Fukami M - Search Results

1

Endometrial preparation methods for frozen-thawed embryo transfer are associated with altered risks of hypertensive disorders of pregnancy, placenta accreta, and gestational diabetes mellitus.

Saito K, Kuwahara A, Ishikawa T, Morisaki N, Miyado M, Miyado K, Fukami M, Miyasaka N, Ishihara O, Irahara M, Saito H. Saito K, et al. Among authors: fukami m. Hum Reprod. 2019 Aug 1;34(8):1567-1575. doi: 10.1093/humrep/dez079. Hum Reprod. 2019. PMID: 31299081

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

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.

4

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.

5

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.

6

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 Free article.

7

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.

8

Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplification.

Saito K, Miyado M, Kobori Y, Tanaka Y, Ishikawa H, Yoshida A, Katsumi M, Saito H, Kubota T, Okada H, Ogata T, Fukami M. Saito K, et al. Among authors: fukami m. J Hum Genet. 2015 Mar;60(3):127-31. doi: 10.1038/jhg.2014.115. Epub 2015 Jan 8. J Hum Genet. 2015. PMID: 25566757

9

Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients.

Kon M, Suzuki E, Dung VC, Hasegawa Y, Mitsui T, Muroya K, Ueoka K, Igarashi N, Nagasaki K, Oto Y, Hamajima T, Yoshino K, Igarashi M, Kato-Fukui Y, Nakabayashi K, Hayashi K, Hata K, Matsubara Y, Moriya K, Ogata T, Nonomura K, Fukami M. Kon M, et al. Among authors: fukami m. Hum Reprod. 2015 Mar;30(3):499-506. doi: 10.1093/humrep/deu364. Epub 2015 Jan 20. Hum Reprod. 2015. PMID: 25605705

10

Microhomology-mediated microduplication in the y chromosomal azoospermia factor a region in a male with mild asthenozoospermia.

Katsumi M, Ishikawa H, Tanaka Y, Saito K, Kobori Y, Okada H, Saito H, Nakabayashi K, Matsubara Y, Ogata T, Fukami M, Miyado M. Katsumi M, et al. Among authors: fukami m. Cytogenet Genome Res. 2014;144(4):285-9. doi: 10.1159/000377649. Epub 2015 Mar 6. Cytogenet Genome Res. 2014. PMID: 25765000

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