PubMed

Genetic analysis of albuminuria in aging mice and concordance with loci for human diabetic nephropathy found in a genome-wide association scan.

Tsaih SW, Pezzolesi MG, Yuan R, Warram JH, Krolewski AS, Korstanje R.

Kidney Int. 2009 Nov 18. [Epub ahead of print]PMID: 19924099 [PubMed - as supplied by publisher]Related articles

confirmation of genetic associations at ELMO1 in the GoKinD collection supports its role as a susceptibility gene in diabetic nephropathy.

Pezzolesi MG, Katavetin P, Kure M, Poznik GD, Skupien J, Mychaleckyj JC, Rich SS, Warram JH, Krolewski AS.

Diabetes. 2009 Nov;58(11):2698-702. Epub 2009 Aug 3.PMID: 19651817 [PubMed - in process]Related articles

Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.

Pezzolesi MG, Poznik GD, Mychaleckyj JC, Paterson AD, Barati MT, Klein JB, Ng DP, Placha G, Canani LH, Bochenski J, Waggott D, Merchant ML, Krolewski B, Mirea L, Wanic K, Katavetin P, Kure M, Wolkow P, Dunn JS, Smiles A, Walker WH, Boright AP, Bull SB; DCCT/EDIC Research Group, Doria A, Rogus JJ, Rich SS, Warram JH, Krolewski AS.

Diabetes. 2009 Jun;58(6):1403-10. Epub 2009 Feb 27.PMID: 19252134 [PubMed - indexed for MEDLINE]Related articlesFree article

High-density single nucleotide polymorphism genome-wide linkage scan for susceptibility genes for diabetic nephropathy in type 1 diabetes: discordant sibpair approach.

Rogus JJ, Poznik GD, Pezzolesi MG, Smiles AM, Dunn J, Walker W, Wanic K, Moczulski D, Canani L, Araki S, Makita Y, Warram JH, Krolewski AS.

Diabetes. 2008 Sep;57(9):2519-26. Epub 2008 Jun 16.PMID: 18559660 [PubMed - indexed for MEDLINE]Related articlesFree article

Differential expression of PTEN-targeting microRNAs miR-19a and miR-21 in Cowden syndrome.

Pezzolesi MG, Platzer P, Waite KA, Eng C.

Am J Hum Genet. 2008 May;82(5):1141-9.PMID: 18460397 [PubMed - indexed for MEDLINE]Related articlesFree article

Cowden syndrome-affected patients with PTEN promoter mutations demonstrate abnormal protein translation.

Teresi RE, Zbuk KM, Pezzolesi MG, Waite KA, Eng C.

Am J Hum Genet. 2007 Oct;81(4):756-67. Epub 2007 Aug 15.PMID: 17847000 [PubMed - indexed for MEDLINE]Related articlesFree article

Comparative genomic and functional analyses reveal a novel cis-acting PTEN regulatory element as a highly conserved functional E-box motif deleted in Cowden syndrome.

Pezzolesi MG, Zbuk KM, Waite KA, Eng C.

Hum Mol Genet. 2007 May 1;16(9):1058-71. Epub 2007 Mar 6.PMID: 17341483 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.

Pezzolesi MG, Li Y, Zhou XP, Pilarski R, Shen L, Eng C.

Am J Hum Genet. 2006 Nov;79(5):923-34. Epub 2006 Sep 29.PMID: 17033968 [PubMed - indexed for MEDLINE]Related articlesFree article

Examination of PPP1R3B as a candidate gene for the type 2 diabetes and MODY loci on chromosome 8p23.

Dunn JS, Mlynarski WM, Pezzolesi MG, Borowiec M, Powers C, Krolewski AS, Doria A.

Ann Hum Genet. 2006 Sep;70(Pt 5):587-93.PMID: 16907705 [PubMed - indexed for MEDLINE]Related articles

Examination of candidate chromosomal regions for type 2 diabetes reveals a susceptibility locus on human chromosome 8p23.1.

Pezzolesi MG, Nam M, Nagase T, Klupa T, Dunn JS, Mlynarski WM, Rich SS, Warram JH, Krolewski AS.

Diabetes. 2004 Feb;53(2):486-91.PMID: 14747302 [PubMed - indexed for MEDLINE]Related articlesFree article

A method for developing high-density SNP maps and its application at the type 1 angiotensin II receptor (AGTR1) locus.

Antonellis A, Rogus JJ, Canani LH, Makita Y, Pezzolesi MG, Nam M, Ng D, Moczulski D, Warram JH, Krolewski AS.

Genomics. 2002 Mar;79(3):326-32.PMID: 11863362 [PubMed - indexed for MEDLINE]Related articles