Udaka T - Search Results

1

Comprehensive screening of the thiopurine methyltransferase polymorphisms by denaturing high-performance liquid chromatography.

Udaka T, Torii C, Takahashi D, Mori T, Aramaki M, Kosaki R, Tanigawara Y, Takahashi T, Kosaki K. Udaka T, et al. Genet Test. 2005 Summer;9(2):85-92. doi: 10.1089/gte.2005.9.85. Genet Test. 2005. PMID: 15943548

2

Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography.

Udaka T, Samejima H, Kosaki R, Kurosawa K, Okamoto N, Mizuno S, Makita Y, Numabe H, Toral JF, Takahashi T, Kosaki K. Udaka T, et al. Congenit Anom (Kyoto). 2005 Dec;45(4):125-31. doi: 10.1111/j.1741-4520.2005.00081.x. Congenit Anom (Kyoto). 2005. PMID: 16359492

3

Screening for CHARGE syndrome mutations in the CHD7 gene using denaturing high-performance liquid chromatography.

Aramaki M, Udaka T, Torii C, Samejima H, Kosaki R, Takahashi T, Kosaki K. Aramaki M, et al. Among authors: udaka t. Genet Test. 2006 Winter;10(4):244-51. doi: 10.1089/gte.2006.10.244. Genet Test. 2006. PMID: 17253929

4

Screening for partial deletions in the CREBBP gene in Rubinstein-Taybi syndrome patients using multiplex PCR/liquid chromatography.

Udaka T, Kurosawa K, Izumi K, Yoshida S, Tsukahara M, Okamoto N, Torii C, Kosaki R, Masuno M, Hosokai N, Takahashi T, Kosaki K. Udaka T, et al. Genet Test. 2006 Winter;10(4):265-71. doi: 10.1089/gte.2006.10.265. Genet Test. 2006. PMID: 17253932

5

Multiplex PCR/liquid chromatography assay for screening of subtelomeric rearrangements.

Udaka T, Imoto I, Aizu Y, Torii C, Izumi K, Kosaki R, Takahashi T, Hayashi S, Inazawa J, Kosaki K. Udaka T, et al. Genet Test. 2007 Fall;11(3):241-8. doi: 10.1089/gte.2007.9993. Genet Test. 2007. PMID: 17949285

6

DHPLC in clinical molecular diagnostic services.

Kosaki K, Udaka T, Okuyama T. Kosaki K, et al. Among authors: udaka t. Mol Genet Metab. 2005 Sep-Oct;86(1-2):117-23. doi: 10.1016/j.ymgme.2005.07.033. Mol Genet Metab. 2005. PMID: 16202954 Review.

7

An Alu retrotransposition-mediated deletion of CHD7 in a patient with CHARGE syndrome.

Udaka T, Okamoto N, Aramaki M, Torii C, Kosaki R, Hosokai N, Hayakawa T, Takahata N, Takahashi T, Kosaki K. Udaka T, et al. Am J Med Genet A. 2007 Apr 1;143A(7):721-6. doi: 10.1002/ajmg.a.31441. Am J Med Genet A. 2007. PMID: 17334995

8

Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.

Aramaki M, Udaka T, Kosaki R, Makita Y, Okamoto N, Yoshihashi H, Oki H, Nanao K, Moriyama N, Oku S, Hasegawa T, Takahashi T, Fukushima Y, Kawame H, Kosaki K. Aramaki M, et al. Among authors: udaka t. J Pediatr. 2006 Mar;148(3):410-4. doi: 10.1016/j.jpeds.2005.10.044. J Pediatr. 2006. PMID: 16615981

9

Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndrome.

Aramaki M, Kimura T, Udaka T, Kosaki R, Mitsuhashi T, Okada Y, Takahashi T, Kosaki K. Aramaki M, et al. Among authors: udaka t. Birth Defects Res A Clin Mol Teratol. 2007 Jan;79(1):50-7. doi: 10.1002/bdra.20330. Birth Defects Res A Clin Mol Teratol. 2007. PMID: 17149726

10

Identification of a prosencephalic-specific enhancer of SALL1: comparative genomic approach using the chick embryo.

Izumi K, Aramaki M, Kimura T, Naito Y, Udaka T, Uchikawa M, Kondoh H, Suzuki H, Cho G, Okada Y, Takahashi T, Golden JA, Kosaki K. Izumi K, et al. Among authors: udaka t. Pediatr Res. 2007 Jun;61(6):660-5. doi: 10.1203/pdr.0b013e318053423a. Pediatr Res. 2007. PMID: 17426652

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