Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Yu Liang Jiang"'
Autor:
Rui Yun Zhang, Peng Cai, Ting Ting Zhang, Jie Zhu, Jian Lei Chen, Hao Wei Zhao, Yu Liang Jiang, Qi Wang, Meng Lei Zhu, Xiao Gang Zhou, Xian Lan Xiang, Fei Long Hu, Zhi Cheng Gu, Zhen Wei Zhu
Publikováno v:
BMC Pediatrics, Vol 23, Iss 1, Pp 1-10 (2023)
Abstract Background/aims To investigate the clinical situation, treatment methods, and clinical predictors of surgical intervention in children with magnetic foreign bodies in the digestive tract. Materials and methods From January 2019 to June 2022,
Externí odkaz:
https://doaj.org/article/015f961f25ee4162b67dd161c5b82f76
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-6 (2021)
Abstract Objective To report Peutz–Jeghers syndrome (PJS) cases with non-definitive clues in the family or personal history and finally diagnosed through pathological examination and STK11 gene mutation test. Clinical presentation and intervention
Externí odkaz:
https://doaj.org/article/1fbae9a5cf684cc19bd1f6ff2123ffdf
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
Publikováno v:
Shock and Vibration, Vol 2020 (2020)
Intelligent mechanical fault diagnosis has developed very fast in recent years due to the advancement and application of deep learning technologies. Thus, there are many deep learning network models that have been explored in fault classification and
Externí odkaz:
https://doaj.org/article/2b5618a9e874432180384cd67a989ad8
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
Autor:
Jie, Zhu, Xian-Lan, Xiang, Peng, Cai, Yu-Liang, Jiang, Zhen-Wei, Zhu, Fei-Long, Hu, Jiang, Wang
Publikováno v:
Transl Pediatr
BACKGROUND: Circulating RNAs (Circ-RNAs) are tightly related to the processes of neuroblastoma. The circ-ACAP2 has been reported as dysregulated in various cancers; however, its biological roles and mechanisms in neuroblastoma remain largely unclear.
Autor:
Rui-Yun Zhang, Zhenwei Zhu, Qi Wang, Jun-Gang Zhao, Xian-Lan Xiang, Zhicheng Gu, Jianlei Chen, Hao-Wei Zhao, Jie Zhu, Peng Cai, Yu-Liang Jiang, Meng-Lei Zhu
Publikováno v:
World Journal of Clinical Cases
Background Congenital biliary atresia is a type of obstruction of the bile ducts inside and outside the liver, which can lead to cholestatic liver cirrhosis and eventually liver failure. The preduodenal portal vein (PD-PV) is a rare developmental mal
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-6 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Objective To report Peutz–Jeghers syndrome (PJS) cases with non-definitive clues in the family or personal history and finally diagnosed through pathological examination and STK11 gene mutation test. Clinical presentation and intervention PJS was s