AGCOH
Other names: atlasgeneticsoncology
The Atlas of Genetics and Cytogenetics in Oncology and Haematology is a peer-reviewed internet journal/encyclopaedia/database focused on genes implicated in cancer, cytogenetics and clinical entities in cancer and cancer-prone hereditary diseases. The main goal of the Atlas is to provide review articles that describe complementary topics, namely, genes, genetic abnormalities, histopathology, clinical diagnoses and a large iconography.
Description
More detailed information about this field from each metasource.
The Atlas of Genetics and Cytogenetics in Oncology and Haematology is a peer-reviewed internet journal/encyclopaedia/database focused on genes implicated in cancer, cytogenetics and clinical entities in cancer and cancer-prone hereditary diseases. The main goal of the Atlas is to provide review articles that describe complementary topics, namely, genes, genetic abnormalities, histopathology, clinical diagnoses and a large iconography.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:32:32.141250
Webpage:
http://atlasgeneticsoncology.orgWebpage
More detailed information about this field from each metasource.
http://atlasgeneticsoncology.org
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:32:32.141250
Licence:
Name: CC-BY-NC-ND-2.0Licence name
More detailed information about this field from each metasource.
Publications:
Publications
More detailed information about this field from each metasource.
Atlas of genetics and cytogenetics in oncology and haematology in 2013
PMID: 23161685
metasource: bio.tools
version: extracted_at: 2022-11-04T11:32:32.141250
Atlas of Genetics and Cytogenetics in Oncology and Haematology, year 2003
PMID: 12520000
metasource: bio.tools
version: extracted_at: 2022-11-04T11:32:32.141250
Publications
More detailed information about this field from each metasource.
Atlas of genetics and cytogenetics in oncology and haematology in 2013
PMID: 23161685
metasource: bio.tools
version: extracted_at: 2022-11-04T11:32:32.141250
Atlas of Genetics and Cytogenetics in Oncology and Haematology, year 2003
PMID: 12520000
metasource: bio.tools
version: extracted_at: 2022-11-04T11:32:32.141250
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Atlas of genetics and cytogenetics in oncology and haematology in 2013
PubMed citations: 68.
68 articles citing: Atlas of genetics and cytogenetics in oncology and haematology in 2013
Myeloid neoplasms and clonal hematopoiesis from the RUNX1 perspective. PMID:35354921
Role and Involvement of TENM4 and miR-708 in Breast Cancer Development and Therapy. PMID:35011736
Distinction of lymphoid and myeloid clonal hematopoiesis. PMID:34663986
Integrated genomics point to immune vulnerabilities in pleural mesothelioma. PMID:34580349
Altered neuronal physiology, development, and function associated with a common chromosome 15 duplication involving CHRNA7. PMID:34320968
A Novel Signature of CCNF-Associated E3 Ligases Collaborate and Counter Each Other in Breast Cancer. PMID:34201347
Reduction of RUNX1 transcription factor activity by a CBFA2T3-mimicking peptide: application to B cell precursor acute lymphoblastic leukemia. PMID:33743795
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers. PMID:33704937
Teneurins: Role in Cancer and Potential Role as Diagnostic Biomarkers and Targets for Therapy. PMID:33652578
Concurrent Central Diabetes Insipidus and Acute Myeloid Leukemia. PMID:33643671
Alterations of 5-hydroxymethylation in circulating cell-free DNA reflect molecular distinctions of subtypes of non-Hodgkin lymphoma. PMID:33574286
Cytogenomic characteristics of murine breast cancer cell line JC. PMID:33526060
MarkerDB: an online database of molecular biomarkers. PMID:33245771
A comprehensive pan-cancer study of fibroblast growth factor receptor aberrations in Chinese cancer patients. PMID:33209870
Proline rich 11 (PRR11) overexpression amplifies PI3K signaling and promotes antiestrogen resistance in breast cancer. PMID:33127913
Chromosomal abnormality, laboratory techniques, tools and databases in molecular Cytogenetics. PMID:33104991
Systems Biology and Experimental Model Systems of Cancer. PMID:33086677
Deficiency of Meis1, a transcriptional regulator, in mice and worms: Neurochemical and behavioral characterizations with implications in the restless legs syndrome. PMID:32910473
ECRG2, a novel transcriptional target of p53, modulates cancer cell sensitivity to DNA damage. PMID:32681017
Molecular Cytogenomic Characterization of the Murine Breast Cancer Cell Lines C-127I, EMT6/P and TA3 Hauschka. PMID:32630352
Role of Anillin in Tumour: From a Prognostic Biomarker to a Novel Target. PMID:32560530
CRISPR Gene Editing of Murine Blood Stem and Progenitor Cells Induces MLL-AF9 Chromosomal Translocation and MLL-AF9 Leukaemogenesis. PMID:32549410
Understanding and Modeling Metastasis Biology to Improve Therapeutic Strategies for Combating Osteosarcoma Progression. PMID:32082995
Development of a Precision Medicine Workflow in Hematological Cancers, Aalborg University Hospital, Denmark. PMID:32013121
TCGA-TCIA Impact on Radiogenomics Cancer Research: A Systematic Review. PMID:31795520
Recurrent Rearrangements in PRKACA and PRKACB in Intraductal Oncocytic Papillary Neoplasms of the Pancreas and Bile Duct. PMID:31678302
Circular RNA differential expression in blood cell populations and exploration of circRNA deregulation in pediatric acute lymphoblastic leukemia. PMID:31605010
Characterization of thyroid cancer driven by known and novel ALK fusions. PMID:31539879
Differential associations of allergic disease genetic variants with developmental profiles of eczema, wheeze and rhinitis. PMID:31441980
BCR: a promiscuous fusion partner in hematopoietic disorders. PMID:31105873
Analysis of Expression Pattern of snoRNAs in Different Cancer Types with Machine Learning Algorithms. PMID:31052553
A distinct epigenetic program underlies the 1;7 translocation in myelodysplastic syndromes. PMID:30923319
Detection of novel fusion-transcripts by RNA-Seq in T-cell lymphoblastic lymphoma. PMID:30914738
A patient with a diagnosis of nodal marginal zone B-cell lymphoma and a t(2;14)(p24;q32) involving MYCN and IGH. PMID:30733831
GLIS Rearrangement is a Genomic Hallmark of Hyalinizing Trabecular Tumor of the Thyroid Gland. PMID:30648929
Teneurins: An Integrative Molecular, Functional, and Biomedical Overview of Their Role in Cancer. PMID:30618566
SeqVItA: Sequence Variant Identification and Annotation Platform for Next Generation Sequencing Data. PMID:30487811
High-resolution architecture and partner genes of MYC rearrangements in lymphoma with DLBCL morphology. PMID:30348671
An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia. PMID:30008805
The Reprimo Gene Family: A Novel Gene Lineage in Gastric Cancer with Tumor Suppressive Properties. PMID:29941787
Clinically actionable mutation profiles in patients with cancer identified by whole-genome sequencing. PMID:29610388
The amino acid transporter SLC7A5 confers a poor prognosis in the highly proliferative breast cancer subtypes and is a key therapeutic target in luminal B tumours. PMID:29566741
Translocation Breakpoints Preferentially Occur in Euchromatin and Acrocentric Chromosomes. PMID:29316705
Identification of large rearrangements in cancer genomes with barcode linked reads. PMID:29186506
WNT signaling, the development of the sympathoadrenal-paraganglionic system and neuroblastoma. PMID:29058015
Metabolic Reprogramming in Glioma. PMID:28491867
Whole-genome sequencing identifies homozygous BRCA2 deletion guiding treatment in dedifferentiated prostate cancer. PMID:28487881
Ultra-High Mass Resolution MALDI Imaging Mass Spectrometry of Proteins and Metabolites in a Mouse Model of Glioblastoma. PMID:28377615
Combination Therapy Targeting BCL6 and Phospho-STAT3 Defeats Intratumor Heterogeneity in a Subset of Non-Small Cell Lung Cancers. PMID:28377453
Impact of RNA degradation on fusion detection by RNA-seq. PMID:27765019
Phenotypic and Cytogenetic Characterization of Mesenchymal Stromal Cells in De Novo Myelodysplastic Syndromes. PMID:27660743
The integrated stress response. PMID:27629041
Discretization of Gene Expression Data Unmasks Molecular Subgroups Recurring in Different Human Cancer Types. PMID:27537329
Challenges in identifying cancer genes by analysis of exome sequencing data. PMID:27417679
Identification of Cancer Related Genes Using a Comprehensive Map of Human Gene Expression. PMID:27322383
Regulation of hematopoietic development by ZBTB transcription factors. PMID:27250345
A Novel Method for Gene-Specific Enhancement of Protein Translation by Targeting 5'UTRs of Selected Tumor Suppressors. PMID:27171412
ERG Is a Useful Immunohistochemical Marker to Distinguish Leukemia Cutis From Nonneoplastic Leukocytic Infiltrates in the Skin. PMID:26909589
Rare double-hit with two translocations involving IGH both, with BCL2 and BCL3, in a monoclonal B-cell lymphoma/leukemia. PMID:26719766
Cytogenetic and Molecular Findings in Children with Acute Lymphoblastic Leukemia: Experience of a Single Institution in Argentina. PMID:26648836
A novel locus in the oxidative stress-related gene ALOX12 moderates the association between PTSD and thickness of the prefrontal cortex. PMID:26372769
Atlas of Cancer Signalling Network: a systems biology resource for integrative analysis of cancer data with Google Maps. PMID:26192618
Dysregulated transcription across diverse cancer types reveals the importance of RNA-binding protein in carcinogenesis. PMID:26100984
Carrageenan Inhibits Insulin Signaling through GRB10-mediated Decrease in Tyr(P)-IRS1 and through Inflammation-induced Increase in Ser(P)307-IRS1. PMID:25784556
Single nucleotide polymorphisms in microRNA binding sites: implications in colorectal cancer. PMID:25654126
Diversity of breakpoints of variant Philadelphia chromosomes in chronic myeloid leukemia in Brazilian patients. PMID:25638762
Cancer cytogenetics: methodology revisited. PMID:25368816
The 2013 Nucleic Acids Research Database Issue and the online molecular biology database collection. PMID:23203983 -
Atlas of Genetics and Cytogenetics in Oncology and Haematology, year 2003
PubMed citations: 22.
22 articles citing: Atlas of Genetics and Cytogenetics in Oncology and Haematology, year 2003
Chromosomal abnormality, laboratory techniques, tools and databases in molecular Cytogenetics. PMID:33104991
Determining the Cause of Recurrent Miscarriages in a Couple: Importance of NOR in the Era of NGS. PMID:31058056
A distinct epigenetic program underlies the 1;7 translocation in myelodysplastic syndromes. PMID:30923319
Identification of miRNA-mRNA Modules in Colorectal Cancer Using Rough Hypercuboid Based Supervised Clustering. PMID:28220871
Role of matrix metalloproteinases (MMPs) and MMP inhibitors on intracranial aneurysms: a review article. PMID:24926188
Genes dysregulated to different extent or oppositely in estrogen receptor-positive and estrogen receptor-negative breast cancers. PMID:23875016
Identification of lung-cancer-related genes with the shortest path approach in a protein-protein interaction network. PMID:23762832
Large scale chromosomal mapping of human microRNA structural clusters. PMID:23444140
Identification of ovarian cancer associated genes using an integrated approach in a Boolean framework. PMID:23383610
Atlas of genetics and cytogenetics in oncology and haematology in 2013. PMID:23161685
Gene Fusion Markup Language: a prototype for exchanging gene fusion data. PMID:23072312
Identification of colorectal cancer related genes with mRMR and shortest path in protein-protein interaction network. PMID:22496748
A Boolean-based systems biology approach to predict novel genes associated with cancer: Application to colorectal cancer. PMID:21352556
Amplification of the 20q chromosomal arm occurs early in tumorigenic transformation and may initiate cancer. PMID:21297939
iCOD: an integrated clinical omics database based on the systems-pathology view of disease. PMID:21143802
BRCA1-mutated and basal-like breast cancers have similar aCGH profiles and a high incidence of protein truncating TP53 mutations. PMID:21118481
Cross-species comparison of aCGH data from mouse and human BRCA1- and BRCA2-mutated breast cancers. PMID:20735817
Extracting consistent knowledge from highly inconsistent cancer gene data sources. PMID:20137077
Network of Cancer Genes: a web resource to analyze duplicability, orthology and network properties of cancer genes. PMID:19906700
Scanning the human genome at kilobase resolution. PMID:18292219
MethyCancer: the database of human DNA methylation and cancer. PMID:17890243
ChimerDB--a knowledgebase for fusion sequences. PMID:16381848
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