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 *

290 related articles for article (PubMed ID: 34161864)

  • 1. A case of digenic maturity onset diabetes of the young with heterozygous variants in both HNF1Α and HNF1Β genes.
    Patouni K; Cinek O; Pruhova S; Elblova L; Xatzipsalti M; Sertedaki A; Vazeou A
    Eur J Med Genet; 2021 Sep; 64(9):104264. PubMed ID: 34161864
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Next generation sequencing targeted gene panel in Greek MODY patients increases diagnostic accuracy.
    Tatsi EB; Kanaka-Gantenbein C; Scorilas A; Chrousos GP; Sertedaki A
    Pediatr Diabetes; 2020 Feb; 21(1):28-39. PubMed ID: 31604004
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5: A pedigree-based case report.
    Tao T; Yang Y; Hu Z
    Medicine (Baltimore); 2020 Jul; 99(31):e21438. PubMed ID: 32756155
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening of diabetes of youth for hepatocyte nuclear factor 1 mutations: clinical phenotype of HNF1β-related maturity-onset diabetes of the young and HNF1α-related maturity-onset diabetes of the young in Japanese.
    Horikawa Y; Enya M; Fushimi N; Fushimi Y; Takeda J
    Diabet Med; 2014 Jun; 31(6):721-7. PubMed ID: 24905847
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Unexpected finding of a whole HNF1B gene deletion during the screening of rare MODY types in a series of Brazilian patients negative for GCK and HNF1A mutations.
    Dotto RP; Giuffrida FM; Franco L; Mathez AL; Weinert LS; Silveiro SP; Sa JR; Reis AF; Dias-da-Silva MR
    Diabetes Res Clin Pract; 2016 Jun; 116():100-4. PubMed ID: 27321323
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of the promoter regions of disease-causing genes in maturity-onset diabetes of the young patients.
    Komazec J; Ristivojevic B; Zukic B; Zdravkovic V; Karan-Djurasevic T; Pavlovic S; Ugrin M
    Mol Biol Rep; 2020 Sep; 47(9):6759-6768. PubMed ID: 32860162
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Maturity Onset Diabetes of the Young due to Glucokinase, HNF1-A, HNF1-B, and HNF4-A Mutations in a Cohort of Turkish Children Diagnosed as Type 1 Diabetes Mellitus.
    Ozsu E; Cizmecioglu FM; Yesiltepe Mutlu G; Yuksel AB; Calıskan M; Yesilyurt A; Hatun S
    Horm Res Paediatr; 2018; 90(4):257-265. PubMed ID: 30481753
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Co-inheritance of HNF1a and GCK mutations in a family with maturity-onset diabetes of the young (MODY): implications for genetic testing.
    López-Garrido MP; Herranz-Antolín S; Alija-Merillas MJ; Giralt P; Escribano J
    Clin Endocrinol (Oxf); 2013 Sep; 79(3):342-7. PubMed ID: 23009393
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case series of maturity-onset diabetes of the young highlighting atypical presentations and the implications of genetic diagnosis.
    Narasimhegowda M; Nagarajappa VH; Palany R
    Arch Endocrinol Metab; 2024; 68():e230239. PubMed ID: 39420905
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Examining the clinical and genetic spectrum of maturity-onset diabetes of the young (MODY) in Iran.
    Asgarian S; Lanjanian H; Rahimipour Anaraki S; Hadaegh F; Moazzam-Jazi M; Najd-Hassan-Bonab L; Masjoudi S; Zahedi AS; Zarkesh M; Shalbafan B; Akbarzadeh M; Tehrani Fateh S; Khalili D; Momenan A; Sarbazi N; Hedayati M; Azizi F; Daneshpour MS
    Sci Rep; 2024 Aug; 14(1):19860. PubMed ID: 39191897
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An Italian MODY family with proband and son carrying variants in GCK and HFN1A: is it a true case of digenic MODY?
    Lucchesi D; Randazzo E; Del Prato S; Bianchi C
    Acta Diabetol; 2024 Jan; 61(1):131-134. PubMed ID: 37730861
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel insights into genetics and clinics of the HNF1A-MODY.
    Valkovicova T; Skopkova M; Stanik J; Gasperikova D
    Endocr Regul; 2019 Apr; 53(2):110-134. PubMed ID: 31517624
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A case of a novel mutation in HNF1β-related maturity-onset diabetes of the young type 5 with diabetic kidney disease complication in a Chinese family.
    Wang Y; Zhao Y; Zhang J; Yang Y; Liu F
    J Diabetes Complications; 2017 Jul; 31(7):1243-1246. PubMed ID: 28502589
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Frequency and characterization of mutations in genes in a large cohort of patients referred to MODY registry.
    Breidbart E; Deng L; Lanzano P; Fan X; Guo J; Leibel RL; LeDuc CA; Chung WK
    J Pediatr Endocrinol Metab; 2021 May; 34(5):633-638. PubMed ID: 33852230
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic and Clinical Characterization of Patients with Maturity-Onset of Diabetes of the Young (MODY): Identification of Novel Variations.
    Ateş EA; Üstay Ö; Polat H; Apaydın T; Elbasan O; Yıldırım Ö; Güney Aİ
    Balkan Med J; 2021 Sep; 38(5):272-277. PubMed ID: 34462253
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Low genetic confirmation rate in South Indian subjects with a clinical diagnosis of maturity-onset diabetes of the young (MODY) who underwent targeted next-generation sequencing for 13 genes.
    Sampathkumar G; Valiyaparambil PP; Kumar H; Bhavani N; Nair V; Menon U; Menon A; Abraham N; Chapla A; Thomas N
    J Endocrinol Invest; 2022 Mar; 45(3):607-615. PubMed ID: 34741762
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maturity onset diabetes of the young due to
    Pavić T; Juszczak A; Pape Medvidović E; Burrows C; Šekerija M; Bennett AJ; Ćuća Knežević J; Gloyn AL; Lauc G; McCarthy MI; Gornik O; Owen KR
    Biochem Med (Zagreb); 2018 Jun; 28(2):020703. PubMed ID: 29666556
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus.
    Yorifuji T; Fujimaru R; Hosokawa Y; Tamagawa N; Shiozaki M; Aizu K; Jinno K; Maruo Y; Nagasaka H; Tajima T; Kobayashi K; Urakami T
    Pediatr Diabetes; 2012 Feb; 13(1):26-32. PubMed ID: 22060211
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes.
    Svalastoga P; Kaci A; Molnes J; Solheim MH; Johansson BB; Krogvold L; Skrivarhaug T; Valen E; Johansson S; Molven A; Sagen JV; Søfteland E; Bjørkhaug L; Tjora E; Aukrust I; Njølstad PR
    Diabetologia; 2023 Dec; 66(12):2226-2237. PubMed ID: 37798422
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.