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 related neoplastic disorders, including Cowden disease.
2 irm the role of this gene in the etiology of Cowden disease.
3 ient with a clinical history consistent with Cowden disease.
4 in the germ line of patients with hereditary Cowden disease.
5            This area overlaps the region for Cowden disease, a distinct hamartomatous intestinal poly
6  also identified as the gene predisposing to Cowden disease, an autosomal dominant cancer predisposit
7  a region harboring the gene responsible for Cowden disease, an autosomal dominant hamartoma syndrome
8 ral familial neoplastic disorders, including Cowden disease and Bannayan-Zonana syndrome.
9 utations in PTEN have also been described in Cowden disease and in a small number of patients with ju
10 d provide novel clues to the pathogenesis of Cowden Disease and sporadic nontoxic goiter.
11  hereditary cancer predisposition syndromes, Cowden disease, and Bannayan-Zonana syndrome, wherein br
12 y cancer syndromes such as Gardner syndrome, Cowden disease, and other rare syndromes.
13                                              Cowden disease (CD) is an autosomal dominant cancer pred
14 m-line mutations in PTEN are responsible for Cowden disease (CD), a rare autosomal dominant multiple-
15                  The susceptibility gene for Cowden disease (CD), an autosomal dominant inherited can
16  related human autosomal dominant disorders, Cowden disease (CD), Lhermitte-Duclos disease (LDD) and
17 Bannayan-Riley-Ruvalcaba syndrome (BRRS) and Cowden disease (CD).
18 eptibility gene for two hamartoma syndromes: Cowden disease (CD; MIM 158350) and Bannayan-Zonana (BZS
19 tified, including BRCA1, BRCA2, p53, and the Cowden disease gene PTEN/MMAC1.
20 n PTEN, PTEN-G129E, which is observed in two Cowden disease kindreds, specifically ablates the abilit
21 en described as different disorders, such as Cowden disease, Lhermitte-Duclos disease, and Bannayan-Z
22 lcaba syndrome, juvenile polyposis coli, and Cowden disease, may share the same genetic defect becaus
23 ion for the chemoprevention and treatment of Cowden disease patients and others tumor syndromes that
24                                              Cowden Disease patients, who harbor germ-line PTEN mutat
25  syndrome, juvenile intestinal polyposis and Cowden disease, respectively.
26 l dominant familial cancer syndrome known as Cowden disease, which includes breast cancer among its c

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。