Benilde Teresa-De

Mexico City, DIF, Mexico

Last Updated: 09/26/2026

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Found 11 publications

Dyskeratosis Congenita with Pigmentary Mosaicism and Hematopoietic Trisomy 9 in a Female Associated with a de novo DKC1 Variant and Markedly Skewed X Chromosome Inactivation.

Dyskeratosis Congenita with Pigmentary Mosaicism and Hematopoietic Trisomy 9 in a Female Associated with a de novo DKC1 Variant and Markedly Skewed X Chromosome Inactivation.

Journal: NPJ genomic medicine

Published: December 15, 2025

The tight bond between Fanconi anemia and aging.

The tight bond between Fanconi anemia and aging.

Journal: Frontiers in aging

Published: November 22, 2025

Analysis of BRCA1, BRCA2 and PALB2 related Fanconi anemia identifies scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes.

Analysis of BRCA1, BRCA2 and PALB2 related Fanconi anemia identifies scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes.

Journal: medRxiv : the preprint server for health sciences

Published: June 26, 2025

BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes.

BRCA1-, BRCA2-, and PALB2-related Fanconi anemia: Scope to expand disease phenotypic features and predict breast cancer risk in heterozygotes.

Journal: American journal of human genetics

Published: May 15, 2025

High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone Marrow.

High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone Marrow.

Journal: Cancers

Published: March 16, 2025

A Boolean network model of the double-strand break repair pathway choice.

A Boolean network model of the double-strand break repair pathway choice.

Journal: Journal of theoretical biology

Published: April 11, 2023

Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences.

Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences.

Journal: Genes

Published: November 19, 2020

Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia.

Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia.

Journal: Experimental hematology

Published: July 29, 2020

MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia.

MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia.

Journal: Cell stem cell

Published: February 21, 2020

Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.

Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.

Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology

Published: March 20, 2019

WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways.

WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways.

Journal: Frontiers in genetics

Published: November 02, 2018

Showing 1-11 of 11

Last Updated: 09/26/2026