- SVEP1 promoter regulation by methylation of CpG sites
[作者：Glait-Santar, C; Benayahu, D,期刊：Gene, 页码：6-14 , 文章类型： Article，,卷期：2011年490-40910]
- SVEP1 gene encodes a cell adhesion molecule (CAM) that was previously shown to be expressed by cells related to skeletal tissues. Here we focus on SVEP1 expression regulation in pre-osteoblastic MBA-15 and mammary adenoc...
- Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant
[作者：Goumy, C; Kemeny, S; Eymard-Pierre, E; Richard, C; Gouas, L; Combes, P; Gay-Bellile, M; Gallot, D; Tchirkov, A; Vago, P,期刊：Gene, 页码：15-17 , 文章类型： Article，,卷期：2011年490-40910]
- Cytogenetic heteromorphisms are described as heritable variations at specific chromosomal regions without phenotypic effect. Polymorphisms of the size of heterochromatic centromeric regions of chromosomes 1,9 and 16 have...
- A novel splice site mutation in gene C2orf37 underlying Woodhouse-Sakati syndrome (WSS) in a consanguineous family of Pakistani origin
[作者：Habib, R; Basit, S; Khan, S; Khan, MN; Ahmad, W,期刊：Gene, 页码：26-31 , 文章类型： Article，,卷期：2011年490-40910]
- Woodhouse-Sakati Syndrome (WSS) is a rare autosomal recessive multisystemic disorder that is marked by hypogonadism, alopecia, intellectual disability, deafness, diabetes mellitus and progressive extrapyramidal defects. ...
- Significant differences in gene expression of GABA receptors in peripheral blood leukocytes of migraineurs
[作者：Plummer, PN; Colson, NJ; Lewohl, JM; MacKay, RK; Fernandez, F; Haupt, LM; Griffiths, LR,期刊：Gene, 页码：32-36 , 文章类型： Article，,卷期：2011年490-40910]
- Migraine is a debilitating neurovascular disorder, with a substantial genetic component. The exact cause of a migraine attack is unknown; however cortical hyperexcitability is thought to play a role. As Gamma-aminobutyri...
- Identification of porcine polycystic kidney disease 1 (PKD1) gene: Molecular cloning, expression profile, and implication in disease model
[作者：He, J; Wang, QS; Ye, JH; Hu, XX; Li, N,期刊：Gene, 页码：37-46 , 文章类型： Article，,卷期：2011年490-40910]
- The polycystic kidney disease 1 (PKD1) gene, which accounts for similar to 85% of human autosomal dominant polycystic kidney disease (ADPKD) cases, has been extensively studied in human and mouse. Much information about ...
- Molecular characterization of relatedness among colour variants of Asian Arowana (Scleropages formosus)
[作者：Mohd-Shamsudin, MI; Fard, MZ; Mather, PB; Suleiman, Z; Hassan, R; Othman, RY; Bhassu, S,期刊：Gene, 页码：47-53 , 文章类型： Article，,卷期：2011年490-40910]
- Morphological identification of fish taxa can sometimes prove difficult because phenotypic variation is either being affected by environmental factors, phenotypic characters are highly conserved or marker selection has b...
- Effect of probiotic fermented milk and chlorophyllin on gene expressions and genotoxicity during AFB(1)-induced hepatocellular carcinoma
[作者：Kumar, M; Verma, V; Nagpal, R; Kumar, A; Gautam, SK; Behare, PV; Grover, CR; Aggarwal, PK,期刊：Gene, 页码：54-59 , 文章类型： Article，,卷期：2011年490-40910]
- The aim of this study was to investigate the chemopreventive effect of probiotic fermented milk and chlorophyllin on aflatoxin B(1) (AFB(1)) induced hepatocellular carcinoma. In vivo trials were conducted on 200 Wistar r...
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