Kato F - Search Results

1

Mutation analysis of FGFR1-3 in 11 Japanese patients with syndromic craniosynostoses.

Ohishi A, Nishimura G, Kato F, Ono H, Maruwaka K, Ago M, Suzumura H, Hirose E, Uchida Y, Fukami M, Ogata T. Ohishi A, et al. Among authors: kato f. Am J Med Genet A. 2017 Jan;173(1):157-162. doi: 10.1002/ajmg.a.37992. Epub 2016 Sep 28. Am J Med Genet A. 2017. PMID: 27683237

2

Transactivation function of an approximately 800-bp evolutionarily conserved sequence at the SHOX 3' region: implication for the downstream enhancer.

Fukami M, Kato F, Tajima T, Yokoya S, Ogata T. Fukami M, et al. Among authors: kato f. Am J Hum Genet. 2006 Jan;78(1):167-70. doi: 10.1086/499254. Am J Hum Genet. 2006. PMID: 16385461 Free PMC article. No abstract available.

3

Mastermind-like domain-containing 1 (MAMLD1 or CXorf6) transactivates the Hes3 promoter, augments testosterone production, and contains the SF1 target sequence.

Fukami M, Wada Y, Okada M, Kato F, Katsumata N, Baba T, Morohashi K, Laporte J, Kitagawa M, Ogata T. Fukami M, et al. Among authors: kato f. J Biol Chem. 2008 Feb 29;283(9):5525-32. doi: 10.1074/jbc.M703289200. Epub 2007 Dec 27. J Biol Chem. 2008. PMID: 18162467 Free article.

4

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.

Kagami M, Sekita Y, Nishimura G, Irie M, Kato F, Okada M, Yamamori S, Kishimoto H, Nakayama M, Tanaka Y, Matsuoka K, Takahashi T, Noguchi M, Tanaka Y, Masumoto K, Utsunomiya T, Kouzan H, Komatsu Y, Ohashi H, Kurosawa K, Kosaki K, Ferguson-Smith AC, Ishino F, Ogata T. Kagami M, et al. Among authors: kato f. Nat Genet. 2008 Feb;40(2):237-42. doi: 10.1038/ng.2007.56. Epub 2008 Jan 6. Nat Genet. 2008. PMID: 18176563

5

Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Léri-Weill dyschondrosteosis.

Fukami M, Dateki S, Kato F, Hasegawa Y, Mochizuki H, Horikawa R, Ogata T. Fukami M, et al. Among authors: kato f. J Hum Genet. 2008;53(5):454-459. doi: 10.1007/s10038-008-0269-z. Epub 2008 Mar 6. J Hum Genet. 2008. PMID: 18322641

6

The IG-DMR and the MEG3-DMR at human chromosome 14q32.2: hierarchical interaction and distinct functional properties as imprinting control centers.

Kagami M, O'Sullivan MJ, Green AJ, Watabe Y, Arisaka O, Masawa N, Matsuoka K, Fukami M, Matsubara K, Kato F, Ferguson-Smith AC, Ogata T. Kagami M, et al. Among authors: kato f. PLoS Genet. 2010 Jun 17;6(6):e1000992. doi: 10.1371/journal.pgen.1000992. PLoS Genet. 2010. PMID: 20585555 Free PMC article.

7

GATA3 abnormalities in six patients with HDR syndrome.

Fukami M, Muroya K, Miyake T, Iso M, Kato F, Yokoi H, Suzuki Y, Tsubouchi K, Nakagomi Y, Kikuchi N, Horikawa R, Ogata T. Fukami M, et al. Among authors: kato f. Endocr J. 2011;58(2):117-21. doi: 10.1507/endocrj.k10e-234. Epub 2011 Jan 13. Endocr J. 2011. PMID: 21242646 Free article.

8

Aromatase excess syndrome: identification of cryptic duplications and deletions leading to gain of function of CYP19A1 and assessment of phenotypic determinants.

Fukami M, Shozu M, Soneda S, Kato F, Inagaki A, Takagi H, Hanaki K, Kanzaki S, Ohyama K, Sano T, Nishigaki T, Yokoya S, Binder G, Horikawa R, Ogata T. Fukami M, et al. Among authors: kato f. J Clin Endocrinol Metab. 2011 Jun;96(6):E1035-43. doi: 10.1210/jc.2011-0145. Epub 2011 Apr 6. J Clin Endocrinol Metab. 2011. PMID: 21470988

9

Relative frequency of underlying genetic causes for the development of UPD(14)pat-like phenotype.

Kagami M, Kato F, Matsubara K, Sato T, Nishimura G, Ogata T. Kagami M, et al. Among authors: kato f. Eur J Hum Genet. 2012 Sep;20(9):928-32. doi: 10.1038/ejhg.2012.26. Epub 2012 Feb 22. Eur J Hum Genet. 2012. PMID: 22353941 Free PMC article.

10

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: kato f. Epigenetics. 2012 Oct;7(10):1142-50. doi: 10.4161/epi.21937. Epub 2012 Aug 23. Epigenetics. 2012. PMID: 22917972 Free PMC article.

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