Fulton Wong
Overview
Explore the profile of Fulton Wong including associated specialties, affiliations and a list of published articles.
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Articles
25
Citations
444
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0
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Recent Articles
1.
Lu Z, Hu X, Reilly J, Jia D, Liu F, Yu S, et al.
J Biol Chem
. 2019 Nov;
294(45):17167.
PMID: 31704775
No abstract available.
2.
Lu Z, Hu X, Reilly J, Jia D, Liu F, Yu S, et al.
J Biol Chem
. 2019 Aug;
294(38):13953-13963.
PMID: 31362982
Mutations in human prominin 1 (), encoding a transmembrane glycoprotein localized mainly to plasma membrane protrusions, have been reported to cause retinitis pigmentosa, macular degeneration, and cone-rod dystrophy. Although the...
3.
Qu Z, Yimer T, Xie S, Wong F, Yu S, Liu X, et al.
Biochim Biophys Acta Mol Basis Dis
. 2019 Jul;
1865(10):2694-2705.
PMID: 31348989
Leber congenital amaurosis (LCA) is the most serious form of inherited retinal dystrophy that leads to blindness or severe visual impairment within a few months after birth. Approximately 1-2% of...
4.
Xie S, Han S, Qu Z, Liu F, Li J, Yu S, et al.
Biochim Biophys Acta Mol Basis Dis
. 2019 Jan;
1865(6):1273-1283.
PMID: 30684641
Mutations in the photoreceptor cell-specific nuclear receptor gene Nr2e3 increased the number of S-cone photoreceptors in human and murine retinas and led to retinal degeneration that involved photoreceptor and non-photoreceptor...
5.
Yu S, Li C, Biswas L, Hu X, Liu F, Reilly J, et al.
Hum Mol Genet
. 2017 Apr;
26(12):2335-2345.
PMID: 28398482
In humans, CERKL mutations cause widespread retinal degeneration: early dysfunction and loss of rod and cone photoreceptors in the outer retina and, progressively, death of cells in the inner retina....
6.
7.
Shah S, Wong F, Sharp D, Vincent A
Ophthalmic Genet
. 2014 Jun;
35(4):241-7.
PMID: 24918165
Identification and classification of all retinitis pigmentosa (RP) causing mutations contribute to a better understanding of disease variants. In this report we describe a New Zealand family, of European heritage,...
8.
Li C, Wang L, Zhang J, Huang M, Wong F, Liu X, et al.
Biochim Biophys Acta
. 2014 Apr;
1842(7):1121-9.
PMID: 24735978
Mutations in the ceramide kinase-like gene (CERKL) are associated with severe retinal degeneration. However, the exact function of the encoded protein (CERKL) remains unknown. Here we show that CERKL interacts...
9.
Vincent A, Carroll J, Fishman G, Sauer A, Sharp D, Summerfelt P, et al.
Transl Vis Sci Technol
. 2013 Sep;
2(2):4.
PMID: 24049715
Purpose: To ascertain the potential pathogenicity of a retinitis pigmentosa (RP)-causing F45L allele in a family affected by congenital achromatopsia (ACHM). Methods: Case series/observational study that included two patients with...
10.
Liu F, Li P, Liu Y, Li W, Wong F, Du R, et al.
Mol Vis
. 2013 Apr;
19:695-701.
PMID: 23559863
Purpose: To identify the disease-causing mutation(s) in a Chinese family with autosomal recessive Usher syndrome type 1 (USH1). Methods: An ophthalmic examination and an audiometric test were conducted to ascertain...