Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Shou Bin Ning"'
Publikováno v:
Gut Pathogens, Vol 16, Iss 1, Pp 1-13 (2024)
Abstract Background Recently, the oral oncobacterium Fusobacterium nucleatum (F. nucleatum), has been linked with ulcerative colitis (UC). Here, we aim to investigate whether Fecal Microbiota Transplantation (FMT) can alleviate UC by restoring gut mi
Externí odkaz:
https://doaj.org/article/57fe804a9a044157bf1d555ef321138e
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Parkinson’s disease (PD) and inflammatory bowel disease (IBD) are chronic diseases affecting the central nervous system and gastrointestinal tract, respectively. Recent research suggests a bidirectional relationship between neurodegenerati
Externí odkaz:
https://doaj.org/article/ebd22968589940eb83db7298b1dbe429
Autor:
Xin Li, Qian Wang, Li Ding, Yu-Xing Wang, Zhi-Dong Zhao, Ning Mao, Chu-Tse Wu, Hua Wang, Heng Zhu, Shou-Bin Ning
Publikováno v:
Stem Cell Research & Therapy, Vol 10, Iss 1, Pp 1-11 (2019)
Abstract Background To investigate the therapeutic effect of intercellular adhesion molecule (ICAM)-1-modified mesenchymal stem cells (MSCs) in a mouse model of inflammatory bowel disease (IBD) induced by dextran sulfate sodium. Methods Primary MSCs
Externí odkaz:
https://doaj.org/article/8366e7d965fc41b4989c6a423e728bcb
Autor:
Yu-Liang Jiang, Zi-Ye Zhao, Bai-Rong Li, Jing Li, Xiao-Wei Jin, En-Da Yu, Xiao-Dong Xu, Shou-Bin Ning
Publikováno v:
BMC Gastroenterology, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Peutz-Jeghers syndrome (PJS) is a Mendelian disease, whose causative gene is STK11, mainly characterized by gastrointestinal polyposis and increased cancer risk. Clinical observation reveals intussusception in childhood are more f
Externí odkaz:
https://doaj.org/article/381bfea82c784b8f9d25a26536963b0e
Autor:
Yu-Liang Jiang, Zi-Ye Zhao, Bai-Rong Li, Fu Yang, Jing Li, Xiao-Wei Jin, Hao Wang, En-Da Yu, Shu-Han Sun, Shou-Bin Ning
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background Peutz-Jeghers syndrome (PJS) is caused by mutations in serine/threonine kinase 11 (STK11) gene. The increased cancer risk has been connected to P53 pathway. Methods PJS probands with STK11 mutation were included in the function an
Externí odkaz:
https://doaj.org/article/2868c0ad04004740af160e85a4c1bd18
Publikováno v:
BMC Surgery, Vol 18, Iss 1, Pp 1-5 (2018)
Abstract Background Peutz-Jeghers syndrome (PJS) is a Mendelian disease characterized by gastrointestinal hamartomas, mucocutaneous pigmentation (MP), and increased cancer risk. Serine/threonine kinase 11 (STK11) is the only validated causative gene
Externí odkaz:
https://doaj.org/article/e2cf48625a5f4d01b5db6b9e2ed6905f
Autor:
Zi-Ye Zhao, Yu-Liang Jiang, Bai-Rong Li, Fu Yang, Jing Li, Xiao-Wei Jin, Shou-Bin Ning, Shu-Han Sun
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-6 (2017)
Abstract Background Peutz-Jeghers syndrome (PJS) is caused by mutations in the tumor suppressor gene, STK11, and is characterized by gastrointestinal hamartomas, melanin spots on the lips and the extremities, and an increased risk of developing cance
Externí odkaz:
https://doaj.org/article/5c6c6abd25424732ad7943191a21f44d
Publikováno v:
Journal of Digestive Diseases. 23:310-317
Linked color imaging (LCI) is a recently developed technique that emphasizes differences in mucosal color. In this study we aimed to develop a LCI classification based on the Narrow-band Imaging International Colorectal Endoscopic Classification for
Autor:
Hong-Yu Chen, Xiao-Wei Jin, Bai-Rong Li, Ming Zhu, Jing Li, Gao-Ping Mao, Ya-Fei Zhang, Shou-Bin Ning
Publikováno v:
Tumor Biology, Vol 39 (2017)
Peutz–Jeghers syndrome is a rare autosomal dominant inherited disorder characterized by mucocutaneous pigmentation and hamartomatous gastrointestinal polyposis. A growing body of evidence has shown that Peutz–Jeghers syndrome could cause an incre
Externí odkaz:
https://doaj.org/article/1a53dab67e78461ba1eb3e4d8f7e70cf
Autor:
Tao Sun, Hong-Yu Chen, Zhi-Bo Xia, Xin Yin, Bai-Rong Li, Shou-Bin Ning, Jing Zhang, Xiao-Peng Zhang, Xiao-Wei Jin
Publikováno v:
World Journal of Clinical Cases
BACKGROUND Most small intestinal lipomas are treated surgically, and some require repeated surgeries for multiple lipomas. However, application of endoscopic submucosal dissection (ESD) technology in the deep small intestine is rarely reported owing