268 related articles for article (PubMed ID: 16550171)
1. Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome.
Coucke PJ; Willaert A; Wessels MW; Callewaert B; Zoppi N; De Backer J; Fox JE; Mancini GM; Kambouris M; Gardella R; Facchetti F; Willems PJ; Forsyth R; Dietz HC; Barlati S; Colombi M; Loeys B; De Paepe A
Nat Genet; 2006 Apr; 38(4):452-7. PubMed ID: 16550171
[TBL] [Abstract][Full Text] [Related]
2. Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families.
Callewaert BL; Willaert A; Kerstjens-Frederikse WS; De Backer J; Devriendt K; Albrecht B; Ramos-Arroyo MA; Doco-Fenzy M; Hennekam RC; Pyeritz RE; Krogmann ON; Gillessen-kaesbach G; Wakeling EL; Nik-zainal S; Francannet C; Mauran P; Booth C; Barrow M; Dekens R; Loeys BL; Coucke PJ; De Paepe AM
Hum Mutat; 2008 Jan; 29(1):150-8. PubMed ID: 17935213
[TBL] [Abstract][Full Text] [Related]
3. Absence of arterial phenotype in mice with homozygous slc2A10 missense substitutions.
Callewaert BL; Loeys BL; Casteleyn C; Willaert A; Dewint P; De Backer J; Sedlmeier R; Simoens P; De Paepe AM; Coucke PJ
Genesis; 2008 Aug; 46(8):385-9. PubMed ID: 18693279
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the SLC2A10 gene cause arterial abnormalities in mice.
Cheng CH; Kikuchi T; Chen YH; Sabbagha NG; Lee YC; Pan HJ; Chang C; Chen YT
Cardiovasc Res; 2009 Feb; 81(2):381-8. PubMed ID: 19028722
[TBL] [Abstract][Full Text] [Related]
5. Glucose transporter 10 and arterial tortuosity syndrome: the vitamin C connection.
Segade F
FEBS Lett; 2010 Jul; 584(14):2990-4. PubMed ID: 20547159
[TBL] [Abstract][Full Text] [Related]
6. Two novel SLC2A10/GLUT10 mutations in a patient with arterial tortuosity syndrome.
Drera B; Guala A; Zoppi N; Gardella R; Franceschini P; Barlati S; Colombi M
Am J Med Genet A; 2007 Jan; 143A(2):216-8. PubMed ID: 17163528
[No Abstract] [Full Text] [Related]
7. Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio.
Chiarelli N; Ritelli M; Zoppi N; Benini A; Borsani G; Barlati S; Colombi M
Int J Dev Biol; 2011; 55(2):229-36. PubMed ID: 21553381
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.
Lee YC; Huang HY; Chang CJ; Cheng CH; Chen YT
Hum Mol Genet; 2010 Oct; 19(19):3721-33. PubMed ID: 20639396
[TBL] [Abstract][Full Text] [Related]
9. A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome.
Faiyaz-Ul-Haque M; Zaidi SH; Al-Sanna N; Alswaid A; Momenah T; Kaya N; Al-Dayel F; Bouhoaigah I; Saliem M; Tsui LC; Teebi AS
Atherosclerosis; 2009 Apr; 203(2):466-71. PubMed ID: 18774132
[TBL] [Abstract][Full Text] [Related]
10. New insights in the pathogenesis of aortic aneurysms.
Loeys B; De Paepe A
Verh K Acad Geneeskd Belg; 2008; 70(2):69-84. PubMed ID: 18630721
[TBL] [Abstract][Full Text] [Related]
11. Sequence and functional analysis of GLUT10: a glucose transporter in the Type 2 diabetes-linked region of chromosome 20q12-13.1.
Dawson PA; Mychaleckyj JC; Fossey SC; Mihic SJ; Craddock AL; Bowden DW
Mol Genet Metab; 2001; 74(1-2):186-99. PubMed ID: 11592815
[TBL] [Abstract][Full Text] [Related]
12. Molecular cloning of a novel member of the GLUT family of transporters, SLC2a10 (GLUT10), localized on chromosome 20q13.1: a candidate gene for NIDDM susceptibility.
McVie-Wylie AJ; Lamson DR; Chen YT
Genomics; 2001 Feb; 72(1):113-7. PubMed ID: 11247674
[TBL] [Abstract][Full Text] [Related]
13. Comprehensive in silico Study of GLUT10: Prediction of Possible Substrate Binding Sites and Interacting Molecules.
Hosen MJ; Hasan M; Chakraborty S; Abir RA; Zubaer A; Coucke P
Curr Pharm Biotechnol; 2020; 21(2):117-130. PubMed ID: 31203799
[TBL] [Abstract][Full Text] [Related]
14. Arterial Tortuosity Syndrome: homozygosity for two novel and one recurrent SLC2A10 missense mutations in three families with severe cardiopulmonary complications in infancy and a literature review.
Ritelli M; Chiarelli N; Dordoni C; Reffo E; Venturini M; Quinzani S; Monica MD; Scarano G; Santoro G; Russo MG; Calzavara-Pinton P; Milanesi O; Colombi M
BMC Med Genet; 2014 Nov; 15():122. PubMed ID: 25373504
[TBL] [Abstract][Full Text] [Related]
15. Arterial Tortuosity Syndrome: An Ascorbate Compartmentalization Disorder?
Boel A; Veszelyi K; Németh CE; Beyens A; Willaert A; Coucke P; Callewaert B; Margittai É
Antioxid Redox Signal; 2021 Apr; 34(11):875-889. PubMed ID: 31621376
[No Abstract] [Full Text] [Related]
16. Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families.
Faiyaz-Ul-Haque M; Zaidi SH; Wahab AA; Eltohami A; Al-Mureikhi MS; Al-Thani G; Peltekova VD; Tsui LC; Teebi AS
Clin Genet; 2008 Aug; 74(2):189-93. PubMed ID: 18565096
[No Abstract] [Full Text] [Related]
17. GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling.
Willaert A; Khatri S; Callewaert BL; Coucke PJ; Crosby SD; Lee JG; Davis EC; Shiva S; Tsang M; De Paepe A; Urban Z
Hum Mol Genet; 2012 Mar; 21(6):1248-59. PubMed ID: 22116938
[TBL] [Abstract][Full Text] [Related]
18. Adult presentation of arterial tortuosity syndrome in a 51-year-old woman with a novel homozygous c.1411+1G>A mutation in the SLC2A10 gene.
Castori M; Ritelli M; Zoppi N; Molisso L; Chiarelli N; Zaccagna F; Grammatico P; Colombi M
Am J Med Genet A; 2012 May; 158A(5):1164-9. PubMed ID: 22488877
[TBL] [Abstract][Full Text] [Related]
19. A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13.
Zaidi SH; Peltekova V; Meyer S; Lindinger A; Paterson AD; Tsui LC; Faiyaz-Ul-Haque M; Teebi AS
Clin Genet; 2005 Feb; 67(2):183-8. PubMed ID: 15679832
[TBL] [Abstract][Full Text] [Related]
20. GLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts.
Zoppi N; Chiarelli N; Cinquina V; Ritelli M; Colombi M
Hum Mol Genet; 2015 Dec; 24(23):6769-87. PubMed ID: 26376865
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
