Fran Martínez-Jiménez
@franmj88.bsky.social
950 followers
660 following
11 posts
Group Leader of Computational Immunogenomics group at VHIO |
Data Mining lead at HartwigMedicalFoundation | Personal account | Advocate for social and environmental justice 🌍
https://www.franmartinezlab.com/
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Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Ivano Amelio
@ivanoamelio.bsky.social
· Jul 19
Aberrant basal cell clonal dynamics shape early lung carcinogenesis
Preinvasive squamous lung lesions are precursors of lung squamous cell carcinoma (LUSC). The cellular events underlying lesion formation are unknown. Using a carcinogen-induced model of LUSC with no a...
www.science.org
Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Ewan Birney
@ewanbirney.bsky.social
· Jun 20
Reposted by Fran Martínez-Jiménez
Lars Velten
@larsplus.bsky.social
· May 21
Clonal tracing with somatic epimutations reveals dynamics of blood ageing - Nature
The discovery that DNA methylation of different CpG sites can serve as digital barcodes of clonal identity led to the development of EPI-Clone, an algorithm that enables single-cell lineage tracing th...
doi.org
Reposted by Fran Martínez-Jiménez
Ana Dueso-Barroso
@aduesoba.bsky.social
· May 16
Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Mariona Graupera
@grauperalab.bsky.social
· Mar 28
Somatic uniparental disomy of PTEN in endothelial cells causes vascular malformations in patients with PTEN Hamartoma Tumor Syndrome
Abstract. PTEN Hamartoma Tumor Syndrome (PHTS) is a rare tumor risk disorder caused by germline loss-of-function mutations in PTEN. Half of these patients develop vascular malformations, a hamartoma c...
aacrjournals.org
Reposted by Fran Martínez-Jiménez
Reposted by Fran Martínez-Jiménez
Mariona Graupera
@grauperalab.bsky.social
· Feb 26
Context-dependent response of endothelial cells to PIK3CA mutation
Cancer mutations in the PIK3CA gene cause congenital disorders. The endothelium is among the most frequently affected tissues in these disorders, displaying aberrant vascular overgrowth in the form of...
bit.ly