Hajrah Sarkar

Mile End Road, E1 4NS
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 17 publications

Oxidative Stress, Inflammation and Altered Glucose Metabolism Contribute to the Retinal Phenotype in the Choroideremia Zebrafish.

Oxidative Stress, Inflammation and Altered Glucose Metabolism Contribute to the Retinal Phenotype in the Choroideremia Zebrafish.

Journal: Antioxidants (Basel, Switzerland)
Published: November 30, 2024

Dominant RDH12-retinitis pigmentosa impairs photoreceptor development and implicates cone involvement in retinal organoids.

Dominant RDH12-retinitis pigmentosa impairs photoreceptor development and implicates cone involvement in retinal organoids.

Journal: Frontiers in cell and developmental biology
Published: October 14, 2024

Oxidative and Endoplasmic Reticulum Stress Represent Novel Therapeutic Targets for Choroideremia.

Oxidative and Endoplasmic Reticulum Stress Represent Novel Therapeutic Targets for Choroideremia.

Journal: Antioxidants (Basel, Switzerland)
Published: July 24, 2023

Loss of REP1 impacts choroidal melanogenesis and vasculogenesis in choroideremia.

Loss of REP1 impacts choroidal melanogenesis and vasculogenesis in choroideremia.

Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: June 15, 2023

Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugs.

Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugs.

Journal: Molecular therapy. Nucleic acids
Published: May 26, 2022

Choroideremia: molecular mechanisms and therapies.

Choroideremia: molecular mechanisms and therapies.

Journal: Trends in molecular medicine
Published: January 28, 2022

Identification of 4 novel human ocular coloboma genes ANK3, BMPR1B, PDGFRA, and CDH4 through evolutionary conserved vertebrate gene analysis.

Identification of 4 novel human ocular coloboma genes ANK3, BMPR1B, PDGFRA, and CDH4 through evolutionary conserved vertebrate gene analysis.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 17, 2021

Involvement of Oxidative and Endoplasmic Reticulum Stress in RDH12-Related Retinopathies.

Involvement of Oxidative and Endoplasmic Reticulum Stress in RDH12-Related Retinopathies.

Journal: International journal of molecular sciences
Published: July 20, 2021

Generation of two human iPSC lines from patients with autosomal dominant retinitis pigmentosa (UCLi014-A) and autosomal recessive Leber congenital amaurosis (UCLi015-A), associated with RDH12 variants.

Generation of two human iPSC lines from patients with autosomal dominant retinitis pigmentosa (UCLi014-A) and autosomal recessive Leber congenital amaurosis (UCLi015-A), associated with RDH12 variants.

Journal: Stem cell research
Published: May 04, 2021

Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditions.

Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditions.

Journal: Stem cell research
Published: November 21, 2020

Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6.

Generation of human iPSC line (UCLi013-A) from a patient with microphthalmia and aniridia, carrying a heterozygous missense mutation c.372C>A p.(Asn124Lys) in PAX6.

Journal: Stem cell research
Published: November 17, 2020

Novel Heterozygous Deletion in Retinol Dehydrogenase 12 (RDH12) Causes Familial Autosomal Dominant Retinitis Pigmentosa.

Novel Heterozygous Deletion in Retinol Dehydrogenase 12 (RDH12) Causes Familial Autosomal Dominant Retinitis Pigmentosa.

Journal: Frontiers in genetics
Published: January 22, 2020
Showing 1-12 of 17

Last Updated: 09/26/2026