| アイテムタイプ |
文献 / Documents(1) |
| 公開日 |
2019-05-27 |
| アクセス権 |
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アクセス権 |
open access |
| 資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
| 出版社版DOI |
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関連識別子 |
https://doi.org/10.1111/j.1365-2265.2006.02534.x |
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関連名称 |
10.1111/j.1365-2265.2006.02534.x |
| 出版タイプ |
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出版タイプ |
AM |
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出版タイプResource |
http://purl.org/coar/version/c_ab4af688f83e57aa |
| タイトル |
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タイトル |
Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome |
| タイトル別表記 |
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その他のタイトル |
Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumor syndrome |
| タイトル別表記 |
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その他のタイトル |
Germline mutation of HRPT2 in patients with hyperparathyroidism |
| タイトル別表記 |
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その他のタイトル |
Germline mutation of HRPT2 in patients with HPT |
| 著者 |
水澤, 典子
ウチノ, シンヤ
岩田, 武男
WEKO
1264
e-Rad_Researcher
10350399
| ja |
岩田, 武男
岩田, 武男
ISNI
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| ja-Kana |
イワタ, タケオ
イワタ, タケオ
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| en |
Iwata, Takeo
Iwata, Takeo
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Search repository
ツユグチ, マサル
スズキ, ヤスヨ
ミズコシ, ツネノリ
ヤマシタ, ヨシオ
サクライ, アキヒロ
スズキ, シンイチ
ベニコ, ムツオ
タハラ, ヒデキ
フジサワ, マサト
鎌田, 伸之
藤澤, 健司
WEKO
1692
e-Rad_Researcher
40228979
| ja |
藤澤, 健司
藤澤, 健司
ISNI
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| ja-Kana |
フジサワ, ケンジ
フジサワ, ケンジ
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| en |
Fujisawa, Kenji
Fujisawa, Kenji
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Search repository
ヤシロ, トオル
長尾, 大輔
Golam, Hossain Md.
佐野, 壽昭
ノグチ, シロウ
吉本, 勝彦
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| 抄録 |
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内容記述 |
Background
A subset of familial isolated primary hyperparathyroidism (FIHP) is a variant of hyperparathyroidism-jaw tumor syndrome (HPT-JT).
Aim/Patients and Methods
We investigated the involvement of the HRPT2, MEN1, and CASR genes in provisional 11 FIHP families and 2 HPT-JT families.
Results
Germline mutations of HRPT2 were found in 2 of 11 FIHP families and 1 of 2 HPT-JT families. One FIHP family with parathyroid carcinoma and atypical adenomas, and another FIHP family with cystic parathyroid adenoma had novel frameshift mutations of 518-521del and 62-66del, respectively. In a patient with HPT-JT, a de novo germline mutation of 39delC was detected. Novel somatic HRPT2 mutations of 70-73del and 95-102del were found in 2 of 5 parathyroid tumors in a family with 518-521del mutation. Biallelic inactivation of HRPT2 by a combination of germline mutation and somatic mutation was confirmed in parathyroid tumors. The finding that 2 families diagnosed with FIHP carried HRPT2 mutations suggests that they have occult HPT-JT. In the remaining 10 families, one family had a missense MEN1 mutation. No mutations of CASR were detected.
Conclusion
Our results confirm the need to test for HRPT2 in FIHP families, especially in those with parathyroid carcinomas, atypical adenomas, or adenomas with cystic change. |
| キーワード |
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主題 |
HPT-JT |
| キーワード |
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主題 |
HRPT2 |
| キーワード |
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主題 |
FIHP |
| キーワード |
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主題 |
parathyroid tumor |
| キーワード |
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主題 |
jaw tumor |
| 書誌情報 |
en : Clinical Endocrinology
巻 65,
号 1,
p. 9-16,
発行日 2006-05-25
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| 収録物ID |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
03000664 |
| 収録物ID |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
13652265 |
| 収録物ID |
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収録物識別子タイプ |
NCID |
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収録物識別子 |
AA00607669 |
| 出版者 |
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出版者 |
John Wiley & Sons |
| 権利情報 |
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権利情報 |
This is the peer reviewed version of the following article: Mizusawa N, Uchino S, Iwata T, Tsuyuguchi M, Suzuki Y, Mizukoshi T, Yamashita Y, Sakurai A, Suzuki S, Beniko M, Tahara H, Fujisawa M, Kamata N, Fujisawa K, Yashiro T, Nagao D, Golam HM, Sano T, Noguchi S, Yoshimoto K. Clin Endocrinol. 2006;65:9-16., which has been published in final form at https://doi.org/10.1111/j.1365-2265.2006.02534.x. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. |
| EID |
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識別子 |
162688 |
| 言語 |
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言語 |
eng |
ce_65_1_9.pdf (1.19 MB)
