BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

471 related articles for article (PubMed ID: 32164158)

  • 21. First report of a novel missense CLDN19 mutations causing familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a Chinese family.
    Yuan T; Pang Q; Xing X; Wang X; Li Y; Li J; Wu X; Li M; Wang O; Jiang Y; Dong J; Xia W
    Calcif Tissue Int; 2015 Apr; 96(4):265-73. PubMed ID: 25555744
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Deletion of claudin-10 (Cldn10) in the thick ascending limb impairs paracellular sodium permeability and leads to hypermagnesemia and nephrocalcinosis.
    Breiderhoff T; Himmerkus N; Stuiver M; Mutig K; Will C; Meij IC; Bachmann S; Bleich M; Willnow TE; Müller D
    Proc Natl Acad Sci U S A; 2012 Aug; 109(35):14241-6. PubMed ID: 22891322
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage.
    Klar J; Piontek J; Milatz S; Tariq M; Jameel M; Breiderhoff T; Schuster J; Fatima A; Asif M; Sher M; Mäbert K; Fromm A; Baig SM; Günzel D; Dahl N
    PLoS Genet; 2017 Jul; 13(7):e1006897. PubMed ID: 28686597
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Disease-associated mutations affect intracellular traffic and paracellular Mg2+ transport function of Claudin-16.
    Kausalya PJ; Amasheh S; Günzel D; Wurps H; Müller D; Fromm M; Hunziker W
    J Clin Invest; 2006 Apr; 116(4):878-91. PubMed ID: 16528408
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Salt and acid-base metabolism in claudin-16 knockdown mice: impact for the pathophysiology of FHHNC patients.
    Himmerkus N; Shan Q; Goerke B; Hou J; Goodenough DA; Bleich M
    Am J Physiol Renal Physiol; 2008 Dec; 295(6):F1641-7. PubMed ID: 18784260
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Claudins in barrier and transport function-the kidney.
    Gong Y; Hou J
    Pflugers Arch; 2017 Jan; 469(1):105-113. PubMed ID: 27878608
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis associated with CLDN16 mutations.
    Kang JH; Choi HJ; Cho HY; Lee JH; Ha IS; Cheong HI; Choi Y
    Pediatr Nephrol; 2005 Oct; 20(10):1490-3. PubMed ID: 16047219
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: unusual clinical associations and novel claudin16 mutation in an Egyptian family.
    Al-Haggar M; Bakr A; Tajima T; Fujieda K; Hammad A; Soliman O; Darwish A; Al-Said A; Yahia S; Abdel-Hady D
    Clin Exp Nephrol; 2009 Aug; 13(4):288-294. PubMed ID: 19165416
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Function and regulation of claudins in the thick ascending limb of Henle.
    Günzel D; Yu AS
    Pflugers Arch; 2009 May; 458(1):77-88. PubMed ID: 18795318
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations.
    Godron A; Harambat J; Boccio V; Mensire A; May A; Rigothier C; Couzi L; Barrou B; Godin M; Chauveau D; Faguer S; Vallet M; Cochat P; Eckart P; Guest G; Guigonis V; Houillier P; Blanchard A; Jeunemaitre X; Vargas-Poussou R
    Clin J Am Soc Nephrol; 2012 May; 7(5):801-9. PubMed ID: 22422540
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Claudin-19 localizes to the thick ascending limb where its expression is required for junctional claudin-16 localization.
    Dimke H; Griveau C; Ling WE; Brideau G; Cheval L; Muthan P; Müller D; Al-Shebel A; Houillier P; Prot-Bertoye C
    Ann N Y Acad Sci; 2023 Aug; 1526(1):126-137. PubMed ID: 37344378
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC): report of three cases with a novel mutation in CLDN19 gene.
    Al-Shibli A; Konrad M; Altay W; Al Masri O; Al-Gazali L; Al Attrach I
    Saudi J Kidney Dis Transpl; 2013 Mar; 24(2):338-44. PubMed ID: 23538362
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: report of three Turkish siblings.
    Peru H; Akin F; Elmas S; Elmaci AM; Konrad M
    Pediatr Nephrol; 2008 Jun; 23(6):1009-12. PubMed ID: 18253757
    [TBL] [Abstract][Full Text] [Related]  

  • 34. One gene, two paracellular ion channels-claudin-10 in the kidney.
    Milatz S; Breiderhoff T
    Pflugers Arch; 2017 Jan; 469(1):115-121. PubMed ID: 27942952
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Renal localization and function of the tight junction protein, claudin-19.
    Angelow S; El-Husseini R; Kanzawa SA; Yu AS
    Am J Physiol Renal Physiol; 2007 Jul; 293(1):F166-77. PubMed ID: 17389678
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: a case report.
    Lu J; Zhao X; Paiardini A; Lang Y; Bottillo I; Shao L
    BMC Nephrol; 2018 Jul; 19(1):181. PubMed ID: 30005619
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Phosphorylated claudin-16 interacts with Trpv5 and regulates transcellular calcium transport in the kidney.
    Hou J; Renigunta V; Nie M; Sunq A; Himmerkus N; Quintanova C; Bleich M; Renigunta A; Wolf MTF
    Proc Natl Acad Sci U S A; 2019 Sep; 116(38):19176-19186. PubMed ID: 31488724
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Methods to analyze subcellular localization and intracellular trafficking of Claudin-16.
    Kausalya PJ; Hunziker W
    Methods Mol Biol; 2011; 762():129-46. PubMed ID: 21717354
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Physiological roles of claudins in kidney tubule paracellular transport.
    Muto S
    Am J Physiol Renal Physiol; 2017 Jan; 312(1):F9-F24. PubMed ID: 27784693
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Claudin 19-based familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a sibling pair.
    Sharma S; Place E; Lord K; Leroy BP; Falk MJ; Pradhan M
    Clin Nephrol; 2016 Jun; 85(6):346-52. PubMed ID: 27007868
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 24.