Lee-Chen GJ - Search Results

1

Using ΔK280 Tau_RD Folding Reporter Cells to Screen TRKB Agonists as Alzheimer's Disease Treatment Strategy.

Weng ZK, Lin TH, Chang KH, Chiu YJ, Lin CH, Tseng PH, Sun YC, Lin W, Lee-Chen GJ, Chen CM. Weng ZK, et al. Among authors: lee chen gj. Biomolecules. 2023 Jan 23;13(2):219. doi: 10.3390/biom13020219. Biomolecules. 2023. PMID: 36830589 Free PMC article.

2

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease.

Ross OA, Wu YR, Lee MC, Funayama M, Chen ML, Soto AI, Mata IF, Lee-Chen GJ, Chen CM, Tang M, Zhao Y, Hattori N, Farrer MJ, Tan EK, Wu RM. Ross OA, et al. Ann Neurol. 2008 Jul;64(1):88-92. doi: 10.1002/ana.21405. Ann Neurol. 2008. PMID: 18412265

3

Characterization of a novel p.S305P and a known c.1006+5G>C splice site mutation in human iduronate-2-sulfatase associated with mucopolysaccharidosis type II.

Chang JH, Lee-Chen GJ, Lin SP, Chuang CK. Chang JH, et al. Clin Chim Acta. 2007 Sep;384(1-2):167-70. doi: 10.1016/j.cca.2007.06.014. Epub 2007 Jun 28. Clin Chim Acta. 2007. PMID: 17655837 No abstract available.

4

Analysis of heat-shock protein 70 gene polymorphisms and the risk of Parkinson's disease.

Wu YR, Wang CK, Chen CM, Hsu Y, Lin SJ, Lin YY, Fung HC, Chang KH, Lee-Chen GJ. Wu YR, et al. Hum Genet. 2004 Feb;114(3):236-41. doi: 10.1007/s00439-003-1050-1. Epub 2003 Nov 6. Hum Genet. 2004. PMID: 14605873

5

Dystonia as a presenting sign of spinocerebellar ataxia type 1.

Wu YR, Lee-Chen GJ, Lang AE, Chen CM, Lin HY, Chen ST. Wu YR, et al. Mov Disord. 2004 May;19(5):586-7. doi: 10.1002/mds.10708. Mov Disord. 2004. PMID: 15133826

6

Markedly asymmetrical parkinsonism as a leading feature of adult-onset Huntington's disease.

Wang SC, Lee-Chen GJ, Wang CK, Chen CM, Tang LM, Wu YR. Wang SC, et al. Mov Disord. 2004 Jul;19(7):854-856. doi: 10.1002/mds.20093. Mov Disord. 2004. PMID: 15254954

7

Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathy.

Ro LS, Lee-Chen GJ, Lin TC, Wu YR, Chen CM, Lin CY, Chen ST. Ro LS, et al. Arch Neurol. 2004 Oct;61(10):1594-9. doi: 10.1001/archneur.61.10.1594. Arch Neurol. 2004. PMID: 15477515

8

Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophrenia.

Chen CM, Lane HY, Wu YR, Ro LS, Chen FL, Hung WL, Hou YT, Lin CY, Huang SY, Chen IC, Soong BW, Li ML, Hsieh-Li HM, Su MT, Lee-Chen GJ. Chen CM, et al. Schizophr Res. 2005 Oct 15;78(2-3):131-6. doi: 10.1016/j.schres.2005.06.018. Schizophr Res. 2005. PMID: 16054804

9

Recurrent cerebral venous thrombosis: an Arg359X mutation in the antithrombin gene in a Taiwanese family.

Chen CM, Lee-Chen GJ, Wu YR, Lin CY, Chen CJ, Chen IC, Ro LS. Chen CM, et al. Thromb Res. 2006;118(2):235-40. doi: 10.1016/j.thromres.2005.07.019. Epub 2005 Sep 8. Thromb Res. 2006. PMID: 16154182 No abstract available.

10

Analysis of the PINK1 gene in a cohort of patients with sporadic early-onset parkinsonism in Taiwan.

Fung HC, Chen CM, Hardy J, Singleton AB, Lee-Chen GJ, Wu YR. Fung HC, et al. Neurosci Lett. 2006 Feb 6;394(1):33-6. doi: 10.1016/j.neulet.2005.10.005. Epub 2005 Oct 27. Neurosci Lett. 2006. PMID: 16257123

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