Accès ouvert
2024
article
OpenAlex
Cheng Fu, Nan Yang, Jen-Zen Chuang, Nobuyuki Nakajima et autres
Abstract Vacuolar protein sorting 35 (VPS35), the core component of the retromer complex which regulates endosomal trafficking, is genetically linked with Parkinson’s disease (PD). Impaired vision is a common non-motor manifestation of PD. Here, we show mouse retinas with VPS35-deficient rods exhibit …
us, jp
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Eunice Sze Yin Ng, Jane Hu, Zhichun Jiang, Roxana A. Radu
Abstract Recessive Stargardt disease (STGD1) is an inherited juvenile maculopathy caused by mutations in the ABCA4 gene, for which there is no suitable treatment. Loss of functional ABCA4 in the retinal pigment epithelium (RPE) alone, without contribution from photoreceptor cells, was shown …
us
(code pays fourni par la source)
Accès ouvert
2024
article
OpenAlex
Ala Morshedian, Zhichun Jiang, Roxana A. Radu, Gordon Fain et autres
Though rod and cone photoreceptors use similar phototransduction mechanisms, previous model calculations have indicated that the most important differences in their light responses are likely to be differences in amplification of the G-protein cascade, different decay rates of phosphodiesterase (PDE) and pigment …
us
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
Eunice Ng, Nermin Kady, Jane Hu, Arpita Dave et autres
gene. The ABCA4 protein is a phospholipid-retinoid flippase in the outer segments of photoreceptors and the internal membranes of retinal pigment epithelial (RPE) cells. Here, we show that RPE cells derived via induced pluripotent stem-cell from a molecularly and clinically diagnosed STGD1 …
us, Égypte
(code pays fourni par la source)
2022
conference-paper
OpenAlex
Zhichun Jiang, Juan Li, Junfeng Wu
This paper takes 265 districts divided by New York City as the study unit and uses one month's taxi operation data of New York City to analyze the taxi travel mode and urban functional pattern of New York residents. In the orbit …
cn
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
Ailís Moran, Stephen P. Carter, Joanna J. Kaylor, Zhichun Jiang et autres
RAB28 is a farnesylated, ciliary G-protein. Patient variants in RAB28 are causative of autosomal recessive cone-rod dystrophy (CRD), an inherited human blindness. In rodent and zebrafish models, the absence of Rab28 results in diminished dawn, photoreceptor, outer segment phagocytosis (OSP). Here, we …
ie, us, nl, es
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
Anna Matynia, Jun Wang, Sangbae Kim, Yumei Li et autres
Purpose: Modern molecular genetics has revolutionized gene discovery, genetic diagnoses, and precision medicine yet many patients remain unable to benefit from these advances as disease-causing variants remain elusive for up to half of Mendelian genetic disorders. Patient-derived induced pluripotent stem (iPS) cells …
us
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Chendong Pan, Kalpita Banerjee, Guillermo L. Lehmann, Dena Almeida et autres
Lipofuscin granules enclose mixtures of cross-linked proteins and lipids in proportions that depend on the tissue analyzed. Retinal lipofuscin is unique in that it contains mostly lipids with very little proteins. However, retinal lipofuscin also presents biological and physicochemical characteristics indistinguishable from …
us, es
(code pays fourni par la source)
Accès ouvert
2021
conference-paper
OpenAlex
Yiheng Peng, Zhichun Jiang
Accurate keypoint positioning is necessary for bottom-up multi-person pose estimation methods to handle scale variation and crowdedness. In this paper, we present DoubleHigherNet: a novel network learning scale-aware and precise heatmap representation for bottom-up process using double high-resolution feature pyramids and coarse-to-fine …
cn, gb
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Arpita R. Dave, Eunice Sze Yin Ng, Zhichun Jiang, Jane Hu et autres
us
(code pays fourni par la source)
Accès ouvert
2021
article
OpenAlex
Eunice Sze Yin Ng, Jane Hu, Zhichun Jiang, Michael B. Gorin et autres
Accès ouvert
2020
article
OpenAlex
Yuan Fang, Alexander Tschulakow, Tatjana Taubitz, Barbara Illing et autres
Abstract Stargardt disease (STGD1), known as inherited retinal dystrophy, is caused by ABCA4 mutations. The pigmented Abca4 −/− mouse strain only reflects the early stage of STGD1 since it is devoid of retinal degeneration. This blue light‐illuminated pigmented Abca4 −/− mouse model …
de, us
(code pays fourni par la source)