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Human Genetics   Research Article

Detection of targets and their mechanisms for early diagnosis of traumatic deep vein thrombosis

Authors: J.W. Mo, D-F. Zhang, G.L. Ji, X.-Z. Liu and B. Fan

The purpose of this investigation was to identify targets for the early diagnosis and predictors of deep venous thrombosis (DVT) and the role of these targets in the formation of venous thrombosis. A model of DVT was constructed in rats. Thromboses and venous walls were sampled for reverse transcription polymerase chain reaction study, and blood was sampl.. Read More»

Genet. Mol. Res. 14(1):
http://dx.doi.org/2015.March.27.26
DOI:
http://dx.doi.org/10.4238/2015.March.27.26
Human Genetics   Research Article

Development and characterization of novel EST-SSR markers and their application for genetic diversity analysis of Jerusalem artichoke (Helianthus tuberosus L.)

Authors: T. Mornkham, P.P. Wangsomnuk, X.C. Mo, F.O. Francisco, L.Z. Gao and H. Kurzweil

Jerusalem artichoke (Helianthus tuberosus L.) is a perennial tuberous plant and a traditional inulin-rich crop in Thailand. It has become the most important source of inulin and has great potential for use in chemical and food industries. In this study, expressed sequence tag (EST)-based simple sequence repeat (SSR) markers we.. Read More»

Genet. Mol. Res. 15(4):
gmr15048857
DOI:
10.4238/gmr15048857
Medical Genetics   Research Article

Pterostilbene as treatment for severe acute pancreatitis

Authors: Y.J. Lin, Y. Ding, J. Wu and B.T. Ning

Acute pancreatitis (AP) has a fast onset and progression, which lead to an unfavorable prognosis. Therefore, the development of novel drugs for its treatment is critical. As a homologous derivative of resveratrol, pterostilbene exerts a variety of effects including anti-inflammatory, antioxidant, and antitumor effects. This study investigated the potentia.. Read More»

Genet. Mol. Res. 15(3):
gmr.15038330
DOI:
10.4238/gmr.15038330
Human Genetics   Research Article

A novel polymorphic Alu insertion embedded in a LINE 1 retrotransposon in the human X chromosome (DXS225): identification and worldwide population study

Authors: Rinaldo Wellerson Pereira, Simone Silva dos Santos and S�©rgio Danilo Junho Pena

We describe a novel polymorphic Alu insertion (DXS225) on the human X chromosome (Xq21.3) embedded into an L1 retrotransposon. The DXS225 polymorphism was genotyped in 684 males from the CEPH Human Genome Diversity Panel. This insertion was found in all regions of the globe, suggesting that it took place before modern humans s.. Read More»

Genet. Mol. Res. 5(1):
Plant Genetics   Research Article

Using the attract method to identify core pathways in juvenile idiopathic arthritis

Authors: J.S. Li, X.L. Gao, Y.R. Liu and Y. Dong

The aim of this study was to identify core pathways associated with juvenile idiopathic arthritis (JIA) using the attract method. Kyoto Encyclopedia of Genes and Genomes pathways were determined using the GSEA-ANOVA method, based on the gene expression data of JIA. Syn-expression groups within core attractor pathways were identified by hierarchical cluste.. Read More»

Genet. Mol. Res. 15(3):
gmr.15038331
DOI:
10.4238/gmr.15038331
Human Genetics   Research Article

Genomic lesions and colorectal carcinogenesis: the effects of protein-calorie restriction and inulin supplementation on deficiency statuses

Authors: W.B. Cantero, N.A. Takahachi, M.O. Mauro, J.R. Pesarini,A.P.M. Rabacow, A.C.M.B. Antoniolli and R.J. Oliveira

The present study investigated the effects of restricting protein and calories and supplementation of inulin, a fiber comprising a linear type of polydisperse carbohydrates composed primarily of fructil-fructose bonds (β-(2→1), on the deficiency statuses of animals in which genomic lesion development and colorectal carcinogenesis had been induce.. Read More»

Genet. Mol. Res. 14(1):
http://dx.doi.org/2015.March.27.27
DOI:
http://dx.doi.org/10.4238/2015.March.27.27
Human Genetics   Research Article

Micronucleus test on gas station attendants

Authors: Cibelem Iribarrem Benites, L�­lian Lund Amado, Rita Aloma Packeiser Vianna and Maria da Gra�§a Martino-Roth

In the present study, the micronucleus test was applied in exfoliated cells of buccal mucosa to assess the mutagenicity risk associated with occupational exposure for gas station attendants. For each individual, 2000 exfoliated buccal cells were analyzed for micronucleus frequency. A highly significant difference was found bet.. Read More»

Genet. Mol. Res. 5(1):
Medical Genetics   Review Article

The time has come: a new scene for PKU treatment

Authors: Luciana Lara dos Santos, Myrian de Castro Magalh�£es, Jos�© N�©lio Janu�¡rio, Marcos Jos�© Burle de Aguiar and Maria Raquel Santos Carvalho

Phenylketonuria (PKU) is one of the few genetic diseases in which mental retardation can be prevented. Hence, diagnosis and treatment must be established early. PKU treatment consists of a phenylalanine-restricted diet supplemented with a phenylalanine-free mixture of amino acids. However, it is difficult to adhere to this die.. Read More»

Genet. Mol. Res. 5(1):
Animal Genetics   Research Article

Well-balanced commensal microbiota contributes to anti-cancer response in a lung cancer mouse model

Authors: Q.-F. Gui, H.-F. Lu, C.-X. Zhang, Z.-R. Xu and Y.-M. Yang

The intestinal microflora affects inflammation and immunity, not only locally at the mucosal level but also systemically, raising the question of whether the microflora affects inflammatory processes that contribute to cancer and its therapy. Prebiotics have also been found to play an antitumor role that is not limited to the gut. We investigated the anti.. Read More»

Genet. Mol. Res. 14(2):
2015.May.25.16
DOI:
10.4238/2015.May.25.16
Medical Genetics   Research Article

Frequencies of phenylalanine hydroxylase mutations I65T, R252W, R261Q, R261X, IVS10nt11, V388M, R408W, Y414C, and IVS12nt1 in Minas Gerais, Brazil

Authors: Luciana Lara dos Santos, Myrian de Castro Magalh�£es, Adriana de Oliveira Reis, Ana L�ºcia Pimenta Starling, Jos�© N�©lio Janu�¡rio, Cleusa Gra�§a da Fonseca, Marcos Jos�© Burle de Aguiar and Maria Raquel Santos Carvalho

In order to determine the phenylketonuria (PKU) mutation spectrum in the population of Minas Gerais State, Brazil, 78 unrelated PKU patients found by the neonatal screening program from 1993 to 2003 were tested for nine phenylalanine hydroxylase mutations. These mutations were selected due to their high frequencies in other Br.. Read More»

Genet. Mol. Res. 5(1):