ライフサイエンスコーパス: Werner's syndrome

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1 cs of cells from individuals with Bloom's or Werner's syndrome.

2 fibroblasts cultured from an individual with Werner's syndrome.

3 national registry for molecular diagnosis of Werner's syndrome, 26 (20%) had wildtype WRN coding regi

4 Mutations in WRN result in Werner's syndrome, a disease with symptoms resembling pr

5 es associated with premature ageing, such as Werner's syndrome and Hutchinson-Gilford progeria syndro

6 damage that has previously been observed for Werner's syndrome cells.

7 members include the Bloom's syndrome and the Werner's syndrome gene products.

8 the human Bloom's syndrome gene BLM and the Werner's syndrome gene WRN.

9 Mutants for sgs1, the yeast homolog of the Werner's syndrome gene, accumulate ERCs more rapidly, le

10 family helicases encoded by the Bloom's and Werner's syndrome genes are likely to act in concert wit

11 BLM and WRN, the products of the Bloom's and Werner's syndrome genes, are members of the RecQ family

12 e products of the human Bloom's syndrome and Werner's syndrome genes.

13 d the products of human Bloom's syndrome and Werner's syndrome genes.

14 m, Cockayne's syndrome, Bloom's syndrome and Werner's syndrome, have been linked to defects in specif

15 es, such as human Bloom's syndrome and human Werner's syndrome helicases.

16 ma pigmentosum and Bloom syndrome as well as Werner's syndrome, in which patients age prematurely, an

17 Werner's syndrome is a progeroid syndrome caused by muta

18 Our findings indicate that Werner's syndrome is molecularly heterogeneous, and a su

19 s, including the WRN protein associated with Werner's syndrome, might also adopt ring structures.

20 ions and were categorised as having atypical Werner's syndrome on the basis of molecular criteria.

21 Acrolein decreased Werner's syndrome protein (WRN), a member of the RecQ he

22 RecQ helicases such as the human Bloom's and Werner's syndrome proteins and that copies of the helica

23 that includes the human Bloom's syndrome and Werner's syndrome proteins.

24 utated in patients with Bloom's syndrome and Werner's syndrome respectively.

25 cQ helicases, which are mutated in Bloom and Werner's syndrome, respectively, and associated with chr

26 In four (15%) of 26 patients with atypical Werner's syndrome, we noted heterozygosity for novel mis

27 ve implications for the basis of Bloom's and Werner's syndromes, which are caused by mutations in DNA

28 sequenced LMNA in individuals with atypical Werner's syndrome (wild-type WRN).

29 Individuals with atypical Werner's syndrome with mutations in LMNA had a more seve

30 Werner's syndrome (WS) and Bloom's syndrome (BS) are can

31 Werner's syndrome (WS) is a human disease with manifesta

32 Werner's syndrome (WS) is an autosomal recessive disorde

33 Werner's syndrome (WS) is an inherited disease character

34 Werner's syndrome (WS) is an inherited disease with clin

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