Fu YH - Search Results

1

Genetic insights on sleep schedules: this time, it's PERsonal.

Chong SY, Ptáček LJ, Fu YH. Chong SY, et al. Among authors: fu yh. Trends Genet. 2012 Dec;28(12):598-605. doi: 10.1016/j.tig.2012.08.002. Epub 2012 Aug 28. Trends Genet. 2012. PMID: 22939700 Free PMC article. Review.

2

Molecular biology of episodic movement disorders.

Ptácek LJ, Fu YH. Ptácek LJ, et al. Among authors: fu yh. Adv Neurol. 2002;89:453-8. Adv Neurol. 2002. PMID: 11968469 Review. No abstract available.

3

Polyglutamine-expanded ataxin-7 promotes non-cell-autonomous purkinje cell degeneration and displays proteolytic cleavage in ataxic transgenic mice.

Garden GA, Libby RT, Fu YH, Kinoshita Y, Huang J, Possin DE, Smith AC, Martinez RA, Fine GC, Grote SK, Ware CB, Einum DD, Morrison RS, Ptacek LJ, Sopher BL, La Spada AR. Garden GA, et al. Among authors: fu yh. J Neurosci. 2002 Jun 15;22(12):4897-905. doi: 10.1523/JNEUROSCI.22-12-04897.2002. J Neurosci. 2002. PMID: 12077187 Free PMC article.

4

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).

Tristani-Firouzi M, Jensen JL, Donaldson MR, Sansone V, Meola G, Hahn A, Bendahhou S, Kwiecinski H, Fidzianska A, Plaster N, Fu YH, Ptacek LJ, Tawil R. Tristani-Firouzi M, et al. Among authors: fu yh. J Clin Invest. 2002 Aug;110(3):381-8. doi: 10.1172/JCI15183. J Clin Invest. 2002. PMID: 12163457 Free PMC article.

5

A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures.

Nakayama J, Fu YH, Clark AM, Nakahara S, Hamano K, Iwasaki N, Matsui A, Arinami T, Ptácek LJ. Nakayama J, et al. Among authors: fu yh. Ann Neurol. 2002 Nov;52(5):654-7. doi: 10.1002/ana.10347. Ann Neurol. 2002. PMID: 12402266

6

Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice.

Libby RT, Monckton DG, Fu YH, Martinez RA, McAbney JP, Lau R, Einum DD, Nichol K, Ware CB, Ptacek LJ, Pearson CE, La Spada AR. Libby RT, et al. Among authors: fu yh. Hum Mol Genet. 2003 Jan 1;12(1):41-50. doi: 10.1093/hmg/ddg006. Hum Mol Genet. 2003. PMID: 12490531

7

A novel central nervous system-enriched spinocerebellar ataxia type 7 gene product.

Einum DD, Clark AM, Townsend JJ, Ptacek LJ, Fu YH. Einum DD, et al. Among authors: fu yh. Arch Neurol. 2003 Jan;60(1):97-103. doi: 10.1001/archneur.60.1.97. Arch Neurol. 2003. PMID: 12533095

8

What's new in epilepsy genetics?

Ptácek LJ, Fu YH. Ptácek LJ, et al. Among authors: fu yh. Mol Psychiatry. 2003 May;8(5):463-5. doi: 10.1038/sj.mp.4001292. Mol Psychiatry. 2003. PMID: 12808423 Review. No abstract available.

9

Defective potassium channel Kir2.1 trafficking underlies Andersen-Tawil syndrome.

Bendahhou S, Donaldson MR, Plaster NM, Tristani-Firouzi M, Fu YH, Ptácek LJ. Bendahhou S, et al. Among authors: fu yh. J Biol Chem. 2003 Dec 19;278(51):51779-85. doi: 10.1074/jbc.M310278200. Epub 2003 Oct 1. J Biol Chem. 2003. PMID: 14522976 Free article.

10

Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity.

Donaldson MR, Yoon G, Fu YH, Ptacek LJ. Donaldson MR, et al. Among authors: fu yh. Ann Med. 2004;36 Suppl 1:92-7. doi: 10.1080/17431380410032490. Ann Med. 2004. PMID: 15176430 Free article. Review.

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