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Hajrah Sarkar

Showing results (1-10 of 16) with videos related to

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Trends in Molecular Medicine|March 28, 2022
Choroideremia: molecular mechanisms and therapiesHajrah Sarkar, Mariya Moosajee
Experimental Eye Research|September 11, 2019
Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectivesHajrah Sarkar, Mariya Moosajee
International Journal of Molecular Sciences|August 27, 2021
Involvement of Oxidative and Endoplasmic Reticulum Stress in <i>RDH12</i>-Related RetinopathiesHajrah Sarkar, Maria Toms, Mariya Moosajee
Antioxidants (Basel, Switzerland)|September 28, 2023
Oxidative and Endoplasmic Reticulum Stress Represent Novel Therapeutic Targets for ChoroideremiaHajrah Sarkar, Manuela Lahne, Neelima Nair, et al.
Frontiers in Genetics|April 24, 2020
Novel Heterozygous Deletion in Retinol Dehydrogenase 12 (<i>RDH12</i>) Causes Familial Autosomal Dominant Retinitis PigmentosaHajrah Sarkar, Adam M Dubis, Susan Downes, et al.
Molecular Therapy. Nucleic Acids|July 24, 2023
Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugsDulce Lima Cunha, Hajrah Sarkar, Jonathan Eintracht, et al.
Angewandte Chemie (International Ed. in English)|July 13, 2017
Dynamic Equilibrium of the Aurora A Kinase Activation Loop Revealed by Single-Molecule SpectroscopyJames A H Gilburt, Hajrah Sarkar, Peter Sheldrake, et al.
Stem Cell Research|December 29, 2020
Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditionsCécile Méjécase, Philippa Harding, Hajrah Sarkar, et al.
Stem Cell Research|February 1, 2021
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 PAX6Philippa Harding, Dulce Lima Cunha, Cécile Méjécase, et al.
Stem Cell Research|July 3, 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 variantsHajrah Sarkar, Cécile Méjécase, Philippa Harding, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Trends in Molecular Medicine|March 28, 2022
Choroideremia: molecular mechanisms and therapiesHajrah Sarkar, Mariya Moosajee
Experimental Eye Research|September 11, 2019
Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectivesHajrah Sarkar, Mariya Moosajee
International Journal of Molecular Sciences|August 27, 2021
Involvement of Oxidative and Endoplasmic Reticulum Stress in <i>RDH12</i>-Related RetinopathiesHajrah Sarkar, Maria Toms, Mariya Moosajee
Antioxidants (Basel, Switzerland)|September 28, 2023
Oxidative and Endoplasmic Reticulum Stress Represent Novel Therapeutic Targets for ChoroideremiaHajrah Sarkar, Manuela Lahne, Neelima Nair, et al.
Frontiers in Genetics|April 24, 2020
Novel Heterozygous Deletion in Retinol Dehydrogenase 12 (<i>RDH12</i>) Causes Familial Autosomal Dominant Retinitis PigmentosaHajrah Sarkar, Adam M Dubis, Susan Downes, et al.
Molecular Therapy. Nucleic Acids|July 24, 2023
Restoration of functional PAX6 in aniridia patient iPSC-derived ocular tissue models using repurposed nonsense suppression drugsDulce Lima Cunha, Hajrah Sarkar, Jonathan Eintracht, et al.
Angewandte Chemie (International Ed. in English)|July 13, 2017
Dynamic Equilibrium of the Aurora A Kinase Activation Loop Revealed by Single-Molecule SpectroscopyJames A H Gilburt, Hajrah Sarkar, Peter Sheldrake, et al.
Stem Cell Research|December 29, 2020
Generation of two human control iPS cell lines (UCLi016-A and UCLi017-A) from healthy donors with no known ocular conditionsCécile Méjécase, Philippa Harding, Hajrah Sarkar, et al.
Stem Cell Research|February 1, 2021
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 PAX6Philippa Harding, Dulce Lima Cunha, Cécile Méjécase, et al.
Stem Cell Research|July 3, 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 variantsHajrah Sarkar, Cécile Méjécase, Philippa Harding, et al.
Pageof 2