has been cited by the following articles in journals that are participating in CrossRef's forward linking service: |
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| Identification of ARHGEF17, DENND2D, FGFR3, and RB1 mutations in melanoma by inhibition of nonsense-mediated mRNA decay Sandra Bloethner, Arne Mould, Mitchell Stark, and Nicholas K. Hayward Genes Chromosomes and Cancer (2008) : NA Link to Article |
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| Human INT6/eIF3e is required for nonsense-mediated mRNA decay Christelle Morris, Jürgen Wittmann, Hans-Martin Jäck, and Pierre Jalinot EMBO Reports (2007) 8: 596 Link to Article |
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| An alternative branch of the nonsense-mediated decay pathway Wai-Kin Chan, Lulu Huang, Jayanthi P Gudikote, Yao-Fu Chang, J Saadi Imam, James A MacLean, and Miles F Wilkinson The EMBO Journal (2007) 26: 1820 Link to Article |
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| Internal ribosome entry sequence-mediated translation initiation triggers nonsense-mediated decay Jill A Holbrook, Gabriele Neu-Yilik, Niels H Gehring, Andreas E Kulozik, and Matthias W Hentze EMBO Reports (2006) 7: 722 Link to Article |
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| Early nonsense: mRNA decay solves a translational problem Nadia Amrani, Matthew S. Sachs, and Allan Jacobson Nature Reviews Molecular Cell Biology (2006) 7: 415 Link to Article |
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| The position of premature termination codons in the hepatocyte nuclear factor −1 beta gene determines susceptibility to nonsense-mediated
decay L. W. Harries, Coralie Bingham, Christine Bellanne-Chantelot, A. T. Hattersley, and Sian Ellard Human Genetics (2005) 118: 214 Link to Article |
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| Polypeptide chain termination and stop codon readthrough on eukaryotic ribosomes S. Rospert, M. Rakwalska, and Y. Dubaquié Reviews of Physiology Biochemistry and Pharmacology (2005) Link to Article |
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| The emerging roles of translation factor eIF4E in the nucleus S. Strudwick and K. L. B. Borden Differentiation (2002) 70: 10 Link to Article |
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| Killing the messenger: new insights into nonsense-mediated mRNA decay Peter H. Byers Journal of Clinical Investigation (2002) 109: 3 Link to Article |
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| MECHANISMS OF mRNA SURVILLENCE IN EUKARYOTES P Hilleren and R Parker Annual Review of Genetics (1999) 33: 229 Link to Article |
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| Correction of genetic disease by making sense from nonsense Randal J. Kaufman Journal of Clinical Investigation (1999) 104: 367 Link to Article |
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| POTENT Reconstruction from Mark III Velocities A. Dekel, A. Eldar, T. Kolatt, A. Yahil, J. A. Willick, S. M. Faber, S. Courteau, and D. Burstein The Astrophysical Journal (1999) 522: 1 Link to Article |
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| Molecular heterogeneity in deficiency of complement protein C2 type I WANG, CIRCOLO, LOKKI, SHACKELFORD, WETSEL*, and COLTEN Immunology (1998) 93: 184 Link to Article |
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| Tay-Sachs disease-causing mutations and neutral polymorphisms in the Hex A gene Rachel Myerowitz Human Mutation (1997) 9: 195 Link to Article |
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| Nonstop treatment of cystic fibrosis Harry C. Dietz and Ada Hamosh Nature Medicine (1996) 2: 608 Link to Article |
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| Reply to “Nonstop treatment of cystic fibrosis” David M. Bedwell, Marybeth Howard, and Raymond A. Frizzell Nature Medicine (1996) 2: 608 Link to Article |
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| Detection of 12 novel mutations in the collagenous domain of the COL4A5 gene in Alport syndrome patients Eileen Boye, Frances Flinter, Jing Zhou, Karl Tryggvason, Martin Bobrow, and Ann Harris Human Mutation (1995) 5: 197 Link to Article |
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| The molecular genetic basis of myophosphorylase deficiency (McArdle's disease) Seiichi Tsujino, Sara Shanske, Ikuya Nonaka, and Salvatore DiMauro Muscle & Nerve (1995) 18: S23 Link to Article |
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| Searching for the 1 in 2,400,000: A review of dystrophin gene point mutations Roland G. Roberts, Rebecca J. Gardner, and Martin Bobrow Human Mutation (1994) 4: 1 Link to Article |
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| Maintenance of an open reading frame as an additional level of scrutiny during splice site selection Harry C. Dietz and Raymond J. Kendzior Nature Genetics (1994) 8: 183 Link to Article |
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