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Nature Publishing Group | 論文
- Non-incidental coamplification of Myc and ERBB2, and Myc and EGFR, in gastric adenocarcinomas
- Genetic variation of genes for xenobiotic-metabolizing enzymes and risk of bronchial asthma : the importance of gene-gene and gene-environment interactions for disease susceptibility
- Gingival epithelial cells heterozygous for Toll-like receptor 4 polymorphisms Asp299Gly and Thr399Ile are hypo-responsive to Porphyromonas gingivalis
- Urokinase-targeted fusion by oncolytic sendai virus eradicates orthotopic glioblastomas by pronounced synergy with interferon-β gene
- Sulphate-climate coupling over the past 300,000 years in inland Antarctica
- The relationship of serum and salivary cortisol levels to male sexual dysfunction as measured by the international index of erectile function
- The functional significance of microRNA-375 in human squamous cell carcinoma : aberrant expression and effects on cancer pathways
- Therapeutic effect of suicide gene-transferred mesenchymal stem cells in a rat model of glioma
- Genome-wide profiling of promoter methylation in human
- Development of basophils in mongolian gerbils: Formation of basophilic cell clusters in the bone marrow after Nippostrongylus brasiliensis infection
- Cerebral hemorrhage in Fabry's disease
- Nemo-like kinase suppresses Notch signalling by interfering with formation of the Notch active transcriptional complex
- Structures and physiological roles of 13 integral lipids of bovine heart cytochrome c oxidase
- Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair
- Hypophosphatasia now draws more attention of both clinicians and researchers : A Commentary on prevelance of c. 1559deIT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasias in Japanese and effects of the mutation on he
- Factor V Leiden mutation in Arabs in Kuwait by real-time PCR : different values for different Arabs
- MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma : association between SNP309 GG genotype and tumor Breslow thickness
- The heritability of risk and age at onset of Parkinson's disease after accounting for known genetic risk factors
- Acquisition of inverted GSTM exons by an intron of primate GSTM5 gene
- pHCR : a Parallel Haplotype Configuration Reduction algorithm for haplotype interaction analysis