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PUBMED FOR HANDHELDS

Journal Abstract Search


226 related items for PubMed ID: 15557430

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  • 2. Expression of wild type and mutant ELOVL4 in cell culture: subcellular localization and cell viability.
    Karan G, Yang Z, Zhang K.
    Mol Vis; 2004 Mar 31; 10():248-53. PubMed ID: 15073583
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  • 3. Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein.
    Ambasudhan R, Wang X, Jablonski MM, Thompson DA, Lagali PS, Wong PW, Sieving PA, Ayyagari R.
    Genomics; 2004 Apr 31; 83(4):615-25. PubMed ID: 15028284
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  • 8. A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.
    Zhang K, Kniazeva M, Han M, Li W, Yu Z, Yang Z, Li Y, Metzker ML, Allikmets R, Zack DJ, Kakuk LE, Lagali PS, Wong PW, MacDonald IM, Sieving PA, Figueroa DJ, Austin CP, Gould RJ, Ayyagari R, Petrukhin K.
    Nat Genet; 2001 Jan 31; 27(1):89-93. PubMed ID: 11138005
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  • 9. Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4.
    Grayson C, Molday RS.
    J Biol Chem; 2005 Sep 16; 280(37):32521-30. PubMed ID: 16036915
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  • 11. [Comparative study of eukaryotic cell expression of wild-type and Pro370Leu mutation type myocilin gene].
    Wang JW, Sun HM, Ji J, Li XR, Zheng JQ.
    Zhonghua Yi Xue Za Zhi; 2006 Mar 14; 86(10):700-4. PubMed ID: 16681932
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  • 12. Mutant ELOVL4 that causes autosomal dominant stargardt-3 macular dystrophy is misrouted to rod outer segment disks.
    Agbaga MP, Tam BM, Wong JS, Yang LL, Anderson RE, Moritz OL.
    Invest Ophthalmol Vis Sci; 2014 May 15; 55(6):3669-80. PubMed ID: 24833735
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  • 16. Dominant-negative effects of episodic ataxia type 2 mutations involve disruption of membrane trafficking of human P/Q-type Ca2+ channels.
    Jeng CJ, Sun MC, Chen YW, Tang CY.
    J Cell Physiol; 2008 Feb 15; 214(2):422-33. PubMed ID: 17654512
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  • 18. Dominant Stargardt Macular Dystrophy (STGD3) and ELOVL4.
    Logan S, Anderson RE.
    Adv Exp Med Biol; 2014 Feb 15; 801():447-53. PubMed ID: 24664730
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