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Abbravation: Journal of Human Genetics

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Nature Publishing Group

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DOI

10.1007/s12161-010-9135-7

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1435-232X

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Novel polymorphism in the 5′untranslated region o

Authors: Akira Takabayashi Kenji Ihara Yuka Sasaki Koichi Kusuhara Sankei Nishima Toshiro Hara
Publish Date: 1999/08
Volume: 44, Issue: 5, Pages: 352-
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Abstract

Thank you for visiting naturecom You are using a browser version with limited support for CSS To obtain the best experience we recommend you use a more up to date browser or turn off compatibility mode in Internet Explorer In the meantime to ensure continued support we are displaying the site without styles and JavaScriptWe found a novel polymorphism C/T change at position 34 counting from the first ATG codon of the interleukin4 IL4 gene located between the TATA box and the first ATG on exon 1 The allelic frequency of this C/T polymorphism in 64 independent Japanese samples was 037 063 In addition PCRrestriction fragment length polymorphism analysis revealed that the 34T/T polymorphism was always associated with 590T/T a known polymorphism that increases IL4 transcriptional activity

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  2. Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications
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  7. Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence
  8. Isolation of human chromosome 21-specific cosmids and their uses in mapping of cosmid contigs on chromosomal subregions
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  10. Dynamin 2 gene is a novel susceptibility gene for late-onset Alzheimer disease in non- APOE -ε4 carriers
  11. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan
  12. The hOGG1 Ser 326 Cys gene polymorphism is associated with decreased insulin sensitivity in subjects with normal glucose tolerance
  13. Concordance and discordance of anencephaly in 109 twin pairs in Japan
  14. Molecular cloning of a novel human gene ( SIRP-B2 ) which encodes a new member of the SIRP/SHPS-1 protein family
  15. Genomic imprinting and its relevance to genetic diseases
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