Masuzaki H - Search Results

1

A case of Kallmann syndrome carrying a missense mutation in alternatively spliced exon 8A encoding the immunoglobulin-like domain IIIb of fibroblast growth factor receptor 1.

Miura K, Miura S, Yoshiura K, Seminara S, Hamaguchi D, Niikawa N, Masuzaki H. Miura K, et al. Among authors: masuzaki h. Hum Reprod. 2010 Apr;25(4):1076-80. doi: 10.1093/humrep/deq006. Epub 2010 Feb 6. Hum Reprod. 2010. PMID: 20139426 Free PMC article.

2

Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid.

Miura S, Miura K, Masuzaki H, Miyake N, Yoshiura KI, Sosonkina N, Harada N, Shimokawa O, Nakayama D, Yoshimura S, Matsumoto N, Niikawa N, Ishimaru T. Miura S, et al. Among authors: masuzaki h. J Hum Genet. 2006;51(5):412-417. doi: 10.1007/s10038-006-0376-7. Epub 2006 Apr 19. J Hum Genet. 2006. PMID: 16622586

3

A strong association between human earwax-type and apocrine colostrum secretion from the mammary gland.

Miura K, Yoshiura K, Miura S, Shimada T, Yamasaki K, Yoshida A, Nakayama D, Shibata Y, Niikawa N, Masuzaki H. Miura K, et al. Among authors: masuzaki h. Hum Genet. 2007 Jun;121(5):631-3. doi: 10.1007/s00439-007-0356-9. Epub 2007 Mar 30. Hum Genet. 2007. PMID: 17394018

4

The possibility of microarray-based analysis using cell-free placental mRNA in maternal plasma.

Miura K, Miura S, Yamasaki K, Shimada T, Kinoshita A, Niikawa N, Yoshiura K, Masuzaki H. Miura K, et al. Among authors: masuzaki h. Prenat Diagn. 2010 Sep;30(9):849-61. doi: 10.1002/pd.2570. Prenat Diagn. 2010. PMID: 20665716

5

Epidemiology of human papillomavirus genotypes in pregnant Japanese women.

Yamasaki K, Miura K, Shimada T, Miura S, Abe S, Murakami M, Sameshima T, Fujishita A, Kotera K, Kinoshita A, Yoshiura K, Masuzaki H. Yamasaki K, et al. Among authors: masuzaki h. J Hum Genet. 2011 Apr;56(4):313-5. doi: 10.1038/jhg.2011.11. Epub 2011 Feb 10. J Hum Genet. 2011. PMID: 21307859

6

Clinical application of fetal sex determination using cell-free fetal DNA in pregnant carriers of X-linked genetic disorders.

Miura K, Higashijima A, Shimada T, Miura S, Yamasaki K, Abe S, Jo O, Kinoshita A, Yoshida A, Yoshimura S, Niikawa N, Yoshiura K, Masuzaki H. Miura K, et al. Among authors: masuzaki h. J Hum Genet. 2011 Apr;56(4):296-9. doi: 10.1038/jhg.2011.7. Epub 2011 Feb 10. J Hum Genet. 2011. PMID: 21307866

7

Copy number variation of the antimicrobial-gene, defensin beta 4, is associated with susceptibility to cervical cancer.

Abe S, Miura K, Kinoshita A, Mishima H, Miura S, Yamasaki K, Hasegawa Y, Higashijima A, Jo O, Sasaki K, Yoshida A, Yoshiura K, Masuzaki H. Abe S, et al. Among authors: masuzaki h. J Hum Genet. 2013 May;58(5):250-3. doi: 10.1038/jhg.2013.7. Epub 2013 Mar 7. J Hum Genet. 2013. PMID: 23466823

8

A significant association between rs8067378 at 17q12 and invasive cervical cancer originally identified by a genome-wide association study in Han Chinese is replicated in a Japanese population.

Miura K, Mishima H, Yasunami M, Kaneuchi M, Kitajima M, Abe S, Higashijima A, Fuchi N, Miura S, Yoshiura K, Masuzaki H. Miura K, et al. Among authors: masuzaki h. J Hum Genet. 2016 Sep;61(9):793-6. doi: 10.1038/jhg.2016.50. Epub 2016 May 19. J Hum Genet. 2016. PMID: 27193219

9

Clinical applications of plasma circulating mRNA analysis in cases of gestational trophoblastic disease.

Masuzaki H, Miura K, Yamasaki K, Miura S, Yoshiura K, Yoshimura S, Nakayama D, Mapendano CK, Niikawa N, Ishimaru T. Masuzaki H, et al. Clin Chem. 2005 Jul;51(7):1261-3. doi: 10.1373/clinchem.2005.050666. Epub 2005 Apr 28. Clin Chem. 2005. PMID: 15860565 No abstract available.

10

Origin and mechanisms of formation of fetus-in-fetu: two cases with genotype and methylation analyses.

Miura S, Miura K, Yamamoto T, Yamanaka M, Saito K, Hirabuki T, Kurosawa K, Harada N, Ishizaki-Yamasaki Y, Matsumoto N, Hirahara F, Yoshiura K, Masuzaki H, Niikawa N. Miura S, et al. Among authors: masuzaki h. Am J Med Genet A. 2006 Aug 15;140(16):1737-43. doi: 10.1002/ajmg.a.31362. Am J Med Genet A. 2006. PMID: 16835914

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