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Profil bibliographique

Zhichun Jiang

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

37Publications signalées
1307Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Retinal Development and DisordersRetinal Diseases and TreatmentsReceptor Mechanisms and SignalingConnexins and lens biologyNeuroscience and Neuropharmacology Research

Les publications récentes

Accès ouvert 2024 article OpenAlex

Mutant mice with rod-specific VPS35 deletion exhibit retinal α-synuclein pathology-associated degeneration

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)

8 citations Nature Communications
Accès ouvert 2024 article OpenAlex

Impaired cathepsin D in retinal pigment epithelium cells mediates Stargardt disease pathogenesis

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)

9 citations The FASEB Journal
Accès ouvert 2024 article OpenAlex

Genetic manipulation of rod-cone differences in mouse retina

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)

1 citation PLoS ONE
Accès ouvert 2022 article OpenAlex

Membrane Attack Complex Mediates Retinal Pigment Epithelium Cell Death in Stargardt Macular Degeneration

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)

27 citations Cells
2022 conference-paper OpenAlex

Research on spatial and temporal characteristics of taxi based on improved K-means with entropy weight: a perspective combined with urban functional area

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)

1 citation International Conference on Cloud Computing, Internet of Things, and Computer Applications (CICA 2022)
Accès ouvert 2022 article OpenAlex

Dawn and dusk peaks of outer segment phagocytosis, and visual cycle function require Rab28

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)

14 citations The FASEB Journal
Accès ouvert 2022 article OpenAlex

Assessing Variant Causality and Severity Using Retinal Pigment Epithelial Cells Derived from Stargardt Disease Patients

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)

10 citations Translational Vision Science & Technology
Accès ouvert 2021 article OpenAlex

Lipofuscin causes atypical necroptosis through lysosomal membrane permeabilization

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)

104 citations Proceedings of the National Academy of Sciences
Accès ouvert 2021 conference-paper OpenAlex

DoubleHigherNet: Coarse-to-Fine Precise Heatmap Bottom- Up Dynamic Pose Computer Intelligent Estimation

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)

1 citation Journal of Physics Conference Series
Accès ouvert 2020 article OpenAlex

Fundus autofluorescence, spectral‐domain optical coherence tomography, and histology correlations in a Stargardt disease mouse model

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)

21 citations The FASEB Journal

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