Výsledky vyhledávání - "Ruhong Cheng"

Akademický článek

Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case report

Autor: Zhe Sun, Ruoqu Wei, Chaolan Pan, Cheng Ni, Xue Zhang, Wenbin Guan, Ruhong Cheng, Yan Gu, Hong Yu, Kejun He, Zhen Zhang, Xia Yu, Zhirong Yao

Publikováno v: Frontiers in Immunology, Vol 15 (2024)

Dedicator of cytokinesis 8 (DOCK8) deficiency represents a primary immunodeficiency with a wide range of clinical symptoms, including recurrent infections, atopy, and increased malignancy risk. This study presents a case of a 6-year-old girl with DOC

Externí odkaz: https://doaj.org/article/c115c9c292154f138b18ec37bdaa3cf8

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Akademický článek

S1P defects cause a new entity of cataract, alopecia, oral mucosal disorder, and psoriasis‐like syndrome

Publikováno v: EMBO Molecular Medicine, Vol 14, Iss 5, Pp 1-17 (2022)

Abstract In this report, we discovered a new entity named cataract, alopecia, oral mucosal disorder, and psoriasis‐like (CAOP) syndrome in two unrelated and ethnically diverse patients. Furthermore, patient 1 failed to respond to regular treatment.

Externí odkaz: https://doaj.org/article/d3fe84912aa441e5b83b8222e5b3f3c6

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Akademický článek

Exploring the SiCCT Gene Family and Its Role in Heading Date in Foxtail Millet

Autor: Congcong Li, Jian Ma, Genping Wang, Haiquan Li, Hailong Wang, Guoliang Wang, Yanmiao Jiang, Yanan Liu, Guiming Liu, Guoqing Liu, Ruhong Cheng, Huan Wang, Jianhua Wei, Lei Yao

Publikováno v: Frontiers in Plant Science, Vol 13 (2022)

CCT transcription factors are involved in the regulation of photoperiod and abiotic stress in Arabidopsis and rice. It is not clear that how CCT gene family expand and regulate heading date in foxtail millet. In this study, we conducted a systematic

Externí odkaz: https://doaj.org/article/a6364d2793d04d5da9fb1dbfb201cbf6

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Akademický článek

The first case of a mosaic superficial epidermolytic ichthyosis diagnosed by Ultra‐Deep Sequence

Autor: Yue Li, Ruhong Cheng, Jianying Liang, Zhirong Yao, Ming Li

Publikováno v: Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)

Abstract Background Superficial epidermolytic ichthyosis (SEI), known as ichthyosis bullosa of Siemens (IBS; OMIM No. 146800) before, is a type of keratinopathic ichthyosis due to the KRT2 mutations (NM_000423.3; OMIM No. 600194). Here, we report the

Externí odkaz: https://doaj.org/article/baf1146912564fd482f8ac7154ebda6d

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Akademický článek

Hypoglycemic Effect of Prolamin from Cooked Foxtail Millet (Setaria italic) on Streptozotocin-Induced Diabetic Mice

Autor: Yongxia Fu, Ruiyang Yin, Zhenyu Liu, Yan Niu, Erhu Guo, Ruhong Cheng, Xianmin Diao, Yong Xue, Qun Shen

Publikováno v: Nutrients, Vol 12, Iss 11, p 3452 (2020)

Millet proteins have been demonstrated to possess glucose-lowering and lipid metabolic disorder modulation functions against diabetes; however, the molecular mechanisms underlying their anti-diabetic effects remain unclear. The present study aimed to

Externí odkaz: https://doaj.org/article/1789b347a92149cf9ae891a77ad6f36e

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Akademický článek

Common FLG mutation K4671X not associated with atopic dermatitis in Han Chinese in a family association study.

Autor: Ruhong Cheng, Ming Li, Hui Zhang, Yifeng Guo, Xilan Chen, Jianfeng Tao, Aifang Jiang, Jiecheng Gan, Huaishan Qi, Hong Yu, Wanqing Liao, Zhirong Yao

Publikováno v: PLoS ONE, Vol 7, Iss 11, p e49158 (2012)

BACKGROUND: Filaggrin gene (FLG) mutations have been identified as the cause of ichthyosis vulgaris (IV) and major predisposing factors for atopic dermatitis (AD). The relationship among AD, IV and FLG mutations has not been clarified yet. Mutations

Externí odkaz: https://doaj.org/article/247218051c774e3bb4db94f77484a464

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