Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jindi Su"'
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background Hereditary hearing loss is a highly heterogeneous disorder. This study aimed to identify the genetic cause of a Chinese family with autosomal recessive non-syndromic sensorineural hearing loss (ARNSHL). Methods Clinical informatio
Externí odkaz:
https://doaj.org/article/bf632ff08bc44a9b8111e25f1762ab84
Autor:
Xi Li, Liping Lai, Jindi Su, Shiguo Chen, Sheng Lin, Baojiang Wang, Jian Gao, Linghua Zhang, Keqin Yao, Shan Duan
Publikováno v:
Journal of Diabetes Investigation, Vol 12, Iss 11, Pp 2062-2070 (2021)
Abstract Aims/Introduction Emerging evidence suggests that expression quantitative trait loci (eQTLs) are more likely to associate with complex diseases. Transient receptor potential cation channel subfamily M member 5 (TRPM5) is a ubiquitously expre
Externí odkaz:
https://doaj.org/article/94f8bb2acee64f9c9f84908d9aabf568
Autor:
Xi Li, Jindi Su, Shiguo Chen, Sheng Lin, Xiujie Zheng, Baojiang Wang, Keqin Yao, Liping Lai, Shan Duan
Publikováno v:
BMC Research Notes, Vol 13, Iss 1, Pp 1-5 (2020)
Abstract Objective The arachidonate 5-lipoxygenase (ALOX5) pathway has been investigated in diverse chronic inflammatory diseases including metabolic disorders. Recently, the ALOX5 polymorphism rs4987105 was identified to confer susceptibility to typ
Externí odkaz:
https://doaj.org/article/415bf018f15e4892a99442ee764ba551
Publikováno v:
Frontiers in Medicine, Vol 8 (2022)
Purpose: To describe the longitudinal structural changes of myopic traction maculopathy (MTM) based on optical coherence tomography (OCT) and to detect biomarkers in the evolution of MTM.Methods: A retrospective study was conducted on patients with M
Externí odkaz:
https://doaj.org/article/4f8bb82138d54a7fbc5d575a212ca19a
Autor:
Shiguo Chen, Jian Gao, Qunyan Wu, Xi Li, Sheng Lin, Jindi Su, Kaifeng Zheng, Zhaopeng Guo, Jilong Yao, Shan Duan
Publikováno v:
Human heredity.
Objective: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked genetic disorder that results in impaired enzyme activity. The G6PD/6PGD ratio assay was routinely used for G6PD deficiency screening in China, but there is an apparent def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9b44aeef7bc0d20c378dcc66af640ea
https://pubmed.ncbi.nlm.nih.gov/36315991
https://pubmed.ncbi.nlm.nih.gov/36315991
Autor:
Liping Lai, Xi Li, Xiujie Zheng, Baojiang Wang, Shiguo Chen, Keqin Yao, Sheng Lin, Jindi Su, Shan Duan
Publikováno v:
BMC Research Notes, Vol 13, Iss 1, Pp 1-5 (2020)
BMC Research Notes
BMC Research Notes
Objective The arachidonate 5-lipoxygenase (ALOX5) pathway has been investigated in diverse chronic inflammatory diseases including metabolic disorders. Recently, the ALOX5 polymorphism rs4987105 was identified to confer susceptibility to type 2 diabe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8b59c934cad3f714ee49678e8caec55
http://link.springer.com/article/10.1186/s13104-020-04953-2
http://link.springer.com/article/10.1186/s13104-020-04953-2
Autor:
Shiguo Chen, Jindi Su, Jian Gao, Qunyan Wu, Kaifeng Zheng, Duan Shan, Lin Sheng, Zhaopeng Guo
Publikováno v:
Human heredity. 85(3-6)
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is caused by one or more mutations in the G6PD gene on chromosome X. This study aimed to characterize the G6PD gene variant distribution in Shenzhen of Guangdong province. Methods: A tot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::152336101cdc0d7d91d80ac60e8c629b
https://pubmed.ncbi.nlm.nih.gov/34134107
https://pubmed.ncbi.nlm.nih.gov/34134107
Autor:
Xi, Li, Jindi, Su, Kaifeng, Zheng, Sheng, Lin, Shiguo, Chen, Baojiang, Wang, Liping, Lai, Shan, Duan
Publikováno v:
Nagoya Journal of Medical Science
Estrogen has an important role in regulating glucose homeostasis, and existing evidence indicates that it might be involved in the development of hyperglycemia in pregnancy. It mediates its effect through estrogen receptors including the nuclear rece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::37566ae81837b12bda860da98457f210
https://pubmed.ncbi.nlm.nih.gov/33311801
https://pubmed.ncbi.nlm.nih.gov/33311801
Publikováno v:
Journal of Physics: Conference Series. 1802:022054
In this paper,a convolution-mixing model of vibration signal is established according to the actual vibration signals collected by the sensor. This model is simulated and separated in P-waves and S-waves by using the frequency domain convolution blin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d088ae586d70fa92ae0585d8ba184dbc
https://doi.org/10.1088/1742-6596/1802/2/022054
https://doi.org/10.1088/1742-6596/1802/2/022054
Autor:
Madelyn Reynolds, Lindsay M. Stoy, Jindi Sun, Prince Emmanuel Opoku Amponsah, Lin Li, Misael Soto, Shang Song
Publikováno v:
Gels, Vol 10, Iss 2, p 115 (2024)
Conductive hydrogels are highly attractive for biomedical applications due to their ability to mimic the electrophysiological environment of biological tissues. Although conducting polymer polythiophene-poly-(3,4-ethylenedioxythiophene) (PEDOT) and p
Externí odkaz:
https://doaj.org/article/a03210401ade42809064d181d88564d5