Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Marusia, Lilova"'
Autor:
Marusia Lilova, Alojz Gregoric, Rezan Topaloglu, Katerina Popovska-Jankovic, Esra Baskin, Emilija Golubovic, Dijana Plaseska-Karanfilska, Marjan Saraga, Velibor Tasic, Predrag Miljkovic, Radovan Bogdanovic, Ipek Akil, Alper Soylu, Emilija Sukarova Stefanovska, Snezana Pavicevic
Publikováno v:
Urolithiasis. 41:21-30
Cystinuria is an autosomal recessive disorder caused by defective transport of cystine and dibasic amino acids in the proximal renal tubules and small intestine. So far, more than 128 mutations in SLC3A1 gene, and 93 in SLC7A9 gene have been describe
Autor:
Zhizhuang Joe Zhao, Ming-Zhi Zhang, Sae Youll Cho, Ingyu Kim, Robert J. Coffey, Jikui Wang, Gilbert W. Moeckel, Dianqing Wu, Weiyi Mai, Raymond C. Harris, Matthew D. Breyer, James A. McKanna, Chuan-Ming Hao, Yasunori Sato, York Pei, Song Li, Marusia Lilova, Cunxi Li, Runxiang Zhao, Huaqi Xiong, Yasuni Nakanuma, Le Sun, Xing-Zhen Chen, Hong Wang, Yizhong Wu, Guanqing Wu
Publikováno v:
Proceedings of the National Academy of Sciences. 101:2311-2316
Mutations of the polycystic kidney and hepatic disease 1 ( PKHD1 ) gene have been shown to cause autosomal recessive polycystic kidney disease (ARPKD), but the cellular functions of the gene product (PKHD1) remain uncharacterized. To illuminate its p
Autor:
Marusia, Lilova
Publikováno v:
The Turkish journal of pediatrics.
Systemic hypertension (HTN) is one of the major problems associated with chronic renal failure (CRF). HTN is a symptom and complication of CRF. The prevalence of HTN varies with the cause of CRF. The incidence of HTN increased up to 90% with progress