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 *

194 related articles for article (PubMed ID: 33633681)

  • 1. Identification of Maturity-Onset Diabetes of the Young Caused by Mutation in
    Zhong L; Zhao Z; Hu Q; Li Y; Zhao W; Li C; Xu Y; Rong R; Zhang J; Zhang Z; Li N; Liu Z
    Front Endocrinol (Lausanne); 2020; 11():534362. PubMed ID: 33633681
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular diagnosis of maturity-onset diabetes of the young in a cohort of Chinese children.
    Xu A; Lin Y; Sheng H; Cheng J; Mei H; Ting TH; Zeng C; Liang C; Zhang W; Li C; Li X; Liu L
    Pediatr Diabetes; 2020 May; 21(3):431-440. PubMed ID: 31957151
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism.
    Johnson SR; Leo PJ; McInerney-Leo AM; Anderson LK; Marshall M; McGown I; Newell F; Brown MA; Conwell LS; Harris M; Duncan EL
    Pediatr Diabetes; 2018 Jun; 19(4):656-662. PubMed ID: 29417725
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular and phenotypic characteristics of maturity-onset diabetes of the young compared with early onset type 2 diabetes in China.
    Zhang M; Zhou JJ; Cui W; Li Y; Yang P; Chen X; Sheng C; Li H; Qu S
    J Diabetes; 2015 Nov; 7(6):858-63. PubMed ID: 25588466
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical whole exome sequencing in early onset diabetes patients.
    Kwak SH; Jung CH; Ahn CH; Park J; Chae J; Jung HS; Cho YM; Lee DH; Kim JI; Park KS
    Diabetes Res Clin Pract; 2016 Dec; 122():71-77. PubMed ID: 27810688
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients.
    Butnariu LI; Bizim DA; Oltean C; Rusu C; Pânzaru MC; Păduraru G; Gimiga N; Ghiga G; Moisă ȘM; Țarcă E; Starcea IM; Popa S; Trandafir LM
    Int J Mol Sci; 2024 Jun; 25(12):. PubMed ID: 38928025
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes.
    Ming-Qiang Z; Yang-Li D; Ke H; Wei W; Jun-Fen F; Chao-Chun Z; Guan-Ping D
    J Pediatr Endocrinol Metab; 2019 Jul; 32(7):759-765. PubMed ID: 31216263
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exome sequencing in children with clinically suspected maturity-onset diabetes of the young.
    Tosur M; Soler-Alfonso C; Chan KM; Khayat MM; Jhangiani SN; Meng Q; Refaey A; Muzny D; Gibbs RA; Murdock DR; Posey JE; Balasubramanyam A; Redondo MJ; Sabo A
    Pediatr Diabetes; 2021 Nov; 22(7):960-968. PubMed ID: 34387403
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High prevalence of copy number variations in the Japanese participants with suspected MODY.
    Tanaka S; Akagawa H; Azuma K; Higuchi S; Ujiie A; Hashimoto K; Iwasaki N
    Clin Genet; 2024 Sep; 106(3):293-304. PubMed ID: 38733153
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Whole-exome sequencing identifies the first French MODY 6 family with a new mutation in the NEUROD1 gene.
    Bouillet B; Crevisy E; Baillot-Rudoni S; Gallegarine D; Jouan T; Duffourd Y; Petit JM; Vergès B; Callier P
    Diabetes Metab; 2020 Oct; 46(5):400-402. PubMed ID: 32184107
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene.
    Bonnefond A; Philippe J; Durand E; Dechaume A; Huyvaert M; Montagne L; Marre M; Balkau B; Fajardy I; Vambergue A; Vatin V; Delplanque J; Le Guilcher D; De Graeve F; Lecoeur C; Sand O; Vaxillaire M; Froguel P
    PLoS One; 2012; 7(6):e37423. PubMed ID: 22701567
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new screening strategy and whole-exome sequencing for the early diagnosis of maturity-onset diabetes of the young.
    Liu Y; Xie Z; Sun X; Wang Y; Xiao Y; Luo S; Huang G; Li X; Xia Y; Zhou Z
    Diabetes Metab Res Rev; 2021 Jul; 37(5):e3381. PubMed ID: 32621647
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic testing for monogenic diabetes using targeted next-generation sequencing in patients with maturity-onset diabetes of the young.
    Szopa M; Ludwig-Gałęzowska A; Radkowski P; Skupień J; Zapała B; Płatek T; Klupa T; Kieć-Wilk B; Borowiec M; Młynarski W; Wołkow P; Małecki MT
    Pol Arch Med Wewn; 2015; 125(11):845-51. PubMed ID: 26552609
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic basis of early-onset, maturity-onset diabetes of the young-like diabetes in Japan and features of patients without mutations in the major MODY genes: Dominance of maternal inheritance.
    Yorifuji T; Higuchi S; Kawakita R; Hosokawa Y; Aoyama T; Murakami A; Kawae Y; Hatake K; Nagasaka H; Tamagawa N
    Pediatr Diabetes; 2018 Nov; 19(7):1164-1172. PubMed ID: 29927023
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening of HNF1A and HNF4A mutation and clinical phenotype analysis in a large cohort of Chinese patients with maturity-onset diabetes of the young.
    Wang X; Wang T; Yu M; Zhang H; Ping F; Zhang Q; Xu J; Feng K; Xiao X
    Acta Diabetol; 2019 Mar; 56(3):281-288. PubMed ID: 30293189
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing.
    Shim YJ; Kim JE; Hwang SK; Choi BS; Choi BH; Cho EM; Jang KM; Ko CW
    Horm Res Paediatr; 2015; 83(4):242-51. PubMed ID: 25765181
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of a novel mutation site in maturity‑onset diabetes of the young in a Chinese family by whole‑exome sequencing.
    Yu H; Liu J; Li X; Miao F; Yang Y
    Mol Med Rep; 2019 Sep; 20(3):2373-2380. PubMed ID: 31322178
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of Maturity-Onset-Diabetes of the Young (MODY) mutations in a country where diabetes is endemic.
    Al-Kandari H; Al-Abdulrazzaq D; Davidsson L; Nizam R; Jacob S; Melhem M; John SE; Al-Mulla F
    Sci Rep; 2021 Aug; 11(1):16060. PubMed ID: 34373539
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.