BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 26235987)

  • 1. Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development.
    Vivante A; Kleppa MJ; Schulz J; Kohl S; Sharma A; Chen J; Shril S; Hwang DY; Weiss AC; Kaminski MM; Shukrun R; Kemper MJ; Lehnhardt A; Beetz R; Sanna-Cherchi S; Verbitsky M; Gharavi AG; Stuart HM; Feather SA; Goodship JA; Goodship TH; Woolf AS; Westra SJ; Doody DP; Bauer SB; Lee RS; Adam RM; Lu W; Reutter HM; Kehinde EO; Mancini EJ; Lifton RP; Tasic V; Lienkamp SS; Jüppner H; Kispert A; Hildebrandt F
    Am J Hum Genet; 2015 Aug; 97(2):291-301. PubMed ID: 26235987
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations
    Vivante A; Mann N; Yonath H; Weiss AC; Getwan M; Kaminski MM; Bohnenpoll T; Teyssier C; Chen J; Shril S; van der Ven AT; Ityel H; Schmidt JM; Widmeier E; Bauer SB; Sanna-Cherchi S; Gharavi AG; Lu W; Magen D; Shukrun R; Lifton RP; Tasic V; Stanescu HC; Cavaillès V; Kleta R; Anikster Y; Dekel B; Kispert A; Lienkamp SS; Hildebrandt F
    J Am Soc Nephrol; 2017 Aug; 28(8):2364-2376. PubMed ID: 28381549
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Proteomic analysis identifies ZMYM2 as endogenous binding partner of TBX18 protein in 293 and A549 cells.
    Lüdtke TH; Kleppa MJ; Rivera-Reyes R; Qasrawi F; Connaughton DM; Shril S; Hildebrandt F; Kispert A
    Biochem J; 2022 Jan; 479(1):91-109. PubMed ID: 34935912
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tbx18 expression demarcates multipotent precursor populations in the developing urogenital system but is exclusively required within the ureteric mesenchymal lineage to suppress a renal stromal fate.
    Bohnenpoll T; Bettenhausen E; Weiss AC; Foik AB; Trowe MO; Blank P; Airik R; Kispert A
    Dev Biol; 2013 Aug; 380(1):25-36. PubMed ID: 23685333
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
    Connaughton DM; Dai R; Owen DJ; Marquez J; Mann N; Graham-Paquin AL; Nakayama M; Coyaud E; Laurent EMN; St-Germain JR; Blok LS; Vino A; Klämbt V; Deutsch K; Wu CW; Kolvenbach CM; Kause F; Ottlewski I; Schneider R; Kitzler TM; Majmundar AJ; Buerger F; Onuchic-Whitford AC; Youying M; Kolb A; Salmanullah D; Chen E; van der Ven AT; Rao J; Ityel H; Seltzsam S; Rieke JM; Chen J; Vivante A; Hwang DY; Kohl S; Dworschak GC; Hermle T; Alders M; Bartolomaeus T; Bauer SB; Baum MA; Brilstra EH; Challman TD; Zyskind J; Costin CE; Dipple KM; Duijkers FA; Ferguson M; Fitzpatrick DR; Fick R; Glass IA; Hulick PJ; Kline AD; Krey I; Kumar S; Lu W; Marco EJ; Wentzensen IM; Mefford HC; Platzer K; Povolotskaya IS; Savatt JM; Shcherbakova NV; Senguttuvan P; Squire AE; Stein DR; Thiffault I; Voinova VY; Somers MJG; Ferguson MA; Traum AZ; Daouk GH; Daga A; Rodig NM; Terhal PA; van Binsbergen E; Eid LA; Tasic V; Rasouly HM; Lim TY; Ahram DF; Gharavi AG; Reutter HM; Rehm HL; MacArthur DG; Lek M; Laricchia KM; Lifton RP; Xu H; Mane SM; Sanna-Cherchi S; Sharrocks AD; Raught B; Fisher SE; Bouchard M; Khokha MK; Shril S; Hildebrandt F
    Am J Hum Genet; 2020 Oct; 107(4):727-742. PubMed ID: 32891193
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SIX1 acts synergistically with TBX18 in mediating ureteral smooth muscle formation.
    Nie X; Sun J; Gordon RE; Cai CL; Xu PX
    Development; 2010 Mar; 137(5):755-65. PubMed ID: 20110314
    [TBL] [Abstract][Full Text] [Related]  

  • 7. T-Box Genes in the Kidney and Urinary Tract.
    Kispert A
    Curr Top Dev Biol; 2017; 122():245-278. PubMed ID: 28057266
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Permissive ureter specification by TBX18-mediated repression of metanephric gene expression.
    Weiss AC; Blank E; Bohnenpoll T; Kleppa MJ; Rivera-Reyes R; Taketo MM; Trowe MO; Kispert A
    Development; 2023 Mar; 150(6):. PubMed ID: 36960826
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tbx18 Regulates the Differentiation of Periductal Smooth Muscle Stroma and the Maintenance of Epithelial Integrity in the Prostate.
    Bolt CC; Negi S; Guimarães-Camboa N; Zhang H; Troy JM; Lu X; Kispert A; Evans SM; Stubbs L
    PLoS One; 2016; 11(4):e0154413. PubMed ID: 27120339
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT).
    Brockschmidt A; Chung B; Weber S; Fischer DC; Kolatsi-Joannou M; Christ L; Heimbach A; Shtiza D; Klaus G; Simonetti GD; Konrad M; Winyard P; Haffner D; Schaefer F; Weber RG
    Nephrol Dial Transplant; 2012 Jun; 27(6):2355-64. PubMed ID: 22146311
    [TBL] [Abstract][Full Text] [Related]  

  • 11. COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.
    Kitzler TM; Schneider R; Kohl S; Kolvenbach CM; Connaughton DM; Dai R; Mann N; Nakayama M; Majmundar AJ; Wu CW; Kari JA; El Desoky SM; Senguttuvan P; Bogdanovic R; Stajic N; Valivullah Z; Lek M; Mane S; Lifton RP; Tasic V; Shril S; Hildebrandt F
    Hum Genet; 2019 Oct; 138(10):1105-1115. PubMed ID: 31230195
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract.
    Zheng B; Seltzsam S; Wang C; Schierbaum L; Schneider S; Wu CW; Dai R; Connaughton DM; Nakayama M; Mann N; Stajic N; Mane S; Bauer SB; Tasic V; Nam HJ; Shril S; Hildebrandt F
    Nephrol Dial Transplant; 2022 Sep; 37(10):1833-1843. PubMed ID: 34473308
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations.
    Kosfeld A; Brand F; Weiss AC; Kreuzer M; Goerk M; Martens H; Schubert S; Schäfer AK; Riehmer V; Hennies I; Bräsen JH; Pape L; Amann K; Krogvold L; Bjerre A; Daniel C; Kispert A; Haffner D; Weber RG
    Hum Mol Genet; 2017 May; 26(9):1716-1731. PubMed ID: 28334964
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.
    Kohl S; Hwang DY; Dworschak GC; Hilger AC; Saisawat P; Vivante A; Stajic N; Bogdanovic R; Reutter HM; Kehinde EO; Tasic V; Hildebrandt F
    J Am Soc Nephrol; 2014 Sep; 25(9):1917-22. PubMed ID: 24700879
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ontogeny of congenital anomalies of the kidney and urinary tract, CAKUT.
    Miyazaki Y; Ichikawa I
    Pediatr Int; 2003 Oct; 45(5):598-604. PubMed ID: 14521544
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract.
    Gimelli S; Caridi G; Beri S; McCracken K; Bocciardi R; Zordan P; Dagnino M; Fiorio P; Murer L; Benetti E; Zuffardi O; Giorda R; Wells JM; Gimelli G; Ghiggeri GM
    Hum Mutat; 2010 Dec; 31(12):1352-9. PubMed ID: 20960469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CAKUT and Autonomic Dysfunction Caused by Acetylcholine Receptor Mutations.
    Mann N; Kause F; Henze EK; Gharpure A; Shril S; Connaughton DM; Nakayama M; Klämbt V; Majmundar AJ; Wu CW; Kolvenbach CM; Dai R; Chen J; van der Ven AT; Ityel H; Tooley MJ; Kari JA; Bownass L; El Desoky S; De Franco E; Shalaby M; Tasic V; Bauer SB; Lee RS; Beckel JM; Yu W; Mane SM; Lifton RP; Reutter H; Ellard S; Hibbs RE; Kawate T; Hildebrandt F
    Am J Hum Genet; 2019 Dec; 105(6):1286-1293. PubMed ID: 31708116
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inflammation-like changes in the urothelium of Lifr-deficient mice and LIFR-haploinsufficient humans with urinary tract anomalies.
    Christians A; Weiss AC; Martens H; Klopf MG; Hennies I; Haffner D; Kispert A; Weber RG
    Hum Mol Genet; 2020 May; 29(7):1192-1204. PubMed ID: 32179912
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
    De Tomasi L; David P; Humbert C; Silbermann F; Arrondel C; Tores F; Fouquet S; Desgrange A; Niel O; Bole-Feysot C; Nitschké P; Roume J; Cordier MP; Pietrement C; Isidor B; Khau Van Kien P; Gonzales M; Saint-Frison MH; Martinovic J; Novo R; Piard J; Cabrol C; Verma IC; Puri R; Journel H; Aziza J; Gavard L; Said-Menthon MH; Heidet L; Saunier S; Jeanpierre C
    Am J Hum Genet; 2017 Nov; 101(5):803-814. PubMed ID: 29100091
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.