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Items: 1 to 20 of 142

1.

Identification of MEN1 gene mutations in families with MEN 1 and related disorders.

Bergman L, Teh B, Cardinal J, Palmer J, Walters M, Shepherd J, Cameron D, Hayward N.

Br J Cancer. 2000 Oct;83(8):1009-14.

2.

Identification of five novel germline mutations of the MEN1 gene in Japanese multiple endocrine neoplasia type 1 (MEN1) families.

Sato M, Matsubara S, Miyauchi A, Ohye H, Imachi H, Murao K, Takahara J.

J Med Genet. 1998 Nov;35(11):915-9.

3.

Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism.

Cetani F, Pardi E, Giovannetti A, Vignali E, Borsari S, Golia F, Cianferotti L, Viacava P, Miccoli P, Gasperi M, Pinchera A, Marcocci C.

Clin Endocrinol (Oxf). 2002 Apr;56(4):457-64.

PMID:
11966738
4.

Multiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region.

Karges W, Jostarndt K, Maier S, Flemming A, Weitz M, Wissmann A, Feldmann B, Dralle H, Wagner P, Boehm BO.

J Endocrinol. 2000 Jul;166(1):1-9.

5.

Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.

Giraud S, Zhang CX, Serova-Sinilnikova O, Wautot V, Salandre J, Buisson N, Waterlot C, Bauters C, Porchet N, Aubert JP, Emy P, Cadiot G, Delemer B, Chabre O, Niccoli P, Leprat F, Duron F, Emperauger B, Cougard P, Goudet P, Sarfati E, Riou JP, Guichard S, Rodier M, Meyrier A, Caron P, Vantyghem MC, Assayag M, Peix JL, Pugeat M, Rohmer V, Vallotton M, Lenoir G, Gaudray P, Proye C, Conte-Devolx B, Chanson P, Shugart YY, Goldgar D, Murat A, Calender A.

Am J Hum Genet. 1998 Aug;63(2):455-67.

6.

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states.

Agarwal SK, Kester MB, Debelenko LV, Heppner C, Emmert-Buck MR, Skarulis MC, Doppman JL, Kim YS, Lubensky IA, Zhuang Z, Green JS, Guru SC, Manickam P, Olufemi SE, Liotta LA, Chandrasekharappa SC, Collins FS, Spiegel AM, Burns AL, Marx SJ.

Hum Mol Genet. 1997 Jul;6(7):1169-75.

7.

A large germline deletion of the MEN1 gene in a family with multiple endocrine neoplasia type 1.

Kishi M, Tsukada T, Shimizu S, Futami H, Ito Y, Kanbe M, Obara T, Yamaguchi K.

Jpn J Cancer Res. 1998 Jan;89(1):1-5.

PMID:
9510467
8.

Somatic mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in patients with sporadic, nonfamilial primary hyperparathyroidism.

Sato K, Yamazaki K, Zhu H, Kanbe M, Iihara M, Wada Y, Tanaka R, Okamoto T, Ito Y, Obara T.

Surgery. 2000 Mar;127(3):337-41.

PMID:
10715991
9.

Germline mutation of the multiple endocrine neoplasia type 1 (MEN1) gene in a family with primary hyperparathyroidism.

Ohye H, Sato M, Matsubara S, Miyauchi A, Imachi H, Murao K, Takahara J.

Endocr J. 1998 Dec;45(6):719-23.

10.

The MEN1 gene and associated diseases: an update.

Tsukada T, Yamaguchi K, Kameya T.

Endocr Pathol. 2001 Fall;12(3):259-73. Review.

PMID:
11740047
11.

Menin mutations in the diagnosis and prediction of multiple endocrine neoplasia type 1.

Karges W, Ludwig L, Kessler H, Wissmann A, Wagner PK, Boehm BO.

Langenbecks Arch Surg. 1998 Apr;383(2):183-6.

PMID:
9641896
12.
13.

Mutation analysis of the MEN1 gene in Israeli patients with MEN1 and familial isolated hyperprolactinemia.

Jakobovitz-Picard O, Olchovsky D, Berezin M, Ghodsizade A, Zahavi Z, Karasik A, Rechavi G, Friedman E.

Hum Mutat. 2000 Sep;16(3):269.

PMID:
10980535
14.

Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families.

Agarwal SK, Debelenko LV, Kester MB, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Heppner C, Crabtree JS, Lubensky IA, Zhuang Z, Kim YS, Chandrasekharappa SC, Collins FS, Liotta LA, Spiegel AM, Burns AL, Emmert-Buck MR, Marx SJ.

Hum Mutat. 1998;12(2):75-82.

PMID:
9671267
15.

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism.

Pannett AA, Kennedy AM, Turner JJ, Forbes SA, Cavaco BM, Bassett JH, Cianferotti L, Harding B, Shine B, Flinter F, Maidment CG, Trembath R, Thakker RV.

Clin Endocrinol (Oxf). 2003 May;58(5):639-46.

PMID:
12699448
16.

Germline and somatic mutation of the gene for multiple endocrine neoplasia type 1 (MEN1).

Marx SJ, Agarwal SK, Kester MB, Heppner C, Kim YS, Emmert-Buck MR, Debelenko LV, Lubensky IA, Zhuang Z, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Doppman JL, Alexander RH, Liotta LA, Collins FS, Chandrasekharappa SC, Spiegel AM, Burns AL.

J Intern Med. 1998 Jun;243(6):447-53.

17.

Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders.

Park JH, Kim IJ, Kang HC, Lee SH, Shin Y, Kim KH, Lim SB, Kang SB, Lee K, Kim SY, Lee MS, Lee MK, Park JH, Moon SD, Park JG.

Clin Genet. 2003 Jul;64(1):48-53.

PMID:
12791038
18.

A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing.

Cardinal JW, Bergman L, Hayward N, Sweet A, Warner J, Marks L, Learoyd D, Dwight T, Robinson B, Epstein M, Smith M, Teh BT, Cameron DP, Prins JB.

J Med Genet. 2005 Jan;42(1):69-74.

19.

Familial isolated primary hyperparathyroidism--a multiple endocrine neoplasia type 1 variant?

Miedlich S, Lohmann T, Schneyer U, Lamesch P, Paschke R.

Eur J Endocrinol. 2001 Aug;145(2):155-60. Review.

20.

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.

Balogh K, Hunyady L, Patocs A, Gergics P, Valkusz Z, Toth M, Racz K.

Clin Endocrinol (Oxf). 2007 Nov;67(5):727-34.

PMID:
17953629
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