| scholarly article | Q13442814 |
| P2093 | author name string | K Yamaguchi | |
| M Kishi | |||
| T Tsukada | |||
| Y Ito | |||
| S Shimizu | |||
| M Kanbe | |||
| T Obara | |||
| H Futami | |||
| P2860 | cites work | Isolation and characterization of human TR3 receptor: a member of steroid receptor superfamily | Q24338717 |
| 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 gene inducible by serum growth factors encodes a member of the steroid and thyroid hormone receptor superfamily | Q33669766 | ||
| Founding mutations and Alu-mediated recombination in hereditary colon cancer | Q34297390 | ||
| An improved method of competitive PCR for quantitation of gene copy number | Q35860321 | ||
| Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci | Q44872297 | ||
| A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13. | Q48048567 | ||
| 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 | ||
| Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1. | Q55099861 | ||
| Determination of Gene Dosage by a Quantitative Adaptation of the Polymerase Chain Reaction (gd-PCR): Rapid Detection of Deletions and Duplications of Gene Sequences | Q57162217 | ||
| A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locus | Q57266953 | ||
| Clinical studies of multiple endocrine neoplasia type 1 (MEN1) | Q71777163 | ||
| Multiple endocrine neoplasia type 1 | Q72143709 | ||
| Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states | Q73494435 | ||
| A 3-Mb sequence-ready contig map encompassing the multiple disease gene cluster on chromosome 11q13.1-q13.3. | Q73957286 | ||
| Multiple endocrine neoplasia type 1 presented with manic-depressive disorder: a case report with an identified MEN1 gene mutation | Q74073443 | ||
| P433 | issue | 1 | |
| P921 | main subject | multiple endocrine neoplasia | Q1553018 |
| P1104 | number of pages | 5 | |
| P304 | page(s) | 1-5 | |
| P577 | publication date | 1998-01-01 | |
| P1433 | published in | Japanese Journal of Cancer Research | Q26842384 |
| P1476 | title | A large germline deletion of the MEN1 gene in a family with multiple endocrine neoplasia type 1. | |
| P478 | volume | 89 |
| Q78054901 | A novel splicing mutation (894-9 G --> A) of the MEN1 gene responsible for multiple endocrine neoplasia type 1 |
| Q73035230 | Analysis of the MEN1 gene in sporadic pituitary adenomas from Japanese patients |
| Q40912570 | Characterization of the MEN1 gene product, menin, by site-specific polyclonal antibodies |
| Q47914008 | Clinical and genetic features of patients with multiple endocrine tumors who have neither family history nor MEN1 germline mutations |
| Q53914105 | Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1. |
| Q37245547 | Copy number variations and cancer |
| Q37642520 | Copy number variations and cancer susceptibility |
| Q37517700 | DNA-based test: when and why to apply it to primary hyperparathyroidism clinical phenotypes |
| Q62579276 | Deletion of exons 1–3 of the MEN1 gene in a large Italian family causes the loss of menin expression |
| Q51788318 | 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. |
| Q33983834 | Gene diagnosis and clinical management of multiple endocrine neoplasia type 1 (MEN1). |
| Q34386474 | Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders |
| Q53312970 | Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein. |
| Q36622013 | Identification of MEN1 gene mutations in families with MEN 1 and related disorders |
| Q37345051 | MEN1 gene and its mutations: basic and clinical implications |
| Q73083013 | Multiple endocrine neoplasia type 1 |
| Q37630910 | Multiple endocrine neoplasia type 1 (MEN1): not only inherited endocrine tumors |
| Q42695925 | Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features. |
| Q74181220 | Novel deletional mutation of the MEN 1 gene in a kindred with multiple endocrine neoplasia type 1 |
| Q28210134 | The MEN1 gene and associated diseases: an update |
| Q50651420 | Type 1 multiple endocrine neoplasia (MEN1): contribution of genetic analysis to the screening and follow-up of a large French kindred. |
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