Laran T Jensen
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Explore the profile of Laran T Jensen including associated specialties, affiliations and a list of published articles.
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39
Citations
909
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Recent Articles
1.
Sangthong J, Thuwajit C, Jensen L, Komyod W, Yuvaniyama J, Ponglikitmongkol M
Biol Cell
. 2024 Mar;
116(4):e202300072.
PMID: 38514439
Background Information: The precise etiology of breast cancer is not completely understood, although women with BRCA1 gene mutations have a significantly increased risk of developing the disease. In addition, sporadic...
2.
Wongkittichote P, Chhay C, Zerafati-Jahromi G, Weisenberg J, Mian A, Jensen L, et al.
Mol Genet Metab
. 2023 Jan;
138(3):107373.
PMID: 36680912
Multiple mitochondrial enzymes employ lipoic acid as a coenzyme. Pathogenic variants in LIAS, encoding lipoic acid synthase (LIAS), are associated with autosomal recessive LIAS-related disorder (OMIM# 614462). This disorder is...
3.
Thosapornvichai T, Huangteerakul C, Jensen A, Jensen L
Environ Toxicol Pharmacol
. 2022 Oct;
96:104000.
PMID: 36252730
Toxicity resulting from off-target effects, beyond acetylcholine esterase inhibition, for the commonly used organophosphate (OP) insecticides chlorpyrifos (CPS) and malathion (MA) was investigated using Saccharomyces cerevisiae and Caenorhabditis elegans model...
4.
Huangteerakul C, Aung H, Thosapornvichai T, Duangkaew M, Jensen A, Sukrong S, et al.
Molecules
. 2021 Mar;
26(5).
PMID: 33668176
Colorectal cancer is a common cancer worldwide and reduced expression of the DNA repair endonuclease XPF (xeroderma pigmentosum complementation group F) is associated with colorectal cancer. extracts were previously found...
5.
Novel Mutations in Waardenburg Syndrome: Functional Characterization and Genotype-Phenotype Analysis
Thongpradit S, Jinawath N, Javed A, Jensen L, Chunsuwan I, Rojnueangnit K, et al.
Front Genet
. 2020 Dec;
11:589784.
PMID: 33362852
Waardenburg syndrome (WS) is a prevalent hearing loss syndrome, concomitant with focal skin pigmentation abnormalities, blue iris, and other abnormalities of neural crest-derived cells, including Hirschsprung's disease. WS is clinically...
6.
Jain A, Nilatawong P, Mamak N, Jensen L, Jensen A
Cell Biosci
. 2020 Sep;
10:105.
PMID: 32944219
Background: Shwachman-Diamond syndrome (SDS) is a congenital disease that affects the bone marrow, skeletal system, and pancreas. The majority of patients with SDS have mutations in the gene, involved in...
7.
Thongpradit S, Jinawath N, Javed A, Noojarern S, Khongkraparn A, Tim-Aroon T, et al.
Sci Rep
. 2020 Jul;
10(1):12712.
PMID: 32728090
MITF is a known gene underlying autosomal dominant hearing loss, Waardenburg syndrome (WS). Biallelic MITF mutations have been found associated with a rare hearing loss syndrome consisting eye abnormalities and...
8.
Songdech P, Ruchala J, Semkiv M, Jensen L, Sibirny A, Ratanakhanokchai K, et al.
Biotechnol J
. 2020 Mar;
15(7):e1900492.
PMID: 32196937
Saccharomyces cerevisiae offers an attractive platform for synthesis of biofuels and biochemical; however, robust strains that can withstand high substrate concentration and fermentation conditions are required. To improve the yield...
9.
Chalermwat C, Thosapornvichai T, Jensen L, Wattanasirichaigoon D
Diseases
. 2020 Jan;
8(1).
PMID: 31936501
Citrin is a liver-specific mitochondrial aspartate-glutamate carrier encoded by . Citrin deficiency caused by mutation results in carbohydrate toxicity, citrullinemia type II, and fatty liver diseases, the mechanisms of some...
10.
Chalermwat C, Thosapornvichai T, Wongkittichote P, Phillips J, Cox J, Jensen A, et al.
FEMS Yeast Res
. 2019 Nov;
19(8).
PMID: 31711143
PEX34, encoding a peroxisomal protein implicated in regulating peroxisome numbers, was identified as a high copy suppressor, capable of bypassing impaired acetate utilization of agc1∆ yeast. However, improved growth of...