Ying Hsu

发表

The BBSome regulates mitochondria dynamics and function

V. Sheffield, D. Thedens, K. Rahmouni, 2022, Molecular metabolism.

A mouse model of Bardet-Biedl Syndrome has impaired fear memory, which is rescued by lithium treatment

V. Sheffield, J. Wemmie, C. Carter, 2020, bioRxiv.

Retinal ciliopathies through the lens of Bardet-Biedl Syndrome: Past, present and future

V. Sheffield, T. Scheetz, M. L. Tung, 2021, Progress in Retinal and Eye Research.

Photoreceptor cilia, in contrast to primary cilia, grant entry to a partially assembled BBSome.

V. Sheffield, Seongjin Seo, Ying Hsu, 2021, Human molecular genetics.

The absence of BBSome function decreases synaptogenesis and causes ectopic synapse formation in the retina

V. Sheffield, Seongjin Seo, Janelle E Garrison, 2020, Scientific Reports.

BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segment

V. Sheffield, D. Nishimura, Seongjin Seo, 2017, PLoS genetics.

Subretinal gene therapy delays vision loss in a Bardet-Biedl Syndrome type 10 mouse model

V. Sheffield, L. Vandenberghe, A. Drack, 2022, Molecular therapy. Nucleic acids.

Progressive retinal degeneration of rods and cones in a Bardet-Biedl syndrome type 10 mouse model

V. Sheffield, A. Drack, Seongjin Seo, 2022, Disease models & mechanisms.

Knockout of Bbs10 results in lack of cone electrical function and progressive retinal degeneration of rods and cones

V. Sheffield, A. Drack, Seongjin Seo, 2022, bioRxiv.

Progressive retinal degeneration of rods and cones in a Bardet-Biedl syndrome type 10 mouse model

V. Sheffield, A. Drack, Seongjin Seo, 2022, Disease Models & Mechanisms.