in 1p and 19q Deletions in Oligodendrogliomas

BMC Clinical Pathology
Forensic MedicinePathologyHistology
2003English

Original Article Loss of Genetic Material Within 1p and 19q Chromosomal Arms in Low Grade Gliomas of Central Nervous System

Folia Neuropathologica
Forensic MedicinePathologyNeurology
2013English

Detailed Assessment of Copy Number Alterations Revealing Homozygous Deletions in 1p and 13q in Mantle Cell Lymphoma

Leukemia Research
Cancer ResearchOncologyHematology
2007English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy