𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Decreased Expression of Lysosomal Alpha-Galactosiase A Gene in Sporadic Parkinson’s Disease

✍ Scribed by Guanghua Wu; Jian Huang; Xungang Feng; Aimei Zhang; Jifeng Li; Shuchao Pang; Kejin Gu; Haixin Dong; Junping Zhang; Huijie Gao; Bo Yan

Publisher
Springer
Year
2011
Tongue
English
Weight
205 KB
Volume
36
Category
Article
ISSN
0364-3190

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Alpha-synuclein mRNA expression in spora
Alpha-synuclein mRNA expression in sporadic Parkinson's disease
✍ Eng-King Tan; Van R. Chandran; Stephanie Fook-Chong; Hui Shen; Kenneth Yew; Mei- 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 79 KB 👁 1 views

## Abstract The expression of α‐synuclein gene can be influenced by the genomic load and/or epigenetic factors. By using quantitative real‐time polymerase chain reaction techniques, we demonstrated that the α‐synuclein gene mRNA expression in sporadic PD did not differ from healthy controls (median

Haplotype analysis of the PARK 11 gene,
Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's disease
✍ Greg T. Sutherland; Gerhard A. Siebert; Jeremy R. B. Newman; Peter A. Silburn; R 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 905 KB

## Abstract Familial Parkinsonism (__PARK__) genes are strong candidates for conferring susceptibility to common forms of PD. However, most studies to date have provided little evidence that their common variants substantially influence disease risk. Recently, mutations were described in the gene,

Identification of a risk haplotype of th
Identification of a risk haplotype of the α-synuclein gene in Japanese with sporadic Parkinson's disease
✍ Hideaki Kobayashi; Hiroshi Ujike; Junko Hasegawa; Mitsutoshi Yamamoto; Akihiro K 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 140 KB

## Abstract α‐Synuclein is one of the main components of Lewy bodies, a pathological marker of Parkinson's disease (PD). Certain missense mutations of the α‐synuclein gene cause familial PD, but the role of the gene in sporadic PD is still controversial. We scrutinized polymorphisms of the α‐synucl

Analysis of PARK2 gene exon rearrangemen
Analysis of PARK2 gene exon rearrangements in Russian patients with sporadic Parkinson's disease
✍ Elena V. Semenova; Maria I. Shadrina; Pyotr A. Slominsky; Irina A. Ivanova-Smole 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 1006 KB

## Abstract ## Background: Deletions and duplications of single exons or exon groups account for a large proportion of the __PARK2__ gene mutations described in juvenile autosomal recessive Parkinson's disease (PD). ## Methods: We analyzed rearrangements in exons 1 to 12 of the __PARK2__ gene in