Zobrazeno 1 - 10
of 313
pro vyhledávání: '"WenXia Song"'
Publikováno v:
Lipids in Health and Disease, Vol 23, Iss 1, Pp 1-15 (2024)
Abstract Background Gestational diabetes mellitus (GDM) is a common complication of mid–to-late pregnancy. Here, we constructed a predictive model for GDM based on a combination of clinical characteristics and relevant serum markers. Methods Data f
Externí odkaz:
https://doaj.org/article/8e976664fc0f43b58063168029131c7b
Autor:
Xiufang Feng, Jiangyuan Ping, Shan Gao, Dong Han, Wenxia Song, Xiaoze Li, Yilun Tao, Lihong Wang
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract Alagille Syndrome (ALGS) is a complex genetic disorder characterized by cholestasis, congenital cardiac anomalies, and butterfly vertebrae. The variable phenotypic expression of ALGS can lead to challenges in accurately diagnosing affected i
Externí odkaz:
https://doaj.org/article/1bc3d3cdf42e418b9de68d11607b776b
Publikováno v:
eLife, Vol 12 (2023)
Antigen-induced B-cell receptor (BCR) signaling is critical for initiating and regulating B-cell activation. The actin cytoskeleton plays essential roles in BCR signaling. Upon encountering cell-surface antigens, actin-driven B-cell spreading amplifi
Externí odkaz:
https://doaj.org/article/e4b2c0ae34a5410b8a168f0863cce1c7
Publikováno v:
Drug Delivery, Vol 30, Iss 1 (2023)
AbstractRheumatoid arthritis (RA), an autoimmune disease, is characterized by inflammatory cell infiltration that damages cartilage, disrupts bone, and impairs joint function. The therapeutic efficacy of RA treatments with the severely affected side
Externí odkaz:
https://doaj.org/article/bde61f84c1f24b9f94a73dd6aaf63103
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome is an infrequent autosomal dominant genetic disorder caused by haploinsufficiency of the GATA binding protein 3 (GATA3) gene. In this report, we present a case study of a 6-year-old fem
Externí odkaz:
https://doaj.org/article/54906215d0ca470aaeaa4b0f651005b7
Publikováno v:
Medicine; 8/16/2024, Vol. 103 Issue 33, p1-4, 4p
Publikováno v:
Journal of Medical Genetics; Aug2024, Vol. 61 Issue 8, p777-779, 20p
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Pantothenate kinase-associated neurodegeneration (PKAN) is a rare genetic neurodegenerative disorder with brain iron accumulation characterized as dysarthria, spasticity, cognitive impairment, parkinsonism, and retinopathy. PKAN is caused by bialleli
Externí odkaz:
https://doaj.org/article/d338bfb2d0b94bb6b8706f7495f27b5e
Publikováno v:
Engineering Microbiology, Vol 2, Iss 3, Pp 100038- (2022)
The recently discovered type IX secretion system (T9SS) is limited to the Bacteroidetes phylum. Cytophaga hutchinsonii, a member of the Bacteroidetes phylum widely spread in soil, has complete orthologs of T9SS components and many T9SS substrates. C.
Externí odkaz:
https://doaj.org/article/830ce76c607941ef938d3dcbd6b9c409
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 12 (2022)
Externí odkaz:
https://doaj.org/article/aed6b0d8a06e42b3b2e48b2bbec77ea9