Inazawa J - Search Results

1

HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome.

Niihori T, Aoki Y, Okamoto N, Kurosawa K, Ohashi H, Mizuno S, Kawame H, Inazawa J, Ohura T, Arai H, Nabatame S, Kikuchi K, Kuroki Y, Miura M, Tanaka T, Ohtake A, Omori I, Ihara K, Mabe H, Watanabe K, Niijima S, Okano E, Numabe H, Matsubara Y. Niihori T, et al. Among authors: inazawa j. J Hum Genet. 2011 Oct;56(10):707-15. doi: 10.1038/jhg.2011.85. Epub 2011 Aug 18. J Hum Genet. 2011. PMID: 21850009

2

Isolation and characterization of a novel gene deleted in DiGeorge syndrome.

Kurahashi H, Akagi K, Inazawa J, Ohta T, Niikawa N, Kayatani F, Sano T, Okada S, Nishisho I. Kurahashi H, et al. Among authors: inazawa j. Hum Mol Genet. 1995 Apr;4(4):541-9. doi: 10.1093/hmg/4.4.541. Hum Mol Genet. 1995. PMID: 7633402

3

Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors.

Hatada I, Inazawa J, Abe T, Nakayama M, Kaneko Y, Jinno Y, Niikawa N, Ohashi H, Fukushima Y, Iida K, Yutani C, Takahashi S, Chiba Y, Ohishi S, Mukai T. Hatada I, et al. Among authors: inazawa j. Hum Mol Genet. 1996 Jun;5(6):783-8. doi: 10.1093/hmg/5.6.783. Hum Mol Genet. 1996. PMID: 8776593

4

Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1).

Tanaka T, Inazawa J, Nakamura Y. Tanaka T, et al. Among authors: inazawa j. Genomics. 1996 Feb 15;32(1):128-30. doi: 10.1006/geno.1996.0087. Genomics. 1996. PMID: 8786100

5

Molecular cloning of a human cDNA encoding putative cysteine protease (PRSC1) and its chromosome assignment to 14q32.1.

Tanaka T, Inazawa J, Nakamura Y. Tanaka T, et al. Among authors: inazawa j. Cytogenet Cell Genet. 1996;74(1-2):120-3. doi: 10.1159/000134397. Cytogenet Cell Genet. 1996. PMID: 8893817

6

Identification of a gene disrupted by inv(11)(q13.5;q25) in a patient with left-right axis malformation.

Iida A, Emi M, Matsuoka R, Hiratsuka E, Okui K, Ohashi H, Inazawa J, Fukushima Y, Imai T, Nakamura Y. Iida A, et al. Among authors: inazawa j. Hum Genet. 2000 Mar;106(3):277-87. doi: 10.1007/s004390051038. Hum Genet. 2000. PMID: 10798355

7

Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization.

Hayashi S, Kurosawa K, Imoto I, Mizutani S, Inazawa J. Hayashi S, et al. Among authors: inazawa j. Am J Med Genet A. 2005 Nov 15;139(1):32-6. doi: 10.1002/ajmg.a.30982. Am J Med Genet A. 2005. PMID: 16222686

8

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.

Hayashi S, Honda S, Minaguchi M, Makita Y, Okamoto N, Kosaki R, Okuyama T, Imoto I, Mizutani S, Inazawa J. Hayashi S, et al. Among authors: inazawa j. J Hum Genet. 2007;52(5):397-405. doi: 10.1007/s10038-007-0127-4. Epub 2007 Apr 4. J Hum Genet. 2007. PMID: 17406783

9

22q13 Microduplication in two patients with common clinical manifestations: a recognizable syndrome?

Okamoto N, Kubota T, Nakamura Y, Murakami R, Nishikubo T, Tanaka I, Takahashi Y, Hayashi S, Imoto I, Inazawa J, Hosokai N, Kohsaka S, Uchino S. Okamoto N, et al. Among authors: inazawa j. Am J Med Genet A. 2007 Dec 1;143A(23):2804-9. doi: 10.1002/ajmg.a.31771. Am J Med Genet A. 2007. PMID: 17975801

10

The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardation.

Hayashi S, Mizuno S, Migita O, Okuyama T, Makita Y, Hata A, Imoto I, Inazawa J. Hayashi S, et al. Among authors: inazawa j. Am J Med Genet A. 2008 Aug 15;146A(16):2145-51. doi: 10.1002/ajmg.a.32433. Am J Med Genet A. 2008. PMID: 18629876

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