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1 ubiquitin ligase Parkin have been linked to familial Parkinson's disease.
2 inase 2 (LRRK2) are the most common cause of familial Parkinson's disease.
3 n ligase parkin were shown to associate with familial Parkinson's disease.
4 tations in it were identified as a cause for familial Parkinson's disease.
5 residues, as the germline mutations causing familial Parkinson's disease.
6 urons, and its mutations are associated with familial Parkinson's disease.
7 at kinase 2 (LRRK2) cause autosomal-dominant familial Parkinson's disease.
8 nd Ala30--> Pro) occur in autosomal dominant familial Parkinson's disease.
9 synuclein, which is a mutant associated with familial Parkinson's disease.
10 2 in 117 other smaller British kindreds with familial Parkinson's disease.
11 tions in parkin are the predominant cause of familial Parkinson's disease.
12 an autosomal recessive, early onset form of familial Parkinson's disease.
13 in parkin are the major cause of early-onset familial Parkinson's disease.
14 urther evidence for genetic heterogeneity in familial Parkinson's disease.
15 d a synuclein mutant that is associated with familial Parkinson's disease.
16 d in the pathogenesis of autosomal recessive familial Parkinson's disease.
17 ciated with rare autosomal dominant forms of familial Parkinson's disease.
18 -L1) genes have been linked to some cases of familial Parkinson's disease.
19 erest, this mutation is a very rare cause of familial Parkinson's disease.
20 Leigh syndrome and in a Drosophila model of familial Parkinson's disease.
21 ubiquitin ligase Parkin have been linked to familial Parkinson's disease.
23 wo mutant forms of alpha-synuclein linked to familial Parkinson's disease (Ala30 --> Pro and Ala53 --
24 ns in the alpha-synuclein gene are linked to familial Parkinson's disease and alpha-synuclein accumul
25 ded by genetic linkage between this gene and familial Parkinson's disease and by neurodegeneration in
26 e gene mutations have now been identified in familial Parkinson's disease and important environmental
27 s including the A53T that has been linked to familial Parkinson's disease, and including five substit
28 n that a mutation in NACP is associated with familial Parkinson's disease, and that Lewy bodies are i
29 ha-synuclein mutations are found in cases of familial Parkinson's disease, and transgenic overexpress
31 l death and the pathogenesis of sporadic and familial Parkinson's disease are creating new opportunit
32 Rare mutations in Nurr1 are associated with familial Parkinson's disease, but the underlying basis f
33 equency of a novel mutation (Gly2019 ser) in familial Parkinson's disease by screening genomic DNA of
35 s disease, amyotrophic lateral sclerosis and familial Parkinson's disease, defects arise at different
36 Parkin, the most commonly mutated gene in familial Parkinson's disease, encodes an E3 ubiquitin li
37 inhibition in mammals represents a cause of familial Parkinson's disease has not been established.
38 arkin, a E3 ubiquitin ligase associated with familial Parkinson's disease, has been implicated in mit
39 clein gene recently has been associated with familial Parkinson's disease in the Spellman-Muenter kin
42 y by wild-type (wt) alpha-synuclein, and its familial Parkinson's disease linked mutants A30P and A53
43 ransgenic mice expressing human wild-type or familial Parkinson's disease-linked A53T or A30P mutant
46 an chromosome 2q37 within a region linked to familial Parkinson's disease (PARK11 locus), and associa
47 ) have been identified as a genetic cause of familial Parkinson's disease (PD) and have also been fou
48 (LRRK2) cause late-onset, autosomal dominant familial Parkinson's disease (PD) and variation at the L
50 Studies of several genes associated with familial Parkinson's disease (PD) have implicated aberra
51 uclein (alphaS) gene mutations occur in rare familial Parkinson's disease (PD) kindreds, and wild-typ
52 ynuclein gene (SNCA) have been implicated in familial Parkinson's disease (PD) while certain polymorp
53 mutations in the alpha-synuclein gene cause familial Parkinson's disease (PD), and alpha-synuclein i
54 lterations in alpha-synuclein dosage lead to familial Parkinson's disease (PD), and its accumulation
55 otein alpha-synuclein in the pathogenesis of familial Parkinson's disease (PD), and the aggregation o
56 he parkin gene are common in early-onset and familial Parkinson's disease (PD), and the parkin protei
57 RK2) contribute to development of late-onset familial Parkinson's disease (PD), with clinical feature
59 Recent studies delineate a pathway involving familial Parkinson's disease (PD)-related proteins PINK1
72 n SNCA have been identified in some cases of familial Parkinson's disease, presenting numerous new ar
75 soluble fraction of brain from patients with familial Parkinson's disease (synuclein A53T mutation) a
76 alphaS and two mutational variants linked to familial Parkinson's disease to describe the structural
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