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Journal Abstract Search

224 related items for PubMed ID: 15333588

  • 1. A molecular pathogenesis for transcription factor associated poly-alanine tract expansions.
    Albrecht AN, Kornak U, Böddrich A, Süring K, Robinson PN, Stiege AC, Lurz R, Stricker S, Wanker EE, Mundlos S.
    Hum Mol Genet; 2004 Oct 15; 13(20):2351-9. PubMed ID: 15333588
    [Abstract] [Full Text] [Related]

  • 2. A recurrent polyalanine expansion in the transcription factor FOXL2 induces extensive nuclear and cytoplasmic protein aggregation.
    Caburet S, Demarez A, Moumné L, Fellous M, De Baere E, Veitia RA.
    J Med Genet; 2004 Dec 15; 41(12):932-6. PubMed ID: 15591279
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  • 3. A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?
    Utsch B, Becker K, Brock D, Lentze MJ, Bidlingmaier F, Ludwig M.
    Hum Genet; 2002 May 15; 110(5):488-94. PubMed ID: 12073020
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  • 4. The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes.
    Bruneau S, Johnson KR, Yamamoto M, Kuroiwa A, Duboule D.
    Dev Biol; 2001 Sep 15; 237(2):345-53. PubMed ID: 11543619
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  • 5. [HOXD13 polyalanine tract expansion in synpolydactyly: mutation detection and prenatal diagnosis in a large Chinese family].
    Zhao XL, Meng JP, Sun M, Ao Y, Wu AH, Lo HY, Zhang X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb 15; 22(1):5-9. PubMed ID: 15696469
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  • 7. Induction of expression and co-localization of heat shock polypeptides with the polyalanine expansion mutant of poly(A)-binding protein N1 after chemical stress.
    Wang Q, Bag J.
    Biochem Biophys Res Commun; 2008 May 23; 370(1):11-5. PubMed ID: 18343218
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  • 9. Shh, Fgf4 and Hoxd gene expression in the mouse limb mutant hypodactyly.
    Robertson KE, Tickle C, Darling SM.
    Int J Dev Biol; 1997 Oct 23; 41(5):733-6. PubMed ID: 9415493
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  • 10. Polyalanine repeat expansion mutations in the HOXD13 gene in Pakistani families with synpolydactyly.
    Wajid M, Ishii Y, Kurban M, Dua-Awereh MB, Shimomura Y, Christiano AM.
    Clin Genet; 2009 Sep 23; 76(3):300-2. PubMed ID: 19686284
    [No Abstract] [Full Text] [Related]

  • 11. Polyalanine expansion mutations in the X-linked hypopituitarism gene SOX3 result in aggresome formation and impaired transactivation.
    Wong J, Farlie P, Holbert S, Lockhart P, Thomas PQ.
    Front Biosci; 2007 Jan 01; 12():2085-95. PubMed ID: 17127446
    [Abstract] [Full Text] [Related]

  • 12. Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophy.
    Abu-Baker A, Messaed C, Laganiere J, Gaspar C, Brais B, Rouleau GA.
    Hum Mol Genet; 2003 Oct 15; 12(20):2609-23. PubMed ID: 12944420
    [Abstract] [Full Text] [Related]

  • 13. Inactivating Pit-1 mutations alter subnuclear dynamics suggesting a protein misfolding and nuclear stress response.
    Sharp ZD, Stenoien DL, Mancini MG, Ouspenski II, Mancini MA.
    J Cell Biochem; 2004 Jul 01; 92(4):664-78. PubMed ID: 15211565
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  • 15. HOXD13 polyalanine tract expansion in classical synpolydactyly type Vordingborg.
    Kjaer KW, Hedeboe J, Bugge M, Hansen C, Friis-Henriksen K, Vestergaard MB, Tommerup N, Opitz JM.
    Am J Med Genet; 2002 Jun 15; 110(2):116-21. PubMed ID: 12116248
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  • 16. Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism induced by polyalanine expansion mutations associated with congenital central hypoventilation syndrome.
    Di Lascio S, Bachetti T, Saba E, Ceccherini I, Benfante R, Fornasari D.
    Neurobiol Dis; 2013 Feb 15; 50():187-200. PubMed ID: 23103552
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  • 18. Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion.
    Horsnell K, Ali M, Malik S, Wilson L, Hall C, Debeer P, Crow Y.
    Eur J Med Genet; 2006 Feb 15; 49(5):396-401. PubMed ID: 16497573
    [Abstract] [Full Text] [Related]

  • 19. Heat shock transcription factor (Hsf)-4b recruits Brg1 during the G1 phase of the cell cycle and regulates the expression of heat shock proteins.
    Tu N, Hu Y, Mivechi NF.
    J Cell Biochem; 2006 Aug 15; 98(6):1528-42. PubMed ID: 16552721
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