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1.
Integrating leiomyoma genetics, epigenomics, and single-cell transcriptomics reveals causal genetic variants, genes, and cell types.
Nat Commun
; 15(1): 1169, 2024 Feb 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-38326302
2.
Engineered MED12 mutations drive uterine fibroid-like transcriptional and metabolic programs by altering the 3D genome compartmentalization.
Res Sq
; 2023 Feb 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-36798375
3.
Engineered MED12 mutations drive leiomyoma-like transcriptional and metabolic programs by altering the 3D genome compartmentalization.
Nat Commun
; 14(1): 4057, 2023 07 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37429859
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