341 related articles for article (PubMed ID: 21518409)
61. Generation of two human iPSC lines from patients with maturity-onset diabetes of the young type 2 (MODY2) and permanent neonatal diabetes due to mutations in the GCK gene.
Aqel YWA; Ali G; Elsayed AK; Al-Khawaga S; Hussain K; Abdelalim EM
Stem Cell Res; 2020 Oct; 48():101991. PubMed ID: 32971462
[TBL] [Abstract][Full Text] [Related]
62. Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene.
Borowiec M; Mysliwiec M; Fendler W; Antosik K; Brandt A; Malecki M; Mlynarski W
Acta Diabetol; 2011 Sep; 48(3):203-8. PubMed ID: 21437567
[TBL] [Abstract][Full Text] [Related]
63. [Glucokinase gene mutation as a causative factor of permanent neonatal diabetes mellitus].
Wajda-Cuszlag M; Witkowski D; Piontek E; Wysocka-Mincewicz M; Borowiec M; Młynarski W; Szalecki M
Pediatr Endocrinol Diabetes Metab; 2012; 18(1):45-7. PubMed ID: 22525692
[TBL] [Abstract][Full Text] [Related]
64. Heterogeneity in phenotype of hyperinsulinism caused by activating glucokinase mutations: a novel mutation and its functional characterization.
Martínez R; Gutierrez-Nogués Á; Fernández-Ramos C; Velayos T; Vela A; ; Navas MÁ; Castaño L
Clin Endocrinol (Oxf); 2017 Jun; 86(6):778-783. PubMed ID: 28247534
[TBL] [Abstract][Full Text] [Related]
65. A novel genetic mutation in a Portuguese family with GCK-MODY.
Almeida C; Silva SR; Garcia E; Leite AL; Teles A; Campos RA
J Pediatr Endocrinol Metab; 2014 Jan; 27(1-2):129-33. PubMed ID: 23843579
[TBL] [Abstract][Full Text] [Related]
66. Insights into the pathogenicity of rare missense GCK variants from the identification and functional characterization of compound heterozygous and double mutations inherited in cis.
Beer NL; Osbak KK; van de Bunt M; Tribble ND; Steele AM; Wensley KJ; Edghill EL; Colcough K; Barrett A; Valentínová L; Rundle JK; Raimondo A; Grimsby J; Ellard S; Gloyn AL
Diabetes Care; 2012 Jul; 35(7):1482-4. PubMed ID: 22611063
[TBL] [Abstract][Full Text] [Related]
67. Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).
Boesgaard TW; Pruhova S; Andersson EA; Cinek O; Obermannova B; Lauenborg J; Damm P; Bergholdt R; Pociot F; Pisinger C; Barbetti F; Lebl J; Pedersen O; Hansen T
BMC Med Genet; 2010 Mar; 11():42. PubMed ID: 20226046
[TBL] [Abstract][Full Text] [Related]
68. Identification of GCK-maturity-onset diabetes of the young in cases of neonatal hyperglycemia: A case series and review of clinical features.
Hughes AE; De Franco E; Globa E; Zelinska N; Hilgard D; Sifianou P; Hattersley AT; Flanagan SE
Pediatr Diabetes; 2021 Sep; 22(6):876-881. PubMed ID: 34085361
[TBL] [Abstract][Full Text] [Related]
69. GCK mutations in Chinese MODY2 patients: a family pedigree report and review of Chinese literature.
Ping Xiao Y; Hua Xu X; Lan Fang Y; Jiang L; Chen C; Liang L; Lin Wang C
J Pediatr Endocrinol Metab; 2016 Aug; 29(8):959-64. PubMed ID: 27269892
[TBL] [Abstract][Full Text] [Related]
70. [MODY diabetes--a monogenic developmental and functional disturbance of pancreatic beta cells].
Miettinen PJ; Tuomi T
Duodecim; 2012; 128(19):1989-98. PubMed ID: 23155750
[TBL] [Abstract][Full Text] [Related]
71. A new de novo mutation in the GCK gene causing MODY2.
Cappelli A; Silvestri S; Tumini S; Carinci S; Cipriano P; Massi L; Staffolani P; Pianese L
Diabetes Res Clin Pract; 2011 Jul; 93(1):e41-3. PubMed ID: 21514682
[TBL] [Abstract][Full Text] [Related]
72. Functional analysis of human glucokinase gene mutations causing MODY2: exploring the regulatory mechanisms of glucokinase activity.
García-Herrero CM; Galán M; Vincent O; Flández B; Gargallo M; Delgado-Alvarez E; Blázquez E; Navas MA
Diabetologia; 2007 Feb; 50(2):325-33. PubMed ID: 17186219
[TBL] [Abstract][Full Text] [Related]
73. Permanent neonatal diabetes in an Asian infant.
Porter JR; Shaw NJ; Barrett TG; Hattersley AT; Ellard S; Gloyn AL
J Pediatr; 2005 Jan; 146(1):131-3. PubMed ID: 15644838
[TBL] [Abstract][Full Text] [Related]
74. Heterozygous lys169Glu mutation of glucokinase gene in a Chinese family having glucokinase-maturity-onset diabetes of the young (GCK-MODY).
Zhou W; Chen M; Zhou H; Zhang Z
J Postgrad Med; 2019; 65(4):241-243. PubMed ID: 31571622
[TBL] [Abstract][Full Text] [Related]
75. Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
Shaw-Smith C; Flanagan SE; Patch AM; Grulich-Henn J; Habeb AM; Hussain K; Pomahacova R; Matyka K; Abdullah M; Hattersley AT; Ellard S
Pediatr Diabetes; 2012 Jun; 13(4):314-21. PubMed ID: 22369132
[TBL] [Abstract][Full Text] [Related]
76. A three-step programmed method for the identification of causative gene mutations of maturity onset diabetes of the young (MODY).
Li Q; Cao X; Qiu HY; Lu J; Gao R; Liu C; Yuan MX; Yang GR; Yang JK
Gene; 2016 Aug; 588(2):141-8. PubMed ID: 27185633
[TBL] [Abstract][Full Text] [Related]
77. Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations.
Aykut A; Karaca E; Onay H; Gökşen D; Çetinkalp Ş; Eren E; Ersoy B; Çakır EP; Büyükinan M; Kara C; Anık A; Kırel B; Özen S; Atik T; Darcan Ş; Özkınay F
Gene; 2018 Jan; 641():186-189. PubMed ID: 29056535
[TBL] [Abstract][Full Text] [Related]
78. Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia.
Habeb AM; Al-Magamsi MS; Eid IM; Ali MI; Hattersley AT; Hussain K; Ellard S
Pediatr Diabetes; 2012 Sep; 13(6):499-505. PubMed ID: 22060631
[TBL] [Abstract][Full Text] [Related]
79. Novel deletion mutation in the glucokinase gene from a korean man with GCK-MODY phenotype and situs inversus.
Cho YK; Cho EH; Choi HS; Kim SW
Diabetes Res Clin Pract; 2018 Sep; 143():263-266. PubMed ID: 30086370
[TBL] [Abstract][Full Text] [Related]
80. Insights into pathogenesis of five novel GCK mutations identified in Chinese MODY patients.
Liu L; Liu Y; Ge X; Liu X; Chen C; Wang Y; Li M; Yin J; Zhang J; Chen Y; Zhang R; Jiang Y; Zhao W; Yang D; Zheng T; Lu M; Zhuang L; Jiang M
Metabolism; 2018 Dec; 89():8-17. PubMed ID: 30257192
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
