Lijin Dong
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Explore the profile of Lijin Dong including associated specialties, affiliations and a list of published articles.
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69
Citations
1719
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Recent Articles
11.
Lui J, Wagner J, Zhou E, Dong L, Barnes K, Jee Y, et al.
JCI Insight
. 2023 Mar;
8(9).
PMID: 36927955
Overgrowth syndromes can be caused by pathogenic genetic variants in epigenetic writers, such as DNA and histone methyltransferases. However, no overgrowth disorder has previously been ascribed to variants in a...
12.
Ma Z, Jiao X, Agbaga M, Anderson R, Qian H, Li Q, et al.
Int J Mol Sci
. 2022 Nov;
23(21).
PMID: 36361898
Bietti crystalline corneo-retinal dystrophy (BCD) is an autosomal recessive inherited retinal dystrophy characterized by multiple shimmering yellow-white deposits in the posterior pole of the retina in association with atrophy of...
13.
Boobalan E, Thompson A, Alur R, McGaughey D, Dong L, Shih G, et al.
Invest Ophthalmol Vis Sci
. 2022 Nov;
63(12):5.
PMID: 36326727
Purpose: Uveal coloboma is a congenital eye malformation caused by failure of the optic fissure to close in early human development. Despite significant progress in identifying genes whose regulation is...
14.
Vijayasarathy C, Zeng Y, Marangoni D, Dong L, Pan Z, Simpson E, et al.
Invest Ophthalmol Vis Sci
. 2022 Oct;
63(11):8.
PMID: 36227606
Purpose: Loss of retinoschisin (RS1) function underlies X-linked retinoschisis (XLRS) pathology. In the retina, both photoreceptor inner segments and bipolar cells express RS1. However, the loss of RS1 function causes...
15.
Yu C, Yadav M, Kang M, Jittayasothorn Y, Dong L, Egwuagu C
Int J Mol Sci
. 2022 Jul;
23(15).
PMID: 35897732
Interleukin-27 is constitutively secreted by microglia in the retina or brain, and upregulation of IL-27 during neuroinflammation suppresses encephalomyelitis and autoimmune uveitis. However, while IL-35 is structurally and functionally similar...
16.
Wu K, Shepard R, Castellano D, Han W, Tian Q, Dong L, et al.
Neuropsychopharmacology
. 2022 May;
47(12):2160-2170.
PMID: 35534528
GABA-A receptors (GABARs) are crucial for development and function of the brain. Altered GABAergic transmission is hypothesized to be involved in neurodevelopmental disorders. Recently, we identified Shisa7 as a GABAR...
17.
Smith A, Advani J, Brock D, Nellissery J, Gumerson J, Dong L, et al.
BMC Biol
. 2022 Mar;
20(1):68.
PMID: 35307029
Background: Functional complexity of the eukaryotic mitochondrial proteome is augmented by independent gene acquisition from bacteria since its endosymbiotic origins. Mammalian homologs of many ancestral mitochondrial proteins have uncharacterized catalytic...
18.
Lui J, Raimann A, Hojo H, Dong L, Roschger P, Kikani B, et al.
Nat Commun
. 2022 Feb;
13(1):700.
PMID: 35121733
SP7/Osterix is a transcription factor critical for osteoblast maturation and bone formation. Homozygous loss-of-function mutations in SP7 cause osteogenesis imperfecta type XII, but neomorphic (gain-of-new-function) mutations of SP7 have not...
19.
Jiao X, Ma Z, Lei J, Liu P, Cai X, Shahi P, et al.
Front Cell Dev Biol
. 2022 Jan;
9:810020.
PMID: 35096838
We constructed and characterized knockout and conditional knockout mice for KCNJ13, encoding the inwardly rectifying K channel of the Kir superfamily Kir7.1, mutations in which cause both Snowflake Vitreoretinal Degeneration...
20.
Choi J, Yu C, Bing S, Jittayasothorn Y, Mattapallil M, Kang M, et al.
Proc Natl Acad Sci U S A
. 2021 Nov;
118(47).
PMID: 34782464
Regulatory B cells (Breg cells) that secrete IL-10 or IL-35 (i35-Breg) play key roles in regulating immunity in tumor microenvironment or during autoimmune and infectious diseases. Thus, loss of Breg...