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

Lack of Mutations in POT1 Gene in Selected Families with Familial Non-Medullary Thyroid Cancer.

Hormones & cancer - 1 Apr 2020

Orois Aida, Badenas Celia, Reverter Jordi L, López Verónica, Potrony Miriam, Mora Mireia, Halperin Irene, Oriola Josep

Abstract excerpt

To date, the genes involved in familial non-medullary thyroid cancer (FNMTC) remain poorly understood, with the exception of syndromic cases of FNMTC. It has been proposed that germline mutations in telomere-related genes, such as POT1, described in familial melanoma might also predispose individuals to thyroid cancer, requiring further research. We aimed to identify germline mutations in POT1 in selected FNMTC...

Read the complete abstract on PubMed

Topics

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

Share to High-Throughput Nucleotide Sequencing
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Shelterin Complex

Share to Telomere-Binding Proteins

Share to Thyroid Cancer, Papillary

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 32172474
DOI: 10.1007/s12672-020-00383-5
PMCID: PMC10355240

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lack of Mutations in POT1 Gene in Selected Families with Familial Non-Medullary Thyroid Cancer.PMID 32172474Read ↗

A new POT1 germline mutation-expanding the spectrum of POT1-associated cancers.Semantic proximity Read ↗

A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid CancerSemantic proximity Read ↗

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.Semantic proximity Read ↗

Telomere-lengthening germline variants predispose to a syndromic papillary thyroid cancer subtype.Semantic proximity Read ↗

Germline POT1 Variants: A Critical Perspective on POT1 Tumor Predisposition SyndromeSemantic proximity Read ↗

Association of the POT1 Germline Missense Variant p.I78T With Familial MelanomaSemantic proximity Read ↗

POT1 tumour predisposition: a broader spectrum of associated malignancies and proposal for additional screening program.Semantic proximity Read ↗

POT 1 germline mutations but not TERT promoter mutations are implicated in melanoma susceptibility in a large cohort of Spanish melanoma familiesSemantic proximity Read ↗

Mutations in POT1 predispose to familial cutaneous malignant melanoma.Semantic proximity Read ↗

A novel germline mutation in the <i>POT1</i> gene predisposes to familial non-medullary thyroid cancerSemantic proximity Read ↗

UK clinical practice guidelines for the management of patients with constitutional POT1 pathogenic variants.Semantic proximity Read ↗

Population-based analysis of<i>POT1</i>variants in a cutaneous melanoma case-control cohortSemantic proximity Read ↗

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