Kagami M - Search Results

1

Genome-wide multilocus imprinting disturbance analysis in Temple syndrome and Kagami-Ogata syndrome.

Kagami M, Matsubara K, Nakabayashi K, Nakamura A, Sano S, Okamura K, Hata K, Fukami M, Ogata T. Kagami M, et al. Genet Med. 2017 Apr;19(4):476-482. doi: 10.1038/gim.2016.123. Epub 2016 Sep 15. Genet Med. 2017. PMID: 27632690 Free PMC article.

2

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T. Sato N, et al. Among authors: kagami m. J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88. doi: 10.1210/jc.2003-030476. J Clin Endocrinol Metab. 2004. PMID: 15001591

3

Segmental and full paternal isodisomy for chromosome 14 in three patients: narrowing the critical region and implication for the clinical features.

Kagami M, Nishimura G, Okuyama T, Hayashidani M, Takeuchi T, Tanaka S, Ishino F, Kurosawa K, Ogata T. Kagami M, et al. Am J Med Genet A. 2005 Oct 1;138A(2):127-32. doi: 10.1002/ajmg.a.30941. Am J Med Genet A. 2005. PMID: 16152632 Review.

4

Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST.

Kagami M, Nagai T, Fukami M, Yamazawa K, Ogata T. Kagami M, et al. J Assist Reprod Genet. 2007 Apr;24(4):131-6. doi: 10.1007/s10815-006-9096-3. Epub 2007 Feb 16. J Assist Reprod Genet. 2007. PMID: 17450433 Free PMC article.

5

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. Nat Genet. 2008 Feb;40(2):237-42. doi: 10.1038/ng.2007.56. Epub 2008 Jan 6. Nat Genet. 2008. PMID: 18176563

6

Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta.

Sekita Y, Wagatsuma H, Nakamura K, Ono R, Kagami M, Wakisaka N, Hino T, Suzuki-Migishima R, Kohda T, Ogura A, Ogata T, Yokoyama M, Kaneko-Ishino T, Ishino F. Sekita Y, et al. Among authors: kagami m. Nat Genet. 2008 Feb;40(2):243-8. doi: 10.1038/ng.2007.51. Epub 2008 Jan 6. Nat Genet. 2008. PMID: 18176565

7

Placental hypoplasia in maternal uniparental disomy for chromosome 7.

Yamazawa K, Kagami M, Ogawa M, Horikawa R, Ogata T. Yamazawa K, et al. Among authors: kagami m. Am J Med Genet A. 2008 Feb 15;146A(4):514-6. doi: 10.1002/ajmg.a.32125. Am J Med Genet A. 2008. PMID: 18203162 No abstract available.

8

Epimutation (hypomethylation) affecting the chromosome 14q32.2 imprinted region in a girl with upd(14)mat-like phenotype.

Hosoki K, Ogata T, Kagami M, Tanaka T, Saitoh S. Hosoki K, et al. Among authors: kagami m. Eur J Hum Genet. 2008 Aug;16(8):1019-23. doi: 10.1038/ejhg.2008.90. Epub 2008 May 14. Eur J Hum Genet. 2008. PMID: 18478039

9

Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas.

Yamazawa K, Kagami M, Nagai T, Kondoh T, Onigata K, Maeyama K, Hasegawa T, Hasegawa Y, Yamazaki T, Mizuno S, Miyoshi Y, Miyagawa S, Horikawa R, Matsuoka K, Ogata T. Yamazawa K, et al. Among authors: kagami m. J Mol Med (Berl). 2008 Oct;86(10):1171-81. doi: 10.1007/s00109-008-0377-4. Epub 2008 Jul 8. J Mol Med (Berl). 2008. PMID: 18607558

10

Placentomegaly in paternal uniparental disomy for human chromosome 14.

Kagami M, Yamazawa K, Matsubara K, Matsuo N, Ogata T. Kagami M, et al. Placenta. 2008 Aug;29(8):760-1. doi: 10.1016/j.placenta.2008.06.001. Epub 2008 Jul 11. Placenta. 2008. PMID: 18619672 No abstract available.

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