Found: 24
Select item for more details and to access through your institution.
Molecular Dynamics Simulations of the STAS Domains of Rat Prestin and Human Pendrin Reveal Conformational Motions in Conserved Flexible Regions.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2014, v. 33, n. 3, p. 605, doi. 10.1159/000358638
- By:
- Publication type:
- Article
Pendrin, a Novel Transcriptional Target of the Uroguanylin System.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2013, v. 32, n. 7, p. 221, doi. 10.1159/000356641
- By:
- Publication type:
- Article
Pendrin, a Novel Transcriptional Target of the Uroguanylin System.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2013, v. 32, p. 221, doi. 10.1159/000356641
- By:
- Publication type:
- Article
Transcriptional Regulation of the Pendrin Gene.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2011, v. 28, n. 3, p. 385, doi. 10.1159/000335100
- By:
- Publication type:
- Article
Pendrin Function and Regulation in Xenopus Oocytes.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2011, v. 28, n. 3, p. 435, doi. 10.1159/000335106
- By:
- Publication type:
- Article
Transcriptional Regulation of the Claudin-16 Gene by MgAvailability.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2010, v. 25, n. 6, p. 705, doi. 10.1159/000315090
- By:
- Publication type:
- Article
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis.
- Published in:
- Nature Genetics, 2004, v. 36, n. 6, p. 579, doi. 10.1038/ng1358
- By:
- Publication type:
- Article
Acute hemodialysis therapy in neonates with inborn errors of metabolism.
- Published in:
- Pediatric Nephrology, 2022, v. 37, n. 11, p. 2725, doi. 10.1007/s00467-022-05507-3
- By:
- Publication type:
- Article
Sodium-coupled amino acid transport in renal tubule.
- Published in:
- Kidney International, 1989, v. 36, n. 3, p. 351, doi. 10.1038/ki.1989.203
- By:
- Publication type:
- Article
Long-term hemodialysis therapy in neonates and infants with end-stage renal disease: a 16-year experience and outcome.
- Published in:
- Pediatric Nephrology, 2016, v. 31, n. 2, p. 305, doi. 10.1007/s00467-015-3214-3
- By:
- Publication type:
- Article
Mysterious hyperkalemia and cardiac arrest in a newborn infant undergoing continuous veno-venous hemofiltration dialysis: question.
- Published in:
- Pediatric Nephrology, 2008, v. 23, n. 7, p. 1053, doi. 10.1007/s00467-008-0805-2
- By:
- Publication type:
- Article
Mysterious hyperkalemia and cardiac arrest in a newborn infant undergoing continuous veno-venous hemofiltration dialysis: answer.
- Published in:
- Pediatric Nephrology, 2008, v. 23, n. 7, p. 1055, doi. 10.1007/s00467-008-0806-1
- By:
- Publication type:
- Article
Neonatal transient renal failure with renal medullary hyperechogenicity: clinical and laboratory features.
- Published in:
- Pediatric Nephrology, 2005, v. 20, n. 7, p. 904, doi. 10.1007/s00467-005-1868-y
- By:
- Publication type:
- Article
Question.
- Published in:
- Pediatric Nephrology, 2002, v. 17, n. 8, p. 695, doi. 10.1007/s00467-002-0856-8
- By:
- Publication type:
- Article
Answer.
- Published in:
- Pediatric Nephrology, 2002, v. 17, n. 8, p. 697, doi. 10.1007/s00467-002-0857-7
- By:
- Publication type:
- Article
MPGN type I induced by granulocyte colony stimulating factor.
- Published in:
- Pediatric Nephrology, 2002, v. 17, n. 5, p. 370, doi. 10.1007/s00467-002-0847-9
- By:
- Publication type:
- Article
Molecular pathophysiology of tubular transport disorders.
- Published in:
- Pediatric Nephrology, 2001, v. 16, n. 11, p. 919, doi. 10.1007/s004670100671
- By:
- Publication type:
- Article
Plasmapheresis in a very young infant with atypical hemolytic uremic syndrome.
- Published in:
- Pediatric Nephrology, 2001, v. 16, n. 1, p. 87, doi. 10.1007/s004670000485
- By:
- Publication type:
- Article
Cholelithiasis following Escherichia coli O157 : H7-associated hemolytic uremic syndrome.
- Published in:
- Pediatric Nephrology, 1998, v. 12, n. 3, p. 222, doi. 10.1007/s004670050442
- By:
- Publication type:
- Article
The claudin-16 channel gene is transcriptionally inhibited by 1,25-dihydroxyvitamin D.
- Published in:
- Experimental Physiology, 2015, v. 100, n. 1, p. 79, doi. 10.1113/expphysiol.2014.083394
- By:
- Publication type:
- Article
An infant with polydactyly and renal anomalies: early diagnosis of a rare syndrome.
- Published in:
- Nephrology Dialysis Transplantation, 2002, v. 17, n. 12, p. 2261, doi. 10.1093/ndt/17.12.2261
- By:
- Publication type:
- Article
Peritonitis in childhood renal disease.
- Published in:
- 1988
- By:
- Publication type:
- journal article
A novel missense mutation inSLC5A2encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria.
- Published in:
- Kidney International, 2005, v. 67, n. 1, p. 34, doi. 10.1111/j.1523-1755.2005.00053.x
- By:
- Publication type:
- Article
A novel mutation in the chloride channel gene, CLCNKB , as a cause of Gitelman and Bartter syndromes.
- Published in:
- Kidney International, 2003, v. 63, n. 1, p. 24, doi. 10.1046/j.1523-1755.2003.00730.x
- By:
- Publication type:
- Article