Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fenglan Peng"'
Autor:
Chang Liu, Cuicui Chen, Fenglan Peng, Huankun Liang, Shuhai Zhong, Tiancai Liu, Laiqing Li, Alexander Boronin, Wenqi Dong
Publikováno v:
BMC Biotechnology, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Carbohydrate antigen 724 (CA724) is a sensitive and specific indicator for multiple malignant tumors. The aim of this study was to establish a Eu-time resolved fluorescence immunochromatography (Eu-TRFICO) method for quantitative
Externí odkaz:
https://doaj.org/article/044d8fdb618f4128acdb15ab04a9e8ed
Autor:
Tian, Qi, Yunping Li, Rizwana Kousar, Guo, Hui, Fenglan Peng, Zheng, Yu, Xiaohua Yang, Zhigao Long, Runyi Tian, Xia, Kun, Haiying Lin, Pan, Qian
The overall statistics for variants of exome sequencing for the affected subject II:3. (DOCX 12 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73bc70792e70e2c96560d00c6b0370ef
Autor:
Tian, Qi, Yunping Li, Rizwana Kousar, Guo, Hui, Fenglan Peng, Zheng, Yu, Xiaohua Yang, Zhigao Long, Runyi Tian, Xia, Kun, Haiying Lin, Pan, Qian
Candidate variations after filtering. (DOCX 12 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b9abdba5b8dcacfd7d976196309c989
Autor:
Tian, Qi, Yunping Li, Rizwana Kousar, Guo, Hui, Fenglan Peng, Zheng, Yu, Xiaohua Yang, Zhigao Long, Runyi Tian, Xia, Kun, Haiying Lin, Pan, Qian
Filtering statistics for the SNVs and InDels called from the exome sequencing data. (DOCX 12 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bcc24680c9ade4c648ad7afeea2c1c7
Publikováno v:
Gene. 506:298-300
Multiple osteochondromas (MO), a dominantly inherited genetic disorder, is characterized by the presence of multiple osteochondromas in the long bones. EXT1 and EXT2 are the causative genes in most MO patients. We have characterized 9 MO families and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5776d46ab7530a38728c5e87cace165b
https://doi.org/10.1016/j.gene.2012.07.006
https://doi.org/10.1016/j.gene.2012.07.006
Autor:
Qi Tian, Yunping Li, Rizwana Kousar, Hui Guo, Fenglan Peng, Yu Zheng, Xiaohua Yang, Zhigao Long, Runyi Tian, Kun Xia, Haiying Lin, Qian Pan
Publikováno v:
BMC Medical Genetics; 1/7/2017, Vol. 18, p1-6, 6p
Autor:
Xiaohua Yang, Zhigao Long, Kun Xia, Qian Pan, Hui Guo, Haiying Lin, Rizwana Kousar, Runyi Tian, Fenglan Peng, Yunping Li, Qi Tian, Yu Zheng
Publikováno v:
BMC Medical Genetics
Background Nance-Horan Syndrome (NHS) (OMIM: 302350) is a rare X-linked developmental disorder characterized by bilateral congenital cataracts, with occasional dental anomalies, characteristic dysmorphic features, brachymetacarpia and mental retardat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4f65b6cdd5b3caeccddc766ea318ace