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    MAGED2 MAGE family member D2 [ Homo sapiens (human) ]

    Gene ID: 10916, updated on 3-Nov-2024

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    Proteomic Analysis Revealed the Potential Role of MAGE-D2 in the Therapeutic Targeting of Triple-Negative Breast Cancer.

    Proteomic Analysis Revealed the Potential Role of MAGE-D2 in the Therapeutic Targeting of Triple-Negative Breast Cancer.
    Shi X, Liu C, Zheng W, Cao X, Li W, Zhang D, Zhu J, Zhang X, Chen Y., Free PMC Article

    02/1/2024
    Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome.

    Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome.
    Yan X, Hu Y, Zhang X, Gao X, Zhao Y, Peng H, Ouyang L, Zhang C., Free PMC Article

    01/31/2024
    MAGED2 Depletion Promotes Stress-Induced Autophagy by Impairing the cAMP/PKA Pathway.

    MAGED2 Depletion Promotes Stress-Induced Autophagy by Impairing the cAMP/PKA Pathway.
    Nasrah S, Radi A, Daberkow JK, Hummler H, Weber S, Seaayfan E, Kömhoff M., Free PMC Article

    09/19/2023
    Reciprocal Regulation of MAGED2 and HIF-1alpha Augments Their Expression under Hypoxia: Role of cAMP and PKA Type II.

    Reciprocal Regulation of MAGED2 and HIF-1α Augments Their Expression under Hypoxia: Role of cAMP and PKA Type II.
    Seaayfan E, Nasrah S, Quell L, Radi A, Kleim M, Schermuly RT, Weber S, Laghmani K, Kömhoff M., Free PMC Article

    11/29/2022
    MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells.

    MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells.
    Reusch B, Bartram MP, Dafinger C, Palacio-Escat N, Wenzel A, Fenton RA, Saez-Rodriguez J, Schermer B, Benzing T, Altmüller J, Beck BB, Rinschen MM.

    03/5/2022
    MAGED2 mutations explained 9% of cases of antenatal Bartter syndrome in a French cohort, and accounted for 38% of patients without other characterized mutations and for 44% of male probands of negative cases.

    Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.
    Legrand A, Treard C, Roncelin I, Dreux S, Bertholet-Thomas A, Broux F, Bruno D, Decramer S, Deschenes G, Djeddi D, Guigonis V, Jay N, Khalifeh T, Llanas B, Morin D, Morin G, Nobili F, Pietrement C, Ryckewaert A, Salomon R, Vrillon I, Blanchard A, Vargas-Poussou R., Free PMC Article

    09/21/2019
    MAGED2 loss of function is the cause of an X-linked transient form of antenatal Bartter's syndrome. Moreover, our findings showed that MAGE-D2 promotes the biogenesis of kidney membrane transporters.

    MAGED2: a novel form of antenatal Bartter's syndrome.
    Kömhoff M, Laghmani K.

    02/2/2019
    Increased expression of MAGE-D2 mRNA was associated with distant metastasis in Gastric Cancer.

    The Expression of Melanoma-Associated Antigen D2 Both in Surgically Resected and Serum Samples Serves as Clinically Relevant Biomarker of Gastric Cancer Progression.
    Kanda M, Nomoto S, Oya H, Takami H, Shimizu D, Hibino S, Hashimoto R, Kobayashi D, Tanaka C, Yamada S, Fujii T, Nakayama G, Sugimoto H, Koike M, Fujiwara M, Kodera Y.

    10/22/2016
    MAGE-D2 is a dynamic protein whose shuttling properties could suggest a role in cell cycle regulation.

    Melanoma antigen-D2: A nucleolar protein undergoing delocalization during cell cycle and after cellular stress.
    Pirlot C, Thiry M, Trussart C, Di Valentin E, Piette J, Habraken Y.

    06/11/2016
    We found that MAGED2 mutations caused X-linked polyhydramnios with prematurity and a severe but transient form of antenatal Bartter's syndrome.

    Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations.
    Laghmani K, Beck BB, Yang SS, Seaayfan E, Wenzel A, Reusch B, Vitzthum H, Priem D, Demaretz S, Bergmann K, Duin LK, Göbel H, Mache C, Thiele H, Bartram MP, Dombret C, Altmüller J, Nürnberg P, Benzing T, Levtchenko E, Seyberth HW, Klaus G, Yigit G, Lin SH, Timmer A, de Koning TJ, Scherjon SA, Schlingmann KP, Bertrand MJ, Rinschen MM, de Backer O, Konrad M, Kömhoff M.

    05/28/2016
    these results identify the expression of MAGE-D2 suppresses TRAIL receptor 2 and protects againstas TRAIL-induced apoptosis

    The melanoma-associated antigen MAGE-D2 suppresses TRAIL receptor 2 and protects against TRAIL-induced apoptosis in human melanoma cells.
    Tseng HY, Chen LH, Ye Y, Tay KH, Jiang CC, Guo ST, Jin L, Hersey P, Zhang XD.

    01/26/2013
    Observational study of gene-disease association. (HuGE Navigator)

    New genetic associations detected in a host response study to hepatitis B vaccine.
    Davila S, Froeling FE, Tan A, Bonnard C, Boland GJ, Snippe H, Hibberd ML, Seielstad M.

    04/7/2010
    Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator)

    Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers.
    Walker LC, Waddell N, Ten Haaf A, kConFab Investigators, Grimmond S, Spurdle AB.

    03/13/2008
    MAGED2, a novel protein, is a p53-dissociator.

    MAGED2: a novel p53-dissociator.
    Papageorgio C, Brachmann R, Zeng J, Culverhouse R, Zhang W, McLeod H.

    01/21/2010
    Maged2 is mainly expressed in tissues of mesodermal origin

    Comparative expression analysis of the MAGED genes during embryogenesis and brain development.
    Bertrand M, Huijbers I, Chomez P, De Backer O.

    01/21/2010
    Expression pattern and further characterization of human MAGED2 and identification of rodent orthologues

    Expression pattern and further characterization of human MAGED2 and identification of rodent orthologues.
    Langnaese K, Kloos DU, Wehnert M, Seidel B, Wieacker P.

    01/21/2010
    Results identified a cDNA clone, corresponding to MAGE D2 mRNA, from primary human bronchial epithelial cells which exhibits increased expression in vitro after treatment with all-trans retinoic acid.

    Identification of a novel MAGE D2 antisense RNA transcript in human tissues.
    Harper R, Xu C, Di P, Chen Y, Privalsky M, Wu R.

    01/21/2010
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