153 related articles for article (PubMed ID: 10664521)
21. 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. PubMed ID: 9215689
[TBL] [Abstract][Full Text] [Related]
22. Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene.
Hannan FM; Nesbit MA; Christie PT; Fratter C; Dudley NE; Sadler GP; Thakker RV
Nat Clin Pract Endocrinol Metab; 2008 Jan; 4(1):53-8. PubMed ID: 18084346
[TBL] [Abstract][Full Text] [Related]
23. A novel six-nucleotide insertion in exon 4 of the MEN1 gene, 878insCTGCAG, in three patients with familial insulinoma and primary hyperparathyroidism.
Okamoto H; Tamada A; Hai N; Doi M; Uchimura I; Hirata Y; Kosugi S
Jpn J Clin Oncol; 2002 Sep; 32(9):368-70. PubMed ID: 12417605
[TBL] [Abstract][Full Text] [Related]
24. Multiple endocrine neoplasia type 1 (MEN1): LOH studies in a affected family and in sporadic cases.
Valdes N; Alvarez V; Diaz-Cadorniga F; Aller J; Villazon F; Garcia I; Herrero A; Coto E
Anticancer Res; 1998; 18(4A):2685-9. PubMed ID: 9703929
[TBL] [Abstract][Full Text] [Related]
25. 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. PubMed ID: 9681842
[TBL] [Abstract][Full Text] [Related]
26. Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism.
Teh BT; Kytölä S; Farnebo F; Bergman L; Wong FK; Weber G; Hayward N; Larsson C; Skogseid B; Beckers A; Phelan C; Edwards M; Epstein M; Alford F; Hurley D; Grimmond S; Silins G; Walters M; Stewart C; Cardinal J; Khodaei S; Parente F; Tranebjaerg L; Jorde R; Salmela P
J Clin Endocrinol Metab; 1998 Aug; 83(8):2621-6. PubMed ID: 9709921
[TBL] [Abstract][Full Text] [Related]
27. A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1.
Cetani F; Pardi E; Cianferotti L; Vignali E; Picone A; Miccoli P; Pinchera A; Marcocci C
Eur J Endocrinol; 1999 May; 140(5):429-33. PubMed ID: 10229909
[TBL] [Abstract][Full Text] [Related]
28. 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. PubMed ID: 17953629
[TBL] [Abstract][Full Text] [Related]
29. A novel mutation of the MEN1 gene in a Chinese kindred with multiple endocrine neoplasia type 1.
Xu L; Li X; Feng B; Ni Y; Wang H; Wang L
Endocr J; 2010; 57(9):839-45. PubMed ID: 20710116
[TBL] [Abstract][Full Text] [Related]
30. Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1.
Hai N; Aoki N; Shimatsu A; Mori T; Kosugi S
Clin Endocrinol (Oxf); 2000 Apr; 52(4):509-18. PubMed ID: 10762295
[TBL] [Abstract][Full Text] [Related]
31. New splicing mutation of MEN1 gene affecting the translocation of menin to the nucleus.
Tala HP; Carvajal CA; González AA; Garrido JL; Tobar J; Solar A; Campino C; Arteaga E; Fardella CE
J Endocrinol Invest; 2006 Nov; 29(10):888-93. PubMed ID: 17185897
[TBL] [Abstract][Full Text] [Related]
32. Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree.
Kassem M; Kruse TA; Wong FK; Larsson C; Teh BT
J Clin Endocrinol Metab; 2000 Jan; 85(1):165-7. PubMed ID: 10634381
[TBL] [Abstract][Full Text] [Related]
33. Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism.
Carling T; Correa P; Hessman O; Hedberg J; Skogseid B; Lindberg D; Rastad J; Westin G; Akerström G
J Clin Endocrinol Metab; 1998 Aug; 83(8):2960-3. PubMed ID: 9709976
[TBL] [Abstract][Full Text] [Related]
34. GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.
Guan B; Welch JM; Sapp JC; Ling H; Li Y; Johnston JJ; Kebebew E; Biesecker LG; Simonds WF; Marx SJ; Agarwal SK
Am J Hum Genet; 2016 Nov; 99(5):1034-1044. PubMed ID: 27745835
[TBL] [Abstract][Full Text] [Related]
35. A novel missense mutation of the MEN1 gene in a multiple endocrine neoplasia type 1 patient associated with carcinoid syndrome.
Ukita C; Yamaguchi M; Tanaka T; Shigeta H; Nishikawa M
Intern Med; 2003 Nov; 42(11):1112-6. PubMed ID: 14686752
[TBL] [Abstract][Full Text] [Related]
36. Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1.
Shimizu S; Tsukada T; Futami H; Ui K; Kameya T; Kawanaka M; Uchiyama S; Aoki A; Yasuda H; Kawano S; Ito Y; Kanbe M; Obara T; Yamaguchi K
Jpn J Cancer Res; 1997 Nov; 88(11):1029-32. PubMed ID: 9439676
[TBL] [Abstract][Full Text] [Related]
37. Different phenotypes of multiple endocrine neoplasia type 1 (MEN1) in monozygotic twins found in a Japanese MEN1 family with MEN1 gene mutation.
Namihira H; Sato M; Miyauchi A; Ohye H; Matsubara S; Bhuiyan MM; Murao K; Ameno S; Ameno K; Ijiri I; Takahara J
Endocr J; 2000 Feb; 47(1):37-43. PubMed ID: 10811291
[TBL] [Abstract][Full Text] [Related]
38. Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.
Simonds WF; Robbins CM; Agarwal SK; Hendy GN; Carpten JD; Marx SJ
J Clin Endocrinol Metab; 2004 Jan; 89(1):96-102. PubMed ID: 14715834
[TBL] [Abstract][Full Text] [Related]
39. MEN1 c.825‑1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report.
Ning Z; Wang O; Meng X; Xing X; Xia W; Jiang Y; Li M; Xu Y
Mol Med Rep; 2015 Oct; 12(4):6152-6. PubMed ID: 26239674
[TBL] [Abstract][Full Text] [Related]
40. Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.
Scarpelli D; D'Aloiso L; Arturi F; Scillitani A; Presta I; Bisceglia M; Cristofaro C; Russo D; Filetti S
J Endocrinol Invest; 2004 Dec; 27(11):1015-21. PubMed ID: 15754732
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]