BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 11073717)

  • 1. Genomic organization, expression, and alternate splicing of the mouse fatty aldehyde dehydrogenase gene.
    Lin Z; Carney G; Rizzo WB
    Mol Genet Metab; 2000 Nov; 71(3):496-505. PubMed ID: 11073717
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sjögren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2).
    Rizzo WB; Carney G
    Hum Mutat; 2005 Jul; 26(1):1-10. PubMed ID: 15931689
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Restoration of fatty aldehyde dehydrogenase deficiency in Sjögren-Larsson syndrome.
    Haug S; Braun-Falco M
    Gene Ther; 2006 Jul; 13(13):1021-6. PubMed ID: 16525484
    [TBL] [Abstract][Full Text] [Related]  

  • 4. RNA-based mutation screening in German families with Sjögren-Larsson syndrome.
    Kraus C; Braun-Quentin C; Ballhausen WG; Pfeiffer RA
    Eur J Hum Genet; 2000 Apr; 8(4):299-306. PubMed ID: 10854114
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genomic organization and tissue-specific expression of splice variants of mouse organic anion transporting polypeptide 2.
    Ogura K; Choudhuri S; Klaassen CD
    Biochem Biophys Res Commun; 2001 Feb; 281(2):431-9. PubMed ID: 11181066
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene.
    De Laurenzi V; Rogers GR; Hamrock DJ; Marekov LN; Steinert PM; Compton JG; Markova N; Rizzo WB
    Nat Genet; 1996 Jan; 12(1):52-7. PubMed ID: 8528251
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fatty aldehyde dehydrogenase: genomic structure, expression and mutation analysis in Sjögren-Larsson syndrome.
    Rizzo WB; Lin Z; Carney G
    Chem Biol Interact; 2001 Jan; 130-132(1-3):297-307. PubMed ID: 11306053
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of the human aldehyde reductase gene and promoter.
    Barski OA; Gabbay KH; Bohren KM
    Genomics; 1999 Sep; 60(2):188-98. PubMed ID: 10486210
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic organization and expression of the human fatty aldehyde dehydrogenase gene (FALDH).
    Rogers GR; Markova NG; De Laurenzi V; Rizzo WB; Compton JG
    Genomics; 1997 Jan; 39(2):127-35. PubMed ID: 9027499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An Indian family with Sjögren-Larsson syndrome caused by a novel ALDH3A2 mutation.
    Sakai K; Akiyama M; Yanagi T; Nampoothiri S; Mampilly T; Sunitha V; Shimizu H
    Int J Dermatol; 2010 Sep; 49(9):1031-3. PubMed ID: 20883264
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Human fatty aldehyde dehydrogenase gene (ALDH10): organization and tissue-dependent expression.
    Chang C; Yoshida A
    Genomics; 1997 Feb; 40(1):80-5. PubMed ID: 9070922
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genomic organization and promoter analysis of the mouse ADP-ribosylarginine hydrolase gene.
    Aoki K; Kato J; Shoemaker MT; Moss J
    Gene; 2005 May; 351():83-95. PubMed ID: 15893437
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Adeno-associated virus vectors are able to restore fatty aldehyde dehydrogenase-deficiency. Implications for gene therapy in Sjogren-Larsson syndrome.
    Haug S; Braun-Falco M
    Arch Dermatol Res; 2005 Jun; 296(12):568-72. PubMed ID: 15834613
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structural organization of the human complexin 2 gene (CPLX2) and aspects of its functional activity.
    Raevskaya NM; Dergunova LV; Vladychenskaya IP; Stavchansky VV; Oborina MV; Poltaraus AB; Limborska SA
    Gene; 2005 Oct; 359():127-37. PubMed ID: 16162394
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genomic organization and structure of the 5'-flanking region of the TEX101 gene: alternative promoter usage and splicing generate transcript variants with distinct 5'-untranslated region.
    Tsukamoto H; Takizawa T; Takamori K; Ogawa H; Araki Y
    Mol Reprod Dev; 2007 Feb; 74(2):154-62. PubMed ID: 16941676
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sjögren-Larsson syndrome: seven novel mutations in the fatty aldehyde dehydrogenase gene ALDH3A2.
    Carney G; Wei S; Rizzo WB
    Hum Mutat; 2004 Aug; 24(2):186. PubMed ID: 15241804
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Human transcription factor Sp3: genomic structure, identification of a processed pseudogene, and transcript analysis.
    Moran KM; Crusio RH; Chan CH; Grekova MC; Richert JR
    Gene; 2004 Oct; 341():235-47. PubMed ID: 15474306
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene structure and expression of the mouse dyskeratosis congenita gene, dkc1.
    Heiss NS; Bächner D; Salowsky R; Kolb A; Kioschis P; Poustka A
    Genomics; 2000 Jul; 67(2):153-63. PubMed ID: 10903840
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The molecular basis of Sjögren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase gene.
    Rizzo WB; Carney G; Lin Z
    Am J Hum Genet; 1999 Dec; 65(6):1547-60. PubMed ID: 10577908
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular cloning, genomic structure, and expression analysis of the mouse transcriptional intermediary factor 1 gamma gene.
    Yan KP; Dollé P; Mark M; Lerouge T; Wendling O; Chambon P; Losson R
    Gene; 2004 Jun; 334():3-13. PubMed ID: 15256250
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.