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 *

280 related articles for article (PubMed ID: 27234567)

  • 21. 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]  

  • 22. Hypertriglyceridemia as a main feature associated with 17q12 deletion syndrome-related hepatocyte nuclear factor 1β-maturity-onset diabetes of the young.
    Thewjitcharoen Y; Nakasatien S; Tsoi TF; Lim CKP; Himathongkam T; Chan JCN
    Endocrinol Diabetes Metab Case Rep; 2022 Sep; 2022():. PubMed ID: 36106561
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Case report: extreme coronary calcifications and hypomagnesemia in a patient with a 17q12 deletion involving HNF1B.
    Li HJ; Groden C; Hoenig MP; Ray EC; Ferreira CR; Gahl W; Novacic D
    BMC Nephrol; 2019 Sep; 20(1):353. PubMed ID: 31500578
    [TBL] [Abstract][Full Text] [Related]  

  • 25.
    Sánchez-Cazorla E; Carrera N; García-González MÁ
    Int J Mol Sci; 2024 Oct; 25(19):. PubMed ID: 39408938
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. [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]  

  • 28. 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]  

  • 29. Could FISH on buccal smears become a new method of screening in children suspect of HNF1B anomaly?
    Laffargue F; Bourthoumieu S; Bellanné-Chantelot C; Guigonis V; Yardin C
    Eur J Med Genet; 2013 Feb; 56(2):93-7. PubMed ID: 23261960
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [HNF1B-related disease: paradigm of a developmental gene and unexpected recognition of a new renal disease].
    Chauveau D; Faguer S; Bandin F; Guigonis V; Chassaing N; Decramer S
    Nephrol Ther; 2013 Nov; 9(6):393-7. PubMed ID: 24119877
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Clinical phenotype and genetic analysis of three pedigrees with 17q12 microdeletion syndrome].
    Wu Q; Yang S; Wang C; Shi H; Kong X; Ren S; Jiao Z; Liu N; Shi P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Apr; 37(4):397-400. PubMed ID: 32219821
    [TBL] [Abstract][Full Text] [Related]  

  • 32. School level of children carrying a HNF1B variant or a deletion.
    Laliève F; Decramer S; Heidet L; Baudouin V; Lahoche A; Llanas B; Cochat P; Tenenbaum J; Lavocat MP; Eckart P; Broux F; Roussey G; Cloarec S; Vrillon I; Dunand O; Bessenay L; Tsimaratos M; Nobili F; Pietrement C; De Parscau L; Bonneville V; Rodier N; Saint-Martin C; Chassaing N; Michel-Calemard L; Moriniere V; Bellanné-Chantelot C; Bahans C; Guigonis V
    Eur J Hum Genet; 2020 Jan; 28(1):56-63. PubMed ID: 31481685
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Accurate diagnosis and heterogeneity analysis of a 17q12 deletion syndrome family with adulthood diabetes onset and complex clinical phenotypes.
    Wu HX; Li L; Zhang H; Tang J; Zhang MB; Tang HN; Guo Y; Zhou ZG; Zhou HD
    Endocrine; 2021 Jul; 73(1):37-46. PubMed ID: 33745123
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The role of hepatocyte nuclear factor 1β in disease and development.
    El-Khairi R; Vallier L
    Diabetes Obes Metab; 2016 Sep; 18 Suppl 1():23-32. PubMed ID: 27615128
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Renal and Extrarenal Phenotypes in Patients With
    Buffin-Meyer B; Richard J; Guigonis V; Weber S; König J; Heidet L; Moussaoui N; Vu JP; Faguer S; Casemayou A; Prakash R; Baudouin V; Hogan J; Alexandrou D; Bockenhauer D; Bacchetta J; Ranchin B; Pruhova S; Zieg J; Lahoche A; Okorn C; Antal-Kónya V; Morin D; Becherucci F; Habbig S; Liebau MC; Mauras M; Nijenhuis T; Llanas B; Mekahli D; Thumfart J; Tönshoff B; Massella L; Eckart P; Cloarec S; Cruz A; Patzer L; Roussey G; Vrillon I; Dunand O; Bessenay L; Taroni F; Zaniew M; Louillet F; Bergmann C; Schaefer F; van Eerde AM; Schanstra JP; Decramer S;
    Kidney Int Rep; 2024 Aug; 9(8):2514-2526. PubMed ID: 39156164
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Chronic renal failure of unknown origin is caused by HNF1B mutations in 9% of adult patients: a single centre cohort analysis.
    Musetti C; Quaglia M; Mellone S; Pagani A; Fusco I; Monzani A; Giordano M; Stratta P
    Nephrology (Carlton); 2014 Apr; 19(4):202-9. PubMed ID: 24387224
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.
    Nagamani SC; Erez A; Shen J; Li C; Roeder E; Cox S; Karaviti L; Pearson M; Kang SH; Sahoo T; Lalani SR; Stankiewicz P; Sutton VR; Cheung SW
    Eur J Hum Genet; 2010 Mar; 18(3):278-84. PubMed ID: 19844256
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series.
    Zhou CX; Zhu XY; Zhu YJ; Gu LL; He LL; Liu W; Yang Y; Wu X; Duan HL; Ru T; Li J
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):232-237. PubMed ID: 33678321
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Recurrent 17q12 microduplications contribute to renal disease but not diabetes.
    Cannon S; Clissold R; Sukcharoen K; Tuke M; Hawkes G; Beaumont RN; Wood AR; Gilchrist M; Hattersley AT; Oram RA; Patel K; Wright C; Weedon MN
    J Med Genet; 2023 May; 60(5):491-497. PubMed ID: 36109160
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.