Fukami M - Search Results

1

Rapid generation of mouse models with defined point mutations by the CRISPR/Cas9 system.

Inui M, Miyado M, Igarashi M, Tamano M, Kubo A, Yamashita S, Asahara H, Fukami M, Takada S. Inui M, et al. Among authors: fukami m. Sci Rep. 2014 Jun 23;4:5396. doi: 10.1038/srep05396. Sci Rep. 2014. PMID: 24953798 Free PMC article.

2

Mamld1 knockdown reduces testosterone production and Cyp17a1 expression in mouse Leydig tumor cells.

Nakamura M, Fukami M, Sugawa F, Miyado M, Nonomura K, Ogata T. Nakamura M, et al. Among authors: fukami m. PLoS One. 2011 Apr 29;6(4):e19123. doi: 10.1371/journal.pone.0019123. PLoS One. 2011. PMID: 21559465 Free PMC article.

3

Complex genomic rearrangement in the SOX9 5' region in a patient with Pierre Robin sequence and hypoplastic left scapula.

Fukami M, Tsuchiya T, Takada S, Kanbara A, Asahara H, Igarashi A, Kamiyama Y, Nishimura G, Ogata T. Fukami M, et al. Am J Med Genet A. 2012 Jul;158A(7):1529-34. doi: 10.1002/ajmg.a.35308. Epub 2012 Apr 23. Am J Med Genet A. 2012. PMID: 22529047

4

Paternal uniparental disomy 14 and related disorders: placental gene expression analyses and histological examinations.

Kagami M, Matsuoka K, Nagai T, Yamanaka M, Kurosawa K, Suzumori N, Sekita Y, Miyado M, Matsubara K, Fuke T, Kato F, Fukami M, Ogata T. Kagami M, et al. Among authors: fukami m. Epigenetics. 2012 Oct;7(10):1142-50. doi: 10.4161/epi.21937. Epub 2012 Aug 23. Epigenetics. 2012. PMID: 22917972 Free PMC article.

5

Mamld1 deficiency significantly reduces mRNA expression levels of multiple genes expressed in mouse fetal Leydig cells but permits normal genital and reproductive development.

Miyado M, Nakamura M, Miyado K, Morohashi K, Sano S, Nagata E, Fukami M, Ogata T. Miyado M, et al. Among authors: fukami m. Endocrinology. 2012 Dec;153(12):6033-40. doi: 10.1210/en.2012-1324. Epub 2012 Oct 18. Endocrinology. 2012. PMID: 23087174 Free PMC article.

6

Submicroscopic deletion involving the fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency.

Fukami M, Iso M, Sato N, Igarashi M, Seo M, Kazukawa I, Kinoshita E, Dateki S, Ogata T. Fukami M, et al. Endocr J. 2013;60(8):1013-20. doi: 10.1507/endocrj.ej13-0023. Epub 2013 May 9. Endocr J. 2013. PMID: 23657145 Free article.

7

Cryptic genomic rearrangements in three patients with 46,XY disorders of sex development.

Igarashi M, Dung VC, Suzuki E, Ida S, Nakacho M, Nakabayashi K, Mizuno K, Hayashi Y, Kohri K, Kojima Y, Ogata T, Fukami M. Igarashi M, et al. Among authors: fukami m. PLoS One. 2013 Jul 8;8(7):e68194. doi: 10.1371/journal.pone.0068194. Print 2013. PLoS One. 2013. PMID: 23861871 Free PMC article.

8

Aromatase excess syndrome in a family with upstream deletion of CYP19A1.

Shihara D, Miyado M, Nakabayashi K, Shozu M, Ogata T, Nagasaki K, Fukami M. Shihara D, et al. Among authors: fukami m. Clin Endocrinol (Oxf). 2014 Aug;81(2):314-6. doi: 10.1111/cen.12329. Epub 2013 Oct 18. Clin Endocrinol (Oxf). 2014. PMID: 24102311 No abstract available.

9

De novo frameshift mutation in fibroblast growth factor 8 in a male patient with gonadotropin deficiency.

Suzuki E, Yatsuga S, Igarashi M, Miyado M, Nakabayashi K, Hayashi K, Hata K, Umezawa A, Yamada G, Ogata T, Fukami M. Suzuki E, et al. Among authors: fukami m. Horm Res Paediatr. 2014;81(2):139-44. doi: 10.1159/000355380. Epub 2013 Nov 20. Horm Res Paediatr. 2014. PMID: 24280688

10

Tamoxifen treatment for pubertal gynecomastia in two siblings with partial androgen insensitivity syndrome.

Saito R, Yamamoto Y, Goto M, Araki S, Kubo K, Kawagoe R, Kawada Y, Kusuhara K, Igarashi M, Fukami M. Saito R, et al. Among authors: fukami m. Horm Res Paediatr. 2014;81(3):211-6. doi: 10.1159/000356923. Epub 2014 Feb 22. Horm Res Paediatr. 2014. PMID: 24577144

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