Studies on differentially methylated parental allele in imprinted genes

Forensic Science International: Genetics Supplement Series

Volumn 1, Issue 1, 2008, Pages 572-573

  Nakayashiki, Nori ^a   Takamiya, Masataka ^a   Shimamoto, Kirito ^a   Aoki, Yasuhiro ^a   Hashiyada, Masaki ^b  

^a IWATE MEDICAL UNIVERSITY   (Japan)

^b TOHOKU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Genomic imprinting; Methylation; Minisequencing; Parental origin; SNP

Indexed keywords

ALLELE; ARTICLE; CONTROLLED STUDY; GENE EXPRESSION; GENETIC ANALYSIS; GENOME IMPRINTING; GENOTYPE; HUMAN; METHYLATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 50349087382     PISSN: 18751768     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fsigss.2007.10.049     Document Type: Article

References (6)

1. Nakayashiki N., Kanetake J., and Aoki Y. A parent-of-origin detectable polymorphism in hypermethylated region upstream of the human H19 gene. Int. J. Legal Med. 118 (2004) 158-162
2. Nakayashiki N., Takamiya M., Kurose N., Aoki Y., and Hashiyada M. Investigation of discrimination method for DMPA (differentially methylated parental allele) II. DNA Polymorphism 14 (2006) 41-45 (in Japanese)
3. Nakayashiki N., Takamiya M., Kumagai A., Aoki Y., and Hashiyada M. Investigation of discrimination method for DMPA (differentially methylated parental allele) III. DNA Polymorphism 15 (2007) 260-263 (in Japanese)
4. Naito E., Dewa K., Fukuda M., Sumi H., Wakabayashi Y., Umetsu K., Yuasa I., and Yamanouchi H. Novel paternity testing by distinguishing parental alleles at a VNTR locus in the differentially methylated region upstream of the human H19 gene. J. Forensic Sci. 48 (2003) 1275-1279
5. Zhao G., Yang Q., Huang D., Yu C., Yang R., Chen H., and Mei K. Study on the application of parent-of-origin specific DNA methylation markers to forensic genetics. Forensic Sci. Int. 154 (2005) 122-127
6. Xu H.-D., Naito E., Dewa K., Fukuda M., Sumi H., Yuasa I., and Yamanouchi H. Parentally imprinted allele typing at a short tandem repeat locus in intron 1a of imprinted gene KCNQ1. Legal Med. 8 (2006) 139-143