These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 20890685)

  • 21. A novel mutation of the HNF1B gene associated with hypoplastic glomerulocystic kidney disease and neonatal renal failure: a case report and mutation update.
    Alvelos MI; Rodrigues M; Lobo L; Medeira A; Sousa AB; Simão C; Lemos MC
    Medicine (Baltimore); 2015 Feb; 94(7):e469. PubMed ID: 25700310
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The Phenotypic Variability Associated with Hepatocyte Nuclear Factor 1B Genetic Defects Poses Challenges in Both Diagnosis and Therapy.
    Petrakis I; Sfakiotaki M; Bitsori M; Drosataki E; Dermitzaki K; Pleros C; Androvitsanea A; Samonakis D; Sertedaki A; Xekouki P; Galanakis E; Stylianou K
    Int J Mol Sci; 2024 Apr; 25(8):. PubMed ID: 38674137
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys.
    Decramer S; Parant O; Beaufils S; Clauin S; Guillou C; Kessler S; Aziza J; Bandin F; Schanstra JP; Bellanné-Chantelot C
    J Am Soc Nephrol; 2007 Mar; 18(3):923-33. PubMed ID: 17267738
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutation of hepatocyte nuclear factor-1beta inhibits Pkhd1 gene expression and produces renal cysts in mice.
    Hiesberger T; Bai Y; Shao X; McNally BT; Sinclair AM; Tian X; Somlo S; Igarashi P
    J Clin Invest; 2004 Mar; 113(6):814-25. PubMed ID: 15067314
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Severe hyperglycemia after renal transplantation in a pediatric patient with a mutation of the hepatocyte nuclear factor-1beta gene.
    Waller SC; Rees L; Woolf AS; Ellard S; Pearson ER; Hattersley AT; Bingham C
    Am J Kidney Dis; 2002 Dec; 40(6):1325-30. PubMed ID: 12460054
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Maturity onset diabetes of the young: clinical characteristics and outcome after kidney and pancreas transplantation in MODY3 and RCAD patients: a single center experience.
    Poitou C; Francois H; Bellanne-Chantelot C; Noel C; Jacquet A; Clauin S; Beaudreuil S; Damieri H; Hebibi H; Hammoudi Y; Benoit G; Charpentier B; Durrbach A
    Transpl Int; 2012 May; 25(5):564-72. PubMed ID: 22432796
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Roles of HNF-1beta in kidney development and congenital cystic diseases.
    Igarashi P; Shao X; McNally BT; Hiesberger T
    Kidney Int; 2005 Nov; 68(5):1944-7. PubMed ID: 16221171
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Case Report: A case of HNF1B mutation patient with first presentation of diabetic ketosis.
    Ge S; Yang M; Gong W; Chen W; Dong J; Liao L
    Front Endocrinol (Lausanne); 2022; 13():917819. PubMed ID: 35992134
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Cystic kidney disease and diabetes--an underdiagnosed monogenic developmental disorder].
    Merenmies J; Ala-Houhala M; Tuomi T
    Duodecim; 2012; 128(19):1999-2006. PubMed ID: 23155751
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Urinary proteome signature of Renal Cysts and Diabetes syndrome in children.
    Ricci P; Magalhães P; Krochmal M; Pejchinovski M; Daina E; Caruso MR; Goea L; Belczacka I; Remuzzi G; Umbhauer M; Drube J; Pape L; Mischak H; Decramer S; Schaefer F; Schanstra JP; Cereghini S; Zürbig P
    Sci Rep; 2019 Feb; 9(1):2225. PubMed ID: 30778115
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations in the hepatocyte nuclear factor-1beta gene are associated with familial hypoplastic glomerulocystic kidney disease.
    Bingham C; Bulman MP; Ellard S; Allen LI; Lipkin GW; Hoff WG; Woolf AS; Rizzoni G; Novelli G; Nicholls AJ; Hattersley AT
    Am J Hum Genet; 2001 Jan; 68(1):219-24. PubMed ID: 11085914
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cystic kidney disease, chromophobe renal cell carcinoma and TCF2 (HNF1 beta) mutations.
    Lebrun G; Vasiliu V; Bellanné-Chantelot C; Bensman A; Ulinski T; Chrétien Y; Grünfeld JP
    Nat Clin Pract Nephrol; 2005 Dec; 1(2):115-9. PubMed ID: 16932376
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Growth hormone therapy-related hyperglycaemia in a boy with renal cystic hypodysplasia and a new mutation of the HNF1 beta gene.
    Giglio S; Contini E; Toni S; Pela I
    Nephrol Dial Transplant; 2010 Sep; 25(9):3116-9. PubMed ID: 20543213
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations.
    Bellanné-Chantelot C; Chauveau D; Gautier JF; Dubois-Laforgue D; Clauin S; Beaufils S; Wilhelm JM; Boitard C; Noël LH; Velho G; Timsit J
    Ann Intern Med; 2004 Apr; 140(7):510-7. PubMed ID: 15068978
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Role of the hepatocyte nuclear factor-1beta (HNF-1beta) C-terminal domain in Pkhd1 (ARPKD) gene transcription and renal cystogenesis.
    Hiesberger T; Shao X; Gourley E; Reimann A; Pontoglio M; Igarashi P
    J Biol Chem; 2005 Mar; 280(11):10578-86. PubMed ID: 15647252
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical manifestations of a sporadic maturity-onset diabetes of the young (MODY) 5 with a whole deletion of HNF1B based on 17q12 microdeletion.
    Omura Y; Yagi K; Honoki H; Iwata M; Enkaku A; Takikawa A; Kuwano T; Watanabe Y; Nishimura A; Liu J; Chujo D; Fujisaka S; Enya M; Horikawa Y; Tobe K
    Endocr J; 2019 Dec; 66(12):1113-1116. PubMed ID: 31391355
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of HNF1B-associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome?
    Vasileiou G; Hoyer J; Thiel CT; Schaefer J; Zapke M; Krumbiegel M; Kraus C; Zweier M; Uebe S; Ekici AB; Schneider M; Wiesener M; Rauch A; Faschingbauer F; Reis A; Zweier C; Popp B
    Prenat Diagn; 2019 Nov; 39(12):1136-1147. PubMed ID: 31498910
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hypomagnesemia as First Clinical Manifestation of ADTKD-HNF1B: A Case Series and Literature Review.
    van der Made CI; Hoorn EJ; de la Faille R; Karaaslan H; Knoers NV; Hoenderop JG; Vargas Poussou R; de Baaij JH
    Am J Nephrol; 2015; 42(1):85-90. PubMed ID: 26340261
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1 beta.
    Bingham C; Ellard S; Allen L; Bulman M; Shepherd M; Frayling T; Berry PJ; Clark PM; Lindner T; Bell GI; Ryffel GU; Nicholls AJ; Hattersley AT
    Kidney Int; 2000 Mar; 57(3):898-907. PubMed ID: 10720943
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.