BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

254 related articles for article (PubMed ID: 20155289)

  • 1. HNF1B alterations associated with congenital anomalies of the kidney and urinary tract.
    Nakayama M; Nozu K; Goto Y; Kamei K; Ito S; Sato H; Emi M; Nakanishi K; Tsuchiya S; Iijima K
    Pediatr Nephrol; 2010 Jun; 25(6):1073-9. PubMed ID: 20155289
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Criteria for HNF1B analysis in patients with congenital abnormalities of kidney and urinary tract.
    Raaijmakers A; Corveleyn A; Devriendt K; van Tienoven TP; Allegaert K; Van Dyck M; van den Heuvel L; Kuypers D; Claes K; Mekahli D; Levtchenko E
    Nephrol Dial Transplant; 2015 May; 30(5):835-42. PubMed ID: 25500806
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases.
    Heidet L; Decramer S; Pawtowski A; Morinière V; Bandin F; Knebelmann B; Lebre AS; Faguer S; Guigonis V; Antignac C; Salomon R
    Clin J Am Soc Nephrol; 2010 Jun; 5(6):1079-90. PubMed ID: 20378641
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical characteristics of HNF1B-related disorders in a Japanese population.
    Nagano C; Morisada N; Nozu K; Kamei K; Tanaka R; Kanda S; Shiona S; Araki Y; Ohara S; Matsumura C; Kasahara K; Mori Y; Seo A; Miura K; Washiyama M; Sugimoto K; Harada R; Tazoe S; Kourakata H; Enseki M; Aotani D; Yamada T; Sakakibara N; Yamamura T; Minamikawa S; Ishikura K; Ito S; Hattori M; Iijima K
    Clin Exp Nephrol; 2019 Sep; 23(9):1119-1129. PubMed ID: 31131422
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract.
    Kołbuc M; Kołek MF; Motyka R; Bieniaś B; Habbig S; Burgmaier K; Prikhodina L; Papizh S; Tasic V; Okorn C; Szczepańska M; Kiliś-Pstrusińska K; Wasilewska A; Adamczyk P; Tkaczyk M; Pańczyk-Tomaszewska M; Miklaszewska M; Pawlaczyk K; Bukowska-Olech E; Jamsheer A; Jankauskiene A; König J; Cheong HI; Ahn YH; Kaspar S; Sikora P; Beck BB; Zaniew M
    Pediatr Nephrol; 2024 Jun; 39(6):1847-1858. PubMed ID: 38196016
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Clinical phenotypes of hepatocyte nuclear factor 1 homeobox b-associated disease].
    Wang F; Yao Y; Yang HX; Shi CY; Zhang XX; Xiao HJ; Zhang HW; Su BG; Zhang YQ; Guo JF; Ding J
    Zhonghua Er Ke Za Zhi; 2017 Sep; 55(9):658-662. PubMed ID: 28881510
    [No Abstract]   [Full Text] [Related]  

  • 7. New-onset diabetes after renal transplantation in a patient with a novel HNF1B mutation.
    Kanda S; Morisada N; Kaneko N; Yabuuchi T; Nawashiro Y; Tada N; Nishiyama K; Miyai T; Sugawara N; Ishizuka K; Chikamoto H; Akioka Y; Iijima K; Hattori M
    Pediatr Transplant; 2016 May; 20(3):467-71. PubMed ID: 26899772
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Copy-number variation analysis in familial nonsyndromic congenital anomalies of the kidney and urinary tract: Evidence for the causative role of a transposable element-associated genomic rearrangement.
    Siomou E; Mitsioni AG; Giapros V; Bouba I; Noutsopoulos D; Georgiou I
    Mol Med Rep; 2017 Jun; 15(6):3631-3636. PubMed ID: 28440405
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Detection of mutations of the HNF1B gene in children with congenital anomalies of the kidney and urinary tract].
    Bascur P MN; Ceballos O ML; Farfán U M; Gajardo H I; López C J
    Rev Chil Pediatr; 2018 Dec; 89(6):741-746. PubMed ID: 30725063
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder.
    Clissold RL; Shaw-Smith C; Turnpenny P; Bunce B; Bockenhauer D; Kerecuk L; Waller S; Bowman P; Ford T; Ellard S; Hattersley AT; Bingham C
    Kidney Int; 2016 Jul; 90(1):203-11. PubMed ID: 27234567
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations.
    Oram RA; Edghill EL; Blackman J; Taylor MJ; Kay T; Flanagan SE; Ismail-Pratt I; Creighton SM; Ellard S; Hattersley AT; Bingham C
    Am J Obstet Gynecol; 2010 Oct; 203(4):364.e1-5. PubMed ID: 20633866
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Different phenotypes of HNF1ß deletion mutants in familial multicystic dysplastic kidneys.
    Hasui M; Kaneko K; Tsuji S; Isozaki Y; Kimata T; Nozu Y; Nozu K; Iijima K
    Clin Nephrol; 2013 Jun; 79(6):484-7. PubMed ID: 23725647
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.
    Thomas R; Sanna-Cherchi S; Warady BA; Furth SL; Kaskel FJ; Gharavi AG
    Pediatr Nephrol; 2011 Jun; 26(6):897-903. PubMed ID: 21380624
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion.
    Clissold RL; Ashfield B; Burrage J; Hannon E; Bingham C; Mill J; Hattersley A; Dempster EL
    Clin Epigenetics; 2018 Jul; 10(1):97. PubMed ID: 30021660
    [TBL] [Abstract][Full Text] [Related]  

  • 16. HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum.
    Clissold RL; Hamilton AJ; Hattersley AT; Ellard S; Bingham C
    Nat Rev Nephrol; 2015 Feb; 11(2):102-12. PubMed ID: 25536396
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deciphering the mutation spectrum in south Indian children with congenital anomalies of the kidney and urinary tract.
    Narikot A; Pardeshi VC; Shubha AM; Iyengar A; Vasudevan A
    BMC Nephrol; 2022 Jan; 23(1):1. PubMed ID: 34979951
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hnf1b haploinsufficiency differentially affects developmental target genes in a new renal cysts and diabetes mouse model.
    Niborski LL; Paces-Fessy M; Ricci P; Bourgeois A; Magalhães P; Kuzma-Kuzniarska M; Lesaulnier C; Reczko M; Declercq E; Zürbig P; Doucet A; Umbhauer M; Cereghini S
    Dis Model Mech; 2021 May; 14(5):. PubMed ID: 33737325
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hnf1b and Pax2 cooperate to control different pathways in kidney and ureter morphogenesis.
    Paces-Fessy M; Fabre M; Lesaulnier C; Cereghini S
    Hum Mol Genet; 2012 Jul; 21(14):3143-55. PubMed ID: 22511595
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood.
    Faguer S; Decramer S; Chassaing N; Bellanné-Chantelot C; Calvas P; Beaufils S; Bessenay L; Lengelé JP; Dahan K; Ronco P; Devuyst O; Chauveau D
    Kidney Int; 2011 Oct; 80(7):768-76. PubMed ID: 21775974
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.