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| description
| - artículu científicu espublizáu en 1999 (ast)
- vědecký článek publikovaný v roce 1999 (cs)
- 1999 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած (hyw)
- наукова стаття, опублікована в жовтні 1999 (uk)
- vedecký článok (publikovaný 1999/10/01) (sk)
- 1999 թվականի հոտեմբերին հրատարակված գիտական հոդված (hy)
- مقالة علمية (نشرت في أكتوبر 1999) (ar)
- научни чланак (објављен 1999/10/01) (sr)
- article scientifique publié en 1999 (fr)
- wetenschappelijk artikel (gepubliceerd op 1999/10/01) (nl)
- scientific journal article (en)
- im Oktober 1999 veröffentlichter wissenschaftlicher Artikel (de)
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| cites work
| - Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer
- Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2
- Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
- Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive
- Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride cotransporter
- Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
- Quality control in the secretory pathway: retention of a misfolded viral membrane glycoprotein involves cycling between the ER, intermediate compartment, and Golgi apparatus
- Localization of the thiazide sensitive Na-Cl cotransporter, rTSC1 in the rat kidney
- Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
- Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2
- Subunit stoichiometry of a mammalian K+ channel determined by construction of multimeric cDNAs.
- Rabbit distal convoluted tubule coexpresses NaCl cotransporter and 11 beta-hydroxysteroid dehydrogenase II mRNA.
- Molecular cloning and functional expression of the K-Cl cotransporter from rabbit, rat, and human. A new member of the cation-chloride cotransporter family
- Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain.
- Ion transporter mutations in Gitelman's and Bartter's syndromes
- Gitelman’s syndrome is genetically distinct from other forms of Bartter’s syndrome
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| author name string
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| author name string
| - R. F. Reilly
- P. Bernstein
- H. Velázquez
- D. H. Ellison
- G. V. Desir
- J. Berkman
- M. Palcso
- S. Kunchaparty
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| rdfs:label
| - Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (en)
- Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (nl)
- Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (ast)
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| skos:prefLabel
| - Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (en)
- Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (nl)
- Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (ast)
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| name
| - Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (en)
- Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (nl)
- Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (ast)
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| title
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| title
| - Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome (en)
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| DOI
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| DOI
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| DOI
| - 10.1152/AJPRENAL.1999.277.4.F643
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