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

Stem cell pluripotency factor NANOG is expressed in human fetal gonocytes, testicular carcinoma <i>in situ</i> and germ cell tumours

27 Jun 2005

Abstract excerpt

AIMS: NANOG is a key regulator of embryonic stem cell (ESC) self-renewal and pluripotency. Our recent genome-wide gene expression profiling study of the precursor of testicular germ cell tumours, carcinoma in situ testis (CIS), showed close similarity between ESC and CIS, including high NANOG expression. In the present study we analysed the protein expression of NANOG during normal development of human testis and...

Read the complete abstract on PubMed

Topics

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

Share to Neuroblastoma Research and Treatments
Share to Pluripotent Stem Cells Research
Share to Testicular diseases and treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 15982323
DOI: 10.1111/j.1365-2559.2005.02182.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Stem cell pluripotency factor NANOG is expressed in human fetal gonocytes, testicular carcinoma <i>in situ</i> and germ cell tumoursPMID 15982323Read ↗

The pluripotency homeobox gene <i>NANOG</i> is expressed in human germ cell tumorsSemantic proximity Read ↗

Analysis of SOX2 expression in developing human testis and germ cell neoplasiaSemantic proximity Read ↗

NANOG controls testicular germ cell tumour stemness through regulation of MIR9-2Semantic proximity Read ↗

Functional Evidence that the Self-Renewal Gene <i>NANOG</i> Regulates Human Tumor DevelopmentSemantic proximity Read ↗

Expression and interdependencies of pluripotency factors LIN28, OCT3/4, NANOG and SOX2 in human testicular germ cells and tumours of the testisSemantic proximity Read ↗

Differential expression of SOX17 and SOX2 in germ cells and stem cells has biological and clinical implicationsSemantic proximity Read ↗

Human embryonic stem cell genes <i>OCT4, NANOG, STELLAR</i>, and <i>GDF3</i> are expressed in both seminoma and breast carcinomaSemantic proximity Read ↗

A Distinct Expression Pattern in Mammalian Testes Indicates a Conserved Role for NANOG in SpermatogenesisSemantic proximity Read ↗

MicroRNA expression profiling of carcinoma in situ cells of the testisSemantic proximity Read ↗

Analysis of Gene Expression Profiles of Microdissected Cell Populations Indicates that Testicular Carcinoma <i>In situ</i> Is an Arrested GonocyteSemantic proximity Read ↗

The emerging phenotype of the testicular carcinoma in situ germ cell.Semantic proximity Read ↗

Developmental model for the pathogenesis of testicular carcinoma <i>in situ</i> : genetic and environmental aspectsSemantic proximity Read ↗

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