BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

62 related articles for article (PubMed ID: 23380319)

  • 1. Evolutionary genetic analyses of MEF2C gene: implications for learning and memory in Homo sapiens.
    Kalmady SV; Venkatasubramanian G; Arasappa R; Rao NP
    Asian J Psychiatr; 2013 Feb; 6(1):56-9. PubMed ID: 23380319
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Vertebrate paralogous MEF2 genes: origin, conservation, and evolution.
    Wu W; de Folter S; Shen X; Zhang W; Tao S
    PLoS One; 2011 Mar; 6(3):e17334. PubMed ID: 21394201
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Properties comparing and evolutionary analysis of MEF2 of Homo sapiens based on bioinformatic methods].
    Guo XJ
    Yi Chuan; 2011 Sep; 33(9):975-81. PubMed ID: 21951798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The MEF2C gene-microdeletion 5q14.3 dilemma and three axioms for molecular syndromology.
    Wilson GN
    Am J Med Genet A; 2013 Apr; 161A(4):916-7. PubMed ID: 23495102
    [No Abstract]   [Full Text] [Related]  

  • 5. Functional diversification of B MADS-box homeotic regulators of flower development: Adaptive evolution in protein-protein interaction domains after major gene duplication events.
    Hernández-Hernández T; Martínez-Castilla LP; Alvarez-Buylla ER
    Mol Biol Evol; 2007 Feb; 24(2):465-81. PubMed ID: 17135333
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Late-onset gain of skills and peculiar jugular pit in an 11-year-old girl with 5q14.3 microdeletion including MEF2C.
    Berland S; Houge G
    Clin Dysmorphol; 2010 Oct; 19(4):222-224. PubMed ID: 20729728
    [No Abstract]   [Full Text] [Related]  

  • 7. Maximum likelihood analysis of mammalian p53 indicates the presence of positively selected sites and higher tumorigenic mutations in purifying sites.
    Khan MM; Rydén AM; Chowdhury MS; Hasan MA; Kazi JU
    Gene; 2011 Sep; 483(1-2):29-35. PubMed ID: 21640173
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Refining the phenotype associated with MEF2C point mutations.
    Bienvenu T; Diebold B; Chelly J; Isidor B
    Neurogenetics; 2013 Feb; 14(1):71-5. PubMed ID: 23001426
    [TBL] [Abstract][Full Text] [Related]  

  • 9. MEF2C mutations are a rare cause of Rett or severe Rett-like encephalopathies.
    Lambert L; Bienvenu T; Allou L; Valduga M; Echenne B; Diebold B; Mignot C; Héron D; Roth V; Saunier A; Moustaïne A; Jonveaux P; Philippe C
    Clin Genet; 2012 Nov; 82(5):499-501. PubMed ID: 22449245
    [No Abstract]   [Full Text] [Related]  

  • 10. Phylogenetic analysis and positive-selection site detecting of vascular endothelial growth factor family in vertebrates.
    He W; Tang Y; Qi B; Lu C; Qin C; Wei Y; Yi J; Chen M
    Gene; 2014 Feb; 535(2):345-52. PubMed ID: 24200960
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Refining the phenotype associated with MEF2C haploinsufficiency.
    Novara F; Beri S; Giorda R; Ortibus E; Nageshappa S; Darra F; Dalla Bernardina B; Zuffardi O; Van Esch H
    Clin Genet; 2010 Nov; 78(5):471-7. PubMed ID: 20412115
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evolution of plant MADS box transcription factors: evidence for shifts in selection associated with early angiosperm diversification and concerted gene duplications.
    Shan H; Zahn L; Guindon S; Wall PK; Kong H; Ma H; DePamphilis CW; Leebens-Mack J
    Mol Biol Evol; 2009 Oct; 26(10):2229-44. PubMed ID: 19578156
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Conservation and evolution in and among SRF- and MEF2-type MADS domains and their binding sites.
    Wu W; Huang X; Cheng J; Li Z; de Folter S; Huang Z; Jiang X; Pang H; Tao S
    Mol Biol Evol; 2011 Jan; 28(1):501-11. PubMed ID: 20724380
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 5q14.3 neurocutaneous syndrome: a novel continguous gene syndrome caused by simultaneous deletion of RASA1 and MEF2C.
    Carr CW; Zimmerman HH; Martin CL; Vikkula M; Byrd AC; Abdul-Rahman OA
    Am J Med Genet A; 2011 Jul; 155A(7):1640-5. PubMed ID: 21626678
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression.
    Zweier M; Gregor A; Zweier C; Engels H; Sticht H; Wohlleber E; Bijlsma EK; Holder SE; Zenker M; Rossier E; Grasshoff U; Johnson DS; Robertson L; Firth HV; ; Ekici AB; Reis A; Rauch A
    Hum Mutat; 2010 Jun; 31(6):722-33. PubMed ID: 20513142
    [TBL] [Abstract][Full Text] [Related]  

  • 16. BCR-ABL mediated repression of miR-223 results in the activation of MEF2C and PTBP2 in chronic myeloid leukemia.
    Agatheeswaran S; Singh S; Biswas S; Biswas G; Chandra Pattnayak N; Chakraborty S
    Leukemia; 2013 Jul; 27(7):1578-80. PubMed ID: 23174904
    [No Abstract]   [Full Text] [Related]  

  • 17. Myocyte enhancer factor 2 acetylation by p300 enhances its DNA binding activity, transcriptional activity, and myogenic differentiation.
    Ma K; Chan JK; Zhu G; Wu Z
    Mol Cell Biol; 2005 May; 25(9):3575-82. PubMed ID: 15831463
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Core promoter short tandem repeats as evolutionary switch codes for primate speciation.
    Ohadi M; Valipour E; Ghadimi-Haddadan S; Namdar-Aligoodarzi P; Bagheri A; Kowsari A; Rezazadeh M; Darvish H; Kazeminasab S
    Am J Primatol; 2015 Jan; 77(1):34-43. PubMed ID: 25099915
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A testis-specific gene within a widely expressed gene: Contrasting evolutionary patterns of two differentially expressed mammalian proteins encoded by a single gene, CAMK4.
    Padhi A; Ma L
    Anim Genet; 2015 Dec; 46(6):683-92. PubMed ID: 26388303
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Variable patterns in the molecular evolution of the hypoxia-inducible factor-1 alpha (HIF-1alpha) gene in teleost fishes and mammals.
    Rytkönen KT; Ryynänen HJ; Nikinmaa M; Primmer CR
    Gene; 2008 Aug; 420(1):1-10. PubMed ID: 18565696
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.