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    CAB39L calcium binding protein 39 like [ Homo sapiens (human) ]

    Gene ID: 81617, updated on 3-Nov-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    Loss of LPAR6 and CAB39L dysregulates the basal-to-luminal urothelial differentiation program, contributing to bladder carcinogenesis.

    Loss of LPAR6 and CAB39L dysregulates the basal-to-luminal urothelial differentiation program, contributing to bladder carcinogenesis.
    Lee S, Bondaruk J, Wang Y, Chen H, Lee JG, Majewski T, Mullen RD, Cogdell D, Chen J, Wang Z, Yao H, Kus P, Jeong J, Lee I, Choi W, Navai N, Guo C, Dinney C, Baggerly K, Mendelsohn C, McConkey D, Behringer RR, Kimmel M, Wei P, Czerniak B., Free PMC Article

    06/14/2024
    Bioinformatics Prediction and Experimental Verification Identify CAB39L as a Diagnostic and Prognostic Biomarker of Kidney Renal Clear Cell Carcinoma.

    Bioinformatics Prediction and Experimental Verification Identify CAB39L as a Diagnostic and Prognostic Biomarker of Kidney Renal Clear Cell Carcinoma.
    Wu Y, Xu Z, Chen X, Fu G, Tian J, Shi Y, Sun J, Jin B., Free PMC Article

    05/3/2023
    Identification of HLA-A*0201-restricted CTL Epitopes for MLAA-34-specific Immunotherapy for Acute Monocytic Leukemia.

    Identification of HLA-A*0201-restricted CTL Epitopes for MLAA-34-specific Immunotherapy for Acute Monocytic Leukemia.
    Bai J, Wang J, Yang Y, Wang F, He A, Zhang W.

    01/22/2022
    Targeted silencing of genes related to acute monocytic leukaemia by CpG(B)-MLAA-34 siRNA conjugates.

    Targeted silencing of genes related to acute monocytic leukaemia by CpG(B)-MLAA-34 siRNA conjugates.
    Huang B, He A, Zhang P, Ma X, Yang Y, Wang J, Wang J, Zhang W.

    08/21/2021
    minimal active region of MLAA-34 located between 402 bp and 200 bp

    [Cloning of New Antigen Gene MLAA-34 Promoter and Identification of Core Region in Acute Monocytic Leukemia].
    Lei B, Zhang WG, He AL, Chen YX, Cao XM, Zhao WH, Wang JL, Liu J, Ma XR, Zhang PY, Bai J.

    07/13/2019
    Our data demonstrate that CAB39L is a novel tumor suppressor in gastric cancer

    CAB39L elicited an anti-Warburg effect via a LKB1-AMPK-PGC1α axis to inhibit gastric tumorigenesis.
    Li W, Wong CC, Zhang X, Kang W, Nakatsu G, Zhao Q, Chen H, Go MYY, Chiu PWY, Wang X, Ji J, Li X, Cai Z, Ng EKW, Yu J., Free PMC Article

    03/2/2019
    Frameshift Mutations of CAB39L are associated with Gastric and Colorectal Cancers.

    Frameshift Mutations of CAB39L, an Activator of LKB1 Tumor Suppressor, in Gastric and Colorectal Cancers.
    Choi MR, An CH, Yoo NJ, Lee SH.

    10/22/2016
    In conclusion, our current results provide new evidence that MLAA-34 may be a novel anti-apoptotic factor in vitro, and the data presented here show a strong correlation between anti-apoptosis with the upregulation of MLAA-34.

    The expression and functional characterization associated with cell apoptosis and proteomic analysis of the novel gene MLAA-34 in U937 cells.
    Zhang WJ, Zhang WG, Zhang PY, Cao XM, He AL, Chen YX, Gu LF.

    06/15/2013
    our data indicate that MLAA-34 may be used as a prognostic marker for treatment decision-making in acute monocytic leukemia

    Quantitative assessment of MLAA-34 expression in diagnosis and prognosis of acute monocytic leukemia.
    Zhao J, He A, Zhang W, Meng X, Gu L., Free PMC Article

    05/21/2011
    Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)

    Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
    Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR., Free PMC Article

    06/30/2010
    It was proposed that a splice variant MLAA-34 of CAB39L associated with acute monocytic leukemia. MLAA-34 was identified and characterized. Identification and functional characterization of the novel acute monocytic leukemia associated antigen MLAA-34

    Identification and functional characterization of the novel acute monocytic leukemia associated antigen MLAA-34.
    Zhang PY, Zhang WG, He AL, Wang JL, Li WB., Free PMC Article

    01/21/2010
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