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2011 | 3 |
2015 | 1 |
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2024 | 0 |
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Page 1
Inflexibility of AMPK-mediated metabolic reprogramming in mitochondrial disease.
Oncotarget. 2017 Sep 1;8(43):73627-73639. doi: 10.18632/oncotarget.20617. eCollection 2017 Sep 26.
Oncotarget. 2017.
PMID: 29088732
Free PMC article.
Mitigation of cerebellar neuropathy in globoid cell leukodystrophy mice by AAV-mediated gene therapy.
Lin DS, Hsiao CD, Lee AY, Ho CS, Liu HL, Wang TJ, Jian YR, Hsu JC, Huang ZD, Lee TH, Chiang MF.
Lin DS, et al. Among authors: jian yr.
Gene. 2015 Oct 15;571(1):81-90. doi: 10.1016/j.gene.2015.06.049. Epub 2015 Jun 23.
Gene. 2015.
PMID: 26115766
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CNS-targeted AAV5 gene transfer results in global dispersal of vector and prevention of morphological and function deterioration in CNS of globoid cell leukodystrophy mouse model.
Lin DS, Hsiao CD, Liau I, Lin SP, Chiang MF, Chuang CK, Wang TJ, Wu TY, Jian YR, Huang SF, Liu HL.
Lin DS, et al. Among authors: jian yr.
Mol Genet Metab. 2011 Aug;103(4):367-77. doi: 10.1016/j.ymgme.2011.05.005. Epub 2011 May 12.
Mol Genet Metab. 2011.
PMID: 21620749
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Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndrome.
Lin DS, Chang JH, Liu HL, Wei CH, Yeung CY, Ho CS, Shu CH, Chiang MF, Chuang CK, Huang YW, Wu TY, Jian YR, Huang ZD, Lin SP.
Lin DS, et al. Among authors: jian yr.
Am J Med Genet A. 2011 Dec;155A(12):3095-9. doi: 10.1002/ajmg.a.34326. Epub 2011 Nov 3.
Am J Med Genet A. 2011.
PMID: 22052856
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A novel mutation in PYCR1 causes an autosomal recessive cutis laxa with premature aging features in a family.
Lin DS, Yeung CY, Liu HL, Ho CS, Shu CH, Chuang CK, Huang YW, Wu TY, Huang ZD, Jian YR, Lin SP.
Lin DS, et al. Among authors: jian yr.
Am J Med Genet A. 2011 Jun;155A(6):1285-9. doi: 10.1002/ajmg.a.33963. Epub 2011 May 12.
Am J Med Genet A. 2011.
PMID: 21567914
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