Recent progress in mitochondrial DNA analysis
スポンサーリンク
概要
- 論文の詳細を見る
- 2005-07-01
著者
-
Yuasa Isao
Division Of Legal Medicine Faculty Of Medicine Tottori University
-
UMETSU Kazuo
Department of Experimental and Forensic Pathology, Faculty of Medicine, Yamagata University
-
Umetsu Kazuo
Department Of Experimental And Forensic Pathology Faculty Of Medicine Yamagata University
関連論文
- 山口県における赤血球酸性フォスファタ-ゼ型の高感度な血中1酸化炭素定量法等電点電気泳動による研究〔英文〕
- 日本人集団におけるGC型遺伝子頻度の地理的勾配--免疫電気泳動によって得られたデ-タの解析〔英文〕
- 各種保存条件が血痕中の型的凝集素におよぼす影響
- Molecular basis of complement factor I (CFI) polymorphism : one of two polymorphic suballeles responsible for CFI A is Japanese-specific
- OCA2^*481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations
- Molecular characterization of four alpha-l-antitrypsin variant alleles found in Japanese population : a mutation hot spot at the codon for amino acid 362
- Characterization of genomic rearrangements of the α_1-acid glycoprotein/orosomucoid gene in Ghanaians
- A new single-nucleotide polymorphism in the seventh component of complement (C7) gene
- 西日本におけるClR型の等電点電気泳動による研究
- 汗斑上の血痕中の同種凝集素の検出
- De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
- Neonatal hyperbilirubinemia and the bilirubin uridine diphosphate-glucuronosyltransferase gene : The common -3263T > G mutation of phenobarbital response enhancer module is not associated with the neonatal hyperbilirubinemia in Japanese
- Sudden Infant Death Syndrome Is Not Associated with the Mutation of PHOX2B Gene, a Major Causative Gene of Congenital Central Hypoventilation Syndrome
- ITIH1^* Q0_, A NULL ALLELE OF INTER-ALPHA-TRYPSIN INHIBITOR H1 CAUSED BY DELETION/FRAMESHIFT MUTATION
- Molecular aspect of biochemical markers
- Recent progress in mitochondrial DNA analysis
- Y-chromosomal STR haplotyping in a Japanese population
- Parentally imprinted allele typing at a short tandem repeat locus in intron 1a of imprinted gene KCNQ1
- Utility of haplogroup determination for forensic mtDNA analysis in the Japanese population
- A Japanese-specific allele in the GALNT11 gene
- Diversification process of stag beetles belonging to the genus Platycerus Geoffroy (Coleoptera : Lucanidae) in Japan based on nuclear and mitochondrial genes
- Polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : rs17884724:A>C is associated with 7-alanine expansion
- The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations
- A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy