Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Houbin Huang"'
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Abstract Background Von Hippel-Lindau (VHL) disease is an autosomal dominant inherited cancer syndrome, and VHL is identified as a tumor suppressor gene. The main objective of this study was to identify disease-causing mutations in a Chinese family a
Externí odkaz:
https://doaj.org/article/bc20ded54d80445994de4d0764f0f4b5
Autor:
Xiaokun Wang, Tiancheng Wang, Jiamin Wang, Yanrui Xu, Xiaojuan Ban, Houbin Huang, Zhihong Zhu, Jian Chang, Jian Jun Zhang
Publikováno v:
Computer Animation and Virtual Worlds.
Publikováno v:
Current Medical Imaging Formerly Current Medical Imaging Reviews. 18:67-73
Background: Dynamic Contrast-enhanced Magnetic Resonance Imaging (DCE-MRI) technique could not only quantify blood-retinal barrier (BRB) breakdown leading to macular edema associated with diabetes, but also provide a two-dimensional imaging method th
Autor:
Anna Majander, Neringa Jurkute, Florence Burté, Kristian Brock, Catarina João, Houbin Huang, Magella M. Neveu, Choi Mun Chan, Holly J. Duncan, Simon Kelly, Emma Burkitt-Wright, Fadil Khoyratty, Yoon Tse Lai, Mala Subash, Patrick F. Chinnery, Maria Bitner-Glindzicz, Gavin Arno, Andrew R. Webster, Anthony T. Moore, Michel Michaelides, Andrew Stockman, Anthony G. Robson, Patrick Yu-Wai-Man
center dot OBJECTIVE: To evaluate the pattern of vision loss and genotype-phenotype correlations in WFS1-associated optic neuropathy (WON).center dot DESIGN: Multicenter cohort study. center dot METHODS: The study involved 37 patients with WON carryi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0bafcd7cbf02be7d371838645096e8
http://hdl.handle.net/10138/346328
http://hdl.handle.net/10138/346328
Autor:
Chongming Song, Yanrui Xu, Xiaokun Wang, Jiamin Wang, Houbin Huang, Zhihong Zhu, Xiaojuan Ban
Publikováno v:
2021 IEEE International Conference on Bioinformatics and Biomedicine (BIBM).
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
BMC Medical Genetics
BMC Medical Genetics
Background Von Hippel-Lindau (VHL) disease is an autosomal dominant inherited cancer syndrome, and VHL is identified as a tumor suppressor gene. The main objective of this study was to identify disease-causing mutations in a Chinese family affected w
Background: Aniridia is a kind of congenital human panocular anomaly, which is related to PAX6 commonly. Methods: A Chinese Aniridia pedigree underwent ophthalmic examinations, including visual acuity, slit lamp and fundoscopy examination. The target
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fed0d7c8c00914e38a014f81cf1f5dc3
https://doi.org/10.21203/rs.3.rs-21412/v2
https://doi.org/10.21203/rs.3.rs-21412/v2
Publikováno v:
BMC Ophthalmology
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-7 (2021)
BMC Ophthalmology, Vol 21, Iss 1, Pp 1-7 (2021)
Background Aniridia is a kind of congenital human pan-ocular anomaly, which is related to PAX6 commonly. Methods The ophthalmic examinations including visual acuity, slit lamp and fundoscopy examination were performed in a Chinese aniridia pedigree.
Publikováno v:
International Journal of Ophthalmology, Vol 11, Iss 12, Pp 1916-1921 (2018)
Aim To recombine the human alpha B-crystallin (αB-crystallin) using gene cloning technology and prokaryotic expression vector and confirm the biological activity of recombinant human αB-crystallin. Methods Cloning the human αB-crystallin cDNA acco
Publikováno v:
Ophthalmic genetics. 39(3)
To describe the clinical characteristics of a Chinese family with peripheral cone dystrophy (PCD) and identify the gene mutations causing PCD.The Chinese PCD pedigree underwent comprehensive ophthalmic examinations, including visual acuity, slit lamp