Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rong‐Biao Ying"'
Autor:
Lin Zheng, Qian‐Qian Yu, Wen‐Bin Ruan, Jin Chen, Qing‐Hua Deng, Ke Zhang, Xu‐Li Jiang, Wen‐Jun Jiang, Dan‐Na Cai, Chen‐Jie He, Yu‐Feng Wang, Shen‐Li Jiang, Rui‐Zhi Ye, Guang‐Xian You, Rong‐Biao Ying, Zhi‐Rui Zhou
Publikováno v:
Cancer Reports, Vol 7, Iss 6, Pp n/a-n/a (2024)
ABSTRACT Background The aim was to identify the nutritional indexes, construct a prognostic model, and develop a nomogram for predicting individual survival probability in pan‐cancers. Methods Nutritional indicators, clinicopathological characteris
Externí odkaz:
https://doaj.org/article/5ee318a96ca745d49cdebcad1bde2669
Autor:
Xiao-Ping Qi, Ju-Ming Ma, Zhen-Fang Du, Rong-Biao Ying, Jun Fei, Hang-Yang Jin, Jian-Shan Han, Jin-Quan Wang, Xiao-Ling Chen, Chun-Yue Chen, Wen-Ting Liu, Jia-Jun Lu, Jian-Guo Zhang, Xian-Ning Zhang
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e20353 (2011)
BackgroundWhole exome sequencing provides a labor-saving and direct means of genetic diagnosis of hereditary disorders in which the pathogenic gene harbors a large cohort of exons. We set out to demonstrate a suitable example of genetic diagnosis of
Externí odkaz:
https://doaj.org/article/8fc832181772457c909b0e2d2860f7de
Autor:
Lin Zheng, Qian-Qian Yu, Wen-Bin Ruan, Jin Chen, Qing-Hua Deng, Ke Zhang, Xu-Li Jiang, Wen-Jun Jiang, Dan-Na Cai, Chen-Jie He, Yu-Feng Wang, Shen-Li Jiang, Ming-Cong Chen, Guang-Xian You, Rong-Biao Ying, Zhi-Rui Zhou
Background We aimed to identify the nutritional indexes, construct a prognostic model, and develop a nomogram for predicting individual survival probability in pan-cancers. Methods We collected nutritional indicators, clinicopathological characterist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8890a158051e91883adef4e7298966f5
https://doi.org/10.21203/rs.3.rs-2681088/v1
https://doi.org/10.21203/rs.3.rs-2681088/v1
miR-215 Inhibits Colorectal Cancer Cell Migration and Invasion via Targeting Stearoyl-CoA Desaturase
Publikováno v:
Computational and Mathematical Methods in Medicine, Vol 2020 (2020)
Computational and Mathematical Methods in Medicine
Computational and Mathematical Methods in Medicine
Background. This study was aimed at exploring the effects of miR-215 and its target gene stearoyl-CoA desaturase (SCD) on colorectal cancer (CRC) cell migration and invasion. Methods. Here, we analyzed the relationship between miR-215 and SCD, as wel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b8b7f3f3c1b22d8b50c6b324827e01a
https://doi.org/10.1155/2020/5807836
https://doi.org/10.1155/2020/5807836
Publikováno v:
Indian Journal of Cancer. 56:173
A 41 year old man presented with a familial history of multiple endocrine neoplasia type 2A (MEN2A) and severe hypertension. Rearranged during transfection (RET) gene sequencing confirmed a Cys634Tyr mutation of TGC to TAC. Total thyroidectomy and bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14a2dc2c4d7a1dfe2cbc54bb2ece84d2
https://doi.org/10.4103/ijc.ijc_472_18
https://doi.org/10.4103/ijc.ijc_472_18
Autor:
You-ping, Yang, Yan, Ding, Ji-rong, Wang, Ling-hui, Zeng, Hong-xia, Lin, Yang-li, Zhu, Hong-wei, Wu, Ruo-yan, Wang, Jian-min, Zhang, Rong-biao, Ying
Publikováno v:
Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences. 43(2)
To construct and identify lentiviral vector containing human ILK-shRNA and mda7 gene.Based on the human ILK gene sequences, RNAi target sequences were designed and cloned into the lentiviral vector pSicoR-eGFP by restriction endonuclease HpaI and Xho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c9a0e1c8fff22feb87b3fc945bdb98a
https://pubmed.ncbi.nlm.nih.gov/24782377
https://pubmed.ncbi.nlm.nih.gov/24782377
Autor:
Xiao-ping, Qi, Zhen-guang, Chen, Hang-yang, Jin, Feng, Li, Jun, Cheng, Rong-biao, Ying, Jian-qiang, Zhao, Ding-gang, Guo, Shi-yun, Luo, Gui-ping, Chen, Xian-ning, Zhang
Publikováno v:
Zhonghua yi xue za zhi. 93(28)
To explore the clinical patterns and clinical significance for RET screening in adrenal pheochromocytoma (PHEO) associated with multiple endocrine neoplasia type 2A (MEN2A).The clinical data of 32 PHEO patients with MEN2A from 13 unrelated MEN2A pedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da78bed8a4305fa51102302411f9af89
https://pubmed.ncbi.nlm.nih.gov/24169328
https://pubmed.ncbi.nlm.nih.gov/24169328
Autor:
Jian-qiang, Zhao, Liang, Guo, Xiao-ping, Qi, Zhen-guang, Chen, Ke-jing, Wang, Jian-lin, Lou, Xiu-hua, Yu, Jun, Cheng, Hang-yang, Jin, Xiao-long, Li, Rong-biao, Ying, Xian-ning, Zhang
Publikováno v:
Zhonghua yi xue za zhi. 93(6)
To explore the clinical characteristics, therapeutic and clinical significance for RET proto-oncogene screening in a pedigree with familial medullary thyroid carcinoma.Comprehensive medical history was obtained from 19 members in a 4-generate souther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::23d4dde33add060156f97fd4857f5397
https://pubmed.ncbi.nlm.nih.gov/23660264
https://pubmed.ncbi.nlm.nih.gov/23660264
Autor:
Yan Zhao, Chun-Yue Chen, Ju-Ming Ma, Wen-Ting Liu, Hu-Ling Jiang, Jin-Quan Wang, Jian-Shan Han, Chang-ping Yang, Jun Fei, Xian-Ning Zhang, Xiao-Ping Qi, Xiao-Ling Chen, Hai-Ping Ke, You-Ping Yang, Qi-Zhe Song, Jun Cheng, Zhen-Guang Chen, Rong-Biao Ying, Zhenfang Du, Hang-Yang Jin
Publikováno v:
Thyroid : official journal of the American Thyroid Association. 22(12)
Genetic screening for germline mutations in the RET proto-oncogene has been extensively exploited worldwide to optimize the diagnostic and clinical management of multiple endocrine neoplasia type 2 (MEN2) patients and their relatives. However, a dist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c2089494aaa2ae7c4f8aa26c77a1864
https://pubmed.ncbi.nlm.nih.gov/23210566
https://pubmed.ncbi.nlm.nih.gov/23210566
Autor:
Jianguo Zhang, Wen-Ting Liu, Zhenfang Du, Hang-Yang Jin, Jun Fei, Xiao-Ping Qi, Chun-Yue Chen, Jia-Jun Lu, Jian-Shan Han, Xiao-Ling Chen, Xian-Ning Zhang, Rong-Biao Ying, Jin-Quan Wang, Ju-Ming Ma
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e20353 (2011)
PLoS ONE
PLoS ONE
BackgroundWhole exome sequencing provides a labor-saving and direct means of genetic diagnosis of hereditary disorders in which the pathogenic gene harbors a large cohort of exons. We set out to demonstrate a suitable example of genetic diagnosis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35b3da365c51fe38d6649ca01d914bf4
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21655256/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21655256/?tool=EBI