Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Yingyuan Guo"'
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Mutations in the STRC (MIM 606440) gene, inducing DFNB16, are considered a major cause of mild–moderate autosomal recessive non-syndromic hearing loss (ARNSHL). We conducted a systematic review and meta-analysis to determine the global
Externí odkaz:
https://doaj.org/article/74566873859a46068093f85d7f68a820
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
Extrapulmonary small cell carcinoma (EPSCC) affecting the external auditory canal (EAC) is uncommon. We herein report a case involving a 56-year-old man with EPSCC of the EAC who had a 48-year history of recurrent purulent discharge in both ears and
Externí odkaz:
https://doaj.org/article/9bf5d7df826c4d3b9f942addaeaf57ab
Publikováno v:
Transl Pediatr
BACKGROUND: Low-grade fibromyxoid sarcoma (LGFMS) is a rare soft tissue tumor with a misleadingly bland histological appearance and fully malignant behavior, typically occurring in the deep soft tissues of the proximal extremities or trunk of young a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4472153b11d7cf522963de664e6a67f
https://europepmc.org/articles/PMC9253951/
https://europepmc.org/articles/PMC9253951/
Autor:
Guofang Guan, Yingyuan Guo, Jingmao Lv, Hongen Xu, Zeming Fu, Shuang Han, Yanru Hao, Fang Guo, Jie Bai, Duo-Jiao Yu, Dejun Zhang
Publikováno v:
Translational Pediatrics. 10:378-387
Background X-linked deafness-4 (DFNX4) caused by the functional loss of the SMPX gene is one form of nonsyndromic hearing loss with postlingual onset. This study aimed to investigate the cause of X-linked inherited sensorineural nonsyndromic hearing
Publikováno v:
Tropical Journal of Pharmaceutical Research. 19:299-304
Purpose: To determine the protective effect of ethosuximide on the hearing of NOD/LtJ mice, and the underlying mechanism of action. Methods: The mice were randomly assigned to control and treatment groups (20 mice per group). Mice in the treatment gr
Publikováno v:
Journal of Cancer
TROP2 (trophoblast cell surface antigen 2) overexpression has been reported in many human cancers. The correlation between TROP2 and tumor aggressiveness has implied it could be a prognostic indicator. However, the roles of TROP2 and their underlying
Publikováno v:
Regenerative Therapy, Vol 11, Iss, Pp 282-289 (2019)
Regenerative Therapy
Regenerative Therapy
Background: Laryngeal squamous cell carcinoma (LSCC) is the common cancer with poor prognosis. Long non-coding RNA (lncRNA) ANRIL has been proven to play an important role in many cancers. However up to now, the role of ANRIL in LSCC is still poorly
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics, Vol 12 (2021)
Background: Mutations in the STRC (MIM 606440) gene, inducing DFNB16, are considered a major cause of mild–moderate autosomal recessive non-syndromic hearing loss (ARNSHL). We conducted a systematic review and meta-analysis to determine the global
Publikováno v:
Journal of Craniofacial Surgery. 31:504-506
Oncocytic Schneiderian papillomas are rare tumours which usually arise in the sinonasal region. This paper presents, to the authors' knowledge, the first reported case of oncocytic Schneiderian papilloma arising primarily from the middle ear and eust
Publikováno v:
Baltic Journal of Management. 14:698-715
Purpose The purpose of this paper is to compare the effects of equity financing and debt financing on technological innovation, and prove that the enhancement of a financing system’s risk tolerance for technological innovation can enhance the innov