Nakabayashi K - Search Results

1

Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues.

Nakabayashi K, Makino S, Minagawa S, Smith AC, Bamforth JS, Stanier P, Preece M, Parker-Katiraee L, Paton T, Oshimura M, Mill P, Yoshikawa Y, Hui CC, Monk D, Moore GE, Scherer SW. Nakabayashi K, et al. J Med Genet. 2004 Aug;41(8):601-8. doi: 10.1136/jmg.2003.014142. J Med Genet. 2004. PMID: 15286155 Free PMC article. No abstract available.

2

The human contactin-associated protein-like 2 gene (CNTNAP2) spans over 2 Mb of DNA at chromosome 7q35.

Nakabayashi K, Scherer SW. Nakabayashi K, et al. Genomics. 2001 Apr 1;73(1):108-12. doi: 10.1006/geno.2001.6517. Genomics. 2001. PMID: 11352571

3

Mutation analysis of the origin recognition complex subunit 5 (ORC5L) gene in adult patients with myeloid leukemias exhibiting deletions of chromosome band 7q22.

Fröhling S, Nakabayashi K, Scherer SW, Döhner H, Döhner K. Fröhling S, et al. Among authors: nakabayashi k. Hum Genet. 2001 Apr;108(4):304-9. doi: 10.1007/s004390100498. Hum Genet. 2001. PMID: 11379876

4

Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.

Cheung J, Petek E, Nakabayashi K, Tsui LC, Vincent JB, Scherer SW. Cheung J, et al. Among authors: nakabayashi k. Genomics. 2001 Nov;78(1-2):7-11. doi: 10.1006/geno.2001.6651. Genomics. 2001. PMID: 11707066

5

Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.

Nakabayashi K, Bentley L, Hitchins MP, Mitsuya K, Meguro M, Minagawa S, Bamforth JS, Stanier P, Preece M, Weksberg R, Oshimura M, Moore GE, Scherer SW. Nakabayashi K, et al. Hum Mol Genet. 2002 Jul 15;11(15):1743-56. doi: 10.1093/hmg/11.15.1743. Hum Mol Genet. 2002. PMID: 12095916

6

Genetic analysis of patients with the Saethre-Chotzen phenotype.

Chun K, Teebi AS, Jung JH, Kennedy S, Laframboise R, Meschino WS, Nakabayashi K, Scherer SW, Ray PN, Teshima I. Chun K, et al. Among authors: nakabayashi k. Am J Med Genet. 2002 Jun 15;110(2):136-43. doi: 10.1002/ajmg.10400. Am J Med Genet. 2002. PMID: 12116251

7

Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome.

Estivill X, Cheung J, Pujana MA, Nakabayashi K, Scherer SW, Tsui LC. Estivill X, et al. Among authors: nakabayashi k. Hum Mol Genet. 2002 Aug 15;11(17):1987-95. doi: 10.1093/hmg/11.17.1987. Hum Mol Genet. 2002. PMID: 12165560

8

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome.

Bentley L, Nakabayashi K, Monk D, Beechey C, Peters J, Birjandi Z, Khayat FE, Patel M, Preece MA, Stanier P, Scherer SW, Moore GE. Bentley L, et al. Among authors: nakabayashi k. J Med Genet. 2003 Apr;40(4):249-56. doi: 10.1136/jmg.40.4.249. J Med Genet. 2003. PMID: 12676894 Free PMC article.

9

Functional and chromosomal clustering of genes responsive to 5-bromodeoxyuridine in human cells.

Minagawa S, Nakabayashi K, Fujii M, Scherer SW, Ayusawa D. Minagawa S, et al. Among authors: nakabayashi k. Exp Gerontol. 2004 Jul;39(7):1069-78. doi: 10.1016/j.exger.2004.03.022. Exp Gerontol. 2004. PMID: 15236766

10

Early BrdU-responsive genes constitute a novel class of senescence-associated genes in human cells.

Minagawa S, Nakabayashi K, Fujii M, Scherer SW, Ayusawa D. Minagawa S, et al. Among authors: nakabayashi k. Exp Cell Res. 2005 Apr 1;304(2):552-8. doi: 10.1016/j.yexcr.2004.10.036. Epub 2004 Dec 15. Exp Cell Res. 2005. PMID: 15748899

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