Proteasome Modulator 9 SNPs are linked to hypertension in type 2 diabetes families

Cardiovascular Diabetology

Volumn 10, Issue , 2011, Pages

  Gragnoli, Claudia ^a,b,c  

^a PENN STATE MILTON S HERSHEY MEDICAL CENTER   (United States)

^b Temple University   (United States)

^c Bios Biotech Multi Diagnostic Health Center   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEASOME; PROTEIN PROTEASOME MODULATOR 9; UNCLASSIFIED DRUG; PSMD9 PROTEIN, HUMAN;

ARTICLE; BLOOD PRESSURE; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC LINKAGE; HUMAN; HYPERTENSION; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; PHENOTYPE; SINGLE NUCLEOTIDE POLYMORPHISM; COMPARATIVE STUDY; GENETICS; ITALY;

DIABETES MELLITUS, TYPE 2; FEMALE; GENETIC LINKAGE; HUMANS; HYPERTENSION; ITALY; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEASOME ENDOPEPTIDASE COMPLEX;

EID: 80052023522     PISSN: None     EISSN: 14752840     Source Type: Journal    
DOI: 10.1186/1475-2840-10-77     Document Type: Article

References (25)

1. Ikram MK, Xueling S, Jensen RA, Cotch MF, Hewitt AW, Ikram MA, Wang JJ, Klein R, Klein BE, Breteler MM, Cheung N, Liew G, Mitchell P, Uitterlinden AG, Rivadeneira F, Hofman A, de Jong PT, van Duijn CM, Kao L, Cheng CY, Smith AV, Glazer NL, Lumley T, McKnight B, Psaty BM, Jonasson F, Eiriksdottir G, Aspelund T, Harris TB, Launer LJ, Taylor KD, Li X, Iyengar SK, Xi Q, Sivakumaran TA, Mackey DA, Macgregor S, Martin NG, Young TL, Bis JC, Wiggins KL, Heckbert SR, Hammond CJ, Andrew T, Fahy S, Attia J, Holliday EG, Scott RJ, Islam FM, Rotter JI, McAuley AK, Boerwinkle E, Tai ES, Gudnason V, Siscovick DS, Vingerling JR, Wong TY. Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet 2010, 6:e1001184. 10.1371/journal.pgen.1001184, 2965750, 21060863.
2. Thomas MKYK, Tenser MS, Wong GG, Habener JF. Bridge-1, a novel PDZ-domain coactivator of E2A-mediated regulation of insulin gene transcription. Mol Cell Biol 1999, 19:8492. 84960, 10567574.
3. Gragnoli C, Cronsell J. PSMD9 gene variants within NIDDM2 may rarely contribute to type 2 diabetes. J Cell Physiol 2007, 212:568. 10.1002/jcp.21127, 17516568.
4. Gragnoli C. PSMD9 gene in the NIDDM2 locus is linked to type 2 diabetes in Italians. J Cell Physiol 2010, 222:265. 10.1002/jcp.21954, 19877155.
5. Gragnoli C. PSMD9 is linked to MODY3. J Cell Physiol 2010, 223:1.
6. Gragnoli C. T2D-nephropathy linkage within 12q24 locus. Diabetes Res Clin Pract 2011, 92:e73. 10.1016/j.diabres.2011.02.026, 21439668.
7. Gragnoli C. PSMD9 is linked to type 2 diabetes neuropathy. J Diabetes Complications 2011,
8. Gragnoli C. Proteasome Modulator 9 gene is linked to diabetic and non-diabetic retinopathy in T2D. Ophthalmic Genet 2011,
9. Gragnoli C. Proteasome Modulator 9 and Carpal Tunnel Syndrome. Diabetes Res Clin Pract 2011 August 19,
10. Gragnoli C. Hypercholesterolemia and a candidate gene within the 12q24 locus. Cardiovasc Diabetol 2011, 10:38. 10.1186/1475-2840-10-38, 3116465, 21554682.
11. Gragnoli C. Proteasome modulator 9 and macrovascular pathology of T2D. Cardiovasc Diabetol 2011, 10:32. 10.1186/1475-2840-10-32, 3102609, 21496327.
12. Gragnoli C. Kir6.2 (KCNJ11) E23K variant in Type 2 Diabetes in Italians. Obesity and Metabolism 2007, 3:97.
13. Gragnoli C. CHOP T/C and C/T haplotypes contribute to early-onset type 2 diabetes in Italians. J Cell Physiol 2008, 217:291. 10.1002/jcp.21553, 18680108.
14. Gragnoli C, Cronsell J. PPARγ P12A variant in Type 2 Diabetes in Italians. Obesity and Metabolism 2007, 3:99.
15. Gragnoli C, Cockburn BN, Chiaramonte F, Gorini A, Marietti G, Marozzi G, Signorini AM. Early-onset Type II diabetes mellitus in Italian families due to mutations in the genes encoding hepatic nuclear factor 1 alpha and glucokinase. Diabetologia 2001, 44:1326. 10.1007/s001250100644, 11692182.
16. Gragnoli C, Cronsell J. Meta-analysis of the IPF1 D76N polymorphism in a worldwide type 2 diabetes population. Minerva Med 2007, 98:163.
17. Gragnoli C, Lindner T, Cockburn BN, Kaisaki PJ, Gragnoli F, Marozzi G, Bell GI. Maturity-onset diabetes of the young due to a mutation in the hepatocyte nuclear factor-4 alpha binding site in the promoter of the hepatocyte nuclear factor-1 alpha gene. Diabetes 1997, 46:1648. 10.2337/diabetes.46.10.1648, 9313764.
18. Gragnoli C, Menzinger Von Preussenthal G, Habener JF. Triple genetic variation in the HNF-4alpha gene is associated with early-onset type 2 diabetes mellitus in a philippino family. Metabolism 2004, 53:959. 10.1016/j.metabol.2004.03.003, 15281001.
19. Gragnoli C, Milord E, Cox N. Worldwide metanalysis of NEUROG3 variants in type 2 diabetes. Obesity and Metabolism 2006, 2:68.
20. Gragnoli C, Milord E, Habener JF. Linkage study of the glucagon receptor gene with type 2 diabetes mellitus in Italians. Metabolism 2005, 54:786. 10.1016/j.metabol.2005.01.022, 15931615.
21. Gragnoli C, Pierpaoli L, Piumelli N, Chiaramonte F. Linkage studies for T2D in Chop and C/EBPbeta chromosomal regions in Italians. J Cell Physiol 2007, 213:552. 10.1002/jcp.21132, 17620318.
22. Gragnoli C, Stanojevic V, Gorini A, Von Preussenthal GM, Thomas MK, Habener JF. IPF-1/MODY4 gene missense mutation in an Italian family with type 2 and gestational diabetes. Metabolism 2005, 54:983. 10.1016/j.metabol.2005.01.037, 16092045.
23. Milord E, Gragnoli C. Chromosome 10 locus in linkage to type 2 diabetes in Italians. Obesity and Metabolism 2007, 3:44.
24. Milord E, Gragnoli C. NEUROG3 variants and type 2 diabetes in Italians. Minerva Med 2006, 97:373.
25. Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002, 30:97. 10.1038/ng786, 11731797.