Search Results - "Furuumi, H."

Molecular Basis of β-Thalassemia in the Maldives by Furuumi, H., Firdous, N., Inoue, T., Ohta, H., Winichagoon, P., Fucharoen, S., Fukumaki, Y.

“…We have systematically analyzed β-thalassemia genes using polymerase chain reaction-related techniques, dot-blot hybridization with oligonucleotide probes,…”
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Molecular analysis of α-thalassemia in Nepal: correlation with malaria endemicity by Sakai, Y, Kobayashi, S, Shibata, H, Furuumi, H, Endo, T, Fucharoen, S, Hamano, S, Acharya, G P, Kawasaki, T, Fukumaki, Y

“…Thalassemia is a prevalent hereditary disorder characterized by impaired synthesis of globin chains. It has been suggested that the high frequency of…”
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Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting by Ishihara, K, Hatano, N, Furuumi, H, Kato, R, Iwaki, T, Miura, K, Jinno, Y, Sasaki, H

“…A differentially methylated region (DMR) and endoderm-specific enhancers, located upstream and downstream of the mouse H19 gene, respectively, are known to be…”
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ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutation by Kubota, Takeo, Furuumi, Hiroyasu, Kamoda, Tomohiro, Iwasaki, Nobuaki, Tobita, Naomi, Fujiwara, Nobuko, Goto, Yu‐ichi, Matsui, Akira, Sasaki, Hiroyuki, Kajii, Tadashi

“…A 3‐year‐old girl with phenotypic and cytogenetic manifestations of the ICF syndrome and DNA hypomethylation but without DNMT3B gene mutation is described. At…”
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Disruption of mesodermal enhancers for Igf2 in the minute mutant by Davies, Karen, Bowden, Lucy, Smith, Paul, Dean, Wendy, Hill, David, Furuumi, Hiroyasu, Sasaki, Hiroyuki, Cattanach, Bruce, Reik, Wolf

“…The radiation-induced mutation minute ( Mnt ) in the mouse leads to intrauterine growth retardation with paternal transmission and has been linked to the…”
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Sequence of a 42-kb mouse region containing the imprinted H19 locus: identification of a novel muscle-specific transcription unit showing biallelic expression by Ishihara, K, Kato, R, Furuumi, H, Zubair, M, Sasaki, H

“…The mouse H19 gene, encoding an untranslated RNA with unknown function, is subject to genomic imprinting and expressed exclusively from the maternal allele…”
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Polymorphism of the cytochrome P450 (CYP) 2C9 gene in Japanese epileptic patients: genetic analysis of the CYP2C9 locus by IMAI, J, ICIRI, I, OTSUBO, K, HIGUCHI, S, MAMIYA, K, MIYAHARA, S, FURUUMI, H, NANBA, E, YAMANE, M, FUKUMAKI, Y, NINOMIYA, H, TASHIRO, N

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Association of polymorphisms in the cytochrome P450 (CYP) 2C19 and 2C18 genes in Japanese epileptic patients by Mamiya, K, Ieiri, I, Miyahara, S, Imai, J, Furuumi, H, Fukumaki, Y, Ninomiya, H, Tashiro, N, Yamada, H, Higuchi, S

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