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Chronic renal failure in a boy with classic Bartter's syndrome due to a novel mutation in CLCNKB coding for the chloride channel.
Lin CM, Tsai JD, Lo YF, Yan MT, Yang SS, Lin SH. Lin CM, et al. Among authors: lo yf. Eur J Pediatr. 2009 Sep;168(9):1129-33. doi: 10.1007/s00431-008-0883-y. Epub 2008 Dec 3. Eur J Pediatr. 2009. PMID: 19050915
Severe metabolic acidosis causes early lethality in NBC1 W516X knock-in mice as a model of human isolated proximal renal tubular acidosis.
Lo YF, Yang SS, Seki G, Yamada H, Horita S, Yamazaki O, Fujita T, Usui T, Tsai JD, Yu IS, Lin SW, Lin SH. Lo YF, et al. Kidney Int. 2011 Apr;79(7):730-41. doi: 10.1038/ki.2010.523. Epub 2011 Jan 12. Kidney Int. 2011. PMID: 21228764
Recurrent deep intronic mutations in the SLC12A3 gene responsible for Gitelman's syndrome.
Lo YF, Nozu K, Iijima K, Morishita T, Huang CC, Yang SS, Sytwu HK, Fang YW, Tseng MH, Lin SH. Lo YF, et al. Clin J Am Soc Nephrol. 2011 Mar;6(3):630-9. doi: 10.2215/CJN.06730810. Epub 2010 Nov 4. Clin J Am Soc Nephrol. 2011. PMID: 21051746 Free PMC article.
SPAK-knockout mice manifest Gitelman syndrome and impaired vasoconstriction.
Yang SS, Lo YF, Wu CC, Lin SW, Yeh CJ, Chu P, Sytwu HK, Uchida S, Sasaki S, Lin SH. Yang SS, et al. Among authors: lo yf. J Am Soc Nephrol. 2010 Nov;21(11):1868-77. doi: 10.1681/ASN.2009121295. Epub 2010 Sep 2. J Am Soc Nephrol. 2010. PMID: 20813865 Free PMC article.
Generation and analysis of the thiazide-sensitive Na+ -Cl- cotransporter (Ncc/Slc12a3) Ser707X knockin mouse as a model of Gitelman syndrome.
Yang SS, Lo YF, Yu IS, Lin SW, Chang TH, Hsu YJ, Chao TK, Sytwu HK, Uchida S, Sasaki S, Lin SH. Yang SS, et al. Among authors: lo yf. Hum Mutat. 2010 Dec;31(12):1304-15. doi: 10.1002/humu.21364. Epub 2010 Oct 14. Hum Mutat. 2010. PMID: 20848653
Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome.
Cheng CJ, Lo YF, Chen JC, Huang CL, Lin SH. Cheng CJ, et al. Among authors: lo yf. J Physiol. 2017 Aug 15;595(16):5573-5586. doi: 10.1113/JP274344. Epub 2017 Jun 27. J Physiol. 2017. PMID: 28555925 Free PMC article.
Genotype and phenotype analysis of patients with sporadic periodic paralysis.
Sung CC, Cheng CJ, Lo YF, Lin MS, Yang SS, Hsu YC, Lin SH. Sung CC, et al. Among authors: lo yf. Am J Med Sci. 2012 Apr;343(4):281-5. doi: 10.1097/MAJ.0b013e31822b430c. Am J Med Sci. 2012. PMID: 21841462
Osteopontin as an injury marker expressing in epithelial hyperplasia lesions helpful in prognosis of focal segmental glomerulosclerosis.
Shui HA, Ka SM, Yang SM, Lin YF, Lo YF, Chen A. Shui HA, et al. Among authors: lo yf. Transl Res. 2007 Oct;150(4):216-22. doi: 10.1016/j.trsl.2007.04.003. Epub 2007 May 25. Transl Res. 2007. PMID: 17900509
WNK4 kinase is a physiological intracellular chloride sensor.
Chen JC, Lo YF, Lin YW, Lin SH, Huang CL, Cheng CJ. Chen JC, et al. Among authors: lo yf. Proc Natl Acad Sci U S A. 2019 Mar 5;116(10):4502-4507. doi: 10.1073/pnas.1817220116. Epub 2019 Feb 14. Proc Natl Acad Sci U S A. 2019. PMID: 30765526 Free PMC article.
First use of artificial canopy bridge by the world's most critically endangered primate the Hainan gibbon Nomascus hainanus.
Chan BPL, Lo YFP, Hong XJ, Mak CF, Ma Z. Chan BPL, et al. Among authors: lo yfp. Sci Rep. 2020 Oct 15;10(1):15176. doi: 10.1038/s41598-020-72641-z. Sci Rep. 2020. PMID: 33060683 Free PMC article.
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