Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Shuzhi Yang"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 12, Pp n/a-n/a (2020)
Abstract Background Waardenburg syndrome (WS) is a highly clinically and genetically heterogeneous disease. The core disease phenotypes of WS are sensorineuronal hearing loss and pigmentary disturbance, which are usually caused by the absence of neur
Externí odkaz:
https://doaj.org/article/992ef3fec5e34881b825b5c5f27ef79d
Autor:
Shuzhi Yang, Pu Dai, Xin Liu, Dongyang Kang, Xin Zhang, Weiyan Yang, Chengyong Zhou, Shiming Yang, Huijun Yuan
Publikováno v:
PLoS ONE, Vol 8, Iss 10, p e77149 (2013)
Waardenburg Syndrome (WS) is an autosomal-dominant disorder characterized by sensorineural hearing loss and pigmentary abnormalities of the eyes, hair, and skin. Microphthalmia-associated transcription factor (MITF) gene mutations account for about 1
Externí odkaz:
https://doaj.org/article/dcab0c2b627d4a3399e48a3bd5066b9a
Publikováno v:
Cellular and Molecular Biology. 68:135-140
Nowadays, the incidence and mortality of head and neck tumors are gradually increasing. Head and neck malignant tumors (such as laryngeal cancer, hypopharyngeal cancer, oral cancer, nasopharyngeal cancer, oropharyngeal cancer, and other head and neck
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84d6a64fdc19fe16b15357c6dd606ebe
https://doi.org/10.14715/cmb/2022.68.5.18
https://doi.org/10.14715/cmb/2022.68.5.18
Publikováno v:
Die Pharmazie. 75(12)
SIRT4 has been reported to be abnormally expressed in many malignant tumor tissues, but data in laryngeal squamous cell carcinoma (LSCC) is lacking. In the present study, we detected the expression of SIRT4 in 168 pairs of LSCC tissues and adjacent n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::addd64993898b55459d3a6623e440413
https://pubmed.ncbi.nlm.nih.gov/33303058
https://pubmed.ncbi.nlm.nih.gov/33303058
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Waardenburg syndrome (WS) is a highly clinically and genetically heterogeneous disease. The core disease phenotypes of WS are sensorineuronal hearing loss and pigmentary disturbance, which are usually caused by the absence of neural crest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50400daff998c950c7d9fab900077c21
https://pubmed.ncbi.nlm.nih.gov/33045145
https://pubmed.ncbi.nlm.nih.gov/33045145
Publikováno v:
Abstract- und Posterband – 91. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Welche Qualität macht den Unterschied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4624a088d7b1c4a47b4e1b8000173cc4
https://doi.org/10.1055/s-0040-1710925
https://doi.org/10.1055/s-0040-1710925
Autor:
Ke Zhou, Bocheng Ning, Zhi Xing, Wen Deng, Lin Zhang, Junliang Yang, Xiaotian Hu, Shuzhi Yang, Yingping Zou, Wei Ma, Bin Yang, Fang Yang, Yong Zhang, Zhaozhao Bi, Yongbo Yuan
Publikováno v:
Solar RRL. 6:2100838
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dffd9980bdac12aae1ded6f183c13844
https://doi.org/10.1002/solr.202100838
https://doi.org/10.1002/solr.202100838
Autor:
Lili Ke, Yongbo Yuan, Hongping Yan, Shaohua Zhang, Lin Zhang, Conghua Zhou, Xiaotian Hu, Xiangchuan Meng, Wei Ma, Shuzhi Yang, Fang Yang
Publikováno v:
Organic Electronics. 89:106027
Regulating the crystallization of donor and acceptor to maintain balanced carrier mobility is of great importance to fabricate efficient organic solar cells (OSCs). Herein, the balanced crystallinity between donor and acceptor was finely controlled i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77b5de79d4165a0fececd4d965ac2f34
https://doi.org/10.1016/j.orgel.2020.106027
https://doi.org/10.1016/j.orgel.2020.106027
Publikováno v:
Hearing Research. 333:283-294
Our previous RNA-sequencing analysis of the rat cochlear genes identified multiple biological processes and molecular pathways in the cochlear response to acoustic overstimulation. However, the biological processes and molecular pathways that are com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a899c10ec6d80ec557d82e9a62667cd
https://doi.org/10.1016/j.heares.2015.10.010
https://doi.org/10.1016/j.heares.2015.10.010
Autor:
Jonathan E. Bard, Bo Hua Hu, Qunfeng Cai, Shuzhi Yang, Weiping Yang, Jianmin Wang, Jennifer Jamison
Publikováno v:
Hearing Research. 330:78-89
Individual variation in the susceptibility of the auditory system to acoustic overstimulation has been well-documented at both the functional and structural levels. However, the molecular mechanism responsible for this variation is unclear. The curre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4b007f50dcf2e6aeba5eee6b84c07ba
https://doi.org/10.1016/j.heares.2015.04.010
https://doi.org/10.1016/j.heares.2015.04.010