Yatsuki H - Search Results

1

Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndrome.

Higashimoto K, Nakabayashi K, Yatsuki H, Yoshinaga H, Jozaki K, Okada J, Watanabe Y, Aoki A, Shiozaki A, Saito S, Koide K, Mukai T, Hata K, Soejima H. Higashimoto K, et al. Among authors: yatsuki h. Am J Med Genet A. 2012 Jul;158A(7):1670-5. doi: 10.1002/ajmg.a.35335. Epub 2012 May 10. Am J Med Genet A. 2012. PMID: 22577095

2

Expression of rat aldolase A gene and analysis of AH promoter region of the gene.

Joh K, Mukai T, Motomura M, Oh-uchida M, Yatsuki H, Hori K. Joh K, et al. Among authors: yatsuki h. Prog Clin Biol Res. 1990;344:53-73. Prog Clin Biol Res. 1990. PMID: 2203054 Review. No abstract available.

3

Human aldolase B gene: characterization of the genomic aldolase B gene and analysis of sequences required for multiple polyadenylations.

Mukai T, Yatsuki H, Arai Y, Joh K, Matsuhashi S, Hori K. Mukai T, et al. Among authors: yatsuki h. J Biochem. 1987 Nov;102(5):1043-51. doi: 10.1093/oxfordjournals.jbchem.a122142. J Biochem. 1987. PMID: 2830249 Free article.

4

Cloning of the Xenopus laevis aldolase C gene and analysis of its promoter function in developing Xenopus embryos and A6 cells.

Yatsuki H, Outida M, Atsuchi Y, Mukai T, Shiokawa K, Hori K. Yatsuki H, et al. Biochim Biophys Acta. 1998 Nov 8;1442(2-3):199-217. doi: 10.1016/s0167-4781(98)00165-1. Biochim Biophys Acta. 1998. PMID: 9804954

5

Functional analysis of the p57KIP2 gene mutation in Beckwith-Wiedemann syndrome.

Bhuiyan ZA, Yatsuki H, Sasaguri T, Joh K, Soejima H, Zhu X, Hatada I, Morisaki H, Morisaki T, Mukai T. Bhuiyan ZA, et al. Among authors: yatsuki h. Hum Genet. 1999 Mar;104(3):205-10. doi: 10.1007/s004390050937. Hum Genet. 1999. PMID: 10323243

6

An NsiI RFLP in the human long QT intronic transcript 1 (LIT1).

Higashimoto K, Soejima H, Yatsuki H, Katsuki T, Mukai T. Higashimoto K, et al. Among authors: yatsuki h. J Hum Genet. 2000;45(2):96-7. doi: 10.1007/s100380050020. J Hum Genet. 2000. PMID: 10721672

7

Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human.

Yatsuki H, Watanabe H, Hattori M, Joh K, Soejima H, Komoda H, Xin Z, Zhu X, Higashimoto K, Nishimura M, Kuratomi S, Sasaki H, Sakaki Y, Mukai T. Yatsuki H, et al. DNA Res. 2000 Jun 30;7(3):195-206. doi: 10.1093/dnares/7.3.195. DNA Res. 2000. PMID: 10907850 Free article.

8

C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5.

Zhu X, Higashimoto K, Soejima H, Yatsuki H, Sugihara H, Mukai T, Joh K. Zhu X, et al. Among authors: yatsuki h. Gene. 2000 Oct 3;256(1-2):311-7. doi: 10.1016/s0378-1119(00)00377-2. Gene. 2000. PMID: 11054561

9

A novel imprinted gene, KCNQ1DN, within the WT2 critical region of human chromosome 11p15.5 and its reduced expression in Wilms' tumors.

Xin Z, Soejima H, Higashimoto K, Yatsuki H, Zhu X, Satoh Y, Masaki Z, Kaneko Y, Jinno Y, Fukuzawa R, Hata Ji, Mukai T. Xin Z, et al. Among authors: yatsuki h. J Biochem. 2000 Nov;128(5):847-53. doi: 10.1093/oxfordjournals.jbchem.a022823. J Biochem. 2000. PMID: 11056398 Free article.

10

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.

Yatsuki H, Joh K, Higashimoto K, Soejima H, Arai Y, Wang Y, Hatada I, Obata Y, Morisaki H, Zhang Z, Nakagawachi T, Satoh Y, Mukai T. Yatsuki H, et al. Genome Res. 2002 Dec;12(12):1860-70. doi: 10.1101/gr.110702. Genome Res. 2002. PMID: 12466290 Free PMC article.

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