Zobrazeno 1 - 4
of 4
pro vyhledávání: '"RONGKUI HUANG"'
Autor:
Haiou Yang, Lili Wang, Juan Geng, Tingting Yu, Ru-en Yao, Yongnian Shen, Lei Yin, Daming Ying, Rongkui Huang, Yunfang Zhou, Huijin Chen, Lanbo Liu, Xi Mo, Yiping Shen, Qihua Fu, Yongguo Yu
Publikováno v:
Cellular Physiology and Biochemistry, Vol 32, Iss 3, Pp 635-644 (2013)
Aims: Hypophosphatasia, a rare inherited disease characterized by defective mineralization of bone and teeth, is caused by various mutations in the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP) gene. Our aim was to determine the mutat
Externí odkaz:
https://doaj.org/article/d7abe83fc69e4dc4a0df770464cf06dc
Autor:
Lei Yin, Fuxiang Chen, Shenmei Wu, Qihua Fu, Rongkui Huang, Yunfang Zhou, Jian Wang, Huijin Chen, Daming Ying, Tingting Yu, Yongnian Shen, Yongguo Yu
Publikováno v:
Molecular Medicine Reports. 9:1191-1196
Osteopetrosis is a heritable bone disorder that exhibits highly clinical and genetical heterogeneity, and is caused by defective osteoclastic resorption. The three main forms are the autosomal recessive severe (ARO), the intermediate autosomal and th
Autor:
Daming Ying, Yongnian Shen, Lili Wang, Lei Yin, Haiou Yang, Qihua Fu, Xi Mo, Yiping Shen, Huijin Chen, Tingting Yu, Yunfang Zhou, Lanbo Liu, Yongguo Yu, Juan Geng, Ruen Yao, Rongkui Huang
Publikováno v:
Cellular Physiology and Biochemistry, Vol 32, Iss 3, Pp 635-644 (2013)
Aims: Hypophosphatasia, a rare inherited disease characterized by defective mineralization of bone and teeth, is caused by various mutations in the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSALP) gene. Our aim was to determine the mutat
Autor:
TINGTING YU, YONGGUO YU, JIAN WANG, LEI YIN, YUNFANG ZHOU, DAMING YING, RONGKUI HUANG, HUIJIN CHEN, SHENMEI WU, YONGNIAN SHEN, QIHUA FU, FUXIANG CHEN
Publikováno v:
Molecular Medicine Reports; 2014, Vol. 9 Issue 4, p1191-1196, 6p