Kagami M - Search Results

1

Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences.

Eggermann T, Yapici E, Bliek J, Pereda A, Begemann M, Russo S, Tannorella P, Calzari L, de Nanclares GP, Lombardi P, Temple IK, Mackay D, Riccio A, Kagami M, Ogata T, Lapunzina P, Monk D, Maher ER, Tümer Z. Eggermann T, et al. Among authors: kagami m. Clin Epigenetics. 2022 Mar 16;14(1):41. doi: 10.1186/s13148-022-01259-x. Clin Epigenetics. 2022. PMID: 35296332 Free PMC article.

2

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.

3

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.

4

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.

5

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

6

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

7

Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14.

Ogata T, Kagami M, Ferguson-Smith AC. Ogata T, et al. Among authors: kagami m. Epigenetics. 2008 Jul-Aug;3(4):181-7. doi: 10.4161/epi.3.4.6550. Epub 2008 Jul 2. Epigenetics. 2008. PMID: 18698157 Review.

8

Monozygotic female twins discordant for Silver-Russell syndrome and hypomethylation of the H19-DMR.

Yamazawa K, Kagami M, Fukami M, Matsubara K, Ogata T. Yamazawa K, et al. Among authors: kagami m. J Hum Genet. 2008;53(10):950-955. doi: 10.1007/s10038-008-0329-4. Epub 2008 Aug 16. J Hum Genet. 2008. PMID: 18709478

9

Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2.

Kobayashi H, Yamada K, Morita S, Hiura H, Fukuda A, Kagami M, Ogata T, Hata K, Sotomaru Y, Kono T. Kobayashi H, et al. Among authors: kagami m. Genomics. 2009 May;93(5):461-72. doi: 10.1016/j.ygeno.2008.12.012. Epub 2009 Feb 4. Genomics. 2009. PMID: 19200453 Free article.

10

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. PLoS Genet. 2010 Jun 17;6(6):e1000992. doi: 10.1371/journal.pgen.1000992. PLoS Genet. 2010. PMID: 20585555 Free PMC article.

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