PubMed (cited) for id: 609526

Year	Number of Results
2005	1
2006	4
2007	1
2024	0

1

Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia.

Amino T, Ishikawa K, Toru S, Ishiguro T, Sato N, Tsunemi T, Murata M, Kobayashi K, Inazawa J, Toda T, Mizusawa H. Amino T, et al. J Hum Genet. 2007;52(8):643-649. doi: 10.1007/s10038-007-0154-1. Epub 2007 Jul 5. J Hum Genet. 2007. PMID: 17611710

2

16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.

Ouyang Y, Sakoe K, Shimazaki H, Namekawa M, Ogawa T, Ando Y, Kawakami T, Kaneko J, Hasegawa Y, Yoshizawa K, Amino T, Ishikawa K, Mizusawa H, Nakano I, Takiyama Y. Ouyang Y, et al. J Neurol Sci. 2006 Sep 25;247(2):180-6. doi: 10.1016/j.jns.2006.04.009. Epub 2006 Jun 15. J Neurol Sci. 2006. PMID: 16780885

3

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.

Lim J, Hao T, Shaw C, Patel AJ, Szabó G, Rual JF, Fisk CJ, Li N, Smolyar A, Hill DE, Barabási AL, Vidal M, Zoghbi HY. Lim J, et al. Cell. 2006 May 19;125(4):801-14. doi: 10.1016/j.cell.2006.03.032. Cell. 2006. PMID: 16713569 Free article.

4

A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.

Ohata T, Yoshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, Mizusawa H, Yoshiura KI, Fukushima Y, Ikeda SI, Matsumoto N. Ohata T, et al. J Hum Genet. 2006;51(5):461-466. doi: 10.1007/s10038-006-0385-6. Epub 2006 Apr 14. J Hum Genet. 2006. PMID: 16614795

5

Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population.

Wieczorek S, Arning L, Alheite I, Epplen JT. Wieczorek S, et al. J Hum Genet. 2006;51(4):363-367. doi: 10.1007/s10038-006-0372-y. Epub 2006 Feb 21. J Hum Genet. 2006. PMID: 16491300

6

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.

Ishikawa K, Toru S, Tsunemi T, Li M, Kobayashi K, Yokota T, Amino T, Owada K, Fujigasaki H, Sakamoto M, Tomimitsu H, Takashima M, Kumagai J, Noguchi Y, Kawashima Y, Ohkoshi N, Ishida G, Gomyoda M, Yoshida M, Hashizume Y, Saito Y, Murayama S, Yamanouchi H, Mizutani T, Kondo I, Toda T, Mizusawa H. Ishikawa K, et al. Am J Hum Genet. 2005 Aug;77(2):280-96. doi: 10.1086/432518. Epub 2005 Jul 6. Am J Hum Genet. 2005. PMID: 16001362 Free PMC article.

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