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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2005 | 1 |
2007 | 2 |
2009 | 1 |
2024 | 0 |
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A porphomethene inhibitor of uroporphyrinogen decarboxylase causes porphyria cutanea tarda.
Proc Natl Acad Sci U S A. 2007 Mar 20;104(12):5079-84. doi: 10.1073/pnas.0700547104. Epub 2007 Mar 9.
Proc Natl Acad Sci U S A. 2007.
PMID: 17360334
Free PMC article.
Substrate shuttling between active sites of uroporphyrinogen decarboxylase is not required to generate coproporphyrinogen.
Phillips JD, Warby CA, Whitby FG, Kushner JP, Hill CP.
Phillips JD, et al.
J Mol Biol. 2009 Jun 5;389(2):306-14. doi: 10.1016/j.jmb.2009.04.013. Epub 2009 Apr 10.
J Mol Biol. 2009.
PMID: 19362562
Free PMC article.
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Two novel uroporphyrinogen decarboxylase (URO-D) mutations causing hepatoerythropoietic porphyria (HEP).
Phillips JD, Whitby FG, Stadtmueller BM, Edwards CQ, Hill CP, Kushner JP.
Phillips JD, et al.
Transl Res. 2007 Feb;149(2):85-91. doi: 10.1016/j.trsl.2006.08.006.
Transl Res. 2007.
PMID: 17240319
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Identification of a novel mutation in the L-ferritin IRE leading to hereditary hyperferritinemia-cataract syndrome.
Phillips JD, Warby CA, Kushner JP.
Phillips JD, et al.
Am J Med Genet A. 2005 Apr 1;134A(1):77-9. doi: 10.1002/ajmg.a.30425.
Am J Med Genet A. 2005.
PMID: 15690351
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