Niida Y - Search Results

1

Inactivation patterns of NF2 and DAL-1/4.1B (EPB41L3) in sporadic meningioma.

Nunes F, Shen Y, Niida Y, Beauchamp R, Stemmer-Rachamimov AO, Ramesh V, Gusella J, MacCollin M. Nunes F, et al. Among authors: niida y. Cancer Genet Cytogenet. 2005 Oct 15;162(2):135-9. doi: 10.1016/j.cancergencyto.2005.04.003. Cancer Genet Cytogenet. 2005. PMID: 16213361

2

Survey of somatic mutations in tuberous sclerosis complex (TSC) hamartomas suggests different genetic mechanisms for pathogenesis of TSC lesions.

Niida Y, Stemmer-Rachamimov AO, Logrip M, Tapon D, Perez R, Kwiatkowski DJ, Sims K, MacCollin M, Louis DN, Ramesh V. Niida Y, et al. Am J Hum Genet. 2001 Sep;69(3):493-503. doi: 10.1086/321972. Epub 2001 Jul 20. Am J Hum Genet. 2001. PMID: 11468687 Free PMC article.

3

Analysis of both TSC1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis.

Niida Y, Lawrence-Smith N, Banwell A, Hammer E, Lewis J, Beauchamp RL, Sims K, Ramesh V, Ozelius L. Niida Y, et al. Hum Mutat. 1999;14(5):412-22. doi: 10.1002/(SICI)1098-1004(199911)14:5<412::AID-HUMU7>3.0.CO;2-K. Hum Mutat. 1999. PMID: 10533067

4

The TSC1 tumor suppressor hamartin interacts with neurofilament-L and possibly functions as a novel integrator of the neuronal cytoskeleton.

Haddad LA, Smith N, Bowser M, Niida Y, Murthy V, Gonzalez-Agosti C, Ramesh V. Haddad LA, et al. Among authors: niida y. J Biol Chem. 2002 Nov 15;277(46):44180-6. doi: 10.1074/jbc.M207211200. Epub 2002 Sep 10. J Biol Chem. 2002. PMID: 12226091 Free article.

5

Superiority of denaturing high performance liquid chromatography over single-stranded conformation and conformation-sensitive gel electrophoresis for mutation detection in TSC2.

Choy YS, Dabora SL, Hall F, Ramesh V, Niida Y, Franz D, Kasprzyk-Obara J, Reeve MP, Kwiatkowski DJ. Choy YS, et al. Among authors: niida y. Ann Hum Genet. 1999 Sep;63(Pt 5):383-91. doi: 10.1046/j.1469-1809.1999.6350383.x. Ann Hum Genet. 1999. PMID: 10735580

6

Mutational analysis of TSC1 and TSC2 in Japanese patients with tuberous sclerosis complex revealed higher incidence of TSC1 patients than previously reported.

Niida Y, Wakisaka A, Tsuji T, Yamada H, Kuroda M, Mitani Y, Okumura A, Yokoi A. Niida Y, et al. J Hum Genet. 2013 Apr;58(4):216-25. doi: 10.1038/jhg.2013.3. Epub 2013 Feb 7. J Hum Genet. 2013. PMID: 23389244

7

Genotype and Phenotype Landscape of 283 Japanese Patients with Tuberous Sclerosis Complex.

Togi S, Ura H, Hatanaka H, Niida Y. Togi S, et al. Among authors: niida y. Int J Mol Sci. 2022 Sep 22;23(19):11175. doi: 10.3390/ijms231911175. Int J Mol Sci. 2022. PMID: 36232477 Free PMC article.

8

A case of solitary subependymal giant cell astrocytoma: two somatic hits of TSC2 in the tumor, without evidence of somatic mosaicism.

Ichikawa T, Wakisaka A, Daido S, Takao S, Tamiya T, Date I, Koizumi S, Niida Y. Ichikawa T, et al. Among authors: niida y. J Mol Diagn. 2005 Oct;7(4):544-9. doi: 10.1016/S1525-1578(10)60586-7. J Mol Diagn. 2005. PMID: 16237225 Free PMC article.

9

Microsatellite analysis of childhood leukemia: correlation of 9p and 12p chromosome abnormalities with expression of related genes.

Nishimura R, Niida Y, Saikawa Y, Goto Y, Noguchi T, Ichihara T, Koizumi S. Nishimura R, et al. Among authors: niida y. Pediatr Int. 1999 Aug;41(4):346-52. doi: 10.1046/j.1442-200x.1999.01088.x. Pediatr Int. 1999. PMID: 10453181

10

TSC2 somatic mosaic mutation, including extra-tumor tissue, may be the developmental cause of solitary subependymal giant cell astrocytoma.

Sasaki T, Uda T, Kuki I, Kunihiro N, Okazaki S, Niida Y, Goto T. Sasaki T, et al. Among authors: niida y. Childs Nerv Syst. 2022 Jan;38(1):77-83. doi: 10.1007/s00381-021-05399-y. Epub 2021 Nov 6. Childs Nerv Syst. 2022. PMID: 34741623

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