Maeda K - Search Results

1

Comprehensive screening of multiple epiphyseal dysplasia mutations in Japanese population.

Itoh T, Shirahama S, Nakashima E, Maeda K, Haga N, Kitoh H, Kosaki R, Ohashi H, Nishimura G, Ikegawa S. Itoh T, et al. Among authors: maeda k. Am J Med Genet A. 2006 Jun 15;140(12):1280-4. doi: 10.1002/ajmg.a.31292. Am J Med Genet A. 2006. PMID: 16691584

2

Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia.

Mabuchi A, Haga N, Maeda K, Nakashima E, Manabe N, Hiraoka H, Kitoh H, Kosaki R, Nishimura G, Ohashi H, Ikegawa S. Mabuchi A, et al. Among authors: maeda k. Hum Mutat. 2004 Nov;24(5):439-40. doi: 10.1002/humu.9286. Hum Mutat. 2004. PMID: 15459972

3

Novel COL9A3 mutation in a family with multiple epiphyseal dysplasia.

Nakashima E, Kitoh H, Maeda K, Haga N, Kosaki R, Mabuchi A, Nishimura G, Ohashi H, Ikegawa S. Nakashima E, et al. Among authors: maeda k. Am J Med Genet A. 2005 Jan 15;132A(2):181-4. doi: 10.1002/ajmg.a.30411. Am J Med Genet A. 2005. PMID: 15551337

4

Mutation in the von Willebrand factor-A domain is not a prerequisite for the MATN3 mutation in multiple epiphyseal dysplasia.

Maeda K, Nakashima E, Horikoshi T, Mabuchi A, Ikegawa S. Maeda K, et al. Am J Med Genet A. 2005 Jul 30;136(3):285-6. doi: 10.1002/ajmg.a.30832. Am J Med Genet A. 2005. PMID: 15948199 No abstract available.

5

A compound heterozygote harboring novel and recurrent DTDST mutations with intermediate phenotype between atelosteogenesis type II and diastrophic dysplasia.

Maeda K, Miyamoto Y, Sawai H, Karniski LP, Nakashima E, Nishimura G, Ikegawa S. Maeda K, et al. Am J Med Genet A. 2006 Jun 1;140(11):1143-7. doi: 10.1002/ajmg.a.31225. Am J Med Genet A. 2006. PMID: 16642506

6

MATN and LAPTM are parts of larger transcription units produced by intergenic splicing: intergenic splicing may be a common phenomenon.

Maeda K, Horikoshi T, Nakashima E, Miyamoto Y, Mabuchi A, Ikegawa S. Maeda K, et al. DNA Res. 2005;12(5):365-72. doi: 10.1093/dnares/dsi017. Epub 2006 Jan 16. DNA Res. 2005. PMID: 16769693 Free article.

7

Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese.

Furuichi T, Maeda K, Chou CT, Liu YF, Liu TC, Miyamoto Y, Takahashi A, Mori K, Ikari K, Kamatani N, Kurosawa H, Inoue H, Tsai SF, Ikegawa S. Furuichi T, et al. Among authors: maeda k. J Hum Genet. 2008;53(5):419-424. doi: 10.1007/s10038-008-0265-3. Epub 2008 Feb 26. J Hum Genet. 2008. PMID: 18299954

8

A large-scale genetic association study of ossification of the posterior longitudinal ligament of the spine.

Horikoshi T, Maeda K, Kawaguchi Y, Chiba K, Mori K, Koshizuka Y, Hirabayashi S, Sugimori K, Matsumoto M, Kawaguchi H, Takahashi M, Inoue H, Kimura T, Matsusue Y, Inoue I, Baba H, Nakamura K, Ikegawa S. Horikoshi T, et al. Among authors: maeda k. Hum Genet. 2006 Jul;119(6):611-6. doi: 10.1007/s00439-006-0170-9. Epub 2006 Apr 12. Hum Genet. 2006. PMID: 16609882

9

Calcium calmodulin kinase IV deficiency in podocytes prevents the development of lupus nephritis.

Bhargava R, Li H, Maeda K, Tsokos MG, Tsokos GC. Bhargava R, et al. Among authors: maeda k. Clin Immunol. 2025 Jan 8:110427. doi: 10.1016/j.clim.2025.110427. Online ahead of print. Clin Immunol. 2025. PMID: 39793862

10

Neuroplasticity in the motor cortex following the achievement of sufficient motor learning.

Mitani A, Shimizu T, Terai J, Maeda K, Suzuki K, Kioka K. Mitani A, et al. Among authors: maeda k. Neurosci Lett. 2025 Jan 7:138117. doi: 10.1016/j.neulet.2025.138117. Online ahead of print. Neurosci Lett. 2025. PMID: 39788482

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