Mukai T - Search Results

1

Assignment of the programmed cell death 4 gene (PDCD4) to human chromosome band 10q24 by in situ hybridization.

Soejima H, Miyoshi O, Yoshinaga H, Masaki Z, Ozaki I, Kajiwara S, Niikawa N, Matsuhashi S, Mukai T. Soejima H, et al. Among authors: mukai t. Cytogenet Cell Genet. 1999;87(1-2):113-4. doi: 10.1159/000015408. Cytogenet Cell Genet. 1999. PMID: 10640828 No abstract available.

2

Cloning and characterization of a novel human gene, TM4SF6, encoding a protein belonging to the transmembrane 4 superfamily, and mapped to Xq22.

Maeda K, Matsuhashi S, Hori K, Xin Z, Mukai T, Tabuchi K, Egashira M, Niikawa N. Maeda K, et al. Among authors: mukai t. Genomics. 1998 Sep 1;52(2):240-2. doi: 10.1006/geno.1998.5415. Genomics. 1998. PMID: 9782095 No abstract available.

3

Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene.

Higashimoto K, Soejima H, Katsuki T, Mukai T. Higashimoto K, et al. Among authors: mukai t. J Hum Genet. 2000;45(1):58-9. doi: 10.1007/s100380050012. J Hum Genet. 2000. PMID: 10697966

4

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: mukai t. Gene. 2000 Oct 3;256(1-2):311-7. doi: 10.1016/s0378-1119(00)00377-2. Gene. 2000. PMID: 11054561

5

Isolation of novel heart-specific genes using the BodyMap database.

Soejima H, Kawamoto S, Akai J, Miyoshi O, Arai Y, Morohka T, Matsuo S, Niikawa N, Kimura A, Okubo K, Mukai T. Soejima H, et al. Among authors: mukai t. Genomics. 2001 May 15;74(1):115-20. doi: 10.1006/geno.2001.6527. Genomics. 2001. PMID: 11374908

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: mukai t. J Hum Genet. 2000;45(2):96-7. doi: 10.1007/s100380050020. J Hum Genet. 2000. PMID: 10721672

7

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: mukai t. J Biochem. 2000 Nov;128(5):847-53. doi: 10.1093/oxfordjournals.jbchem.a022823. J Biochem. 2000. PMID: 11056398 Free article.

8

Gene silencing in DNA damage repair.

Soejima H, Joh K, Mukai T. Soejima H, et al. Among authors: mukai t. Cell Mol Life Sci. 2004 Sep;61(17):2168-72. doi: 10.1007/s00018-004-4178-9. Cell Mol Life Sci. 2004. PMID: 15338047 Free PMC article. Review.

9

Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours.

Satoh Y, Nakadate H, Nakagawachi T, Higashimoto K, Joh K, Masaki Z, Uozumi J, Kaneko Y, Mukai T, Soejima H. Satoh Y, et al. Among authors: mukai t. Br J Cancer. 2006 Aug 21;95(4):541-7. doi: 10.1038/sj.bjc.6603302. Epub 2006 Aug 8. Br J Cancer. 2006. PMID: 16909133 Free PMC article.

10

Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome.

Ohtsuka Y, Higashimoto K, Sasaki K, Jozaki K, Yoshinaga H, Okamoto N, Takama Y, Kubota A, Nakayama M, Yatsuki H, Nishioka K, Joh K, Mukai T, Yoshiura KI, Soejima H. Ohtsuka Y, et al. Among authors: mukai t. Clin Genet. 2015 Sep;88(3):261-6. doi: 10.1111/cge.12496. Epub 2014 Nov 8. Clin Genet. 2015. PMID: 25171146

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