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Hal Dietz - Publications

Affiliations: 
Johns Hopkins University, Baltimore, MD 
Area:
Genetics, Molecular Biology
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30 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Ziegler SG, Ferreira CR, MacFarlane EG, Riddle RC, Tomlinson RE, Chew EY, Martin L, Ma CT, Sergienko E, Pinkerton AB, Millán JL, Gahl WA, Dietz HC. Ectopic calcification in pseudoxanthoma elasticum responds to inhibition of tissue-nonspecific alkaline phosphatase. Science Translational Medicine. 9. PMID 28592560 DOI: 10.1126/Scitranslmed.Aal1669  0.303
2011 Frischmeyer-Guerrerio PA, Montgomery RA, Warren DS, Cooke SK, Lutz J, Sonnenday CJ, Guerrerio AL, Dietz HC. Perturbation of thymocyte development in nonsense-mediated decay (NMD)-deficient mice. Proceedings of the National Academy of Sciences of the United States of America. 108: 10638-43. PMID 21670277 DOI: 10.1073/Pnas.1019352108  0.307
2010 Cooper TK, Zhong Q, Krawczyk M, Tae HJ, Müller GA, Schubert R, Myers LA, Dietz HC, Talan MI, Briest W. The haploinsufficient Col3a1 mouse as a model for vascular Ehlers-Danlos syndrome. Veterinary Pathology. 47: 1028-39. PMID 20587693 DOI: 10.1177/0300985810374842  0.482
2009 Dang Y, Low WK, Xu J, Gehring NH, Dietz HC, Romo D, Liu JO. Inhibition of nonsense-mediated mRNA decay by the natural product pateamine A through eukaryotic initiation factor 4AIII. The Journal of Biological Chemistry. 284: 23613-21. PMID 19570977 DOI: 10.1074/Jbc.M109.009985  0.363
2007 Xie J, Bessling SL, Cooper TK, Dietz HC, McCallion AS, Fisher S. Manipulating mitotic recombination in the zebrafish embryo through RecQ helicases. Genetics. 176: 1339-42. PMID 17483412 DOI: 10.1534/Genetics.107.072983  0.548
2006 Ciaudo C, Bourdet A, Cohen-Tannoudji M, Dietz HC, Rougeulle C, Avner P. Nuclear mRNA degradation pathway(s) are implicated in Xist regulation and X chromosome inactivation. Plos Genetics. 2: e94. PMID 16789828 DOI: 10.1371/Journal.Pgen.0020094  0.339
2006 Habashi JP, Judge DP, Holm TM, Cohn RD, Loeys BL, Cooper TK, Myers L, Klein EC, Liu G, Calvi C, Podowski M, Neptune ER, Halushka MK, Bedja D, Gabrielson K, ... ... Dietz HC, et al. Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome. Science (New York, N.Y.). 312: 117-21. PMID 16601194 DOI: 10.1126/Science.1124287  0.496
2006 Habashi J, Judge D, Holm T, Cohn R, Loeys B, Cooper T, Myers L, Klein E, Liu G, Calvi C, Podowski M, Neptune E, Halushka M, Bedja D, Gabrielson K, ... ... Dietz H, et al. Losartan in Marfan Syndrome—Beyond Blood Pressure Lowering Journal of the American Society of Nephrology. 17: 1759-1764. DOI: 10.1681/Asn.2006050508  0.532
2004 Mendell JT, Sharifi NA, Meyers JL, Martinez-Murillo F, Dietz HC. Nonsense surveillance regulates expression of diverse classes of mammalian transcripts and mutes genomic noise. Nature Genetics. 36: 1073-8. PMID 15448691 DOI: 10.1038/Ng1429  0.671
2004 Judge DP, Biery NJ, Keene DR, Geubtner J, Myers L, Huso DL, Sakai LY, Dietz HC. Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome. The Journal of Clinical Investigation. 114: 172-81. PMID 15254584 DOI: 10.1172/Jci20641  0.31
2002 Mendell JT, ap Rhys CM, Dietz HC. Separable roles for rent1/hUpf1 in altered splicing and decay of nonsense transcripts. Science (New York, N.Y.). 298: 419-22. PMID 12228722 DOI: 10.1126/Science.1074428  0.641
2002 van Hoof A, Frischmeyer PA, Dietz HC, Parker R. Exosome-mediated recognition and degradation of mRNAs lacking a termination codon. Science (New York, N.Y.). 295: 2262-4. PMID 11910110 DOI: 10.1126/Science.1067272  0.383
2002 Frischmeyer PA, van Hoof A, O'Donnell K, Guerrerio AL, Parker R, Dietz HC. An mRNA surveillance mechanism that eliminates transcripts lacking termination codons. Science (New York, N.Y.). 295: 2258-61. PMID 11910109 DOI: 10.1126/Science.1067338  0.412
2002 Mendell JT, Dietz HC. When the message goes awry: disease-producing mutations that influence mRNA content and performance. Cell. 107: 411-4. PMID 11719181 DOI: 10.1016/S0092-8674(01)00583-9  0.605
2001 Noensie EN, Dietz HC. A strategy for disease gene identification through nonsense-mediated mRNA decay inhibition. Nature Biotechnology. 19: 434-9. PMID 11329012 DOI: 10.1038/88099  0.653
2001 Medghalchi SM, Frischmeyer PA, Mendell JT, Kelly AG, Lawler AM, Dietz HC. Rent1, a trans-effector of nonsense-mediated mRNA decay, is essential for mammalian embryonic viability. Human Molecular Genetics. 10: 99-105. PMID 11152657 DOI: 10.1093/Hmg/10.2.99  0.649
2000 Mendell JT, Medghalchi SM, Lake RG, Noensie EN, Dietz HC. Novel Upf2p orthologues suggest a functional link between translation initiation and nonsense surveillance complexes. Molecular and Cellular Biology. 20: 8944-57. PMID 11073994 DOI: 10.1128/Mcb.20.23.8944-8957.2000  0.608
2000 Dietz HC, Mecham RP. Mouse models of genetic diseases resulting from mutations in elastic fiber proteins Matrix Biology. 19: 481-488. PMID 11068202 DOI: 10.1016/S0945-053X(00)00101-3  0.319
1999 Frischmeyer PA, Dietz HC. Nonsense-mediated mRNA decay in health and disease. Human Molecular Genetics. 8: 1893-900. PMID 10469842 DOI: 10.1093/Hmg/8.10.1893  0.423
1999 Biery NJ, Eldadah ZA, Moore CS, Stetten G, Spencer F, Dietz HC. Revised genomic organization of FBN1 and significance for regulated gene expression. Genomics. 56: 70-7. PMID 10036187 DOI: 10.1006/Geno.1998.5697  0.339
1998 Sun X, Perlick HA, Dietz HC, Maquat LE. A mutated human homologue to yeast Upf1 protein has a dominant-negative effect on the decay of nonsense-containing mRNAs in mammalian cells Proceedings of the National Academy of Sciences of the United States of America. 95: 10009-10014. PMID 9707591 DOI: 10.1073/Pnas.95.17.10009  0.417
1998 Czaplinski K, Ruiz-Echevarria MJ, Paushkin SV, Han X, Weng Y, Perlick HA, Dietz HC, Ter-Avanesyan MD, Peltz SW. The surveillance complex interacts with the translation release factors to enhance termination and degrade aberrant mRNAs. Genes & Development. 12: 1665-77. PMID 9620853 DOI: 10.1101/Gad.12.11.1665  0.421
1997 Montgomery RA, Dietz HC. Inhibition of fibrillin 1 expression using U1 snRNA as a vehicle for the presentation of antisense targeting sequence. Human Molecular Genetics. 6: 519-25. PMID 9097954 DOI: 10.1093/Hmg/6.4.519  0.312
1996 Jin Y, Dietz HC, Montgomery RA, Bell WR, McIntosh I, Coller B, Bray PF. Glanzmann thrombasthenia. Cooperation between sequence variants in cis during splice site selection. The Journal of Clinical Investigation. 98: 1745-54. PMID 8878424 DOI: 10.1172/Jci118973  0.326
1996 Perlick HA, Medghalchi SM, Spencer FA, Kendzior RJ, Dietz HC. Mammalian orthologues of a yeast regulator of nonsense transcript stability. Proceedings of the National Academy of Sciences of the United States of America. 93: 10928-32. PMID 8855285 DOI: 10.1073/Pnas.93.20.10928  0.425
1995 Eldadah ZA, Brenn T, Furthmayr H, Dietz HC. Expression of a mutant human fibrillin allele upon a normal human or murine genetic background recapitulates a Marfan cellular phenotype. The Journal of Clinical Investigation. 95: 874-80. PMID 7860770 DOI: 10.1172/Jci117737  0.314
1995 Dietz HC, Kendzior RJ. Maintenance of an open reading frame as an additional level of scrutiny during splice site selection. Nature Genetics. 8: 183-8. PMID 7842017 DOI: 10.1038/Ng1094-183  0.355
1993 Dietz HC, Valle D, Francomano CA, Kendzior RJ, Pyeritz RE, Cutting GR. The skipping of constitutive exons in vivo induced by nonsense mutations. Science (New York, N.Y.). 259: 680-3. PMID 8430317 DOI: 10.1126/Science.8430317  0.34
1993 Dietz HC, McIntosh I, Sakai LY, Corson GM, Chalberg SC, Pyeritz RE, Francomano CA. Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndrome. Genomics. 17: 468-75. PMID 8406497 DOI: 10.1006/Geno.1993.1349  0.346
1993 Dietz HC, Saraiva JM, Pyeritz RE, Cutting GR, Francomano CA. Clustering of fibrillin (FBN1) missense mutations in Marfan syndrome patients at cysteine residues in EGF-like domains. Human Mutation. 1: 366-74. PMID 1301946 DOI: 10.1002/Humu.1380010504  0.309
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