Yuanqing Lu
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Explore the profile of Yuanqing Lu including associated specialties, affiliations and a list of published articles.
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39
Citations
625
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Recent Articles
1.
Baser O, Lu Y, Sepulveda F, Alemzadeh A, Endrizal A
J Health Econ Outcomes Res
. 2025 Mar;
12(1):86-96.
PMID: 40026366
The 2022 US Supreme Court decision in eliminated the constitutional right to abortion and activated trigger laws in 21 states, either banning or significantly restricting abortion access. This study estimated...
2.
Lu Y, Mohammad N, Lee J, Aranyos A, Serban K, Brantly M
PLoS One
. 2024 Sep;
19(9):e0310524.
PMID: 39298444
Background: Alpha-1 antitrypsin deficiency (AATD) is an inherited disease, the common variant caused by a Pi*Z mutation in the SERPINA1 gene. Pi*Z AAT increases the risk of pulmonary emphysema and...
3.
Baser O, Rodchenko K, Vivier E, Baser I, Lu Y, Mohamed M
Expert Opin Pharmacother
. 2024 Aug;
25(11):1565-1573.
PMID: 39129529
Background: Obesity has been established as a significant risk factor for osteoarthritis. Anti-obesity medications (AOMs) have demonstrated efficacy in weight management. However, potential impact on osteoarthritis risk remains uncertain. Methods:...
4.
Agrobacterium-mediated transformation of B. juncea reveals that BjuLKP2 functions in plant yellowing
Zeng J, Zhao L, Lu Y, Zuo T, Huang B, Wang D, et al.
Theor Appl Genet
. 2024 Aug;
137(9):200.
PMID: 39122841
A stable Agrobacterium-mediated transformation system was constructed for B. juncea, and BjuLKP2 was overexpressed, leading to plant yellowing. A stable and efficient transformation system is necessary to verify gene functions...
5.
Lee J, Mohammad N, Lu Y, Oshins R, Aranyos A, Brantly M
Respir Res
. 2023 Dec;
24(1):309.
PMID: 38082274
Alpha-1-antitrypsin deficiency (AATD) is a genetic disorder associated with a 5-tenfold decrease in lung levels of alpha-1-antitrypsin (AAT) and an increased risk for obstructive lung disease. α-defensins are cationic broad-spectrum...
6.
Khodayari N, Oshins R, Aranyos A, Duarte S, Mostofizadeh S, Lu Y, et al.
Am J Physiol Gastrointest Liver Physiol
. 2022 Oct;
323(6):G594-G608.
PMID: 36256438
Alpha-1 antitrypsin deficiency (AATD) is a genetic disease caused by a hepatic accumulation of mutant alpha-1 antitrypsin (ZAAT). Individuals with AATD are prone to develop a chronic liver disease that...
7.
Lu Y, Wang L, Lee J, Mohammad N, Aranyos A, Gould C, et al.
Hepatol Commun
. 2022 Aug;
6(12):3599.
PMID: 36017787
No abstract available.
8.
Lee J, Mohammad N, Lu Y, Kang K, Han K, Brantly M
JCI Insight
. 2022 Jun;
7(12).
PMID: 35730566
α-1 antitrypsin (AAT) is a serine protease inhibitor that plays a pivotal role in maintaining lung homeostasis. The most common AAT allele associated with AAT deficiency (AATD) is PiZ. Z-AAT...
9.
Lu Y, Wang L, Lee J, Mohammad N, Aranyos A, Gould C, et al.
Hepatol Commun
. 2022 May;
6(9):2354-2367.
PMID: 35621045
Alpha-1 antitrypsin (AAT) deficiency (AATD) is an inherited disease caused by mutations in the serpin family A member 1 (SERPINA1, also known as AAT) gene. The most common variant, PI*Z...
10.
Khodayari N, Wang R, Oshins R, Lu Y, Millett M, Aranyos A, et al.
Int J Mol Sci
. 2021 Dec;
22(24).
PMID: 34948056
Alpha-1 antitrypsin deficiency (AATD) is caused by a single mutation in the SERPINA1 gene, which culminates in the accumulation of misfolded alpha-1 antitrypsin (ZAAT) within the endoplasmic reticulum (ER) of...