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1 - 10 of 20 results found for MEN1.

  1. Active Surveillance versus Surgery of Nonfunctioning Pancreatic Neuroendocrine Neoplasms

    http://iris.ucl.ac.uk/iris/publication/1528957/3

  2. Genetic background influences embryonic lethality and the occurrence of neural tube...

    http://iris.ucl.ac.uk/iris/publication/1802069/3

  3. A whole MEN1 gene deletion flanked by Alu repeats in a family with multiple endocrine...

    Multiple endocrine neoplasia type 1 is an autosomal dominant cancer syndrome characterized by pituitary, parathyroid and enteropancreatic endocrine tumors, which is caused by germline mutations of the tumor suppressor gene MEN1. In the case reported

    http://iris.ucl.ac.uk/iris/publication/383374/2

  4. Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).

    The multiple endocrine neoplasia type 1 (MEN1) locus has been previously localised to 11q13 by combined tumour deletion mapping and linkage studies and a 3.8-cM region flanked by PYGM and D11S97 has been defined. The zinc finger in the MEN1 locus

    http://iris.ucl.ac.uk/iris/publication/975758/2

  5. MEN1 gene replacement therapy reduces proliferation rates in a mouse model of pituitary...

    Multiple endocrine neoplasia type 1 (MEN1) is characterized by the combined occurrence of pituitary, pancreatic, and parathyroid tumors showing loss of heterozygosity in the putative tumor suppressor gene MEN1. This gene encodes the protein menin,

    http://iris.ucl.ac.uk/iris/publication/882451/7

  6. MiR-15a/miR-16-1 expression inversely correlates with cyclin D1 levels in Men1 pituitary...

    Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by the combined occurrence of parathyroid, pituitary and pancreatic islet tumours, and is due to mutations of the MEN1 gene, which encodes the tumour

    http://iris.ucl.ac.uk/iris/publication/1802063/1

  7. A 500-kb sequence-ready cosmid contig and transcript map of the MEN1 region on 11q13

    We have generated a transcript map of an approximately 1.2-Mb region from human chromosome band 11q13 between the loci VEGFB and CAPN1, which flank the multiple endocrine neoplasia type 1 (MEN 1) locus. In total, we isolated 144 cosmids from this

    http://iris.ucl.ac.uk/iris/publication/1744437/7

  8. Correlation of mutant menin stability with clinical expression of multiple endocrine...

    Germline mutations of the tumor suppressor gene MEN1 are found not only in typical multiple endocrine neoplasia type 1 (MEN1) but also in its incomplete forms such as familial isolated hyperparathyroidism (FIHP) and apparently sporadic parathyroid

    http://iris.ucl.ac.uk/iris/publication/383418/2

  9. Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and...

    Forty loci (16 polymorphic and 24 non-polymorphic) together with 23 cosmids isolated from a chromosome 11-specific library were used to construct a detailed genetic map of 11p13-11q13. The map was constructed by using a panel of 13 somatic cell

    http://iris.ucl.ac.uk/iris/publication/975761/2

  10. Characterization of mutations in patients with multiple endocrine neoplasia type 1.

    Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by tumors of the parathyroids, pancreatic islets, and anterior pituitary. The MEN1 gene, on chromosome 11q13, has recently been cloned, and mutations have

    http://iris.ucl.ac.uk/iris/publication/975755/2

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