Lista de obras - Meng-Ling Chen - Dominio Público Uruguay

A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing

artículo científico publicado en 2019

A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome

artículo científico publicado en 2010

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

artículo científico publicado en 2008

BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population.

artículo científico publicado en 2013

COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population

artículo científico publicado en 2014

LRRK 2 gene mutations in the pathophysiology of the ROCO domain and therapeutic targets for Parkinson's disease: a review

artículo científico publicado en 2018

Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort.

artículo científico publicado en 2016

Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population

artículo científico publicado en 2017

Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity

artículo científico publicado en 2016

Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease.

artículo científico publicado en 2010

Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study

artículo científico publicado en 2010

Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese population.

artículo científico publicado en 2013

Mutational analysis of angiogenin gene in Parkinson's disease

artículo científico publicado en 2014

Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations.

artículo científico publicado en 2009

Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria.

artículo científico publicado en 2011

RIT2 variant is not associated with Parkinson's disease in a Taiwanese population.

artículo científico publicado en 2013

Reaffirmation of GAK, but not HLA-DRA, as a Parkinson's disease susceptibility gene in a Taiwanese population

artículo científico publicado en 2013

The design, synthesis and biological evaluation of 7-alkoxy-4-heteroarylamino-3-cyanoquinolines as dual inhibitors of c-Src and iNOS.

artículo científico publicado en 2008

Lista de obras de Meng-Ling Chen

A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing

A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome

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

BST1 rs11724635 interacts with environmental factors to increase the risk of Parkinson's disease in a Taiwanese population.

COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population

LRRK 2 gene mutations in the pathophysiology of the ROCO domain and therapeutic targets for Parkinson's disease: a review

Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort.

Lack of TMEM230 mutations in patients with familial and sporadic Parkinson's disease in a Taiwanese population

Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity

Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease.

Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study

Mutational analysis of FBXO7 gene in Parkinson's disease in a Taiwanese population.

Mutational analysis of angiogenin gene in Parkinson's disease

Non-synonymous GIGYF2 variants in Parkinson's disease from two Asian populations.

Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria.

RIT2 variant is not associated with Parkinson's disease in a Taiwanese population.

Reaffirmation of GAK, but not HLA-DRA, as a Parkinson's disease susceptibility gene in a Taiwanese population

The design, synthesis and biological evaluation of 7-alkoxy-4-heteroarylamino-3-cyanoquinolines as dual inhibitors of c-Src and iNOS.