Okamoto T - Search Results

1

Paternal allele of IGF2 gene haplotype CTG is associated with fetal and placental growth in Japanese.

Nagaya K, Makita Y, Taketazu G, Okamoto T, Nakamura E, Hayashi T, Fujieda K. Nagaya K, et al. Among authors: okamoto t. Pediatr Res. 2009 Aug;66(2):135-9. doi: 10.1203/PDR.0b013e3181a9e818. Pediatr Res. 2009. PMID: 19390492

2

Matrix metalloproteinases in infants with posthemorrhagic hydrocephalus.

Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Shirai M, Fujieda K. Okamoto T, et al. Early Hum Dev. 2008 Feb;84(2):137-9. doi: 10.1016/j.earlhumdev.2007.08.006. Epub 2007 Oct 4. Early Hum Dev. 2008. PMID: 17919852

3

Airway humidification with a heated wire humidifier during high-frequency ventilation using Babylog 8000 plus in neonates.

Nagaya K, Okamoto T, Nakamura E, Hayashi T, Fujieda K. Nagaya K, et al. Among authors: okamoto t. Pediatr Pulmonol. 2009 Mar;44(3):260-6. doi: 10.1002/ppul.20990. Pediatr Pulmonol. 2009. PMID: 19208373

4

Transforming growth factor-beta1 induces matrix metalloproteinase-9 expression in human meningeal cells via ERK and Smad pathways.

Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Fujieda K. Okamoto T, et al. Biochem Biophys Res Commun. 2009 Jun 12;383(4):475-9. doi: 10.1016/j.bbrc.2009.04.038. Epub 2009 Apr 14. Biochem Biophys Res Commun. 2009. PMID: 19371720

5

Increased expression of matrix metalloproteinase-9 and hepatocyte growth factor in the cerebrospinal fluid of infants with posthemorrhagic hydrocephalus.

Okamoto T, Takahashi S, Nakamura E, Nagaya K, Hayashi T, Shirai M, Fujieda K. Okamoto T, et al. Early Hum Dev. 2010 Apr;86(4):251-4. doi: 10.1016/j.earlhumdev.2010.03.007. Epub 2010 May 10. Early Hum Dev. 2010. PMID: 20457496

6

5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects.

Nakamura E, Makita Y, Okamoto T, Nagaya K, Hayashi T, Sugimoto M, Manabe H, Taketazu G, Kajino H, Fujieda K. Nakamura E, et al. Among authors: okamoto t. Eur J Med Genet. 2011 May-Jun;54(3):354-6. doi: 10.1016/j.ejmg.2010.12.004. Epub 2010 Dec 21. Eur J Med Genet. 2011. PMID: 21172461

7

Patient reports: Two novel frameshift mutations in the SOX9 gene in two patients with campomelic dysplasia who showed long-term survival.

Okamoto T, Nakamura E, Nagaya K, Hayashi T, Mukai T, Fujieda K. Okamoto T, et al. J Pediatr Endocrinol Metab. 2010 Nov;23(11):1189-93. doi: 10.1515/jpem.2010.187. J Pediatr Endocrinol Metab. 2010. PMID: 21284335 Review.

8

Maternal deletion allele of Angiotensin-converting enzyme gene is associated with fetal growth restriction.

Nakamura E, Okamoto T, Nagaya K, Hayashi T. Nakamura E, et al. Among authors: okamoto t. Pediatr Dev Pathol. 2012 Mar-Apr;15(2):114-7. doi: 10.2350/11-09-1092-OA.1. Epub 2011 Dec 9. Pediatr Dev Pathol. 2012. PMID: 22150532

9

Sequential changes in pathophysiology of systemic inflammatory response in a disseminated neonatal herpes simplex virus (HSV) infection.

Nagamori T, Koyano S, Asai Y, Nohara F, Okamoto T, Nagaya K, Hayashi T, Miura Y, Tsuda N, Iseki K, Azuma H. Nagamori T, et al. Among authors: okamoto t. J Clin Virol. 2012 Mar;53(3):265-7. doi: 10.1016/j.jcv.2011.12.017. Epub 2012 Jan 10. J Clin Virol. 2012. PMID: 22237001

10

Platyspondylic lethal dysplasia torrance type with a heterozygous mutation in the triple helical domain of COL2A1 in two sibs from phenotypically normal parents.

Okamoto T, Nagaya K, Asai H, Tsuchida E, Nohara F, Hayashi T, Yamashita A, Nishimura G, Azuma H. Okamoto T, et al. Am J Med Genet A. 2012 Aug;158A(8):1953-6. doi: 10.1002/ajmg.a.35509. Epub 2012 Jun 18. Am J Med Genet A. 2012. PMID: 22711552

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