Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Nina Pan"'
Autor:
Chenming Xu, Jianli Li, Songchang Chen, Xiaoqiang Cai, Ruilin Jing, Xiaomei Qin, Dong Pan, Xin Zhao, Dongyang Ma, Xiufeng Xu, Xiaojun Liu, Can Wang, Bingxin Yang, Lanlan Zhang, Shuyuan Li, Yiyao Chen, Nina Pan, Ping Tang, Jieping Song, Nian Liu, Chen Zhang, Zhiwei Zhang, Xiang Qiu, Weiliang Lu, Chunmei Ying, Xiaotian Li, Congjian Xu, Yanlin Wang, Yanting Wu, He-Feng Huang, Jinglan Zhang
Publikováno v:
Cell Discovery, Vol 8, Iss 1, Pp 1-22 (2022)
Abstract Current non-invasive prenatal screening (NIPS) analyzes circulating fetal cell-free DNA (cfDNA) in maternal peripheral blood for selected aneuploidies or microdeletion/duplication syndromes. Many genetic disorders are refractory to NIPS larg
Externí odkaz:
https://doaj.org/article/e4dc48cd6d3141a390533b0de953c394
Autor:
Nina Pan, Songchang Chen, Xiaoqiang Cai, Jianli Li, Tao Yu, He‐feng Huang, Jinglan Zhang, Chenming Xu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Background Nicolaides–Baraitser syndrome (NCBRS) is a severe neurodevelopmental disorder with multiple abnormalities. To date, all pathogenic variants in SMARCA2 causing NCBRS are de novo and most are missense variants located in the ATPas
Externí odkaz:
https://doaj.org/article/46c9bb0697304db7b5824c99b51236b4
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e17153 (2011)
Recent studies show that mutations in Leucine Rich Repeat Kinase 2 (LRRK2) are the cause of the most common inherited and some sporadic forms of Parkinson's disease (PD). The molecular mechanism underlying the pathogenic role of LRRK2 mutations in PD
Externí odkaz:
https://doaj.org/article/619458f46bb24823a815ee8740863489
Publikováno v:
PLoS ONE, Vol 6, Iss 7 (2011)
Externí odkaz:
https://doaj.org/article/73ce375ca64a4496a38129cab490bb5c
Autor:
Chenming Xu, Jinglan Zhang, Songchang Chen, Jianli Li, Xiaoqiang Cai, He-Feng Huang, Nina Pan, Tao Yu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 9, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Nicolaides–Baraitser syndrome (NCBRS) is a severe neurodevelopmental disorder with multiple abnormalities. To date, all pathogenic variants in SMARCA2 causing NCBRS are de novo and most are missense variants located in the ATPase domain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64040f39f59382d20e8d4f4f476c3715
https://doaj.org/article/46c9bb0697304db7b5824c99b51236b4
https://doaj.org/article/46c9bb0697304db7b5824c99b51236b4
Autor:
Emmanouela Leandrou, Nicolina Clemente, Adam Schaffner, Iban Ubarretxena-Belandia, Chen Yao, Zhenyu Yue, Xiaoluan Hua, Lianteng Zhi, Hui Zhang, Christopher J. H. Elliott, Nina Pan, Shu G. Chen, Xianting Li, Hardy J. Rideout, Anna Memou, Ming-Ming Zhou, Farinaz Afsari, Keita Morohashi, Yacob Gomez-Llorente, Chunyu Wang
Publikováno v:
Cell Research. 29:313-329
Missense mutations in Leucine-Rich Repeat Kinase 2 (LRRK2) cause the majority of familial and some sporadic forms of Parkinson's disease (PD). The hyperactivity of LRRK2 kinase induced by the pathogenic mutations underlies neurotoxicity, promoting th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8785ec939e0eb3b4d71a9bac98f809c
https://doi.org/10.1038/s41422-019-0153-8
https://doi.org/10.1038/s41422-019-0153-8
Autor:
Ming-Hu Han, Jing Wang, Barbara Juarez, Rachael L. Neve, Jessica J. Walsh, Xianting Li, Nina Pan, David M. Dietz, Allyson K. Friedman, Vincent Vialou, Zhenyu Yue, Dipesh Chaudhury, Stacy M. Ku
Publikováno v:
Science. 344:313-319
Resilient Hyperpolarization Despite constant exposure to all sorts of stressors, most people are resilient and do not develop depression, but we do not understand the neurophysiological underpinnings of stress resilience. Friedman et al. (p. 313 ) st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b41b6c4c12c1d06c114d9df6d3e75469
https://doi.org/10.1126/science.1249240
https://doi.org/10.1126/science.1249240
Publikováno v:
BioMetals. 20:1-11
The mechanism of cytotoxicity on liver carcinoma Bel-7402 cells induced by copper-1,10-phenanthroline, Cu(OP)2, has been studied. Cell viability and apoptotic rate were examined in cells treated with Cu(OP)2 or Cu2+ alone. It was found that the apopt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15d905251fb771aadcd1b079a4701068
https://doi.org/10.1007/s10534-006-9008-0
https://doi.org/10.1007/s10534-006-9008-0
Publikováno v:
Journal of Fluorescence. 15:841-847
Chemical unfolding of bovine testicular hyaluronidase (HAase) has been studied by fluorescence spectroscopy and Fourier transformed infrared spectroscopy (FTIR). Thermodynamic parameters were determined for unfolding HAase from changes in the intrins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6ae097aec9b8a61037b385f8aaa6d2f
https://doi.org/10.1007/s10895-005-0011-6
https://doi.org/10.1007/s10895-005-0011-6
Publikováno v:
Analytical Letters. 38:2151-2164
Adriamycin is a clinically used antitumor anthracycline antibiotic. Histone H1 is a target for the activity of anthracycline drug at the chromatin level. A new optical biosensor technique based on the resonant mirror was used to characterize interact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b79238150670ee9d476dde515771ee9
https://doi.org/10.1080/00032710500259466
https://doi.org/10.1080/00032710500259466