ライフサイエンスコーパス: oculopharyngeal

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 Emery-Dreifuss; distal; facioscapulohumeral; oculopharyngeal; and limb-girdle which is the most heter

2 Oculopharyngeal muscular dystrophy (OPMD) is a late onse

3 Oculopharyngeal muscular dystrophy (OPMD) is a late-onse

4 Oculopharyngeal muscular dystrophy (OPMD) is a late-onse

5 Oculopharyngeal muscular dystrophy (OPMD) is a rare myop

6 Oculopharyngeal muscular dystrophy (OPMD) is an adult-on

7 Oculopharyngeal muscular dystrophy (OPMD) is an autosoma

8 Oculopharyngeal muscular dystrophy (OPMD) is an autosoma

9 Oculopharyngeal muscular dystrophy (OPMD) is an autosoma

10 Oculopharyngeal muscular dystrophy (OPMD) is an autosoma

11 are one of the ultrastructural hallmarks of oculopharyngeal muscular dystrophy (OPMD), a disorder ca

12 ne tract in the N-terminus of PABPN1 lead to oculopharyngeal muscular dystrophy (OPMD), which is an a

13 a specific form of muscular dystrophy termed oculopharyngeal muscular dystrophy (OPMD).

14 nal group is altered in the transcriptome of oculopharyngeal muscular dystrophy (OPMD).

15 ng protein nuclear-1 (PABPN1) protein causes oculopharyngeal muscular dystrophy (OPMD).

16 ed a different chromosomal haplotype for the oculopharyngeal muscular dystrophy alleles than did the

17 expansion in PABPN1 that is thought to cause oculopharyngeal muscular dystrophy cannot completely res

18 Oculopharyngeal muscular dystrophy is a late-onset disea

19 Oculopharyngeal muscular dystrophy is a late-onset, auto

20 A heat-shock response was also seen in an oculopharyngeal muscular dystrophy mouse model expressin

21 Linkage of oculopharyngeal muscular dystrophy to 14q11.2-q13 has be

22 gton's disease (HD), Parkinson's disease and oculopharyngeal muscular dystrophy, are associated with

23 osis type 1, congenital myasthenic syndrome, oculopharyngeal muscular dystrophy, chronic progressive

24 vacuoles is described in autosomal dominant oculopharyngeal muscular dystrophy, the age of onset, th

25 nt progressive external ophthalmoplegia, and oculopharyngeal muscular dystrophy.

26 s 5 multigenerational American families with oculopharyngeal muscular dystrophy.

27 some system, which is highly dysregulated in oculopharyngeal muscular dystrophy.

28 e muscle weakness in the late-onset disorder oculopharyngeal muscular dystrophy.

29 siblings who developed a rapidly progressive oculopharyngeal somatic syndrome, at the ages of 11 and

30 ly is an example of a GCG expansion-negative oculopharyngeal syndrome requiring further genetic inves

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。