These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
449 related items for PubMed ID: 7790377
1. Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders. Wiemer EA, Nuttley WM, Bertolaet BL, Li X, Francke U, Wheelock MJ, Anné UK, Johnson KR, Subramani S. J Cell Biol; 1995 Jul; 130(1):51-65. PubMed ID: 7790377 [Abstract] [Full Text] [Related]
2. The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells--the PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family. McCollum D, Monosov E, Subramani S. J Cell Biol; 1993 May; 121(4):761-74. PubMed ID: 8098333 [Abstract] [Full Text] [Related]
3. Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders. Slawecki ML, Dodt G, Steinberg S, Moser AB, Moser HW, Gould SJ. J Cell Sci; 1995 May; 108 ( Pt 5)():1817-29. PubMed ID: 7544797 [Abstract] [Full Text] [Related]
4. Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants. Otera H, Okumoto K, Tateishi K, Ikoma Y, Matsuda E, Nishimura M, Tsukamoto T, Osumi T, Ohashi K, Higuchi O, Fujiki Y. Mol Cell Biol; 1998 Jan; 18(1):388-99. PubMed ID: 9418886 [Abstract] [Full Text] [Related]
5. Abnormality in catalase import into peroxisomes leads to severe neurological disorder. Sheikh FG, Pahan K, Khan M, Barbosa E, Singh I. Proc Natl Acad Sci U S A; 1998 Mar 17; 95(6):2961-6. PubMed ID: 9501198 [Abstract] [Full Text] [Related]
6. An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes. Braverman N, Dodt G, Gould SJ, Valle D. Hum Mol Genet; 1998 Aug 17; 7(8):1195-205. PubMed ID: 9668159 [Abstract] [Full Text] [Related]
7. PER3, a gene required for peroxisome biogenesis in Pichia pastoris, encodes a peroxisomal membrane protein involved in protein import. Liu H, Tan X, Russell KA, Veenhuis M, Cregg JM. J Biol Chem; 1995 May 05; 270(18):10940-51. PubMed ID: 7738036 [Abstract] [Full Text] [Related]
8. Involvement of Pex13p in Pex14p localization and peroxisomal targeting signal 2-dependent protein import into peroxisomes. Girzalsky W, Rehling P, Stein K, Kipper J, Blank L, Kunau WH, Erdmann R. J Cell Biol; 1999 Mar 22; 144(6):1151-62. PubMed ID: 10087260 [Abstract] [Full Text] [Related]
9. Convergence of model systems for peroxisome biogenesis. Subramani S. Curr Opin Cell Biol; 1996 Aug 22; 8(4):513-8. PubMed ID: 8791450 [Abstract] [Full Text] [Related]
10. A mobile PTS2 receptor for peroxisomal protein import in Pichia pastoris. Elgersma Y, Elgersma-Hooisma M, Wenzel T, McCaffery JM, Farquhar MG, Subramani S. J Cell Biol; 1998 Feb 23; 140(4):807-20. PubMed ID: 9472033 [Abstract] [Full Text] [Related]
11. The Pichia pastoris peroxisomal protein PAS8p is the receptor for the C-terminal tripeptide peroxisomal targeting signal. Terlecky SR, Nuttley WM, McCollum D, Sock E, Subramani S. EMBO J; 1995 Aug 01; 14(15):3627-34. PubMed ID: 7641682 [Abstract] [Full Text] [Related]
12. Identification of a human PTS1 receptor docking protein directly required for peroxisomal protein import. Fransen M, Terlecky SR, Subramani S. Proc Natl Acad Sci U S A; 1998 Jul 07; 95(14):8087-92. PubMed ID: 9653144 [Abstract] [Full Text] [Related]
13. The plant PTS1 receptor: similarities and differences to its human and yeast counterparts. Wimmer C, Schmid M, Veenhuis M, Gietl C. Plant J; 1998 Nov 07; 16(4):453-64. PubMed ID: 9881165 [Abstract] [Full Text] [Related]
14. The ubiquitin-conjugating enzyme Pex4p of Hansenula polymorpha is required for efficient functioning of the PTS1 import machinery. van der Klei IJ, Hilbrands RE, Kiel JA, Rasmussen SW, Cregg JM, Veenhuis M. EMBO J; 1998 Jul 01; 17(13):3608-18. PubMed ID: 9649431 [Abstract] [Full Text] [Related]
15. Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders. Wendland M, Subramani S. J Clin Invest; 1993 Nov 01; 92(5):2462-8. PubMed ID: 7693762 [Abstract] [Full Text] [Related]
16. Disruption of the interaction of the longer isoform of Pex5p, Pex5pL, with Pex7p abolishes peroxisome targeting signal type 2 protein import in mammals. Study with a novel Pex5-impaired Chinese hamster ovary cell mutant. Matsumura T, Otera H, Fujiki Y. J Biol Chem; 2000 Jul 14; 275(28):21715-21. PubMed ID: 10767287 [Abstract] [Full Text] [Related]
17. Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders. Dodt G, Braverman N, Wong C, Moser A, Moser HW, Watkins P, Valle D, Gould SJ. Nat Genet; 1995 Feb 14; 9(2):115-25. PubMed ID: 7719337 [Abstract] [Full Text] [Related]
18. The SH3 domain of the Saccharomyces cerevisiae peroxisomal membrane protein Pex13p functions as a docking site for Pex5p, a mobile receptor for the import PTS1-containing proteins. Elgersma Y, Kwast L, Klein A, Voorn-Brouwer T, van den Berg M, Metzig B, America T, Tabak HF, Distel B. J Cell Biol; 1996 Oct 14; 135(1):97-109. PubMed ID: 8858166 [Abstract] [Full Text] [Related]
19. Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor. Gould SJ, Kalish JE, Morrell JC, Bjorkman J, Urquhart AJ, Crane DI. J Cell Biol; 1996 Oct 14; 135(1):85-95. PubMed ID: 8858165 [Abstract] [Full Text] [Related]
20. Identification of Pex13p a peroxisomal membrane receptor for the PTS1 recognition factor. Erdmann R, Blobel G. J Cell Biol; 1996 Oct 14; 135(1):111-21. PubMed ID: 8858167 [Abstract] [Full Text] [Related] Page: [Next] [New Search]