Papers authored by Curran SP

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Allelic Depletion of grem1 Attenuates Diabetic Kidney Disease.
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Roxburgh SA, Kattla JJ, Curran SP, O'Meara YM, Pollock CA, Goldschmeding R, Godson C, Martin F, and Brazil DP
Diabetes 58(7):1641-50, 2009 Jul - Who cited this? | PubMed ID: 19401426 | Fulltext
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A soma-to-germline transformation in long-lived Caenorhabditis elegans mutants.
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Curran SP, Wu X, Riedel CG, and Ruvkun G
Nature 459(7250):1079-84, 2009 Jun 25 - Who cited this? | PubMed ID: 19506556 | Fulltext
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Lifespan regulation by evolutionarily conserved genes essential for viability.
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Curran SP and Ruvkun G
PLoS genetics 3(4), 2007 Apr 6 - Who cited this? | PubMed ID: 17411345 | Fulltext
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Patterns that define the four domains conserved in known and novel isoforms of the protein import receptor Tom20.
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Likić VA, Perry A, Hulett J, Derby M, Traven A, Waller RF, Keeling PJ, Koehler CM, Curran SP, Gooley PR, and Lithgow T
Journal of molecular biology 347(1):81-93, 2005 Mar 18 - Who cited this? | PubMed ID: 15733919 | Fulltext
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Defective mitochondrial protein translocation precludes normal Caenorhabditis elegans development.
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Curran SP, Leverich EP, Koehler CM, and Larsen PL
The Journal of biological chemistry 279(52):54655-62, 2004 Dec 24 - Who cited this? | PubMed ID: 15485840 | Fulltext
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The role of Hot13p and redox chemistry in the mitochondrial TIM22 import pathway.
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Curran SP, Leuenberger D, Leverich EP, Hwang DK, Beverly KN, and Koehler CM
The Journal of biological chemistry 279(42):43744-51, 2004 Oct 15 - Who cited this? | PubMed ID: 15294910 | Fulltext
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The role of Tim9p in the assembly of the TIM22 import complexes.
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Leuenberger D, Curran SP, Wong D, and Koehler CM
Traffic (Copenhagen, Denmark) 4(3):144-52, 2003 Mar - Who cited this? | PubMed ID: 12656987 | Fulltext
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The role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteins.
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Curran SP, Leuenberger D, Schmidt E, and Koehler CM
The Journal of cell biology 158(6):1017-27, 2002 Sep 16 - Who cited this? | PubMed ID: 12221072 | Fulltext
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Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex.
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Roesch K, Curran SP, Tranebjaerg L, and Koehler CM
Human molecular genetics 11(5):477, 2002 Mar 1 - Who cited this? | PubMed ID: 11875042 | Fulltext
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The Tim9p-Tim10p complex binds to the transmembrane domains of the ADP/ATP carrier.
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Curran SP, Leuenberger D, Oppliger W, and Koehler CM
The EMBO journal 21(5):942-53, 2002 Mar 1 - Who cited this? | PubMed ID: 11867522 | Fulltext
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The essential function of the small Tim proteins in the TIM22 import pathway does not depend on formation of the soluble 70-kilodalton complex.
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Murphy MP, Leuenberger D, Curran SP, Oppliger W, and Koehler CM
Molecular and cellular biology 21(18):6132-8, 2001 Sep - Who cited this? | PubMed ID: 11509656 | Fulltext
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