| scholarly article | Q13442814 |
| P2093 | author name string | S C Guru | |
| J S Crabtree | |||
| L V Debelenko | |||
| P Manickam | |||
| S E Olufemi | |||
| S K Agarwal | |||
| P2860 | cites work | Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector | Q24563904 |
| A transcript map for the 2.8-Mb region containing the multiple endocrine neoplasia type 1 locus | Q24628248 | ||
| 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 | ||
| Definition of the MinimalMEN1Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13 | Q29303492 | ||
| Preparation and screening of an arrayed human genomic library generated with the P1 cloning system | Q35126048 | ||
| A new bacteriophage P1-derived vector for the propagation of large human DNA fragments | Q36745476 | ||
| Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland | Q48038625 | ||
| Eighteen new polymorphic markers in the multiple endocrine neoplasia type 1 (MEN1) region | Q48041395 | ||
| Characterization of a human homolog (OVOL1) of the Drosophila ovo gene, which maps to chromosome 11q13. | Q48042143 | ||
| 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 | ||
| Molecular tools for presymptomatic testing in multiple endocrine neoplasia type 1 | Q57423384 | ||
| P433 | issue | 6 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | multiple endocrine neoplasia | Q1553018 |
| multiple endocrine neoplasia type 1 | Q3347154 | ||
| P304 | page(s) | 433-9 | |
| P577 | publication date | 1998-06-01 | |
| P1433 | published in | Journal of Internal Medicine | Q6295387 |
| P1476 | title | Identification and characterization of the multiple endocrine neoplasia type 1 (MEN1) gene | |
| P478 | volume | 243 |
| Q33747848 | An oncogenic role for the multiple endocrine neoplasia type 1 gene in prostate cancer. |
| Q42757996 | Genetic and epigenetic analysis in korean patients with multiple endocrine neoplasia type 1. |
| Q35908958 | Genetic screening methods for the detection of mutations responsible for multiple endocrine neoplasia type 1. |
| Q42271393 | Germline and somatic genetic changes in multicentric tumors obtained from a patient with multiple endocrine neoplasia type 1. |
| Q36400951 | Insulinoma: pathophysiology, localization and management |
| Q48207494 | Menin Controls the Memory Th2 Cell Function by Maintaining the Epigenetic Integrity of Th2 Cells. |
| Q57600501 | Multiple Endocrine Neoplasia Type-I-like Syndrome in Two Cats |
| Q28266645 | Novel MEN 1 gene findings in rare sporadic insulinoma--a case control study |
| Q35098325 | Parathyroid tumor development involves deregulation of homeobox genes |
| Q36909002 | Pituitary adenomas in childhood: development and diagnosis |
| Q37429020 | Recapitulation of pancreatic neuroendocrine tumors in human multiple endocrine neoplasia type I syndrome via Pdx1-directed inactivation of Men1. |
| Q28510023 | STAT6-mediated displacement of polycomb by trithorax complex establishes long-term maintenance of GATA3 expression in T helper type 2 cells |
| Q38162595 | Stemness of T cells and the hematopoietic stem cells: fate, memory, niche, cytokines |
| Q35131420 | The diffuse endocrine system: from embryogenesis to carcinogenesis. |
| Q38274982 | The role of genetic and epigenetic changes in pituitary tumorigenesis |
| Q34144612 | Trithorax complex component Menin controls differentiation and maintenance of T helper 17 cells. |
| Q49480395 | Two nonsense somatic mutations in MEN1 identified in sporadic insulinomas |
| Q44943256 | Unusual presentation of multiple endocrine neoplasia type 1 in a young woman with a novel mutation of the MEN1 gene |
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