Cargando…

Human retina-in-a-dish: Unlocking the potential to study mechanisms of inherited retinal disease

Detalles Bibliográficos
Autores principales:	Yee, Tiffany, Wert, Katherine J.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	American Society of Gene & Cell Therapy 2023
Materias:	Commentary
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10485576/ https://www.ncbi.nlm.nih.gov/pubmed/37693947 http://dx.doi.org/10.1016/j.omtm.2023.08.019

Ejemplares similares

Base and Prime Editing in the Retina—From Preclinical Research toward Human Clinical Trials
por: Yee, Tiffany, et al.
Publicado: (2022)

Retinal Oxygenation in Inherited Diseases of the Retina
por: Türksever, Cengiz, et al.
Publicado: (2021)

Unlocking the potential of fungi: the QuantFung project
por: Büttel, Zsófia, et al.
Publicado: (2015)

Telling tales: unlocking the potential of AAC technologies
por: Waller, Annalu
Publicado: (2018)

Unlocking the secrets to human NTCP structure
por: Qi, Xiangbing, et al.
Publicado: (2022)

The future of non-viral gene delivery for the treatment of inherited retinal diseases
por: Sharma, Jyoti, et al.
Publicado: (2022)

Unlocking the bovine genome
por: Tellam, Ross L, et al.
Publicado: (2009)

Unlocking the gating mechanism of Kv2.1 using guangxitoxin
por: Navarro, Marco A., et al.
Publicado: (2019)

Unlocking the potential of non-coding RNAs in cancer research and therapy
por: Uppaluri, Kalyan Ram, et al.
Publicado: (2023)

Establishing Functional Retina in a Dish: Progress and Promises of Induced Pluripotent Stem Cell-Based Retinal Neuron Differentiation
por: Wong, Nonthaphat Kent, et al.
Publicado: (2023)

Unlocking the mechanisms of HCN channel gating with locked-open and locked-closed channels
por: Trudeau, Matthew C.
Publicado: (2012)

The Foundation Fighting Blindness Plays an Essential and Expansive Role in Driving Genetic Research for Inherited Retinal Diseases
por: Shaberman, Ben, et al.
Publicado: (2019)

Commentary: CRISPR gene editing for inherited retinal dystrophies: Towards clinical translation
por: Bansal, Mayank, et al.
Publicado: (2022)

Towards effective restriction of unhealthy food marketing to children: unlocking the potential of artificial intelligence
por: Olstad, Dana Lee, et al.
Publicado: (2023)

Powering up antifungal treatment: using small molecules to unlock the potential of existing therapies
por: Shapiro, Rebecca S., et al.
Publicado: (2023)

Many Keys Unlock the Doors for Virus Entry
por: Gallagher, Tom
Publicado: (2022)

Allelic Expression Imbalance in the Human Retinal Transcriptome and Potential Impact on Inherited Retinal Diseases
por: Llavona, Pablo, et al.
Publicado: (2017)

Humans in a Dish: The Potential of Organoids in Modeling Immunity and Infectious Diseases
por: Iakobachvili, Nino, et al.
Publicado: (2017)

Xtreme Everest 2: unlocking the secrets of the Sherpa phenotype?
por: Martin, Daniel S, et al.
Publicado: (2013)

Inherited Retinal Diseases
por: Ben-Yosef, Tamar
Publicado: (2022)

Modelling Charcot-Marie-Tooth disease in a dish reveals common cell type-specific alterations
por: Müller, Juliane S, et al.
Publicado: (2021)

Retinal imaging in inherited retinal diseases
por: Georgiou, Michalis, et al.
Publicado: (2020)

Acupuncture benefits for Flammer syndrome in individuals with inherited diseases of the retina
por: Blechschmidt, Tilo, et al.
Publicado: (2017)

Unlocking the potential of the UK 100,000 Genomes Project—lessons learned from analysis of the “Congenital Malformations caused by Ciliopathies” cohort
por: Best, Sunayna, et al.
Publicado: (2022)

The promise and the challenge of modelling human disease in a dish
por: Gage, Fred
Publicado: (2010)

DISH Phagia!
por: Santosh Rai, P. V.
Publicado: (2009)

Approach to inherited retinal diseases
por: Ratra, Dhanashree, et al.
Publicado: (2022)

Brain Organoids: Studying Human Brain Development and Diseases in a Dish
por: Xu, Jie, et al.
Publicado: (2021)

Primary and Secondary Cone Cell Death Mechanisms in Inherited Retinal Diseases and Potential Treatment Options
por: Brunet, Alicia A., et al.
Publicado: (2022)

Evaluation of gene panels for inherited cardiac disease—is less more?
por: Dooijes, D., et al.
Publicado: (2019)

Applied systems thinking: unlocking theory, evidence and practice for health policy and systems research
por: Kwamie, Aku, et al.
Publicado: (2021)

Patient-specific induced pluripotent stem cells as “disease-in-a-dish” models for inherited cardiomyopathies and channelopathies – 15 years of research
por: Micheu, Miruna Mihaela, et al.
Publicado: (2021)

ATP and Adenosine in the Retina and Retinal Diseases
por: Ye, Shan-Shan, et al.
Publicado: (2021)

Commentary: Change in trends of imaging the retina
por: Ahuja, Ashish Arjun, et al.
Publicado: (2018)

Does COVID-19 Involve the Retina?
por: Karampelas, Michael, et al.
Publicado: (2020)

Unlocking the Potential of the Human Microbiome for Identifying Disease Diagnostic Biomarkers
por: Hajjo, Rima, et al.
Publicado: (2022)

Commentary on “Evidence of complement dysregulation in outer retina of Stargardt disease donor eyes”
por: Dhooge, Patty P.A., et al.
Publicado: (2021)

Gene therapy for inherited retinal diseases
por: Nuzbrokh, Yan, et al.
Publicado: (2021)

Prime Editing for Inherited Retinal Diseases
por: da Costa, Bruna Lopes, et al.
Publicado: (2021)

Structural evaluation in inherited retinal diseases
por: Daich Varela, Malena, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_0nanu710pmjdn2q5ted7dcemu1