Matsuo M - Search Results

1

Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome.

Rossanti R, Shono A, Miura K, Hattori M, Yamamura T, Nakanishi K, Minamikawa S, Fujimura J, Horinouchi T, Nagano C, Sakakibara N, Kaito H, Nagase H, Morisada N, Asanuma K, Matsuo M, Nozu K, Iijima K. Rossanti R, et al. Among authors: matsuo m. J Hum Genet. 2019 Jul;64(7):673-679. doi: 10.1038/s10038-019-0606-4. Epub 2019 Apr 23. J Hum Genet. 2019. PMID: 31015583

2

A novel cryptic exon in intron 3 of the dystrophin gene was incorporated into dystrophin mRNA with a single nucleotide deletion in exon 5.

Suminaga R, Takeshima Y, Adachi K, Yagi M, Nakamura H, Matsuo M. Suminaga R, et al. Among authors: matsuo m. J Hum Genet. 2002;47(4):196-201. doi: 10.1007/s100380200023. J Hum Genet. 2002. PMID: 12166656

3

Two alternative exons can result from activation of the cryptic splice acceptor site deep within intron 2 of the dystrophin gene in a patient with as yet asymptomatic dystrophinopathy.

Yagi M, Takeshima Y, Wada H, Nakamura H, Matsuo M. Yagi M, et al. Among authors: matsuo m. Hum Genet. 2003 Feb;112(2):164-70. doi: 10.1007/s00439-002-0854-8. Epub 2002 Oct 31. Hum Genet. 2003. PMID: 12522557

4

Blockade of TGF-beta action ameliorates renal dysfunction and histologic progression in anti-GBM nephritis.

Zhou A, Ueno H, Shimomura M, Tanaka R, Shirakawa T, Nakamura H, Matsuo M, Iijima K. Zhou A, et al. Among authors: matsuo m. Kidney Int. 2003 Jul;64(1):92-101. doi: 10.1046/j.1523-1755.2003.00045.x. Kidney Int. 2003. PMID: 12787399 Free article.

5

Role of p38 MAP kinase pathway in a toxin-induced model of hemolytic uremic syndrome.

Fu XJ, Iijima K, Nozu K, Hamahira K, Tanaka R, Oda T, Yoshikawa N, Matsuo M. Fu XJ, et al. Among authors: matsuo m. Pediatr Nephrol. 2004 Aug;19(8):844-52. doi: 10.1007/s00467-004-1502-4. Epub 2004 Jun 17. Pediatr Nephrol. 2004. PMID: 15206036

6

Novel double-deletion mutations of the OFD1 gene creating multiple novel transcripts.

Morisawa T, Yagi M, Surono A, Yokoyama N, Ohmori M, Terashi H, Matsuo M. Morisawa T, et al. Among authors: matsuo m. Hum Genet. 2004 Jul;115(2):97-103. doi: 10.1007/s00439-004-1139-1. Epub 2004 Jun 2. Hum Genet. 2004. PMID: 15221448

7

Cyclosporin A absorption profiles in children with nephrotic syndrome.

Nozu K, Iijima K, Sakaeda T, Okumura K, Nakanishi K, Yoshikawa N, Honda M, Ikeda M, Matsuo M. Nozu K, et al. Among authors: matsuo m. Pediatr Nephrol. 2005 Jul;20(7):910-3. doi: 10.1007/s00467-005-1844-6. Epub 2005 Apr 23. Pediatr Nephrol. 2005. PMID: 15856324

8

A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitro.

Thi Tran HT, Takeshima Y, Surono A, Yagi M, Wada H, Matsuo M. Thi Tran HT, et al. Among authors: matsuo m. Mol Genet Metab. 2005 Jul;85(3):213-9. doi: 10.1016/j.ymgme.2005.03.006. Mol Genet Metab. 2005. PMID: 15979033

9

Rituximab treatment for posttransplant lymphoproliferative disorder (PTLD) induces complete remission of recurrent nephrotic syndrome.

Nozu K, Iijima K, Fujisawa M, Nakagawa A, Yoshikawa N, Matsuo M. Nozu K, et al. Among authors: matsuo m. Pediatr Nephrol. 2005 Nov;20(11):1660-3. doi: 10.1007/s00467-005-2013-7. Epub 2005 Aug 16. Pediatr Nephrol. 2005. PMID: 16133051

10

A novel cryptic exon identified in the 3' region of intron 2 of the human dystrophin gene.

Tran VK, Zhang Z, Yagi M, Nishiyama A, Habara Y, Takeshima Y, Matsuo M. Tran VK, et al. Among authors: matsuo m. J Hum Genet. 2005;50(8):425-433. doi: 10.1007/s10038-005-0272-6. Epub 2005 Aug 30. J Hum Genet. 2005. PMID: 16133659

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