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Human Genetics   Research Article

Effect of ARMS2 gene polymorphism on intravitreal ranibizumab treatment for neovascular age-related macular degeneration

Authors: H. Bardak, Y. Bardak, Y. Ercalik, E. Turkseven Kumral, S. Imamoglu, M. Gunay, H. Ozbas and O. Bagci

Age-related macular degeneration (AMD) is a leading cause of blindness in developed countries. The ARMS2 gene has been found to be associated with AMD. Currently, intravitreal ranibizumab (IVR) treatment is one of the widely used treatments for neovascular AMD. The aim of this study was to investigate the association between t.. Read More»

Genet. Mol. Res. 15(4):
gmr15049164
DOI:
10.4238/gmr15049164
Animal Genetics   Research Article

Differential expression of Toll-like receptors in goat dominant and nondominant follicles

Authors: G.X. E, Y.J. Zhao, Y.H. Ma, M.X. Chu, Q.H. Hong, S.J. Lv, L. Zhu, F.K. Li, Y.G. Han, X. Wu5and Y.F. Huang

The mechanism of dominant follicle selection is unclear because of its physiological complexity. However, some studies have reported that the immune system plays an important role in reproductive physiology. The objective of the current study was to investigate the differential expression of Toll-like receptors (TLRs) in the d.. Read More»

Genet. Mol. Res. 15(4):
gmr15049157
DOI:
10.4238/gmr15049157
Animal Genetics   Research Article

Evaluation of crosses of Holstein, Jersey or Brown Swiss sires x Holstein-Friesian/Gir dams. 3. Lifetime performance and economic evaluation

Authors: R.L. Teodoro and F.E. Madalena

Lifetime dairy production, reproduction and growth traits of 75 females sired by Holstein, Jersey or Brown Swiss bulls and Holstein- Friesian x Gir dams of 1/2 to 3/4 Holstein-Friesian fractions were compared. The animals were in a single herd under the same management. Milk, fat and protein yields, concentrates fed, reproduct.. Read More»

Genet. Mol. Res. 4(1):
Plant Genetics   Research Article

Evidence for a natural hybrid of peacock bass (Cichla monoculus vs Cichla temensis) based on esterase electrophoretic patterns

Authors: Aylton Saturnino Teixeira and Suzana da Silva de Oliveira

Esterase (Est) and esterase-D (Est-D) electrophoretic patterns identified by starch gel electrophoresis of skeletal muscle protein extracts of 184 specimens of three species of peacock bass, locally known as tucunarés (Cichla monoculus, C. temensis and Cichla sp), plus four specimens of a supposed hybrid (C. monoculus v.. Read More»

Genet. Mol. Res. 4(1):
Microbial Genetics   Research Article

Specific and straightforward molecular investigation of �²-thalassemia mutations in the Malaysian Malays and Chinese using direct TaqMan genotyping assays

Authors: S.L. Kho, K.H. Chua, E. George and J.A.M.A. Tan

Beta-thalassemia is a life-threatening inherited blood disorder. Rapid characterization of β-globin gene mutations is necessary because of the high frequency of Malaysian β-thalassemia carriers. A combination real-time polymerase chain reaction genotyping assay using TaqMan probes was developed to confirm β-globin gene mutations. In this st.. Read More»

Genet. Mol. Res. 12(3):
2013.February.28.4
DOI:
10.4238/2013.February.28.4
Human Genetics   Research Article

Hereditary hemochromatosis in a Brazilian university hospital in S�£o Paulo State (1990-2000)

Authors: Ana L.C. Martinelli, Rui Filho, Samantha Cruz, Rendrik Franco,Marli Tavella, Marie Secaf, Leandra Ramalho, Sergio Zucoloto, Sandra Rodrigues and Marcos Zago

Hereditary hemochromatosis (HH) is the most common genetic disease among individuals of European descent. Two mutations (845G→A, C282Y and 187C→G, H63D) in the hemochromatosis gene (HFE gene) are associated with HH. About 85-90% of patients of northern European descent with HH are C282Y homozygous. The prevalence of .. Read More»

Genet. Mol. Res. 4(1):
Human Genetics   Research Article

Association between COL9A2 Gln326Arg mutations and the development of intervertebral disc disease in a Chinese population

Authors: T. Meng, Q. Ren, J.M. Wang, H. Shi, S.T. Zhang and M.T. Liu

Intervertebral disc disease is a multifactorial condition, yet disease pathogenesis that can be promoted by a single dominant mutation affecting the expression of susceptibility genes. We performed a case-control study to assess the influence of the COL9A2 Gln326Arg polymorphism on risk of intervertebral disc disease in a Chin.. Read More»

Genet. Mol. Res. 15(4):
gmr15048958
DOI:
10.4238/gmr15048958
Human Genetics   Research Article

No relationship found between -1438A/G polymorphism of the serotonin 2A receptor gene (rs6311) and major depression susceptibility in a northeastern Thai population

Authors: T. Tencomnao, V. Thongrakard, W. Phuchana, T. Sritharathikhun and S. Suttirat

Several lines of evidence suggest a molecular role of -1438A/G single nucleotide polymorphism in the 5-HTR2A gene promoter (rs6311) in regulating the expression of this gene, making rs6311 polymorphism a promising candidate for an association study. We looked for a possible association between rs6311 polymorphism and major dep.. Read More»

Genet. Mol. Res. 9(2):
vol9-2gmr823
DOI:
10.4238/vol9-2gmr823
Microbial Genetics   Research Article

Molecular cloning and characterization of the glyceraldehyde-3-phosphate dehydrogenase gene from Penicillium expansum PE-12

Authors: T. Zhang, Z. Qi, Q.S. Yu and K.X. Tang

Penicillium expansum produces large amounts of lipase, which is widely used in laundry detergent and leather industry. We isolated the glyceraldehyde-3-phosphate dehydrogenase gene (PeGPD) from P. expansum PE-12 through reverse transcriptase PCR and 5êÃ?Â?Ã?Â?-3êÃ?Â?Ã?Â?-rapid amplification of cDNA ends (RACE-PCR). The gene is 1266 bp long, in.. Read More»

Genet. Mol. Res. 12(3):
2013.February.6.2
DOI:
10.4238/2013.February.6.2
Human Genetics   Research Article

Correlation between TRAIL and caspase-8 expression and their relationship with cell proliferation and apoptosis in human osteosarcoma

Authors: X. Ning, X.W. Shang, Y. Zhuang, M. Liu, H. Yang, H. Zhang and M.Z. Huang

Osteosarcoma is a common malignant bone tumor that mainly affects children and adolescents. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a member of the tumor necrosis factor superfamily. Caspase-8 appears in the upstream of apoptosis signaling pathway among caspases. We investigated TRAIL and caspase-8 l.. Read More»

Genet. Mol. Res. 15(4):
gmr15048876
DOI:
10.4238/gmr15048876