BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

124 related articles for article (PubMed ID: 31228576)

  • 1. Expression pattern of Kmt2d in murine craniofacial tissues.
    Dong C; Umar M; Bartoletti G; Gahankari A; Fidelak L; He F
    Gene Expr Patterns; 2019 Dec; 34():119060. PubMed ID: 31228576
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Precocious chondrocyte differentiation disrupts skeletal growth in Kabuki syndrome mice.
    Fahrner JA; Lin WY; Riddle RC; Boukas L; DeLeon VB; Chopra S; Lad SE; Luperchio TR; Hansen KD; Bjornsson HT
    JCI Insight; 2019 Oct; 4(20):. PubMed ID: 31557133
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The KMT2D Kabuki syndrome histone methylase controls neural crest cell differentiation and facial morphology.
    Shpargel KB; Mangini CL; Xie G; Ge K; Magnuson T
    Development; 2020 Jul; 147(21):. PubMed ID: 32541010
    [TBL] [Abstract][Full Text] [Related]  

  • 4. KMT2D deficiency disturbs the proliferation and cell cycle activity of dental epithelial cell line (LS8) partially via Wnt signaling.
    Pang L; Tian H; Gao X; Wang W; Wang X; Zhang Z
    Biosci Rep; 2021 Nov; 41(11):. PubMed ID: 34724040
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Precocious neuronal differentiation and disrupted oxygen responses in Kabuki syndrome.
    Carosso GA; Boukas L; Augustin JJ; Nguyen HN; Winer BL; Cannon GH; Robertson JD; Zhang L; Hansen KD; Goff LA; Bjornsson HT
    JCI Insight; 2019 Oct; 4(20):. PubMed ID: 31465303
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Abnormal Peyer patch development and B-cell gut homing drive IgA deficiency in Kabuki syndrome.
    Pilarowski GO; Cazares T; Zhang L; Benjamin JS; Liu K; Jagannathan S; Mousa N; Kasten J; Barski A; Lindsley AW; Bjornsson HT
    J Allergy Clin Immunol; 2020 Mar; 145(3):982-992. PubMed ID: 31816409
    [TBL] [Abstract][Full Text] [Related]  

  • 7. KMT2D regulates specific programs in heart development via histone H3 lysine 4 di-methylation.
    Ang SY; Uebersohn A; Spencer CI; Huang Y; Lee JE; Ge K; Bruneau BG
    Development; 2016 Mar; 143(5):810-21. PubMed ID: 26932671
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Loss of Function of the Gene Encoding the Histone Methyltransferase KMT2D Leads to Deregulation of Mitochondrial Respiration.
    Pacelli C; Adipietro I; Malerba N; Squeo GM; Piccoli C; Amoresano A; Pinto G; Pucci P; Lee JE; Ge K; Capitanio N; Merla G
    Cells; 2020 Jul; 9(7):. PubMed ID: 32668765
    [No Abstract]   [Full Text] [Related]  

  • 9. Genetic and behavioral characterization of a Kmt2d mouse mutant, a new model for Kabuki Syndrome.
    Yamamoto PK; de Souza TA; Antiorio ATFB; Zanatto DA; Garcia-Gomes MSA; Alexandre-Ribeiro SR; Oliveira NS; Menck CFM; Bernardi MM; Massironi SMG; Mori CMC
    Genes Brain Behav; 2019 Nov; 18(8):e12568. PubMed ID: 30891914
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enhancer Reprogramming Confers Dependence on Glycolysis and IGF Signaling in KMT2D Mutant Melanoma.
    Maitituoheti M; Keung EZ; Tang M; Yan L; Alam H; Han G; Singh AK; Raman AT; Terranova C; Sarkar S; Orouji E; Amin SB; Sharma S; Williams M; Samant NS; Dhamdhere M; Zheng N; Shah T; Shah A; Axelrad JB; Anvar NE; Lin YH; Jiang S; Chang EQ; Ingram DR; Wang WL; Lazar A; Lee MG; Muller F; Wang L; Ying H; Rai K
    Cell Rep; 2020 Oct; 33(3):108293. PubMed ID: 33086062
    [TBL] [Abstract][Full Text] [Related]  

  • 11. KMT2D regulates activation, localization, and integrin expression by T-cells.
    Potter SJ; Zhang L; Kotliar M; Wu Y; Schafer C; Stefan K; Boukas L; Qu'd D; Bodamer O; Simpson BN; Barski A; Lindsley AW; Bjornsson HT
    Front Immunol; 2024; 15():1341745. PubMed ID: 38765012
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Histone H3 lysine 4 methyltransferase KMT2D.
    Froimchuk E; Jang Y; Ge K
    Gene; 2017 Sep; 627():337-342. PubMed ID: 28669924
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans.
    Liu YH; Tang Z; Kundu RK; Wu L; Luo W; Zhu D; Sangiorgi F; Snead ML; Maxson RE
    Dev Biol; 1999 Jan; 205(2):260-74. PubMed ID: 9917362
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development.
    Van Laarhoven PM; Neitzel LR; Quintana AM; Geiger EA; Zackai EH; Clouthier DE; Artinger KB; Ming JE; Shaikh TH
    Hum Mol Genet; 2015 Aug; 24(15):4443-53. PubMed ID: 25972376
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A ketogenic diet rescues hippocampal memory defects in a mouse model of Kabuki syndrome.
    Benjamin JS; Pilarowski GO; Carosso GA; Zhang L; Huso DL; Goff LA; Vernon HJ; Hansen KD; Bjornsson HT
    Proc Natl Acad Sci U S A; 2017 Jan; 114(1):125-130. PubMed ID: 27999180
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Expanding the Oro-Dental and Mutational Spectra of Kabuki Syndrome and Expression of
    Porntaveetus T; Abid MF; Theerapanon T; Srichomthong C; Ohazama A; Kawasaki K; Kawasaki M; Suphapeetiporn K; Sharpe PT; Shotelersuk V
    Int J Biol Sci; 2018; 14(4):381-389. PubMed ID: 29725259
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis.
    Schwenty-Lara J; Nürnberger A; Borchers A
    Dev Dyn; 2019 Jun; 248(6):465-476. PubMed ID: 30980591
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular mechanisms in calvarial bone and suture development, and their relation to craniosynostosis.
    Rice DP; Rice R; Thesleff I
    Eur J Orthod; 2003 Apr; 25(2):139-48. PubMed ID: 12737212
    [TBL] [Abstract][Full Text] [Related]  

  • 19. COMPASS Ascending: Emerging clues regarding the roles of MLL3/KMT2C and MLL2/KMT2D proteins in cancer.
    Fagan RJ; Dingwall AK
    Cancer Lett; 2019 Aug; 458():56-65. PubMed ID: 31128216
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Kabuki syndrome stem cell models reveal locus specificity of histone methyltransferase 2D (KMT2D/MLL4).
    Jefri M; Zhang X; Stumpf PS; Zhang L; Peng H; Hettige N; Theroux JF; Aouabed Z; Wilson K; Deshmukh S; Antonyan L; Ni A; Alsuwaidi S; Zhang Y; Jabado N; Garcia BA; Schuppert A; Bjornsson HT; Ernst C
    Hum Mol Genet; 2022 Oct; 31(21):3715-3728. PubMed ID: 35640156
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.