Fujieda K - 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: fujieda k. Pediatr Res. 2009 Aug;66(2):135-9. doi: 10.1203/PDR.0b013e3181a9e818. Pediatr Res. 2009. PMID: 19390492

2

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. Among authors: fujieda k. 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

3

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. Among authors: fujieda k. 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

4

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. Among authors: fujieda k. J Pediatr Endocrinol Metab. 2010 Nov;23(11):1189-93. doi: 10.1515/jpem.2010.187. J Pediatr Endocrinol Metab. 2010. PMID: 21284335 Review.

5

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: fujieda k. Pediatr Pulmonol. 2009 Mar;44(3):260-6. doi: 10.1002/ppul.20990. Pediatr Pulmonol. 2009. PMID: 19208373

6

Molecular basis of neonatal diabetes in Japanese patients.

Suzuki S, Makita Y, Mukai T, Matsuo K, Ueda O, Fujieda K. Suzuki S, et al. Among authors: fujieda k. J Clin Endocrinol Metab. 2007 Oct;92(10):3979-85. doi: 10.1210/jc.2007-0486. Epub 2007 Jul 17. J Clin Endocrinol Metab. 2007. PMID: 17635943

7

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: fujieda k. 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

8

Leukemia in Cardio-facio-cutaneous (CFC) syndrome: a patient with a germline mutation in BRAF proto-oncogene.

Makita Y, Narumi Y, Yoshida M, Niihori T, Kure S, Fujieda K, Matsubara Y, Aoki Y. Makita Y, et al. Among authors: fujieda k. J Pediatr Hematol Oncol. 2007 May;29(5):287-90. doi: 10.1097/MPH.0b013e3180547136. J Pediatr Hematol Oncol. 2007. PMID: 17483702 Free article.

9

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. Among authors: fujieda k. 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

10

Skewed X chromosome inactivation failed to explain the normal phenotype of a carrier female with MECP2 mutation resulting in Rett syndrome.

Takahashi S, Ohinata J, Makita Y, Suzuki N, Araki A, Sasaki A, Murono K, Tanaka H, Fujieda K. Takahashi S, et al. Among authors: fujieda k. Clin Genet. 2008 Mar;73(3):257-61. doi: 10.1111/j.1399-0004.2007.00944.x. Epub 2007 Jan 8. Clin Genet. 2008. PMID: 18190595

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