Pages that link to "Q22254660"

The following pages link to The human GRAF gene is fused to MLL in a unique t(5;11)(q31;q23) and both alleles are disrupted in three cases of myelodysplastic syndrome/acute myeloid leukemia with a deletion 5q (Q22254660):

Displaying 50 items.

• Rho GTPase activating protein 26 (Q21105473) ‎ (← links)
• A new Purkinje cell antibody (anti-Ca) associated with subacute cerebellar ataxia: immunological characterization (Q21245233) ‎ (← links)
• DLC-1 operates as a tumor suppressor gene in human non-small cell lung carcinomas (Q23910292) ‎ (← links)
• The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia (Q24291407) ‎ (← links)
• DLC-1 gene inhibits human breast cancer cell growth and in vivo tumorigenicity (Q24293186) ‎ (← links)
• A BAR domain-mediated autoinhibitory mechanism for RhoGAPs of the GRAF family (Q24309329) ‎ (← links)
• Integrin engagement-induced inhibition of human myelopoiesis is mediated by proline-rich tyrosine kinase 2 gene products (Q24322005) ‎ (← links)
• Rho GTPases in hematopoiesis and hemopathies (Q24652636) ‎ (← links)
• 'Medusa head ataxia': the expanding spectrum of Purkinje cell antibodies in autoimmune cerebellar ataxia. Part 2: Anti-PKC-gamma, anti-GluR-delta2, anti-Ca/ARHGAP26 and anti-VGCC (Q26786113) ‎ (← links)
• Structure of the BH domain from graf and its implications for Rho GTPase recognition (Q27626985) ‎ (← links)
• Leukemia-associated Rho guanine nucleotide exchange factor, a Dbl family protein found mutated in leukemia, causes transformation by activation of RhoA (Q28190494) ‎ (← links)
• Human RhoGAP domain-containing proteins: structure, function and evolutionary relationships (Q28203687) ‎ (← links)
• Identification and characterization of a gene encoding a putative mouse Rho GTPase activating protein gene 8, Arhgap8 (Q28206274) ‎ (← links)
• RAS diseases in children (Q28252058) ‎ (← links)
• DLC1: a significant GAP in the cancer genome (Q28390592) ‎ (← links)
• MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23). (Q30163820) ‎ (← links)
• GRAF1a is a brain-specific protein that promotes lipid droplet clustering and growth, and is enriched at lipid droplet junctions (Q30425958) ‎ (← links)
• Decreased expression of GRAF1/OPHN-1-L in the X-linked alpha thalassemia mental retardation syndrome. (Q33625532) ‎ (← links)
• BAR the door: cancer suppression by amphiphysin-like genes (Q33870256) ‎ (← links)
• Evolutionary conservation of zebrafish linkage group 14 with frequently deleted regions of human chromosome 5 in myeloid malignancies (Q34028179) ‎ (← links)
• GTPase regulator associated with the focal adhesion kinase (GRAF) transcript was down-regulated in patients with myeloid malignancies (Q34081636) ‎ (← links)
• MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisom (Q34136814) ‎ (← links)
• Activation-induced cytidine deaminase accelerates clonal evolution in BCR-ABL1-driven B-cell lineage acute lymphoblastic leukemia (Q34168766) ‎ (← links)
• Identification of a novel RAS GTPase-activating protein (RASGAP) gene at 9q34 as an MLL fusion partner in a patient with de novo acute myeloid leukemia (Q34300390) ‎ (← links)
• Translocation t(X;11)(q13;q23) in B-cell chronic lymphocytic leukemia disrupts two novel genes (Q34367685) ‎ (← links)
• Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins (Q34405465) ‎ (← links)
• The human orthologue of CdGAP is a phosphoprotein and a GTPase-activating protein for Cdc42 and Rac1 but not RhoA. (Q34499924) ‎ (← links)
• Molecular pathogenesis of MDS. (Q34996338) ‎ (← links)
• Important features of myelodysplastic syndrome (Q34996344) ‎ (← links)
• Chromosomal bands affected by acute oil exposure and DNA repair errors (Q35058557) ‎ (← links)
• ArhGAP9, a novel MAP kinase docking protein, inhibits Erk and p38 activation through WW domain binding (Q35651832) ‎ (← links)
• GRAF1 deficiency blunts sarcolemmal injury repair and exacerbates cardiac and skeletal muscle pathology in dystrophin-deficient mice (Q35753474) ‎ (← links)
• The biological and clinical significance of MLL abnormalities in haematological malignancies (Q35854955) ‎ (← links)
• Molecular classification and pathogenesis of eosinophilic disorders: 2005 update (Q36182741) ‎ (← links)
• Stable RNA markers for identification of blood and saliva stains revealed from whole genome expression analysis of time-wise degraded samples (Q36428637) ‎ (← links)
• Prospective tracing of MLL-FRYL clone with low MEIS1 expression from emergence during neuroblastoma treatment to diagnosis of myelodysplastic syndrome (Q36508959) ‎ (← links)
• Current knowledge of the large RhoGAP family of proteins (Q36707513) ‎ (← links)
• Focal adhesion kinase and p53 signaling in cancer cells (Q36921742) ‎ (← links)
• Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion (Q37260976) ‎ (← links)
• Dual FGF-2 and intergrin alpha5beta1 signaling mediate GRAF-induced RhoA inactivation in a model of breast cancer dormancy (Q37456497) ‎ (← links)
• p200 RhoGAP promotes cell proliferation by mediating cross-talk between Ras and Rho signaling pathways (Q38507110) ‎ (← links)
• Involvement of Rho GAP GRAF1 in maintenance of epithelial phenotype (Q38748555) ‎ (← links)
• A novel infant acute lymphoblastic leukemia cell line with MLL-AF5q31 fusion transcript (Q40625217) ‎ (← links)
• Characterisation of the GRAF gene promoter and its methylation in patients with acute myeloid leukaemia and myelodysplastic syndrome (Q42123629) ‎ (← links)
• Activation of clg, a novel dbl family guanine nucleotide exchange factor gene, by proviral insertion at evi24, a common integration site in B cell and myeloid leukemias (Q42818782) ‎ (← links)
• Use of MLL/GRAF fusion mRNA for measurement of minimal residual disease during chemotherapy in an infant with acute monoblastic leukemia (AML-M5). (Q46456154) ‎ (← links)
• Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures (Q46630788) ‎ (← links)
• Graf regulates hematopoiesis through GEEC endocytosis of EGFR. (Q47586127) ‎ (← links)
• Trisomy 21 with t(5; 11) chromosomal translocation as new unfavorable cytogenetic abnormalities in pediatric acute myeloid leukemia type M2: One case report of nine-year follow-up and literature review (Q50067507) ‎ (← links)
• SEPT2 is a new fusion partner of MLL in acute myeloid leukemia with t(2;11)(q37;q23). (Q54602756) ‎ (← links)