Zobrazeno 1 - 10
of 515
pro vyhledávání: '"Wei L. Fu"'
Autor:
Flores-Hernandez, Hector1 (AUTHOR), Martinez-Ledesma, Emmanuel2,3 (AUTHOR) juanemmanuel@tec.mx
Publikováno v:
Journal of Cheminformatics. 11/18/2024, Vol. 16 Issue 1, p1-25. 25p.
Autor:
Ariga, Katsuhiko1,2 (AUTHOR) ARIGA.Katsuhiko@nims.go.jp
Publikováno v:
Advanced Nanobiomed Research. Nov2024, p1. 23p. 21 Illustrations.
Autor:
Wu, Dan-ni1 (AUTHOR), Zhang, Kang-liang2 (AUTHOR), Chen, Rui-heng1 (AUTHOR), Ye, Wen-sheng1 (AUTHOR), Zheng, Chong1 (AUTHOR), Zheng, Yuan-liang1 (AUTHOR), Zhao, Xiao-dan3 (AUTHOR), Huang, Ri-sheng1 (AUTHOR) hrs9900@wmu.edu.cn
Publikováno v:
BMC Cancer. 10/29/2024, Vol. 24 Issue 1, p1-12. 12p.
Autor:
Yang, Liu1,2,3 (AUTHOR) yangliu_rachel@life.hkbu.edu.hk, Qiao, Shuangying1,2,3 (AUTHOR) qiaosysy@hkbu.edu.hk, Zhang, Ge2,3 (AUTHOR), Lu, Aiping1,2,3 (AUTHOR) aipinglu@hkbu.edu.hk, Li, Fangfei1,2,3 (AUTHOR) aipinglu@hkbu.edu.hk
Publikováno v:
International Journal of Molecular Sciences. Oct2024, Vol. 25 Issue 20, p10991. 16p.
Autor:
Rajala, Raju V. S.1,2,3,4 raju-rajala@ouhsc.edu, Rajala, Ammaji1,4
Publikováno v:
Aging & Disease. Oct2024, Vol. 15 Issue 5, p1994-2002. 9p.
Publikováno v:
Clinica Chimica Acta. 358:75-80
Background Retinoblastoma, an embryonic neoplasm of retinal origin, is the most common and severe intra-ocular tumor affecting infants and young children. Methods Loss of heterozygosity (LOH) on chromosome 13 was investigated in 16 Chinese sporadic R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5b4d0c7419a87b98e147e66bebd33f2
https://doi.org/10.1016/j.cccn.2005.02.013
https://doi.org/10.1016/j.cccn.2005.02.013
Autor:
Becker, Anna-Louisa1 (AUTHOR), Scholle, Leila2 (AUTHOR), Klause, Clara Helene1 (AUTHOR), Staege, Martin Sebastian3 (AUTHOR), Strauss, Christian1 (AUTHOR), Otto, Markus2 (AUTHOR), Rampp, Stefan1,4,5 (AUTHOR), Scheller, Christian1 (AUTHOR), Leisz, Sandra1 (AUTHOR) sandra.leisz@uk-halle.de
Publikováno v:
Cancers. Sep2024, Vol. 16 Issue 17, p3002. 22p.
Autor:
Meng, Xiaoyan1,2 (AUTHOR), Liu, Zhonglong1,2 (AUTHOR), Deng, Liang3,4 (AUTHOR), Yang, Yangzi5 (AUTHOR), Zhu, Yingchun6 (AUTHOR), Sun, Xiaoying7 (AUTHOR) xysun@shu.edu.cn, Hao, Yongqiang3,4 (AUTHOR) HAOYQ1664@sh9hospital.org.cn, He, Yue1,2 (AUTHOR) HEY1683@sh9hospital.org.cn, Fu, Jingke3,4 (AUTHOR) fujingke@sjtu.edu.cn
Publikováno v:
Advanced Science. 7/24/2024, Vol. 11 Issue 28, p1-15. 15p.
Publikováno v:
Life sciences. 78(13)
Retinitis pigmentosa is a very heterogeneous group of retinal degenerations, with multiple genes identified in each mode of inheritance. For autosomal dominant retinitis pigmentosa (ADRP), the most common gene is the rhodopsin (RHO) gene, mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8377b75bd5f06f1e1960ae00f9a7e17c
https://pubmed.ncbi.nlm.nih.gov/16229860
https://pubmed.ncbi.nlm.nih.gov/16229860
Autor:
Grochowski, Przemyslaw1 (AUTHOR) przemyslaw.grochowski@uk-augsburg.de, Grosser, Bianca1 (AUTHOR), Sommer, Florian2 (AUTHOR), Probst, Andreas3 (AUTHOR), Waidhauser, Johanna4 (AUTHOR), Schenkirsch, Gerhard5 (AUTHOR), Reitsam, Nic G.1 (AUTHOR), Märkl, Bruno1 (AUTHOR)
Publikováno v:
BMC Cancer. 6/26/2024, Vol. 24 Issue 1, p1-12. 12p.