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Publikováno v: BMJ: British Medical Journal, 1989 Nov . 299(6711), 1334-1334.

Externí odkaz: https://www.jstor.org/stable/29706131

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Insufficient Mechanical Loading Downregulates Piezo1 in Chondrocytes and Impairs Fracture Healing Through ApoE‐Induced Senescence.

Autor: Jia, Siming^1,2 (AUTHOR), Liu, Weijian³ (AUTHOR), Zhang, Mo^2,4 (AUTHOR), Wang, Lijun^5,6 (AUTHOR), Ren, Chuan¹ (AUTHOR), Feng, Chen¹ (AUTHOR), Zhang, Tao¹ (AUTHOR), Lv, Hongzhi¹ (AUTHOR), Hou, Zhiyong¹ (AUTHOR), Zou, Weiguo^5,6 (AUTHOR), Zhang, Yingze¹ (AUTHOR), Tong, Wei³ (AUTHOR) tongwei312@hust.edu.cn, Wang, Juan¹ (AUTHOR) wangj_heb3y@hebmu.edu.cn, Chen, Wei¹ (AUTHOR) 18101515@hebmu.edu.cn

Publikováno v: Advanced Science. 12/11/2024, Vol. 11 Issue 46, p1-16. 16p.

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The T‐Type Calcium Channel CACNA1H is Required for Smooth Muscle Cytoskeletal Organization During Tracheal Tubulogenesis.

Autor: Liu, Ziying^1,2 (AUTHOR), Lu, Chunyan¹ (AUTHOR), Ma, Li³ (AUTHOR), Li, Changjiang¹ (AUTHOR), Luo, Haiyun¹ (AUTHOR), Liu, Yiqi¹ (AUTHOR), Liu, Xinyuan¹ (AUTHOR), Li, Haiqing¹ (AUTHOR), Cui, Yachao¹ (AUTHOR), Zeng, Jiahang⁴ (AUTHOR), Bottasso‐Arias, Natalia⁵ (AUTHOR), Sinner, Debora⁵ (AUTHOR), Li, Le⁴ (AUTHOR), Wang, Jian¹ (AUTHOR), Stainier, Didier Y. R.⁶ (AUTHOR), Yin, Wenguang^1,2,7,8 (AUTHOR) yin_wenguang@gzhmu.edu.cn

Publikováno v: Advanced Science. Nov2024, Vol. 11 Issue 44, p1-16. 16p.

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Mechanisms of Flavonoids and Their Derivatives in Endothelial Dysfunction Induced by Oxidative Stress in Diabetes.

Autor: Dou, Baolei¹ (AUTHOR), Zhu, Yingying¹ (AUTHOR), Sun, Mengwei¹ (AUTHOR), Wang, Lina¹ (AUTHOR), Tang, Yu¹ (AUTHOR), Tian, Shuo¹ (AUTHOR), Wang, Furong¹ (AUTHOR) 60020029@sdutcm.edu.cn

Publikováno v: Molecules. Jul2024, Vol. 29 Issue 14, p3265. 32p.

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CTLA4 gene and Graves' disease: association of Graves' disease with the CTLA4 exon 1 and intron 1 polymorphisms, but not with the promoter polymorphism

Autor: B, Vaidya, E J C, Oakes, H, Imrie, A J, Dickinson, P, Perros, P, Kendall-Taylor, S H S, Pearce

Publikováno v: Clinical endocrinology. 58(6)

Recent studies have shown that Graves' disease (GD) is linked to and associated with alleles of the cytotoxic T lymphocyte antigen-4 (CTLA4) locus. However, the true pathogenic polymorphism(s) at this locus remains uncertain. Moreover, the associatio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1aa5ede24de358b0388f2842e241f66b
https://pubmed.ncbi.nlm.nih.gov/12780750

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Evidence for a Graves' disease susceptibility locus at chromosome Xp11 in a United Kingdom population

Autor: H, Imrie, B, Vaidya, P, Perros, W F, Kelly, A D, Toft, E T, Young, P, Kendall-Taylor, S H, Pearce

Publikováno v: The Journal of clinical endocrinology and metabolism. 86(2)

Graves' disease (GD), which has a strong female preponderance (female/male ratio,5:1), is inherited as a complex genetic trait. Loci for GD have started to be defined using genome-wide approaches for genetic linkage. To date, 3 loci have been confirm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6f9ce1fbb51c4b92a7c3416ff0933aad
https://pubmed.ncbi.nlm.nih.gov/11158020

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Association analysis of the cytotoxic T lymphocyte antigen-4 (CTLA-4) and autoimmune regulator-1 (AIRE-1) genes in sporadic autoimmune Addison's disease

Autor: B, Vaidya, H, Imrie, D R, Geatch, P, Perros, S G, Ball, P H, Baylis, D, Carr, S J, Hurel, R A, James, W F, Kelly, E H, Kemp, E T, Young, A P, Weetman, P, Kendall-Taylor, S H, Pearce

Publikováno v: The Journal of clinical endocrinology and metabolism. 85(2)

Although autoimmune Addison's disease (AAD) may occur as a component of the monogenic autoimmune polyendocrinopathy type 1 syndrome (APS1), it is most commonly found as an isolated disorder or associated with the autoimmune polyendocrinopathy type 2

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f26b436b23c4e8c4380c03a582483e58
https://pubmed.ncbi.nlm.nih.gov/10690877

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A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients

Autor: E H, Kemp, R A, Ajjan, E S, Husebye, P, Peterson, R, Uibo, H, Imrie, S H, Pearce, P F, Watson, A P, Weetman

Publikováno v: Clinical endocrinology. 49(5)

Recent studies have demonstrated an association between a microsatellite polymorphism of the CTLA-4 gene, specifically a 106 base pair allele, and both Graves' disease and autoimmune hypothyroidism. The aim of the present study was to determine wheth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::16c7dce8b835daf41ac4b1971d70702d
https://pubmed.ncbi.nlm.nih.gov/10197076

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