Suchergebnisse - "PDE6B"

PubPharm (252)

1

Cognitive decline, Aβ pathology, and blood-brain barrier function in aged 5xFAD mice

enthalten in: Fluids and barriers of the CNS | 2024

von Nehra, G. | Promsan, S. | Yubolphan, R. | +6

2

The m6A reader YTHDC2 maintains visual function and retinal photoreceptor survival through modulating translation of PPEF2 and PDE6B

enthalten in: Journal of genetics and genomics = Yi chuan xue bao | 2024

von Yang, Y. | Jiang, X. | Chen, J. | +6

3

Cognitive decline, Aβ pathology, and blood–brain barrier function in aged 5xFAD mice

in: Fluids and Barriers of the CNS | 2024

von Geetika Nehra | Sasivimon Promsan | Ruedeemars Yubolphan | +6

4

Does Background Matter? A Comparative Characterization of Mouse Models of Autosomal Retinitis Pigmentosa rd1 and Pde6b-KO

enthalten in: International journal of molecular sciences | 2023

von Chirinskaite, A. | Rotov, A. | Ermolaeva, M. | +8

5

Identification and Characterization of Retinitis Pigmentosa in a Novel Mouse Model Caused by PDE6B-T592I

enthalten in: Biomedicines | 2023

von Xia, C. | Liu, H. | Li, M. | +3

6

High amplitude pulses on the same charge condition efficiently elicit bipolar cell-mediated retinal ganglion cell responses in the degenerate retina

enthalten in: Biomedical engineering letters | 2023

von Ahn, J. | Jeong, Y. | Cha, S. | +3

7

Characterization of a novel Pde6b-deficient rat model of retinal degeneration and treatment with adeno-associated virus (AAV) gene therapy

enthalten in: Gene therapy | 2023

von Han, I. | Wiley, L. | Ochoa, D. | +6

8

A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family

enthalten in: BMC ophthalmology | 2023

von Aziz, N. | Ullah, M. | Rashid, A. | +6

9

In vivo base editing rescues photoreceptors in a mouse model of retinitis pigmentosa

enthalten in: Molecular therapy. Nucleic acids | 2023

von Su, J. | She, K. | Song, L. | +9

10

Pseudodominant Inheritance of Retinitis Pigmentosa Due to Mutations in the Phosphodiesterase 6B Gene : A Case Report

enthalten in: Cureus | 2023

von Robles Bocanegra, A. | Tato, J. | Molina Thurin, L. | +2

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