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  1.  

    C-type natriuretic peptide improves growth retardation in a mouse model of cardio-facio-cutaneous syndrome

    Inoue, Shin-ichi / Morozumi, Naomi / Yoshikiyo, Kazunori et al. | British Library Online Contents | 2018
  2.  

    Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

    Quinn, Peter M / Mulder, Aat A / Henrique Alves, C et al. | British Library Online Contents | 2018
  3.  

    Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)

    Seo, Aaron / Gulsuner, Suleyman / Pierce, Sarah et al. | British Library Online Contents | 2018
  4.  

    Investigating the impact of cigarette smoking behaviours on DNA methylation patterns in adolescence

    Prince, Claire / Hammerton, Gemma / Taylor, Amy E et al. | British Library Online Contents | 2018
  5.  

    Investigating the impact of cigarette smoking behaviours on DNA methylation patterns in adolescence

    Prince, Claire / Hammerton, Gemma / Taylor, Amy E et al. | British Library Online Contents | 2018
  6.  

    Bezafibrate induces autophagy and improves hepatic lipid metabolism in glycogen storage disease type Ia

    Waskowicz, Lauren R / Zhou, Jin / Landau, Dustin J et al. | British Library Online Contents | 2018
  7.  

    Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype

    Quinn, Peter M / Mulder, Aat A / Henrique Alves, C et al. | British Library Online Contents | 2018
  8.  

    Cordycepin activates autophagy through AMPK phosphorylation to reduce abnormalities in Machado–Joseph disease models

    Marcelo, Adriana / Brito, Filipa / Carmo-Silva, Sara et al. | British Library Online Contents | 2018
  9.  

    A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis

    Jurynec, M. J. / Sawitzke, A. D. / Beals, T. C. et al. | British Library Online Contents | 2018
  10.  

    Noonan syndrome-causing SHP2 mutants impair ERK-dependent chondrocyte differentiation during endochondral bone growth

    Tajan, M. n. / Pernin-Grandjean, J. / Beton, N. et al. | British Library Online Contents | 2018
  11.  

    Facioscapulohumeral dystrophy: activating an early embryonic transcriptional program in human skeletal muscle

    Campbell, A. E. / Belleville, A. E. / Resnick, R. et al. | British Library Online Contents | 2018

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