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Kidney Disease

Human Genetics   Research Article

MicroRNAs as biomarkers of kidney allograft injuries ischemia reperfusion and acute rejection

Authors: Patricia Milhoransa, Carolina Caruccio Montanari, Mariane Dos Santos, Marina Sieber, Roberto Ceratti Manfro

Renal transplantation provides a significant increase in life expectancy for patients with end-stage kidney diseases. Despite the unequivocal progresses made in the last decades, many grafts injuries still jeopardize graft function leading to its loss. Currently, the allograft biopsy is the gold standard for diagnosing such conditions. However, it has man.. Read More»

Genet. Mol. Res. 17(4):
http://dx.doi.org/gmr16039933
DOI:
http://dx.doi.org/10.4238/gmr16039933
Medical Genetics   Research Article

Pulmonary hypertension in patients with stage 1-3 chronic kidney disease

Authors: Q.M. Yang and X.R. Bao

Pulmonary hypertension (PH) secondary to chronic kidney disease (CKD) is common, but in stages 1-3 CKD patients, it remains unclear. We sought to evaluate the prevalence of PH and elucidate the possible pathogenesis in Chinese patients with early stage kidney disease. Doppler-estimated pulmonary systolic artery pressure (PASP).. Read More»

Genet. Mol. Res. 13(3):
2014.July.25.25
DOI:
10.4238/2014.July.25.25
Human Genetics   Research Article

eNOS gene Glu298Asp and 4b/a polymorphisms are associated with renal function parameters in Mexican patients with Fabry disease

Authors: A. Marin-Medina, A.J.L. Brambila-Tapia, V.J. Picos-C�¡rdenas, M.P. Gallegos-Arreola and L.E. Figuera

Fabry disease (FD) is an inherited X-linked lysosomal disease that causes renal failure in a high percentage of affected individuals. The eNOS gene encodes for endothelial nitric oxide synthase, which plays an important role in glomerular hemodynamics. This gene has two main polymorphisms (Glu298Asp and 4b/a) that have been st.. Read More»

Genet. Mol. Res. 15(4):
gmr15047802
DOI:
10.4238/gmr15047802
Animal Genetics   Research Article

Proteomic analysis revealed the altered kidney protein profile of a Cyld knockout mouse model

Authors: Y. Zhao, Y. Zhang, H.B. Song, F. Wu, X.L. Wang, S.-C. Sun, T.X. Cui and D.Q. Tang

The aim of this study was to compare the proteomics pattern of the kidneys from Cyld knockout mice with that from normal mouse kidneys and establish a preliminary understanding of the role of Cyld in the kidney. Proteins from the kidneys of knockout Cyld mice and wild-type mice were extracted, isobaric tags for relative and absolute quantitation (iTRAQ) w.. Read More»

Genet. Mol. Res. 14(2):
2015.June.1.14
DOI:
10.4238/2015.June.1.14
Human Genetics   Case Reports

Whole-exome analysis of a child with polycystic kidney disease and ventriculomegaly

Authors: M.M. Nabhan,H. Abdelaziz,Y. Xu,R. El Sayed,M. Santibanez-Koref,N.A. Soliman and J.A. Sayer

Autosomal recessive polycystic kidney disease (ARPKD) is an inherited ciliopathy leading to progressive kidney and liver disease. Biallelic mutations in the PKHD1 gene underlie this condition. We describe a child with bilaterally enlarged cystic kidneys, portal hypertension, and cerebral ventriculomegaly. Molecular genetic investigations using whole-exome.. Read More»

Genet. Mol. Res. 14(2):
http://dx.doi.org/2015.April.17.11
DOI:
http://dx.doi.org/10.4238/2015.April.17.11