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    MED12 mediator complex subunit 12 [ Homo sapiens (human) ]

    Gene ID: 9968, updated on 5-Jan-2025

    GeneRIFs: Gene References Into Functions

    GeneRIFPubMed TitleDate
    A C->T Variation in 3'-Untranslated Region Elevates MED12 Protein Level in Breast Cancer That Relates to Better Prognosis.

    A C->T Variation in 3'-Untranslated Region Elevates MED12 Protein Level in Breast Cancer That Relates to Better Prognosis.
    Chen J, Wang T, Mu W.

    10/29/2024
    Somatic MED12 Mutations in Myometrial Cells.

    Somatic MED12 Mutations in Myometrial Cells.
    Li Y, Asif H, Feng Y, Kim JJ, Wei JJ., Free PMC Article

    09/17/2024
    MED12 Mutation in Two Families with X-Linked Ohdo Syndrome.

    MED12 Mutation in Two Families with X-Linked Ohdo Syndrome.
    Rocchetti L, Evangelista E, De Falco L, Savarese G, Savarese P, Ruggiero R, D'Amore L, Sensi A, Fico A., Free PMC Article

    08/29/2024
    Interaction between MED12 and DeltaNp63 activates basal identity in pancreatic ductal adenocarcinoma.

    Interaction between MED12 and ΔNp63 activates basal identity in pancreatic ductal adenocarcinoma.
    Maia-Silva D, Cunniff PJ, Schier AC, Skopelitis D, Trousdell MC, Moresco P, Gao Y, Kechejian V, He XY, Sahin Y, Wan L, Alpsoy A, Liverpool J, Krainer AR, Egeblad M, Spector DL, Fearon DT, Dos Santos CO, Taatjes DJ, Vakoc CR.,

    08/13/2024
    MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability.

    MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability.
    Yang JH, Liu ZG, Liu CL, Zhang MR, Jia YL, Zhai QX, He MF, He N, Qiao JD.

    04/15/2024
    Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells.

    Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells.
    Khan NH, McNally R, Kim JJ, Wei JJ.,

    04/3/2024
    The Effect of Race/Ethnicity and MED12 Mutation on the Expression of Long Non-Coding RNAs in Uterine Leiomyoma and Myometrium.

    The Effect of Race/Ethnicity and MED12 Mutation on the Expression of Long Non-Coding RNAs in Uterine Leiomyoma and Myometrium.
    Chuang TD, Ton N, Rysling S, Boos D, Khorram O., Free PMC Article

    02/2/2024
    The Mediator Complex Subunit 12 (MED-12) Gene and Uterine Fibroids: a Systematic Review.

    The Mediator Complex Subunit 12 (MED-12) Gene and Uterine Fibroids: a Systematic Review.
    Amendola ILS, Spann M, Segars J, Singh B.

    02/1/2024
    Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy.

    Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy.
    Ghasemi S, Mahdavi M, Maleki M, Salahshourifar I, Kalayinia S., Free PMC Article

    01/3/2024
    RISING STARS: Role of MED12 mutation in the pathogenesis of uterine fibroids.

    RISING STARS: Role of MED12 mutation in the pathogenesis of uterine fibroids.
    Ishikawa H, Kobayashi T, Kaneko M, Saito Y, Shozu M, Koga K.

    10/2/2023
    Differential Expression of MED12-Associated Coding RNA Transcripts in Uterine Leiomyomas.

    Differential Expression of MED12-Associated Coding RNA Transcripts in Uterine Leiomyomas.
    Chuang TD, Gao J, Quintanilla D, McSwiggin H, Boos D, Yan W, Khorram O., Free PMC Article

    03/23/2023
    Missense MED12 variants in 22 males with intellectual disability: From nonspecific symptoms to complete syndromes.

    Missense MED12 variants in 22 males with intellectual disability: From nonspecific symptoms to complete syndromes.
    Maia N, Ibarluzea N, Misra-Isrie M, Koboldt DC, Marques I, Soares G, Santos R, Marcelis CLM, Keski-Filppula R, Guitart M, Gabau Vila E, Lehman A, Hickey S, Mori M, Terhal P, Valenzuela I, Lasa-Aranzasti A, Cueto-González AM, Chhouk BH, Yeh RC, Neil JE, Abu-Libde B, Kleefstra T, Elting MW, Császár A, Kárteszi J, Bessenyei B, van Bokhoven H, Jorge P, van Hagen JM, de Brouwer APM., Free PMC Article

    03/3/2023
    MED12 mutations in uterine leiomyomas: prediction of volume reduction by gonadotropin-releasing hormone agonists.

    MED12 mutations in uterine leiomyomas: prediction of volume reduction by gonadotropin-releasing hormone agonists.
    Nagai K, Asano R, Sekiguchi F, Asai-Sato M, Miyagi Y, Miyagi E.

    02/4/2023
    XLID syndrome gene Med12 promotes Ig isotype switching through chromatin modification and enhancer RNA regulation.

    XLID syndrome gene Med12 promotes Ig isotype switching through chromatin modification and enhancer RNA regulation.
    Haque F, Honjo T, Begum NA., Free PMC Article

    12/24/2022
    MED12 mutation as a potential predictive biomarker for immune checkpoint inhibitors in pan-cancer.

    MED12 mutation as a potential predictive biomarker for immune checkpoint inhibitors in pan-cancer.
    Zhou Y, Tan Y, Zhang Q, Duan Q, Chen J., Free PMC Article

    11/5/2022
    A mediator complex subunit 12 gain-of-function mutation induces partial leiomyoma cell properties in human uterine smooth muscle cells.

    A mediator complex subunit 12 gain-of-function mutation induces partial leiomyoma cell properties in human uterine smooth muscle cells.
    Takao T, Ono M, Yoshimasa Y, Masuda H, Maruyama T.

    10/22/2022
    Different DNA methylome, transcriptome and histological features in uterine fibroids with and without MED12 mutations.

    Different DNA methylome, transcriptome and histological features in uterine fibroids with and without MED12 mutations.
    Maekawa R, Sato S, Tamehisa T, Sakai T, Kajimura T, Sueoka K, Sugino N., Free PMC Article

    06/11/2022
    The novel mechanism of Med12-mediated drug resistance in a TGFBR2-independent manner.

    The novel mechanism of Med12-mediated drug resistance in a TGFBR2-independent manner.
    Han Y, Dong Q, Liu T, Chen X, Yu C, Zhang Y.

    05/28/2022
    Frequency of MED12 Mutation in Relation to Tumor and Patient's Clinical Characteristics: a Meta-analysis.

    Frequency of MED12 Mutation in Relation to Tumor and Patient's Clinical Characteristics: a Meta-analysis.
    He C, Nelson W, Li H, Xu YD, Dai XJ, Wang YX, Ding YB, Li YP, Li T.

    05/21/2022
    MED12 Regulates Human Adipose-Derived Stem Cell Adipogenesis and Mediator Kinase Subunit Expression in Murine Adipose Depots.

    MED12 Regulates Human Adipose-Derived Stem Cell Adipogenesis and Mediator Kinase Subunit Expression in Murine Adipose Depots.
    Venigalla S, Straub J, Idigo O, Rinderle C, Stephens JM, Newman JJ., Free PMC Article

    05/14/2022
    MED12 Regulates Smooth Muscle Cell Functions and Participates in the Development of Aortic Dissection.

    MED12 Regulates Smooth Muscle Cell Functions and Participates in the Development of Aortic Dissection.
    Zhou Y, Zha L, Wu J, Wang M, Zhou M, Wu G, Cheng X, Huang Z, Xie Q, Tu X., Free PMC Article

    04/30/2022
    Aberrant R-loop-induced replication stress in MED12-mutant uterine fibroids.

    Aberrant R-loop-induced replication stress in MED12-mutant uterine fibroids.
    Muralimanoharan S, Shamby R, Stansbury N, Schenken R, de la Pena Avalos B, Javanmardi S, Dray E, Sung P, Boyer TG., Free PMC Article

    04/30/2022
    Eye and ocular adnexa manifestations of MED12-related disorders.

    Eye and ocular adnexa manifestations of MED12-related disorders.
    Shah A, Bapna M, Al-Saif H, Li R, Couser NL.

    04/23/2022
    Uterine cellular leiomyomas are characterized by common HMGA2 aberrations, followed by chromosome 1p deletion and MED12 mutation: morphological, molecular, and immunohistochemical study of 52 cases.

    Uterine cellular leiomyomas are characterized by common HMGA2 aberrations, followed by chromosome 1p deletion and MED12 mutation: morphological, molecular, and immunohistochemical study of 52 cases.
    Dundr P, Gregová M, Hojný J, Krkavcová E, Michálková R, Němejcová K, Bártů M, Hájková N, Laco J, Mára M, Richtárová A, Zima T, Stružinská I.

    04/16/2022
    Tryptophan 2,3-Dioxygenase-2 in Uterine Leiomyoma: Dysregulation by MED12 Mutation Status.

    Tryptophan 2,3-Dioxygenase-2 in Uterine Leiomyoma: Dysregulation by MED12 Mutation Status.
    Hutchinson AP, Yin P, Neale I, Coon JS 5th, Kujawa SA, Liu S, Bulun SE., Free PMC Article

    03/26/2022
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