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BAALC was identified by gene expression studies in patients with acute myeloid leukemia (AML). 再加上，我们可以发BAALC 蛋白 (8) 和 BAALC 试剂盒 (4)和数多这个蛋白质的别的产品。
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Human Polyclonal BAALC Primary Antibody for EIA, WB - ABIN452776
Kuila, Sahoo, Kumari, Biswas, Patnaik, Pattnayak, Biswas, Chakraborty: EVI1, BAALC and AME: prevalence of the secondary mutations in chronic and accelerated phases of chronic myeloid leukemia patients from eastern India. in Leukemia research 2009
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Human Polyclonal BAALC Primary Antibody for ELISA, WB - ABIN250807
Satoskar, Tanner, Weinstein, Qualman, de la Chapelle: Baalc, a marker of mesoderm and muscle. in Gene expression patterns : GEP 2005
Human Monoclonal BAALC Primary Antibody for ELISA, WB - ABIN529108
Ikeda, Ageta, Tsuchida, Yamada: iTRAQ-based proteomics reveals novel biomarkers of osteoarthritis. in Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2013
BAALC expression-based minimal residual disease detection during therapy may be considered a strategy to identify patients at high risk of relapse.
Study provide evidence for an association of rs62527607 [GT] SNP of BAALC gene with multidrug resistance in childhood ALL.
BAALC and ERG (显示 ERG 抗体) genes are specific significant molecular markers in acute myeloid leukemia (显示 BCL11A 抗体) disease progression, response to treatment and survival.
demonstrated that BAALC blocks ERK (显示 EPHB2 抗体)-mediated monocytic differentiation of acute myeloid leukemia (显示 BCL11A 抗体) cells by trapping Kruppel-like factor 4 (KLF4 (显示 KLF4 抗体)) in the cytoplasm and inhibiting its function in the nucleus
combined determination of both miR (显示 MLXIP 抗体)-3151 and BAALC improved this prognostic stratification, with patients with low levels of both parameters showing a better outcome compared with those patients harboring increased levels of one or both markers
study indicates that overexpression of BAALC serves as an independent prognostic biomarker in acute myeloid leukemia (显示 BCL11A 抗体)
Evaluating WT1 (显示 WT1 抗体) and BAALC gene expression at diagnosis may improve standard risk stratification and possibly refine the therapeutic approach for Myelodysplastic Syndromes patients.
Thus low MDR1 (显示 TBC1D9 抗体)/low BAALC expression identifies a subgroup of intermediate cytogenetic risk AML (显示 RUNX1 抗体) patients with a remarkably good long-term outcome achieved by chemotherapy alone.
miR (显示 MLXIP 抗体)-3151 introns within BAALC have roles in driving leukemogenesis by deregulating the TP53 (显示 TP53 抗体) pathway
Higher BAALC expression and FLT3 (显示 FLT3 抗体)-ITD mutation, both individually and in combination, were associated with worse survival outcomes in CN-AML (显示 RUNX1 抗体), and this was also applicable in NPM1 (显示 NPM1 抗体)-mutated CN-AML (显示 RUNX1 抗体), known as a favorable-risk group.
BAALC/Baalc is a marker of the mesodermal lineage, especially muscle.
This gene was identified by gene expression studies in patients with acute myeloid leukemia (AML). The gene is conserved among mammals and is not found in lower organisms. Tissues that express this gene develop from the neuroectoderm. Multiple alternatively spliced transcript variants that encode different proteins have been described for this gene\; however, some of the transcript variants are found only in AML cell lines.
brain and acute leukemia cytoplasmic protein
, brain and acute leukemia, cytoplasmic