Diana C. Diaz-Sierra
Bogota, DC, Colombia
Last Updated: 09/26/2026
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Found 9 publications
MIEN1 promoter deletion leads to impaired migration and invasion potential via actin cytoskeleton rearrangement in colorectal cancer.
Journal: Scientific reports
Published: April 04, 2025
Integrating next-generation sequencing and artificial intelligence for the identification and validation of pathogenic variants in colorectal cancer.
Journal: Frontiers in oncology
Published: February 19, 2025
Functional Analysis of BRCA1 3'UTR Variants Predisposing to Breast Cancer.
Journal: The application of clinical genetics
Published: November 02, 2023
Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies.
Journal: International journal of molecular sciences
Published: September 24, 2021
DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformation.
Journal: Human genetics
Published: April 21, 2020
Mutant GNLY is linked to Stevens-Johnson syndrome and toxic epidermal necrolysis.
Journal: Human genetics
Published: July 11, 2019
FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia.
Journal: Molecular medicine (Cambridge, Mass.)
Published: March 13, 2019
Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans.
Journal: Open biology
Published: April 13, 2016
Showing 1-9 of 9
Last Updated: 09/26/2026