戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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
9                                              Spinobulbar muscular atrophy and Huntington's disease ar
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
13                                              Spinobulbar muscular atrophy is a neurodegenerative diso
14                                              Spinobulbar muscular atrophy is a progressive motor neur
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
17                                              Spinobulbar muscular atrophy (SBMA) is a neurodegenerati
18                                              Spinobulbar muscular atrophy (SBMA) is an X-linked disea
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
21 ture models of the dominant genetic disorder spinobulbar muscular atrophy (SBMA).
22 uromuscular degeneration in individuals with spinobulbar muscular atrophy (SBMA).

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。