Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jiayan Feng"'
Autor:
Hua Shi, Tianchao Xiang, Jiayan Feng, Xue Yang, Yaqi Li, Ye Fang, Linan Xu, Qi Qi, Jian Shen, Liangfeng Tang, Qian Shen, Xiang Wang, Hong Xu, Jia Rao
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
BackgroundCongenital anomalies of the kidneys and urinary tracts (CAKUT) represent the most prevalent cause for renal failure in children. The RNA epigenetic modification N6-methyladenosine (m6A) methylation modulates gene expression and function pos
Externí odkaz:
https://doaj.org/article/6cdb57e0bf864f8eb57704274433d235
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 4, Pp 447-448 (2021)
Externí odkaz:
https://doaj.org/article/de9f3274c63b484388d6d0f93b0db008
Publikováno v:
PeerJ, Vol 6, p e5665 (2018)
Purpose Most studies on neuroblastoma (NB) have been conducted in Western countries or Japan. The objective of our study was to analyze clinical and pathological features, MYCN status, surgical methods, and prognosis in Chinese NB patients. Methods A
Externí odkaz:
https://doaj.org/article/e71dc2906cc64360a30db575bc90a374
Publikováno v:
Pediatric Blood & Cancer.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ae36cabd4479d9add08cb6cb9773562
https://doi.org/10.1002/pbc.30348
https://doi.org/10.1002/pbc.30348
Publikováno v:
Pediatric Blood & Cancer. 70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7686aa8b80647b9c514adc3ee9ba5e3
https://doi.org/10.1002/pbc.30038
https://doi.org/10.1002/pbc.30038
Publikováno v:
Pediatric Blood & Cancer. 70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ca4789bbf76fd64f17e8b096e71db20
https://doi.org/10.1002/pbc.29935
https://doi.org/10.1002/pbc.29935
Publikováno v:
Pediatric Blood & Cancer. 70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3969f586b689e800713727aa2528b2b
https://doi.org/10.1002/pbc.29843
https://doi.org/10.1002/pbc.29843
Publikováno v:
Clinical Neuropathology. 40:36-45
Aims To analyze the clinicopathological characteristics of poorly differentiated chordomas (PDCs) with SMARCB1/INI1 loss in children. Materials Four cases of PDCs were included in the study. Methods Immunohistochemistry was performed with respect to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7119fad375ca2839a2a952ab5514021
https://doi.org/10.5414/np301277
https://doi.org/10.5414/np301277
Publikováno v:
Clinica Chimica Acta. 489:68-74
Background Sarcoidosis is a chronic noncaseating granulomatous disease with an unknown etiology that can affect multiple organs. Renal involvement in pediatric-onset adult-type sarcoidosis is rare, and only a few cases have been reported. We present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ec014aa85a84813506115669cd570e1
https://doi.org/10.1016/j.cca.2018.11.014
https://doi.org/10.1016/j.cca.2018.11.014
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 4, Pp 447-448 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b3341ad1d5aaf4c03f7530b6a500736
http://www.sciencedirect.com/science/article/pii/S187595722100022X
http://www.sciencedirect.com/science/article/pii/S187595722100022X