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Human Genetics   Research Article

Ability of HMGB1 protein to bind to intrinsically bent and non-bent DNA sites in the AMPD2 gene amplicon

Authors: K.J.R. Passos, A. Fiorini, F.R. Rosado, D.V.B. Freitas, Q.A. Lima Neto, J.R. Pattaro Junior, V.P. Gaspar and M.A. Fernandez

HMGB-like proteins are architectural chromatin factors, and their function is heavily dependent on their ability to interact with DNA (especially non-canonical DNA structures). HMGB1 is involved in many DNA processes, and dysregulation of HMGB protein expression has profound effects on cellular transcription, resulting in seve.. Read More»

Genet. Mol. Res. 15(2):
gmr.15027441
DOI:
10.4238/gmr.15027441
Microbial Genetics   Research Article

Influence of the XbaI polymorphism in the estrogen receptor-�± gene on human spermatogenic defects

Authors: J. Meng, X. Mu and Y.M. Wang

Polymorphisms of estrogen receptor (ER) genes have been implicated in male infertility, but studies of this association have produced conflicting results. The present study was conducted to examine whether polymorphisms within the ERα and ERβ genes are susceptibility factors for human male idiopathic infertility in Chinese men. We investigated .. Read More»

Genet. Mol. Res. 12(2):
2013.June.11.1
DOI:
10.4238/2013.June.11.1
Human Genetics   Research Article

Genetic parameters for carcass traits and body weight using a Bayesian approach in the Canchim cattle

Authors: S.L.C. Meirelles, F.B. Mokry, A.C. Espasand�­n, M.A.D. Dias, M.M. Baena and L.C. de A. Regitano

Correlation between genetic parameters and factors such as backfat thickness (BFT), rib eye area (REA), and body weight (BW) were estimated for Canchim beef cattle raised in natural pastures of Brazil. Data from 1648 animals were analyzed using multi-trait (BFT, REA, and BW) animal models by the Bayesian approach. This model i.. Read More»

Genet. Mol. Res. 15(2):
gmr.15027471
DOI:
10.4238/gmr.15027471
Human Genetics   Research Article

Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia

Authors: F. Richeti, C. Kochi, M.N. Rocha, C. Santâ��Anna Corr�ªa, R. Lazzarini, R.M. Guazzelli, R.F. Mendon�§a, M.R. Melo and C.A. Longui

Normal testosterone levels are frequently observed in women with androgenetic alopecia (AGA), suggesting the involvement of androgen sensitivity in this condition. Androgen sensitivity is related to androgen receptor (AR) messenger RNA (mRNA) production in hair follicles and is negatively related to the number of CAG repeats present in exon 1 of the AR ge.. Read More»

Genet. Mol. Res. 12(2):
2013.February.28.19
DOI:
10.4238/2013.February.28.19
Human Genetics   Research Article

IL-16 rs4778889 polymorphism contribution to the development of renal cell cancer in a Chinese population

Authors: S.X. Yang, F. Chen, J.W. Zhang, Z.Q. Sun and B.P. Chen

IL-16 plays an important role in affect the secretion of tumor-related inflammatory cytokines. We aimed to assess the role of interleukin-16 (IL-16) rs4778889 T/C and rs11556218 T/G polymorphisms in the occurrence of renal cell cancer (RCC). This study is composed of 274 RCC patients and 274 control subjects. Genotyping of pol.. Read More»

Genet. Mol. Res. 15(2):
gmr.15027553
DOI:
10.4238/gmr.15027553
Human Genetics   Research Article

Association between the interleukin-1�² gene -511C/T polymorphism and ischemic stroke: an updated meta-analysis

Authors: W. Yan, Z.Y. Chen, J.Q. Chen and H.M. Chen

Numerous studies have investigated the relationship between the interleukin-1β gene (IL1B) -511C/T polymorphism and ischemic stroke (IS) risk. However, the results are inconsistent. We performed this meta-analysis of all available case-control studies that evaluated the relationship between the IL1B -511C/T polymorphism a.. Read More»

Genet. Mol. Res. 15(2):
gmr.15027580
DOI:
10.4238/gmr.15027580
Plant Genetics   Short communication

Plasticity of Corynebacterium diphtheriae pathogenicity islands revealed by PCR

Authors: S.C. Soares, F.A. Dorella, L.G.C. Pacheco, R. Hirata Jr., A.L. Mattos-Guaraldi, V. Azevedo and A. Miyoshi

Despite the existence of a vaccine against diphtheria, this disease remains endemic and is reemerging in several regions due to many factors, including variations in genes coding for virulence factors. One common feature of virulence factors is their high concentration in pathogenicity islands (PAIs), very unstable regions acq.. Read More»

Genet. Mol. Res. 10(2):
vol10-2gmr1211
DOI:
10.4238/vol10-2gmr1211
Human Genetics   Research Article

Construction of a primary DNA fingerprint database for cotton cultivars

Authors: Y.C. Zhang, M. Kuang, W.H. Yang, H.X. Xu, D.Y. Zhou, Y.Q. Wang, X.A. Feng, C. Su and F. Wang

Forty core primers were used to construct a DNA fingerprint database of 132 cotton species based on multiplex fluorescence detection technology. A high first successful ratio of 99.04% was demonstrated with tetraplex polymerase chain reaction. Forty primer pairs amplified a total of 262 genotypes among 132 species, with an average of 6.55 per primer and v.. Read More»

Genet. Mol. Res. 12(2):
2013.January.30.3
DOI:
10.4238/2013.January.30.3
Bioinformatics   Research Article

Dysregulation of TFDP1 and of the cell cycle pathway in high-grade glioblastoma multiforme: a bioinformatic analysis

Authors: X. Lu, X.D. Lv, Y.H. Ren, W.D. Yang, Z.B. Li, L. Zhang and X.F. Bai

Despite extensive research, the prognosis of high-grade glioblastoma multiforme (GBM) has improved only slightly because of the limited response to standard treatments. Recent advances (discoveries of molecular biomarkers) provide new opportunities for the treatment of GBM. The aim of the present study was to identify diagnost.. Read More»

Genet. Mol. Res. 15(2):
gmr.15027646
DOI:
10.4238/gmr.15027646
Human Genetics   Research Article

Th17/Treg cell expression in children with primary nephritic syndrome and the effects of ox-LDL on Th17/Treg cells

Authors: Y.Y. Li, S.G. Wei, X. Zhao, Y.Z. Jia, Y.F. Zhang and S.Z. Sun

To investigate the role of T-helper cells/Treg (Th17/Treg) and morbidity factors related to primary nephritic syndrome (PNS) in children, as well as the influence of ox-low density lipoprotein (ox-LDL) on Th17/Treg expression in children with PNS. To clarify the pathogenesis of PNS in children, 50 children with PNS treated in .. Read More»

Genet. Mol. Res. 15(2):
gmr.15027669
DOI:
10.4238/gmr.15027669