ライフサイエンスコーパス: peripheral myelin protein 22

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 , three for myelin protein zero, and two for peripheral myelin protein 22.

2 ture suggests that OSP is a CNS homologue of peripheral myelin protein-22.

3 These genes were peripheral myelin protein 22, decorin, transcription fac

4 n the myelin protein zero gene (MPZ) and the peripheral myelin protein 22 gene (PMP22), appear to mak

5 o be caused by an altered copy number of the peripheral myelin protein 22 gene (PMP22), which lies wi

6 to a region on chromosome 11 containing the peripheral myelin protein 22 gene (Pmp22).

7 b region of chromosome 17 which includes the peripheral myelin protein 22 gene (PMP22).

8 ded that the possession of two copies of the peripheral myelin protein 22 gene within the duplicated

9 to result from an altered copy number of the peripheral myelin protein-22 gene, PMP22, which maps wit

10 ication of chromosome 17p11.2 containing the peripheral myelin protein-22 gene.

11 The occurrence of mutations in peripheral myelin protein 22 is one of the genetic mecha

12 utations in the genes encoding protein zero, peripheral myelin protein 22 kDa, and connexin32, all of

13 type 1 (CMT1) is caused by mutations in the peripheral myelin protein, 22 kDa (PMP22) gene, protein

14 ere remyelinated by protein zero (P0)(+) and peripheral myelin protein 22-kDa (PMP22)(+) myelin, norm

15 The peripheral myelin protein 22 mutation W28R was associate

16 ation, 5 a myelin protein zero mutation, 5 a peripheral myelin protein 22 mutation, 1 an early growth

17 ciated with alterations of several proteins: peripheral myelin protein 22, myelin protein zero, conne

18 type 1A (CMT1A) is caused by duplication of peripheral myelin protein 22 (PMP22) and is the most com

19 mutations in the tetraspan membrane protein peripheral myelin protein 22 (PMP22) are known to result

20 lications, deletions, and point mutations in peripheral myelin protein 22 (PMP22) are linked to sever

21 Haploinsufficiency of peripheral myelin protein 22 (PMP22) causes hereditary n

22 nconservative leucine to proline mutation in peripheral myelin protein 22 (PMP22) causes the Trembler

23 athy, is usually caused by overexpression of peripheral myelin protein 22 (PMP22) due to a genomic du

24 Direct sequencing of the candidate peripheral myelin protein 22 (PMP22) gene detected a uni

25 Alterations in peripheral myelin protein 22 (PMP22) gene expression are

26 SMS region of 17p11.2 and a deletion of the peripheral myelin protein 22 (PMP22) gene within 17p12 o

27 pathy is a copy number variant involving the Peripheral Myelin Protein 22 (PMP22) gene, which is loca

28 1A (CMT1A) is linked with duplication of the peripheral myelin protein 22 (PMP22) gene.

29 identified four novel point mutations in the peripheral myelin protein 22 (PMP22) gene.

30 is most commonly caused by overexpression of peripheral myelin protein 22 (PMP22) in Schwann cells of

31 Since peripheral myelin protein 22 (PMP22) is a key component

32 Peripheral myelin protein 22 (PMP22) is a short-lived Sc

33 Peripheral myelin protein 22 (PMP22) is a tetraspan memb

34 Peripheral myelin protein 22 (PMP22) is an integral memb

35 Peripheral myelin protein 22 (PMP22) is associated with

36 An example is found in the relationship of peripheral myelin protein 22 (PMP22) to Charcot-Marie-To

37 Peripheral myelin protein 22 (PMP22) was increased in CM

38 Misexpression and cytosolic retention of peripheral myelin protein 22 (PMP22) within Schwann cell

39 Mutations in the gene encoding the peripheral myelin protein 22 (PMP22), a tetraspan protei

40 Peripheral myelin protein 22 (PMP22), also known as grow

41 Peripheral myelin protein 22 (PMP22), another member of

42 riants of the alpha-helical membrane protein peripheral myelin protein 22 (PMP22), the intracellular

43 lts in an extra copy and increased dosage of peripheral myelin protein 22 (PMP22).

44 major protein components of myelin, such as peripheral myelin protein 22 (PMP22).

45 The peripheral myelin protein-22 (PMP22) gene is associated

46 on on chromosome 17p11.2, which contains the peripheral myelin protein-22 (PMP22) gene.

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。