Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clonality of combined tumors.

Archives of pathology & laboratory medicine - 1 Apr 2002

Huang Jiaoti, Behrens Carmen, Wistuba Ignacio I, Gazdar Adi F, Jagirdar Jaishree

Abstract excerpt

CONTEXT: Tumors with mixed morphologic patterns (combined tumors) are sometimes encountered, and questions often arise regarding the mechanism of molecular pathogenesis of each component and their relationships. OBJECTIVE: To determine whether different components of combined tumors contain the same or different genetic alterations, thus providing evidence for their clonality. MATERIALS AND METHODS: Six combined...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Carcinoma, Neuroendocrine
Share to Carcinoma, Small Cell
Share to Carcinoma, Squamous Cell

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Clone Cells

Share to Colonic Neoplasms

Share to Genes, ras

Share to Loss of Heterozygosity

Share to Neoplasms, Multiple Primary

Source

Identifiers

PMID: 11900568
DOI: 10.5858/2002-126-0437-COCT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clonality of combined tumors.PMID 11900568Read ↗

Colorectal mixed adenoneuroendocrine carcinomas and neuroendocrine carcinomas are genetically closely related to colorectal adenocarcinomas.Semantic proximity Read ↗

The role of next-generation sequencing in the differential diagnosis of composite neoplasms.Semantic proximity Read ↗

Mixed adenoneuroendocrine carcinomas of the gastrointestinal tract: targeted next-generation sequencing suggests a monoclonal origin of the two components.Semantic proximity Read ↗

Molecular Analysis of Mixed Endometrial Carcinomas Shows Clonality in Most Cases.Semantic proximity Read ↗

Monoclonal Origins of Malignant Mixed Tumors (Carcinosarcomas)Semantic proximity Read ↗

Frequent genetic heterogeneity in the clonal evolution of gynecological carcinosarcoma and its influence on phenotypic diversity.Semantic proximity Read ↗

Genetic evidence for the multi-step progression of mixed glandular-neuroendocrine gastric carcinomas.Semantic proximity Read ↗

Origin and evolution of colorectal mixed neuroendocrine-non-neuroendocrine neoplasms (MiNEN).Semantic proximity Read ↗

Molecular Evidence for Independent Origin of Multifocal Neuroendocrine Tumors of the Enteropancreatic AxisSemantic proximity Read ↗

Genetic classification of combined hepatocellular-cholangiocarcinoma.Semantic proximity Read ↗

Identical clonality of both components of mammary carcinosarcoma with differential loss of heterozygosity.Semantic proximity Read ↗

Multiclonal colorectal cancers with divergent histomorphological features and RAS mutations: one cancer or separate cancers?Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.