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Meningioma 1 (MN1) contains two sets of CAG repeats. Additionally we are shipping MN1 Antibodies (34) and and many more products for this protein.
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MN1 gene expression in acute myeloid leukemia (show BCL11A Proteins).
MN1 deletion is associated with Craniofacial Abnormalities.
Chromosome 22q12.1 microdeletions involving the MN1 gene confirm it as a candidate gene for cleft palate.
MLL1 and DOT1L (show DOT1L Proteins) cooperate with meningioma-1 to induce acute myeloid leukemia (show BCL11A Proteins).
genotype-phenotype correlation among our patients and those previously reported with overlapping 22q12 deletions, we identified a 560 kb critical region containing the MN1 gene that is implicated in human cleft palate formation
these results suggest that deregulated MN1 expression contributes to the pathogenesis of pediatric B-ALL.
identified potential driver mutations in NF2 (neurofibromatosis type 2) and MN1 (meningioma 1).
cotransduction of an activated HOX (show MSH2 Proteins) gene (NUP98HOXD13) with MN1 induces a serially transplantable acute myeloid leukemia (show BCL11A Proteins) (AML (show RUNX1 Proteins)).
MN1 overexpression independently predicts bad clinical outcome in CN-AML (show RUNX1 Proteins) patients
High MN1 expression confers worse prognosis in Chinese adult patients with de novo acute myeloid leukemia (show BCL11A Proteins).
Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4\\;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis.
meningioma (translocation balanced)
, meningioma chromosome region 1
, probable tumor suppressor protein MN1