These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 32698523)

  • 1. PCAF Involvement in Lamin A/C-HDAC2 Interplay during the Early Phase of Muscle Differentiation.
    Santi S; Cenni V; Capanni C; Lattanzi G; Mattioli E
    Cells; 2020 Jul; 9(7):. PubMed ID: 32698523
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lamin A/C Assembly Defects in
    Bertrand AT; Brull A; Azibani F; Benarroch L; Chikhaoui K; Stewart CL; Medalia O; Ben Yaou R; Bonne G
    Cells; 2020 Mar; 9(4):. PubMed ID: 32244403
    [No Abstract]   [Full Text] [Related]  

  • 3. Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy.
    Cenni V; Sabatelli P; Mattioli E; Marmiroli S; Capanni C; Ognibene A; Squarzoni S; Maraldi NM; Bonne G; Columbaro M; Merlini L; Lattanzi G
    J Med Genet; 2005 Mar; 42(3):214-20. PubMed ID: 15744034
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Emery-Dreifuss Muscular Dystrophy-Associated Mutant Forms of Lamin A Recruit the Stress Responsive Protein Ankrd2 into the Nucleus, Affecting the Cellular Response to Oxidative Stress.
    Angori S; Capanni C; Faulkner G; Bean C; Boriani G; Lattanzi G; Cenni V
    Cell Physiol Biochem; 2017; 42(1):169-184. PubMed ID: 28531892
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression of a mutant lamin A that causes Emery-Dreifuss muscular dystrophy inhibits in vitro differentiation of C2C12 myoblasts.
    Favreau C; Higuet D; Courvalin JC; Buendia B
    Mol Cell Biol; 2004 Feb; 24(4):1481-92. PubMed ID: 14749366
    [TBL] [Abstract][Full Text] [Related]  

  • 6. FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy.
    Ziat E; Mamchaoui K; Beuvin M; Nelson I; Azibani F; Spuler S; Bonne G; Bertrand AT
    J Neuromuscul Dis; 2016 Nov; 3(4):497-510. PubMed ID: 27911330
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Differentiation of C2C12 myoblasts expressing lamin A mutated at a site responsible for Emery-Dreifuss muscular dystrophy is improved by inhibition of the MEK-ERK pathway and stimulation of the PI3-kinase pathway.
    Favreau C; Delbarre E; Courvalin JC; Buendia B
    Exp Cell Res; 2008 Apr; 314(6):1392-405. PubMed ID: 18294630
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium composition.
    Holt I; Nguyen TM; Wehnert M; Morris GE
    Neuromuscul Disord; 2006 Jun; 16(6):368-73. PubMed ID: 16697197
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
    Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC
    BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy.
    Favreau C; Dubosclard E; Ostlund C; Vigouroux C; Capeau J; Wehnert M; Higuet D; Worman HJ; Courvalin JC; Buendia B
    Exp Cell Res; 2003 Jan; 282(1):14-23. PubMed ID: 12490190
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Laminopathies disrupt epigenomic developmental programs and cell fate.
    Perovanovic J; Dell'Orso S; Gnochi VF; Jaiswal JK; Sartorelli V; Vigouroux C; Mamchaoui K; Mouly V; Bonne G; Hoffman EP
    Sci Transl Med; 2016 Apr; 8(335):335ra58. PubMed ID: 27099177
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical aspects of Emery-Dreifuss muscular dystrophy.
    Madej-Pilarczyk A
    Nucleus; 2018 Jan; 9(1):268-274. PubMed ID: 29633897
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
    Mercuri E; Counsell S; Allsop J; Jungbluth H; Kinali M; Bonne G; Schwartz K; Bydder G; Dubowitz V; Muntoni F
    Neuropediatrics; 2002 Feb; 33(1):10-4. PubMed ID: 11930270
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects.
    Håkelien AM; Delbarre E; Gaustad KG; Buendia B; Collas P
    Exp Cell Res; 2008 May; 314(8):1869-80. PubMed ID: 18396274
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle.
    Mattioli E; Columbaro M; Capanni C; Maraldi NM; Cenni V; Scotlandi K; Marino MT; Merlini L; Squarzoni S; Lattanzi G
    Cell Death Differ; 2011 Aug; 18(8):1305-15. PubMed ID: 21311568
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells.
    Janin A; Bauer D; Ratti F; Valla C; Bertrand A; Christin E; Chopin E; Streichenberger N; Bonne G; Gache V; Cohen T; Méjat A
    Sci Rep; 2018 Apr; 8(1):5618. PubMed ID: 29618840
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.
    Maraldi NM; Lattanzi G; Sabatelli P; Ognibene A; Columbaro M; Capanni C; Rutigliano C; Mattioli E; Squarzoni S
    Eur J Histochem; 2003; 47(1):3-16. PubMed ID: 12685553
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy.
    Wang Y; Herron AJ; Worman HJ
    Hum Mol Genet; 2006 Aug; 15(16):2479-89. PubMed ID: 16825283
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Uncoordinated transcription and compromised muscle function in the lmna-null mouse model of Emery- Emery-Dreyfuss muscular dystrophy.
    Gnocchi VF; Scharner J; Huang Z; Brady K; Lee JS; White RB; Morgan JE; Sun YB; Ellis JA; Zammit PS
    PLoS One; 2011 Feb; 6(2):e16651. PubMed ID: 21364987
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy.
    Motsch I; Kaluarachchi M; Emerson LJ; Brown CA; Brown SC; Dabauvalle MC; Ellis JA
    Eur J Cell Biol; 2005 Sep; 84(9):765-81. PubMed ID: 16218190
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.