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1. 出産時の臍帯血酸塩基分析umbilical cord blood acid base analysis at delivery [show details]
… physiology. This topic will review basic concepts of fetal acid-base physiology and discuss the clinical use of umbilical cord acid-base analysis at delivery. Percutaneous umbilical cord blood sampling and …
2. 遺伝的疾患における褐色細胞腫pheochromocytoma in genetic disorders [show details]
… and SDHAF2 mutation analysis in patients with skull base and neck paragangliomas and SDHB mutation analysis in patients with paragangliomas… The approximate frequency of pheochromocytoma in these disorders is 10 to 20 percent in VHL syndrome,…
3. 遺伝学：用語集genetics glossary of terms [show details]
… (difference in base pair) that affects a single base pair, with a population frequency of at least 1 percent. Single base pair changes that occur at a lower population frequency are called… length, making them useful markers in genetic studies, including genome mapping and family-based linkage analysis. Microsatellites are also known as short tandem repeat markers (STRs) or short tandem repeat …
4. 分娩時胎児心拍数の評価intrapartum fetal heart rate assessment [show details]
…decelerations (frequency and duration of recurrent decelerations). Based on information entered by the clinician, the calculator suggests observation or delivery. The algorithm on which the calculator is based has… and by algorithms for pattern interpretation based on standardization of visual pattern analysis and correlation with fetal scalp blood…
5. 強イオンおよび酸塩基障害の解析（スチュワート法）strong ions and the analysis of acid base disturbances stewart approach [show details]
… Stewart approach to acid-base analysis is that the serum bicarbonate concentration does not alter blood pH. Instead, the independent variables responsible for changes in acid-base balance are the strong …

English Journal

DNA methylation and the frequency of CpG in animal DNA.

, B B, A A, A A.
Nucleic acids research. 1980 Apr;8(7)1499-504.
An analysis of nearest neighbour dinucleotide frequencies and the level of DNA methylation in animals strongly supports the suggestion that 5-methylcytosine (5mC) tends to mutate abnormally frequently to T. This tendency is the likely cause of the CpG deficiency in heavily methylated genomes.
PMID 6253938

Comparison of nucleotide sequences in HeLa cell mRNA and hnRNA.

Fraser NW, Burdon RH, Elton RA.
Nucleic acids research. 1975 Nov;2(11)2131-46.
Nearest neighbour analysis of nucleotides in vertebrate DNA has revealed a marked deficiency in the frequency of occurrence of the sequence CpGp. By use of the fingerprinting technique of Sanger et al. (1965) to characterise the nucleotide sequences of HeLa cell hnRNA after T1 RNAase digestion, we h
PMID 1052534