Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Er-Zhi Gao"'
Autor:
Jian-Hong Liu, Xiu-Xiu Wei, Ang Li, Ying-Xia Cui, Xin-Yi Xia, Wei-Song Qin, Ming-Chao Zhang, Er-Zhi Gao, Jun Sun, Chun-Lin Gao, Feng-Xia Liu, Qiu-Yue Wu, Wei-Wei Li, Asan, Zhi-Hong Liu, Xiao-Jun Li
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177685 (2017)
Alport syndrome (AS) is a clinically and genetically heterogeneous, progressive nephropathy caused by mutations in COL4A3, COL4A4, and COL4A5, which encode type IV collagen. The large sizes of these genes and the absence of mutation hot spots have co
Externí odkaz:
https://doaj.org/article/5d8fd1cbfd01476ca700cca2280e75f4
Autor:
Ying-Xia Cui, Xin-Yi Xia, Xiao-Jun Li, Er-Zhi Gao, Xiu-Xiu Wei, Ang Li, Xing Lv, Zheng-Kun Xia, Zhi-Hong Liu, Chun-Lin Gao, Jian-Hong Liu, Feng-Xia Liu, Asan
Publikováno v:
Cytogenetic and Genome Research. 154:30-36
Thin basement membrane nephropathy (TBMN), autosomal dominant Alport syndrome (ADAS), and focal segmental glomerulosclerosis (FSGS) are kidney diseases that differ in clinical diagnosis, treatment, and prognosis. Nevertheless, they may result from th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d06b584dbd46e4f5909deac556e342b1
https://doi.org/10.1159/000486979
https://doi.org/10.1159/000486979
Autor:
Zhi-Hong Liu, Ying-Xia Cui, Jian-Hong Liu, Asan, Xing Lv, Er-Zhi Gao, Ang Li, Feng-Xia Liu, Xiu-Xiu Wei, Chun-Lin Gao, Zheng-Kun Xia, Xin-Yi Xia, Xiao-Jun Li
Publikováno v:
Cytogenetic and Genome Research. 154:132-136
Mutations in the COL4A5 gene result in X-linked Alport syndrome, homozygous or compound heterozygous mutations in COL4A3 or COL4A4 are responsible for autosomal recessive Alport syndrome, and heterozygous mutations in COL4A3 or COL4A4 cause autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cadacf7bbaa797a42424d38e0bb5c779
https://doi.org/10.1159/000488163
https://doi.org/10.1159/000488163
Autor:
Ang, Li, Ying-Xia, Cui, Xing, Lv, Jian-Hong, Liu, Er-Zhi, Gao, Xiu-Xiu, Wei, Xin-Yi, Xia, Chun-Lin, Gao, Feng-Xia, Liu, Zheng-Kun, Xia, Asan, Zhi-Hong, Liu, Xiao-Jun, Li
Publikováno v:
Cytogenetic and genome research. 154(3)
Mutations in the COL4A5 gene result in X-linked Alport syndrome, homozygous or compound heterozygous mutations in COL4A3 or COL4A4 are responsible for autosomal recessive Alport syndrome, and heterozygous mutations in COL4A3 or COL4A4 cause autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8547d653d4bbb36eb576bafbae0fe15
https://pubmed.ncbi.nlm.nih.gov/29742505
https://pubmed.ncbi.nlm.nih.gov/29742505
Autor:
Ang, Li, Er-Zhi, Gao, Ying-Xia, Cui, Jian-Hong, Liu, Xing, Lv, Xiu-Xiu, Wei, Xin-Yi, Xia, Chun-Lin, Gao, Feng-Xia, Liu, Zheng-Kun, Xia, Asan, Zhi-Hong, Liu, Xiao-Jun, Li
Publikováno v:
Cytogenetic and genome research. 154(1)
Thin basement membrane nephropathy (TBMN), autosomal dominant Alport syndrome (ADAS), and focal segmental glomerulosclerosis (FSGS) are kidney diseases that differ in clinical diagnosis, treatment, and prognosis. Nevertheless, they may result from th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1d64ec8b7105378e91cde0a19f0de667
https://pubmed.ncbi.nlm.nih.gov/29669314
https://pubmed.ncbi.nlm.nih.gov/29669314
Autor:
Xiao-Jun Li, Weisong Qin, Zhihong Liu, Wei-Wei Li, Jun Sun, Jian-Hong Liu, Feng-Xia Liu, Asan, Chun-Lin Gao, Xiu-Xiu Wei, Qiu-Yue Wu, Xin-Yi Xia, Ying-Xia Cui, Ang Li, Mingchao Zhang, Er-Zhi Gao
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177685 (2017)
PLoS ONE
PLoS ONE
Alport syndrome (AS) is a clinically and genetically heterogeneous, progressive nephropathy caused by mutations in COL4A3, COL4A4, and COL4A5, which encode type IV collagen. The large sizes of these genes and the absence of mutation hot spots have co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a21344597366a7da3007a2ed99e37896
https://doi.org/10.1371/journal.pone.0177685
https://doi.org/10.1371/journal.pone.0177685