| P2093 | author name string | Toshihiko Tsukada | |
| | Junko Naito | |
| | Kazuo Chihara | |
| | Hideaki Sowa | |
| | Sohei Kitazawa | |
| | Geoffrey N Hendy | |
| | Hiroshi Kaji | |
| | Toshitsugu Sugimoto | |
| | Riko Kitazawa | |
| P2860 | cites work | Clinical and genetic features of patients with multiple endocrine tumors who have neither family history nor MEN1 germline mutations | Q47914008 |
| | Menin inactivation leads to loss of transforming growth factor beta inhibition of parathyroid cell proliferation and parathyroid hormone secretion | Q47937066 |
| | Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma | Q48100816 |
| | Somatic mutation of the MEN1 gene in parathyroid tumours. | Q50623754 |
| | Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1. | Q53914105 |
| | Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory. | Q54680442 |
| | A large germline deletion of the MEN1 gene in a family with multiple endocrine neoplasia type 1. | Q54960820 |
| | Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1. | Q55099861 |
| | Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing | Q62000559 |
| | Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN1 patients | Q71767618 |
| | Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states | Q73494435 |
| | Heterozygous Men1 mutant mice develop a range of endocrine tumors mimicking multiple endocrine neoplasia type 1 | Q73557853 |
| | Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1) | Q74129471 |
| | Somatic mutations in MEN type 1 tumors, consistent with the Knudson "two-hit" hypothesis | Q74494218 |
| | Alterations of the MEN1 gene in sporadic parathyroid tumors | Q77114024 |
| | Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism | Q77114226 |
| | Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type beta signaling | Q24290996 |
| | Characterization of mutations in patients with multiple endocrine neoplasia type 1. | Q24538768 |
| | Role of transforming growth factor-beta signaling in cancer | Q28145449 |
| | Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1 | Q28243243 |
| | Positional cloning of the gene for multiple endocrine neoplasia-type 1 | Q28307577 |
| | A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors | Q28592210 |
| | In situ analysis of human menin in normal and neoplastic pancreatic tissues: evidence for differential expression in exocrine and endocrine cells | Q30976047 |
| | Guidelines for diagnosis and therapy of MEN type 1 and type 2. | Q34104591 |
| | TGFbeta signaling and cancer | Q34174327 |
| | Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11. | Q35248378 |
| | Mutational and gross deletion study of the MEN1 gene and correlation with clinical features in Spanish patients | Q35442479 |
| | A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing | Q35446790 |
| | Of mice and MEN1: Insulinomas in a conditional mouse knockout | Q35660901 |
| | Hereditary cancer: two hits revisited | Q40970549 |
| | Multiple endocrine neoplasia type 1 with unusual concomitance of various neoplastic disorders | Q44788859 |
| | Comparison of different parathyroid hormone radioimmunoassays in uremic patients with secondary hyperparathyroidism | Q44851899 |
| | Primary hyperparathyroidism associatiated with aldosterone-producing adrenocortical adenoma and breast cancer: relation to MEN1 gene | Q44914823 |
| | Expression of menin in parathyroid tumors | Q46798444 |
| | Differential expression of menin in sporadic pituitary adenomas | Q47429582 |
| P433 | issue | 3 | |
| P921 | main subject | heterozygosity | Q124059385 |
| | multiple endocrine neoplasia | Q1553018 |
| | multiple endocrine neoplasia type 1 | Q3347154 |
| P304 | page(s) | 485-490 | |
| P577 | publication date | 2006-06-01 | |
| P1433 | published in | Endocrine | Q15757048 |
| P1476 | title | Expression and functional analysis of menin in a multiple endocrine neoplasia type 1 (MEN1) patient with somatic loss of heterozygosity in chromosome 11q13 and unidentified germline mutation of the MEN1 gene. | |
| P478 | volume | 29 | |