Absence of germ-line mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in familial pituitary adenoma in contrast to MEN1 in Japanese

Journal of Clinical Endocrinology and Metabolism

Volumn 83, Issue 3, 1998, Pages 960-965

  Tanaka, Chisato ^a   Yoshimoto, Katsuhiko ^a   Yamada, Shozo ^b   Nishioka, Hiroshi ^c   Ii, Setsuko ^a   Moritani, Maki ^a   Yamaoka, Takashi ^a   Itakura, Mitsuo ^a  

^a UNIVERSITY OF TOKUSHIMA   (Japan)

^b TORANOMON HOSPITAL   (Japan)

^c TOKYO MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GERM LINE; HETEROZYGOSITY LOSS; HUMAN; HYPOPHYSIS ADENOMA; JAPAN; MALE; MULTIPLE ENDOCRINE NEOPLASIA; PRIORITY JOURNAL;

ADENOMA; ADULT; AGED; CHROMOSOMES, HUMAN, PAIR 11; DNA; EXONS; FEMALE; GERM-LINE MUTATION; HUMANS; HYPERPARATHYROIDISM; INTRONS; JAPAN; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; PITUITARY NEOPLASMS; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0031760161     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.83.3.960     Document Type: Article

References (20)

1. Ballard HS, Frame B, Hartsock RJ. 1964 Familial multiple endocrine adenomapeptic ulcer complex. Medicine. 43:481-516.
2. Benlian P, Giraud S, Lahlou N, et al. 1995 Familial acromegaly: a specific clinical entity-further evidence from the genetic study of a three-generation family. Eur J Endocrinol. 133:451-456.
3. Yamada S, Yoshimoto K, Sano T, et al. 1997 Inactivation of the tumor suppressor gene on 11q13 in brothers with familial acrogigantism without multiple endocrine neoplasia type 1. J Clin Endocrinol Metab. 82:239-242.
4. Mallette LE. 1994 The functional and pathologic spectrum of parathyroid abnormalities in hyperparathyroidism. In: Bilezikian JP, Marcus R, Levine MA, eds. The parathyroids. New York: Raven Press; 423-455.
5. Szabò J, Heath B, Hill VM, et al. 1995 Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31. Am J Hum Genet. 56:944-950.
6. Wassif WS, Moniz CF, Friedman E, et al. 1993 Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer. J Clin Endocrinol Metab. 77:1485-1489.
7. Kassem M, Zhang X, Brask S, Eriksen EF, Mosekilde L, Kruse TA. 1994 Familial isolated primary hyperparathyroidism. Clin Endocrinol (Oxf). 41:415-420.
8. Larsson C, Skogseid B, Öberg K, Nakamura Y, Nordenskjöld M. 1988 Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature. 332:85-87.
9. Chandrasekharappa SC, Guru SC, Manickam P, et al. 1997 Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science. 276:404-407.
10. Agarwal SK, Kester MB, Debelenko LV, et al. 1997 Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Hum Mol Genet. 6:1169-1175.
11. Lemmens I, Van de Ven WJM, Kas K, et al. 1997 Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. Hum Mol Genet. 6:1177-1183.
12. Yoshimoto K, Endo H, Tsuyuguchi M, et al. Familial isolated primary hyperparathyroidism with parathyroid carcinomas: clinical and molecular features. Clin Endocrinol (Oxf). In press.
13. Kip1 gene and trisomy 12 in a subset of human pituitary adenomas. J Clin Endocrinol Metab. 82:3141-3147.
14. Shintani Y, Yoshimoto K, Hone H, et al. 1995 Two different pituitary adenomas in a patient with multiple endocrine neoplasia type 1 associated with growth hormone-releasing hormone-producing pancreatic tumor: clinical and genetic features. Endocrinol J. 42:331-340.
15. Yoshimoto K, Iwahana H, Kubo K, Saito S, Itakura M. 1991 Allele loss on chromosome 11 in a pituitary tumor from a patient with multiple endocrine neoplasia type 1. Jpn J Cancer Res. 82:886-889.
16. Sarui H, Yoshimoto K, Okumura S, et al. 1997 Cystic glucagonoma with loss of heterozygosity on chromosome 11 in multiple endocrine neoplasia type 1. Clin Endocrinol (Oxf). 46:511-516.
17. Dib C, Fauré S, Fizames C, et al. 1996 A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature. 380:152-154.
18. Gyapay G, Morissette J, Vignal A, et al. 1994 The 1993-94 Généthon human genetic linkage map. Nat Genet. 7:246-339.
19. Iwasaki H, Stewart PW, Dilley WG, et al. 1992 A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95. Genomics. 13:7-15.
20. Xue F, Yu H, Maurer LH, et al. 1994 Germline RET mutations in MEN 2A and FMTC and their detection by simple DNA diagnostic tests. Hum Mol Genet. 3:635-638.