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1 eral sclerosis, spinal muscular atrophy, and spinobulbar muscular atrophy.
2 a fly model of the neurodegenerative disease spinobulbar muscular atrophy.
3 ders such as Huntington disease and X-linked spinobulbar muscular atrophy.
4 to the androgen receptor which is mutated in spinobulbar muscular atrophy.
5 teral sclerosis, spinal muscular atrophy and spinobulbar muscular atrophy.
6 Huntington's disease, hereditary ataxias and spinobulbar muscular atrophy.
7 pansion in the androgen receptor (AR) causes spinobulbar muscular atrophy.
8 ns a polyQ tract associated with the disease spinobulbar muscular atrophy, also known as Kennedy dise
10 olding disorders include Huntington disease, spinobulbar muscular atrophy, dentatorubral-pallidoluysi
11 r (AR), the protein responsible for X-linked spinobulbar muscular atrophy, forms insoluble aggregates
12 inicopathologic features of these disorders (spinobulbar muscular atrophy, Huntington disease, and th
15 rogen receptor (AR) causes Kennedy's disease/spinobulbar muscular atrophy (KD/SBMA) through poorly de
16 llar ataxia type 1, together with studies on spinobulbar muscular atrophy last year, indicate that ho
19 in androgen receptor (AR) is responsible for spinobulbar muscular atrophy (SBMA) that leads to select
20 In polyglutamine diseases such as X-linked spinobulbar muscular atrophy (SBMA), it is unknown wheth
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