Jesus-jose Fernandez-Ferre

Albacete, CM 02008, Spain

Last Updated: 09/26/2026

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Found 13 publications

Exploring Gallium(III) Complexes as Emerging Therapeutic Candidates for Breast Cancer.

Exploring Gallium(III) Complexes as Emerging Therapeutic Candidates for Breast Cancer.

Journal: Journal of medicinal chemistry

Published: April 06, 2026

Displacement of distant regulatory elements of FOXC1 as a potential human disease mechanism.

Displacement of distant regulatory elements of FOXC1 as a potential human disease mechanism.

Journal: Human genomics

Published: January 13, 2025

Transgenic Overexpression of Myocilin Leads to Variable Ocular Anterior Segment and Retinal Alterations Associated with Extracellular Matrix Abnormalities in Adult Zebrafish.

Transgenic Overexpression of Myocilin Leads to Variable Ocular Anterior Segment and Retinal Alterations Associated with Extracellular Matrix Abnormalities in Adult Zebrafish.

Journal: International journal of molecular sciences

Published: July 31, 2022

CRISPR-Cas9-mediated functional dissection of the foxc1 genomic region in zebrafish identifies critical conserved cis-regulatory elements.

CRISPR-Cas9-mediated functional dissection of the foxc1 genomic region in zebrafish identifies critical conserved cis-regulatory elements.

Journal: Human genomics

Published: July 08, 2022

Knockout of myoc Provides Evidence for the Role of Myocilin in Zebrafish Sex Determination Associated with Wnt Signalling Downregulation.

Knockout of myoc Provides Evidence for the Role of Myocilin in Zebrafish Sex Determination Associated with Wnt Signalling Downregulation.

Journal: Biology

Published: December 23, 2020

Disruption of foxc1 genes in zebrafish results in dosage-dependent phenotypes overlapping Axenfeld-Rieger syndrome.

Disruption of foxc1 genes in zebrafish results in dosage-dependent phenotypes overlapping Axenfeld-Rieger syndrome.

Journal: Human molecular genetics

Published: May 21, 2020

Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish.

Role of GUCA1C in Primary Congenital Glaucoma and in the Retina: Functional Evaluation in Zebrafish.

Journal: Genes

Published: March 27, 2020

CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix.

CPAMD8 loss-of-function underlies non-dominant congenital glaucoma with variable anterior segment dysgenesis and abnormal extracellular matrix.

Journal: Human genetics

Published: January 27, 2020

Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma.

Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma.

Journal: PloS one

Published: August 18, 2018

Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development.

Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development.

Journal: Scientific reports

Published: December 01, 2016

Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes.

Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes.

Journal: Acta ophthalmologica

Published: July 27, 2015

The Role of hsa-miR-548l Dysregulation as a Putative Modifier Factor for Glaucoma-Associated FOXC1 Mutations.

The Role of hsa-miR-548l Dysregulation as a Putative Modifier Factor for Glaucoma-Associated FOXC1 Mutations.

Journal: MicroRNA (Shariqah, United Arab Emirates)

Published: January 13, 2015

Showing 1-12 of 13

Last Updated: 09/26/2026