Salvato in:
Dettagli Bibliografici
Autore principale: Mamoor, Shahan
Natura: Recurso digital
Lingua:
Pubblicazione: Zenodo 2025
Accesso online:https://doi.org/10.5281/zenodo.16452472
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!
_version_ 1866902264331894784
author Mamoor, Shahan
author_facet Mamoor, Shahan
contents <p>Membrane expression of receptors in circulating tumor cells remains incompletely defined. We identified enrichment of SMIM38 when studying membrane expression of receptors in circulating tumor cells in humans with metastatic breast cancer. SMIM38 function was studied at the interaction level using proteomics, identifying ETDA and ETDB as protein-protein interaction partners. Both ETDA and ETDB were also transcriptionally active in the circulating tumor cell. SMIM38 functions with ETDA and ETDB in circulation during metastasis in humans with cancer. </p>
format Recurso digital
id zenodo_https___doi_org_10_5281_zenodo_16452472
institution Zenodo
language
publishDate 2025
publisher Zenodo
record_format zenodo
spellingShingle The integral membrane protein SMIM38 is transcriptionally activated in circulating tumor cells in human breast cancer in conjunction with two SMIM38-interacting proteins of undefined function, ETDA and ETDB.
Mamoor, Shahan
<p>Membrane expression of receptors in circulating tumor cells remains incompletely defined. We identified enrichment of SMIM38 when studying membrane expression of receptors in circulating tumor cells in humans with metastatic breast cancer. SMIM38 function was studied at the interaction level using proteomics, identifying ETDA and ETDB as protein-protein interaction partners. Both ETDA and ETDB were also transcriptionally active in the circulating tumor cell. SMIM38 functions with ETDA and ETDB in circulation during metastasis in humans with cancer. </p>
title The integral membrane protein SMIM38 is transcriptionally activated in circulating tumor cells in human breast cancer in conjunction with two SMIM38-interacting proteins of undefined function, ETDA and ETDB.
url https://doi.org/10.5281/zenodo.16452472