Zobrazeno 1 - 10
of 20
pro vyhledávání: '"COX6A1"'
Autor:
Ying Jin, Zhifei Xu, Jinjin Shao, Peihua Luo, Qiaojun He, Nengming Lin, Ying Zhang, Bo Yang, Hao Yan, Jiangxia Du, Xueqin Chen
Publikováno v:
Autophagy
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Liver dysfunction is an outstanding dose-limiting toxicity of gefitinib, an EGFR (epidermal growth factor receptor)-tyrosine kinase inhibitor (TKI), in the treatment of EGFR mutation-positive non-small cell lung cancer (NSCLC). We aimed to elucidate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f9f5b3a3fe3f9d2f82c29313a045049
https://doi.org/10.1080/15548627.2020.1851492
https://doi.org/10.1080/15548627.2020.1851492
Publikováno v:
International Journal of Cancer and Biomedical Research.
Background: Many genes are involved in non-Hodgkin lymphoma (NHL)-associated translocations regulate the cell cycle, apoptosis, and lymphocyte development. NHL commonly occurs along with molecular genetic abnormalities. Certain molecular genetic abno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::454935bb45b1b01e7ad91c6ba76bce66
https://doi.org/10.21608/jcbr.2020.32420.1044
https://doi.org/10.21608/jcbr.2020.32420.1044
Autor:
Qiao Wei, Dian-Fu Chen, Yin Ma, Hong-Fu Li, Zhi-Ying Wu, Hao Yu, Ge Bai, Hai-Lin Dong, Lei Chen, Jia-Qi Li, Gong-Lu Liu
Publikováno v:
Brain : a journal of neurology. 144(8)
Sensory neuronopathies are a rare and distinct subgroup of peripheral neuropathies, characterized by degeneration of the dorsal root ganglia neurons. About 50% of sensory neuronopathies are idiopathic and genetic causes remain to be clarified. Throug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f8c1a07d04630ca3ade4953aee393d5
https://pubmed.ncbi.nlm.nih.gov/36136859
https://pubmed.ncbi.nlm.nih.gov/36136859
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
The aim of current study was to use Weighted Gene Coexpression Network Analysis (WGCNA) to identify hub genes related to the incidence and prognosis of KRAS mutant (MT) lung adenocarcinoma (L
The aim of current study was to use Weighted Gene Coexpression Network Analysis (WGCNA) to identify hub genes related to the incidence and prognosis of KRAS mutant (MT) lung adenocarcinoma (L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55e5eb5a5b496efbc24906c3e17be9f5
https://pubmed.ncbi.nlm.nih.gov/32769881
https://pubmed.ncbi.nlm.nih.gov/32769881
Autor:
Iakes Ezkurdia, Marta Loureiro, José Antonio Enríquez, Jesús Vázquez, Enrique Calvo, Nadia Mercader, Adela Guarás, Carolina García-Poyatos, Rocio Nieto-Arellano, Sara Cogliati
Publikováno v:
Nature. 539:579-582
Respiratory chain complexes can super-assemble into quaternary structures called supercomplexes that optimize cellular metabolism. The interaction between complexes III (CIII) and IV (CIV) is modulated by supercomplex assembly factor 1 (SCAF1, also k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc7f9a6b6b95035d4377098af25feef8
https://doi.org/10.1038/nature20157
https://doi.org/10.1038/nature20157
Akademický článek
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Autor:
Chikahiko Numakura, Atsushi Tanaka, Osamu Onodera, Daijiro Yanagisawa, Nobuhiro Ogawa, Satoshi Makino, Tomoya Terashima, Makiko Hayashi, Hiroshi Maegawa, Chizuru Ito, Akiko Abe, Kiyoshi Hayasaka, Gen Tamiya, Ikuo Tooyama, Masayoshi Tada, Masao Ueki, Kiyotaka Toshimori
Publikováno v:
The American Journal of Human Genetics. 95(3):294-300
Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy characterized by clinical and genetic heterogeneity. Although more than 30 loci harboring CMT-causing mutations have been identified, many other genes still remain to be discov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9992e805b8496b0bdd4eab6f4ff6a3b
Publikováno v:
Clinical Genetics. 89:512-514
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::452d7acecf589e67a0e273bfd973573c
https://doi.org/10.1111/cge.12649
https://doi.org/10.1111/cge.12649
Publikováno v:
Gene. 337:163-171
Cytochrome c oxidase (COX) is a multimeric enzyme consisting of 13 subunits that are encoded in both mitochondrial and nuclear genomes. We analyzed the promoter of the rat gene encoding the liver isoform of COX subunit VIa. Using transiently transfec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::308bd787383c484ccaf4efa2d7cc0636
https://doi.org/10.1016/j.gene.2004.04.024
https://doi.org/10.1016/j.gene.2004.04.024
Publikováno v:
Gene. 247:63-75
The human COX6A1 gene encodes the ubiquitous isoform of cytochrome c oxidase (COX) subunit VIa (VIa-L), and is located in a CpG island on chromosome 12q24.2. We compared the COX6A1 gene with the published cDNA and several ESTs and concluded that subu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::014ed728ef3862e533da2d6fb67c7168
https://doi.org/10.1016/s0378-1119(00)00121-9
https://doi.org/10.1016/s0378-1119(00)00121-9