Arahori H - Search Results

1

An International Aircraft Transport of a Neonate From Georgia to Japan.

Saeki S, Taniguchi H, Arahori H, Kitabatake Y, Ozono K. Saeki S, et al. Among authors: arahori h. Cureus. 2022 Sep 8;14(9):e28952. doi: 10.7759/cureus.28952. eCollection 2022 Sep. Cureus. 2022. PMID: 36225492 Free PMC article.

2

CMV DNA detection in dried blood spots for diagnosing congenital CMV infection in Japan.

Yamagishi Y, Miyagawa H, Wada K, Matsumoto S, Arahori H, Tamura A, Taniguchi H, Kanekiyo T, Sashihara J, Yoda T, Kitagawa M, Ozono K. Yamagishi Y, et al. Among authors: arahori h. J Med Virol. 2006 Jul;78(7):923-5. doi: 10.1002/jmv.20642. J Med Virol. 2006. PMID: 16721859

3

Sonographic femur length to trunk cross area ratio: prediction of fetal outcome in 30 cases in which micromelia was suspected.

Arahori H, Tamura A, Wasada K, Shimoya K, Wada K, Murata Y, Ozono K. Arahori H, et al. J Obstet Gynaecol Res. 2007 Jun;33(3):248-53. doi: 10.1111/j.1447-0756.2007.00519.x. J Obstet Gynaecol Res. 2007. PMID: 17578350

4

Circulating levels of soluble alpha-Klotho are markedly elevated in human umbilical cord blood.

Ohata Y, Arahori H, Namba N, Kitaoka T, Hirai H, Wada K, Nakayama M, Michigami T, Imura A, Nabeshima Y, Yamazaki Y, Ozono K. Ohata Y, et al. Among authors: arahori h. J Clin Endocrinol Metab. 2011 Jun;96(6):E943-7. doi: 10.1210/jc.2010-2357. Epub 2011 Mar 16. J Clin Endocrinol Metab. 2011. PMID: 21411554

5

Systematic Cellular Disease Models Reveal Synergistic Interaction of Trisomy 21 and GATA1 Mutations in Hematopoietic Abnormalities.

Banno K, Omori S, Hirata K, Nawa N, Nakagawa N, Nishimura K, Ohtaka M, Nakanishi M, Sakuma T, Yamamoto T, Toki T, Ito E, Yamamoto T, Kokubu C, Takeda J, Taniguchi H, Arahori H, Wada K, Kitabatake Y, Ozono K. Banno K, et al. Among authors: arahori h. Cell Rep. 2016 May 10;15(6):1228-41. doi: 10.1016/j.celrep.2016.04.031. Epub 2016 Apr 28. Cell Rep. 2016. PMID: 27134169 Free article.

6

A Pair of Maternal Chromosomes Derived from Meiotic Nondisjunction in Trisomy 21 Affects Nuclear Architecture and Transcriptional Regulation.

Omori S, Tanabe H, Banno K, Tsuji A, Nawa N, Hirata K, Kawatani K, Kokubu C, Takeda J, Taniguchi H, Arahori H, Wada K, Kitabatake Y, Ozono K. Omori S, et al. Among authors: arahori h. Sci Rep. 2017 Apr 10;7(1):764. doi: 10.1038/s41598-017-00714-7. Sci Rep. 2017. PMID: 28396582 Free PMC article.

7

Elimination of protein aggregates prevents premature senescence in human trisomy 21 fibroblasts.

Nawa N, Hirata K, Kawatani K, Nambara T, Omori S, Banno K, Kokubu C, Takeda J, Nishimura K, Ohtaka M, Nakanishi M, Okuzaki D, Taniguchi H, Arahori H, Wada K, Kitabatake Y, Ozono K. Nawa N, et al. Among authors: arahori h. PLoS One. 2019 Jul 29;14(7):e0219592. doi: 10.1371/journal.pone.0219592. eCollection 2019. PLoS One. 2019. PMID: 31356639 Free PMC article.

8

4-Phenylbutyrate ameliorates apoptotic neural cell death in Down syndrome by reducing protein aggregates.

Hirata K, Nambara T, Kawatani K, Nawa N, Yoshimatsu H, Kusakabe H, Banno K, Nishimura K, Ohtaka M, Nakanishi M, Taniguchi H, Arahori H, Wada K, Ozono K, Kitabatake Y. Hirata K, et al. Among authors: arahori h. Sci Rep. 2020 Aug 20;10(1):14047. doi: 10.1038/s41598-020-70362-x. Sci Rep. 2020. PMID: 32820178 Free PMC article.

9

A human isogenic iPSC-derived cell line panel identifies major regulators of aberrant astrocyte proliferation in Down syndrome.

Kawatani K, Nambara T, Nawa N, Yoshimatsu H, Kusakabe H, Hirata K, Tanave A, Sumiyama K, Banno K, Taniguchi H, Arahori H, Ozono K, Kitabatake Y. Kawatani K, et al. Among authors: arahori h. Commun Biol. 2021 Jun 14;4(1):730. doi: 10.1038/s42003-021-02242-7. Commun Biol. 2021. PMID: 34127780 Free PMC article.

10

Prenatal diagnosis of fetal intracranial hemorrhage in pregnancy complicated by idiopathic thrombocytopenic purpura.

Koyama S, Tomimatsu T, Sawada K, Kanagawa T, Isobe A, Taniguchi Y, Wada T, Kimura T, Arahori H, Kitabatake Y, Wada K. Koyama S, et al. Among authors: arahori h. Prenat Diagn. 2010 May;30(5):489-91. doi: 10.1002/pd.2518. Prenat Diagn. 2010. PMID: 20440739 Review. No abstract available.

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