Pages that link to "Q42602297"
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The following pages link to Isolation, genomic organization, and expression analysis of Men1, the murine homolog of the MEN1 gene. (Q42602297):
Displaying 27 items.
- A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors (Q28592210) (← links)
- Menin interacts with IQGAP1 to enhance intercellular adhesion of beta-cells (Q30438923) (← links)
- Characterization of a MEN1 ortholog from Drosophila melanogaster (Q32062751) (← links)
- Mouse models of human familial cancer syndromes (Q33204054) (← links)
- Comparison of nonsense-mediated mRNA decay efficiency in various murine tissues (Q33390501) (← links)
- The menin tumor suppressor protein is phosphorylated in response to DNA damage (Q33802663) (← links)
- Sporadic endocrine tumours and their relationship to the hereditary endocrine neoplasia syndromes (Q33940347) (← links)
- Menin: a tumor suppressor that mediates postsynaptic receptor expression and synaptogenesis between central neurons of Lymnaea stagnalis. (Q34408718) (← links)
- Of mice and MEN1: Insulinomas in a conditional mouse knockout (Q35660901) (← links)
- Molecular alterations in sporadic primary hyperparathyroidism (Q35910367) (← links)
- Menin induces endodermal differentiation in aggregated P19 stem cells by modulating the retinoic acid receptors (Q36143068) (← links)
- Multiple endocrine neoplasia type 1 (MEN1) as a cancer predisposition syndrome: clues into the mechanisms of MEN1-related carcinogenesis (Q36973287) (← links)
- Recapitulation of pancreatic neuroendocrine tumors in human multiple endocrine neoplasia type I syndrome via Pdx1-directed inactivation of Men1. (Q37429020) (← links)
- Menin: a scaffold protein that controls gene expression and cell signaling (Q38121288) (← links)
- Tumor suppressor menin is required for subunit-specific nAChR α5 transcription and nAChR-dependent presynaptic facilitation in cultured mouse hippocampal neurons. (Q38790846) (← links)
- Expression and subcellular localization of menin in human cancer cells (Q42324428) (← links)
- Functional studies of the MEN1 gene (Q48245733) (← links)
- Expression of developing neural transcription factors in lung carcinoid tumors (Q51119058) (← links)
- Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice. (Q52543976) (← links)
- Genetic ablation of the tumor suppressor menin causes lethality at mid-gestation with defects in multiple organs. (Q52550786) (← links)
- Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein. (Q53312970) (← links)
- Multiple Endocrine Neoplasia Syndromes from Genetic and Epigenetic Perspectives. (Q55712143) (← links)
- Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type 1 gene, in cell lines and human tissues (Q73527291) (← links)
- Proliferation-associated expression of the MEN1 gene as revealed by in situ hybridization: possible role of the menin as a negative regulator of cell proliferation under DNA damage (Q73952692) (← links)
- Multiple endocrine neoplasia type 1 (Q77164497) (← links)
- Multiple endocrine neoplasia type 1 (Q79172144) (← links)
- Neuron-Specific Menin Deletion Leads to Synaptic Dysfunction and Cognitive Impairment by Modulating p35 Expression (Q90316651) (← links)