BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

277 related articles for article (PubMed ID: 29459093)

  • 1. Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).
    Neirijnck Y; Reginensi A; Renkema KY; Massa F; Kozlov VM; Dhib H; Bongers EMHF; Feitz WF; van Eerde AM; Lefebvre V; Knoers NVAM; Tabatabaei M; Schulz H; McNeill H; Schaefer F; Wegner M; Sock E; Schedl A
    Kidney Int; 2018 May; 93(5):1142-1153. PubMed ID: 29459093
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Development of the urogenital system is regulated via the 3'UTR of GDNF.
    Li H; Jakobson M; Ola R; Gui Y; Kumar A; Sipilä P; Sariola H; Kuure S; Andressoo JO
    Sci Rep; 2019 Mar; 9(1):5302. PubMed ID: 30923332
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tract.
    Du X; Wang C; Liu J; Yu M; Ju H; Xue S; Li Y; Liu J; Dai R; Chen J; Zhai Y; Rao J; Wang X; Sun Y; Sun L; Wu X; Xu H; Shen Q
    Hum Genomics; 2024 Apr; 18(1):41. PubMed ID: 38654324
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Primer on Congenital Anomalies of the Kidneys and Urinary Tracts (CAKUT).
    Murugapoopathy V; Gupta IR
    Clin J Am Soc Nephrol; 2020 May; 15(5):723-731. PubMed ID: 32188635
    [TBL] [Abstract][Full Text] [Related]  

  • 5.
    Le Tanno P; Breton J; Bidart M; Satre V; Harbuz R; Ray PF; Bosson C; Dieterich K; Jaillard S; Odent S; Poke G; Beddow R; Digilio MC; Novelli A; Bernardini L; Pisanti MA; Mackenroth L; Hackmann K; Vogel I; Christensen R; Fokstuen S; Béna F; Amblard F; Devillard F; Vieville G; Apostolou A; Jouk PS; Guebre-Egziabher F; Sartelet H; Coutton C
    J Med Genet; 2017 Jul; 54(7):502-510. PubMed ID: 28270404
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SIX1 gene: absence of mutations in children with isolated congenital anomalies of kidney and urinary tract.
    Negrisolo S; Centi S; Benetti E; Ghirardo G; Della Vella M; Murer L; Artifoni L
    J Nephrol; 2014 Dec; 27(6):667-71. PubMed ID: 24899122
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Uroplakin 1b is critical in urinary tract development and urothelial differentiation and homeostasis.
    Carpenter AR; Becknell MB; Ching CB; Cuaresma EJ; Chen X; Hains DS; McHugh KM
    Kidney Int; 2016 Mar; 89(3):612-24. PubMed ID: 26880456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New congenital anomalies of the kidney and urinary tract and outcomes in Robo2 mutant mice with the inserted piggyBac transposon.
    Liu J; Sun L; Shen Q; Wu X; Xu H
    BMC Nephrol; 2016 Jul; 17(1):98. PubMed ID: 27460642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
    van der Ven AT; Connaughton DM; Ityel H; Mann N; Nakayama M; Chen J; Vivante A; Hwang DY; Schulz J; Braun DA; Schmidt JM; Schapiro D; Schneider R; Warejko JK; Daga A; Majmundar AJ; Tan W; Jobst-Schwan T; Hermle T; Widmeier E; Ashraf S; Amar A; Hoogstraaten CA; Hugo H; Kitzler TM; Kause F; Kolvenbach CM; Dai R; Spaneas L; Amann K; Stein DR; Baum MA; Somers MJG; Rodig NM; Ferguson MA; Traum AZ; Daouk GH; Bogdanović R; Stajić N; Soliman NA; Kari JA; El Desoky S; Fathy HM; Milosevic D; Al-Saffar M; Awad HS; Eid LA; Selvin A; Senguttuvan P; Sanna-Cherchi S; Rehm HL; MacArthur DG; Lek M; Laricchia KM; Wilson MW; Mane SM; Lifton RP; Lee RS; Bauer SB; Lu W; Reutter HM; Tasic V; Shril S; Hildebrandt F
    J Am Soc Nephrol; 2018 Sep; 29(9):2348-2361. PubMed ID: 30143558
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interleukin-10-1082A/G polymorphism is associated with renal parenchymal damage in congenital anomalies of the kidney and urinary tract.
    Miteva LD; Kostadinova ES; Stanilova SA
    Nephrology (Carlton); 2019 Feb; 24(2):213-220. PubMed ID: 29380920
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association between the clinical presentation of congenital anomalies of the kidney and urinary tract (CAKUT) and gene mutations: an analysis of 66 patients at a single institution.
    Ishiwa S; Sato M; Morisada N; Nishi K; Kanamori T; Okutsu M; Ogura M; Sako M; Kosuga M; Kamei K; Ito S; Nozu K; Iijima K; Ishikura K
    Pediatr Nephrol; 2019 Aug; 34(8):1457-1464. PubMed ID: 30937553
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Genetic Basis of Congenital Anomalies of the Kidney and Urinary Tract].
    Bodria M; Sanna-Cherchi S
    G Ital Nefrol; 2015; 32 Suppl 64():. PubMed ID: 26479062
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT).
    Kosfeld A; Kreuzer M; Daniel C; Brand F; Schäfer AK; Chadt A; Weiss AC; Riehmer V; Jeanpierre C; Klintschar M; Bräsen JH; Amann K; Pape L; Kispert A; Al-Hasani H; Haffner D; Weber RG
    Hum Genet; 2016 Jan; 135(1):69-87. PubMed ID: 26572137
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).
    Riedhammer KM; Nguyen TT; Koşukcu C; Calzada-Wack J; Li Y; Assia Batzir N; Saygılı S; Wimmers V; Kim GJ; Chrysanthou M; Bakey Z; Sofrin-Drucker E; Kraiger M; Sanz-Moreno A; Amarie OV; Rathkolb B; Klein-Rodewald T; Garrett L; Hölter SM; Seisenberger C; Haug S; Schlosser P; Marschall S; Wurst W; Fuchs H; Gailus-Durner V; Wuttke M; Hrabe de Angelis M; Ćomić J; Akgün Doğan Ö; Özlük Y; Taşdemir M; Ağbaş A; Canpolat N; Orenstein N; Çalışkan S; Weber RG; Bergmann C; Jeanpierre C; Saunier S; Lim TY; Hildebrandt F; Alhaddad B; Basel-Salmon L; Borovitz Y; Wu K; Antony D; Matschkal J; Schaaf CW; Renders L; Schmaderer C; Rogg M; Schell C; Meitinger T; Heemann U; Köttgen A; Arnold SJ; Ozaltin F; Schmidts M; Hoefele J
    Kidney Int; 2024 Apr; 105(4):844-864. PubMed ID: 38154558
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetics of congenital anomalies of the kidney and urinary tract.
    Song R; Yosypiv IV
    Pediatr Nephrol; 2011 Mar; 26(3):353-64. PubMed ID: 20798957
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).
    Ristoska-Bojkovska N
    Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2017 Mar; 38(1):59-62. PubMed ID: 28593883
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.
    Saisawat P; Kohl S; Hilger AC; Hwang DY; Yung Gee H; Dworschak GC; Tasic V; Pennimpede T; Natarajan S; Sperry E; Matassa DS; Stajić N; Bogdanovic R; de Blaauw I; Marcelis CL; Wijers CH; Bartels E; Schmiedeke E; Schmidt D; Märzheuser S; Grasshoff-Derr S; Holland-Cunz S; Ludwig M; Nöthen MM; Draaken M; Brosens E; Heij H; Tibboel D; Herrmann BG; Solomon BD; de Klein A; van Rooij IA; Esposito F; Reutter HM; Hildebrandt F
    Kidney Int; 2014 Jun; 85(6):1310-7. PubMed ID: 24152966
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Non-canonical Wnt5a/Ror2 signaling regulates kidney morphogenesis by controlling intermediate mesoderm extension.
    Yun K; Ajima R; Sharma N; Costantini F; Mackem S; Lewandoski M; Yamaguchi TP; Perantoni AO
    Hum Mol Genet; 2014 Dec; 23(25):6807-14. PubMed ID: 25082826
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Duplex kidney formation: developmental mechanisms and genetic predisposition.
    Kozlov VM; Schedl A
    F1000Res; 2020; 9():. PubMed ID: 32030122
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Impact of next generation sequencing on our understanding of CAKUT.
    Nigam A; Knoers NVAM; Renkema KY
    Semin Cell Dev Biol; 2019 Jul; 91():104-110. PubMed ID: 30172048
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.