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ARVO Annual Meeting Abstract July 2019

Biophysical characterization of a simultaneous interpenetrating polymer network composed of crosslinked collagen and hyaluronic acid

Krystal Ya-Fong Lai; Hyun Jong Lee; Sarah Hull; Gabriella Fernandes-Cunha; David Myung

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4097. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

Characterization of bioorthogonally crosslinked collagen gels with encapsulated corneal stromal stem cells

Sarah Hull; Gabriella Fernandes-Cunha; Ilham Putra; Medi Eslani; Ali R Djalilian; Sarah Heilshorn; David Myung

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4110. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

Effects of mesenchymal stem cells encapsulated within crosslinked collagen carrier gels on alkali burns in a corneal organ culture model

Ignacio Jesus Blanco; Gabriella Fernandes-Cunha; Sarah Hull; Hyun Jong Lee; Kyung-Sun Na; Ali R Djalilian; David Myung

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):4685. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2019

Leber Congenital Amaurosis associated with GUCY2D variants: A Retrospective Natural History Study in preparation for future Therapies.

ZAINA Ibrahim BOUZIA; Michalis Georgiou; Sarah Hull; Anthony G Robson; Andrew Webster; Alison J Hardcastle; Alessia Fiorentino; Michel Michaelides

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5421. doi: https://doi.org/

ARVO Annual Meeting Abstract July 2018

Effects of engineered cellular microenvironments on the secretome of human mesenchymal stem cells

Sarah Hull; Gabriella Fernandes-Cunha; Hyun Jong Lee; Sarah Heilshorn; David Myung

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2293. doi: https://doi.org/

Genetics November 2016

Mutations in AGBL5 , Encoding α-Tubulin Deglutamylase, Are Associated With Autosomal Recessive Retinitis Pigmentosa

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Galuh D. N. Astuti; Gavin Arno; Sarah Hull; Laurence Pierrache; Hanka Venselaar; Keren Carss; F. Lucy Raymond; Rob W. J. Collin; Sultana M. H. Faradz; L. Ingeborgh van den Born; Andrew R. Webster; Frans P. M. Cremers
TAGS: autosomal recessive inheritance, mutation, retinitis pigmentosa, tubulin, family, genes, proteins
Invest. Ophthalmol. Vis. Sci.. 2016; 57(14):6180-6187. doi: https://doi.org/10.1167/iovs.16-20148

ARVO Annual Meeting Abstract September 2016

Survey of ophthalmic and systemic features in patients with PNPLA6 -related disorders

Robert B Hufnagel; Sarah Hull; Jose Luiz Pedroso; Shuan Dai; Andrea Nemeth; Helene Dollfus; Brian Patrick Brooks; Robert Sisk; Michel Michaelides; Anthony T Moore; Zubair Ahmed

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):6564. doi: https://doi.org/

ARVO Annual Meeting Abstract September 2016

Molecular study of the MFRP gene in patients with posterior microphthalmia (MCOP) supports its role in autosomal recessive MCOP pathogenesis

Basamat Almoallem; Gavin Arno; Julie De Zaeytijd; Sarah Hull; Martina Suzani; Thomy J. L. de Ravel; Andrew Webster; Bart Peter Leroy; Tony Moore; Elfride De Baere

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):6584. doi: https://doi.org/

Genetics September 2016

Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1

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Gavin Arno; Sarah Hull; Keren Carss; Arundhati Dev-Borman; Christina Chakarova; Kinga Bujakowska; L. Ingeborgh van den Born; Anthony G. Robson; Graham E. Holder; Michel Michaelides; Frans P. M. Cremers; Eric Pierce; F. Lucy Raymond; Anthony T. Moore; Andrew R. Webster
TAGS: alleles, mutation, retinal dystrophies, homozygote
Invest. Ophthalmol. Vis. Sci.. 2016; 57(11):4806-4813. doi: https://doi.org/10.1167/iovs.16-19687

Includes: Supplemental Content

Genetics March 2016

Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140

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Sarah Hull; Nicholas Owen; Farrah Islam; Dhani Tracey-White; Vincent Plagnol; Graham E. Holder; Michel Michaelides; Keren Carss; F. Lucy Raymond; Jean-Michel Rozet; Simon C. Ramsden; Graeme C. M. Black; Isabelle Perrault; Ajoy Sarkar; Mariya Moosajee; Andrew R. Webster; Gavin Arno; Anthony T. Moore
TAGS: mutation, biological transport, family, genes, retinal dystrophies
Invest. Ophthalmol. Vis. Sci.. 2016; 57(3):1053-1062. doi: https://doi.org/10.1167/iovs.15-17976

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2015

Molecular investigation of a large UK cohort of early onset retinal dystrophy

Sarah Hull; Robert Henderson; Phillip Moradi; Graham E Holder; Michel Michaelides; Andrew Webster; Donna Mackay; Gavin Arno; Anthony T Moore; Arun Dev Borman

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2867. doi: https://doi.org/

ARVO Annual Meeting Abstract June 2015

Biallelic mutations in RBP3 encoding interphotoreceptor binding protein (IRBP) cause an early onset retinal dystrophy and high myopia

Gavin Arno; Sarah Hull; Anthony G Robson; Graham E Holder; Andrew Webster; Vincent Plagnol; Anthony T Moore

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2892. doi: https://doi.org/

Genetics April 2015

Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal Dystrophy

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Gavin Arno; Sarah Hull; Anthony G. Robson; Graham E. Holder; Michael E. Cheetham; Andrew R. Webster; Vincent Plagnol; Anthony T. Moore
TAGS: e2f1 gene, family, homozygote, mutation, mutation, nonsense, myopia, retinal dystrophies, retinol binding proteins, retinal cone, rod photoreceptors
Invest. Ophthalmol. Vis. Sci.. 2015; 56(4):2358-2365. doi: https://doi.org/10.1167/iovs.15-16520

Genetics October 2014

The Phenotypic Variability of Retinal Dystrophies Associated With Mutations in CRX , With Report of a Novel Macular Dystrophy Phenotype

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Sarah Hull; Gavin Arno; Vincent Plagnol; Sarah Chamney; Isabelle Russell-Eggitt; Dorothy Thompson; Simon C. Ramsden; Graeme C. M. Black; Anthony Robson; Graham E. Holder; Anthony T. Moore; Andrew R. Webster
TAGS: macular dystrophy, mutation, phenotype, retinal dystrophies, family
Invest. Ophthalmol. Vis. Sci.. 2014; 55(10):6934-6944. doi: https://doi.org/10.1167/iovs.14-14715

Includes: Supplemental Content

ARVO Annual Meeting Abstract April 2014

Phenotypic variability of retinal dystrophies associated with mutations in CRX: with report of a novel macular dystrophy phenotype

Sarah Hull; Gavin Arno; Sarah Chamney; Isabelle Russell-Eggitt; Anthony G Robson; Graham E Holder; Andrew Webster; Anthony T Moore

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3279. doi: https://doi.org/

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Biophysical characterization of a simultaneous interpenetrating polymer network composed of crosslinked collagen and hyaluronic acid

Characterization of bioorthogonally crosslinked collagen gels with encapsulated corneal stromal stem cells

Effects of mesenchymal stem cells encapsulated within crosslinked collagen carrier gels on alkali burns in a corneal organ culture model

Leber Congenital Amaurosis associated with GUCY2D variants: A Retrospective Natural History Study in preparation for future Therapies.

Effects of engineered cellular microenvironments on the secretome of human mesenchymal stem cells

Mutations in AGBL5 , Encoding α-Tubulin Deglutamylase, Are Associated With Autosomal Recessive Retinitis Pigmentosa

Survey of ophthalmic and systemic features in patients with PNPLA6 -related disorders

Molecular study of the MFRP gene in patients with posterior microphthalmia (MCOP) supports its role in autosomal recessive MCOP pathogenesis

Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1

Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary Transport Gene IFT140

Molecular investigation of a large UK cohort of early onset retinal dystrophy

Biallelic mutations in RBP3 encoding interphotoreceptor binding protein (IRBP) cause an early onset retinal dystrophy and high myopia

Lack of Interphotoreceptor Retinoid Binding Protein Caused by Homozygous Mutation of RBP3 Is Associated With High Myopia and Retinal Dystrophy

The Phenotypic Variability of Retinal Dystrophies Associated With Mutations in CRX , With Report of a Novel Macular Dystrophy Phenotype

Phenotypic variability of retinal dystrophies associated with mutations in CRX: with report of a novel macular dystrophy phenotype

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