Xuntian Jiang
Overview
Explore the profile of Xuntian Jiang including associated specialties, affiliations and a list of published articles.
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Articles
74
Citations
1987
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0
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Recent Articles
1.
Beecy S, Gross A, Maguire A, Hoffman L, Diffie E, Cuddon P, et al.
Mol Genet Metab
. 2024 Dec;
144(1):108615.
PMID: 39644670
Though it has no catalytic activity toward GM2 ganglioside, the GM2 activator protein (GM2A) is essential for ganglioside hydrolysis by facilitating the action of lysosomal ß-N-acetylhexosaminidase. GM2A deficiency results in...
2.
Mitchell J, Panni U, Fergestrom N, Toriola A, Nywening T, Goedegebuure S, et al.
Ann Surg Oncol
. 2024 Oct;
32(1):537-538.
PMID: 39453587
No abstract available.
3.
Mitchell J, Panni U, Fergestrom N, Toriola A, Nywening T, Goedegebuure S, et al.
Ann Surg Oncol
. 2024 Sep;
31(13):8725-8733.
PMID: 39306621
Background: Pancreatic ductal adenocarcinoma (PDAC) has a high fatality rate, with surgery as the only curative treatment. Identification of new biomarkers related to survival may help guide discovery of new...
4.
Mishra S, Kell P, Scherrer D, Dietzen D, Vite C, Berry-Kravis E, et al.
J Lipid Res
. 2024 Jul;
65(8):100600.
PMID: 39048052
Lysosomal function is impaired in Niemann-Pick disease type C1 (NPC1), a rare and inherited neurodegenerative disorder, resulting in late endosomal/lysosomal accumulation of unesterified cholesterol. The precise pathogenic mechanism of NPC1...
5.
Zatloukal J, Zylla S, Markus M, Ewert R, Glaser S, Volzke H, et al.
Adv Biol (Weinh)
. 2024 Feb;
8(4):e2300633.
PMID: 38342586
Ceramides and cardiorespiratory (CR) fitness are both related to cardiovascular diseases. The associations of three blood plasma ceramides (C16:0, C22:0, and C24:0) with CR fitness in the population-based Study of...
6.
Furderer M, Berhe B, Chen T, Wincovitch S, Jiang X, Tayebi N, et al.
Int J Mol Sci
. 2024 Feb;
25(3).
PMID: 38339105
Gaucher disease (GD) is a lysosomal storage disorder stemming from biallelic mutations in , characterized by glucocerebrosidase dysfunction and glucocerebroside and glucosylsphingosine accumulation. Since phenotypes of murine models of GD...
7.
Kell P, Sidhu R, Qian M, Mishra S, Nicoli E, DSouza P, et al.
EBioMedicine
. 2023 Jun;
92:104627.
PMID: 37267847
Background: GM1 gangliosidosis is a rare, fatal, neurodegenerative disease caused by mutations in the GLB1 gene and deficiency in β-galactosidase. Delay of symptom onset and increase in lifespan in a...
8.
Diaz J, Iannotti L, Dulience S, Vie S, Jiang X, Grigura V, et al.
PLOS Glob Public Health
. 2023 May;
3(5):e0001863.
PMID: 37145992
Background: Diarrheagenic Escherichia coli (DEC) are common pathogens infecting children during their growth and development. Determining the epidemiology and the impact of DEC on child anthropometric measures informs prioritization of...
9.
Gaudioso A, Jiang X, Casas J, Schuchman E, Ledesma M
Cell Death Dis
. 2023 Apr;
14(4):248.
PMID: 37024473
Acid sphingomyelinase deficiency (ASMD) is a lysosomal storage disorder caused by mutations in the SMPD1 gene encoding for the acid sphingomyelinase (ASM). While intravenous infusion of recombinant ASM is an...
10.
Nicoli E, Huebecker M, Han S, Garcia K, Munasinghe J, Lizak M, et al.
Mol Genet Metab
. 2023 Jan;
138(2):107508.
PMID: 36709532
GM1 gangliosidosis is a rare lysosomal storage disorder affecting multiple organ systems, primarily the central nervous system, and is caused by functional deficiency of β-galactosidase (GLB1). Using CRISPR/Cas9 genome editing,...