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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
Sro7p, a Saccharomyces cerevisiae counterpart of the tumor suppressor l(2)gl protein, is related to myosins in function.
Kagami M, Toh-e A, Matsui Y. Kagami M, et al. Genetics. 1998 Aug;149(4):1717-27. Genetics. 1998. PMID: 9691031 Free PMC article.
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.
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.
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
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.
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
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.
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
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