Passos-Bueno MR - Search Results

1

Deletion of the basement membrane heparan sulfate proteoglycan type XVIII collagen causes hypertriglyceridemia in mice and humans.

Bishop JR, Passos-Bueno MR, Fong L, Stanford KI, Gonzales JC, Yeh E, Young SG, Bensadoun A, Witztum JL, Esko JD, Moulton KS. Bishop JR, et al. PLoS One. 2010 Nov 10;5(11):e13919. doi: 10.1371/journal.pone.0013919. PLoS One. 2010. PMID: 21085708 Free PMC article.

2

Cell Type-Dependent Nonspecific Fibroblast Growth Factor Signaling in Apert Syndrome.

Yeh E, Atique R, Fanganiello RD, Sunaga DY, Ishiy FA, Passos-Bueno MR. Yeh E, et al. Stem Cells Dev. 2016 Aug 15;25(16):1249-60. doi: 10.1089/scd.2016.0018. Epub 2016 Jun 23. Stem Cells Dev. 2016. PMID: 27339175

3

Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome.

Yeh E, Fanganiello RD, Sunaga DY, Zhou X, Holmes G, Rocha KM, Alonso N, Matushita H, Wang Y, Jabs EW, Passos-Bueno MR. Yeh E, et al. PLoS One. 2013 Apr 4;8(4):e60439. doi: 10.1371/journal.pone.0060439. Print 2013. PLoS One. 2013. PMID: 23593218 Free PMC article.

4

COL18A1 is highly expressed during human adipocyte differentiation and the SNP c.1136C > T in its "frizzled" motif is associated with obesity in diabetes type 2 patients.

Errera FI, Canani LH, Yeh E, Kague E, Armelin-Corrêa LM, Suzuki OT, Tschiedel B, Silva ME, Sertié AL, Passos-Bueno MR. Errera FI, et al. An Acad Bras Cienc. 2008 Mar;80(1):167-77. doi: 10.1590/s0001-37652008000100012. An Acad Bras Cienc. 2008. PMID: 18345385 Free article.

5

Genetics of craniosynostosis: genes, syndromes, mutations and genotype-phenotype correlations.

Passos-Bueno MR, Sertié AL, Jehee FS, Fanganiello R, Yeh E. Passos-Bueno MR, et al. Front Oral Biol. 2008;12:107-143. doi: 10.1159/000115035. Front Oral Biol. 2008. PMID: 18391498 Review.

6

Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells.

Fanganiello RD, Sertié AL, Reis EM, Yeh E, Oliveira NA, Bueno DF, Kerkis I, Alonso N, Cavalheiro S, Matsushita H, Freitas R, Verjovski-Almeida S, Passos-Bueno MR. Fanganiello RD, et al. Mol Med. 2007 Jul-Aug;13(7-8):422-42. doi: 10.2119/2007–00027.Fanganiello. Mol Med. 2007. PMID: 17622301 Free PMC article.

7

FGFR2 mutation confers a less drastic gain of function in mesenchymal stem cells than in fibroblasts.

Yeh E, Atique R, Ishiy FA, Fanganiello RD, Alonso N, Matushita H, da Rocha KM, Passos-Bueno MR. Yeh E, et al. Stem Cell Rev Rep. 2012 Sep;8(3):685-95. doi: 10.1007/s12015-011-9327-6. Stem Cell Rev Rep. 2012. PMID: 22048896 Free PMC article.

8

Functional vascular endothelial growth factor -634G>C SNP is associated with proliferative diabetic retinopathy: a case-control study in a Brazilian population of European ancestry.

Errera FI, Canani LH, Silva ME, Yeh E, Takahashi W, Santos KG, Souto KE, Tschiedel B, Roisenberg I, Gross JL, Passos-Bueno MR. Errera FI, et al. Diabetes Care. 2007 Feb;30(2):275-9. doi: 10.2337/dc06-1399. Diabetes Care. 2007. PMID: 17259494

9

A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia.

Hu Y, Chen IP, de Almeida S, Tiziani V, Do Amaral CM, Gowrishankar K, Passos-Bueno MR, Reichenberger EJ. Hu Y, et al. PLoS One. 2013 Aug 12;8(8):e73576. doi: 10.1371/journal.pone.0073576. eCollection 2013. PLoS One. 2013. PMID: 23951358 Free PMC article.

10

Effect of polymorphisms of the MTHFR and APOE genes on susceptibility to diabetes and severity of diabetic retinopathy in Brazilian patients.

Errera FI, Silva ME, Yeh E, Maranduba CM, Folco B, Takahashi W, Pereira AC, Krieger JE, Passos-Bueno MR. Errera FI, et al. Braz J Med Biol Res. 2006 Jul;39(7):883-8. doi: 10.1590/s0100-879x2006000700005. Braz J Med Biol Res. 2006. PMID: 16862278 Free article.

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