Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Zi Ye Zhao"'
Autor:
Xian Hua Gao, Juan Li, Zi Ye Zhao, Xiao Dong Xu, Yi Qi Du, Hong Li Yan, Lian Jie Liu, Chen Guang Bai, Wei Zhang
Publikováno v:
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-9 (2020)
Abstract Background Juvenile polyposis syndrome (JPS) is a rare disorder characterized by the presence of multiple juvenile polyps in the gastrointestinal tract, and germline mutations in SMAD4 or BMPR1A. Due to its rarity and complex clinical manife
Externí odkaz:
https://doaj.org/article/1ba96d8183dd4439b26f8c11c5350b9d
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, 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
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:
Zi-Ye Zhao, Ye Lei, Zhao-Ming Wang, Huan Han, Jun-Jie Xing, Xiao-Dong Xu, Xian-Hua Gao, Wei Zhang, En-Da Yu
Publikováno v:
Gastroenterology Report. 11
Background Bone morphogenetic protein receptor type 1A (BMPR1A) is responsible for two individual Mendelian diseases: juvenile polyposis syndrome and hereditary mixed polyposis syndrome 2, which have overlapping phenotypes. This study aimed to elucid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84aa62084f57e20edb29432b4b2da107
https://doi.org/10.1093/gastro/goac082
https://doi.org/10.1093/gastro/goac082
Autor:
Cheng-Long Wang, Zi-Ye Zhao, Jia-Yi Wu, Fei-Hu Yan, Jie Yuan, Jun-Jie Xing, Hao Wang, En-Da Yu
Publikováno v:
Medicine; 8/25/2023, Vol. 102 Issue 34, p1-6, 6p
Autor:
Chen Guang Bai, Hong Li Yan, Xian Hua Gao, Yi Qi Du, Xiao Dong Xu, Juan Li, Wei Zhang, Lian Jie Liu, Zi Ye Zhao
Publikováno v:
BMC Gastroenterology, Vol 20, Iss 1, Pp 1-9 (2020)
BMC Gastroenterology
BMC Gastroenterology
BackgroundJuvenile polyposis syndrome (JPS) is a rare disorder characterized by the presence of multiple juvenile polyps in the gastrointestinal tract, and germline mutations in SMAD4 or BMPR1A. Due to its rarity and complex clinical manifestation, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::843a94559b809744573fe5281bb814a8
http://link.springer.com/article/10.1186/s12876-020-01238-7
http://link.springer.com/article/10.1186/s12876-020-01238-7
Publikováno v:
Gastroenterology Report. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5333b33127f85f9158829389f6d37903
https://doi.org/10.1093/gastro/goac030
https://doi.org/10.1093/gastro/goac030
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e63667402fc31d80891bebe6a786e0b9
https://doi.org/10.1186/s13023-021-01900-7
https://doi.org/10.1186/s13023-021-01900-7
Publikováno v:
Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland. 23(6)
Based on the high prevalence of endometriosis (EM) and the good chance of its deep infiltration, EM is frequently involving the colorectum and found during colonoscopy by accident. However, there are not always classical signs present on the surface
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5296f06f1f2e55df02f148fbb08aec0a
https://pubmed.ncbi.nlm.nih.gov/33751772
https://pubmed.ncbi.nlm.nih.gov/33751772