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1. Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson’s disease*

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2. Spiegelbildliche Mitbewegungen bei Kindern und Jugendlichen mit infantiler Zerebralparese


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3. and TLR2-driven cell activation

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4. Generation of anti-TLR2 intrabody mediating inhibition of macrophage surface TLR2 expression and TLR2-driven cell activation


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5. A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E


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6. Type and frequency of mutations in the LRRK2 gene in familiar and sporadic Parkinson's disease


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7. Generation of anti-TLR2 intrabody mediating inhibition of macrophage surface TLR2 expression and TLR2-driven cell activation

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873280
http://www.ncbi.nlm.nih.gov/pubmed/20388199  
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8. A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3031338
http://www.ncbi.nlm.nih.gov/pubmed/20015959  
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9. A misplaced lncRNA causes brachydactyly in humans

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485082
http://www.ncbi.nlm.nih.gov/pubmed/23093776  
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10. A cis-regulatory site downregulates PTHLH in translocation t(8;12)(q13;p11.2) and leads to Brachydactyly Type E


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