Jane Sowden

Affiliations: 
Institute of Child Health University College London, London, United Kingdom 
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"Jane Sowden"
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Aldunate EZ, Di Foggia V, Di Marco F, et al. (2019) Conditional Dicer1 depletion using Chrnb4-Cre leads to cone cell death and impaired photopic vision. Scientific Reports. 9: 2314
Lakowski J, Welby E, Budinger D, et al. (2018) Isolation of Human Photoreceptor Precursors via a Cell Surface Marker Panel from Stem Cell-derived Retinal Organoids and Fetal Retinae. Stem Cells (Dayton, Ohio)
Waldron PV, Di Marco F, Kruczek K, et al. (2018) Transplanted Donor- or Stem Cell-Derived Cone Photoreceptors Can Both Integrate and Undergo Material Transfer in an Environment-Dependent Manner. Stem Cell Reports
Welby E, Lakowski J, Di Foggia V, et al. (2017) Isolation and Comparative Transcriptome Analysis of Human Fetal and iPSC-Derived Cone Photoreceptor Cells. Stem Cell Reports
Gonzalez-Cordero A, Kruczek K, Naeem A, et al. (2017) Recapitulation of Human Retinal Development from Human Pluripotent Stem Cells Generates Transplantable Populations of Cone Photoreceptors. Stem Cell Reports
Kruczek K, Gonzalez-Cordero A, Goh D, et al. (2017) Differentiation and Transplantation of Embryonic Stem Cell-Derived Cone Photoreceptors into a Mouse Model of End-Stage Retinal Degeneration. Stem Cell Reports
Di Foggia V, Makwana P, Ali RR, et al. (2016) Induced Pluripotent Stem Cell Therapies for Degenerative Disease of the Outer Retina: Disease Modeling and Cell Replacement. Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association For Ocular Pharmacology and Therapeutics
Lakowski J, Gonzalez-Cordero A, West EL, et al. (2015) Transplantation of Photoreceptor Precursors Isolated via a Cell Surface Biomarker Panel From Embryonic Stem Cell-Derived Self-Forming Retina. Stem Cells (Dayton, Ohio). 33: 2469-82
Islam L, Kelberman D, Williamson L, et al. (2015) Functional analysis of FOXE3 mutations causing dominant and recessive ocular anterior segment disease. Human Mutation. 36: 296-300
Kelberman D, Islam L, Lakowski J, et al. (2014) Mutation of SALL2 causes recessive ocular coloboma in humans and mice. Human Molecular Genetics. 23: 2511-26
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