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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 17626896)

  • 1. Functional rescue of elastin insufficiency in mice by the human elastin gene: implications for mouse models of human disease.
    Hirano E; Knutsen RH; Sugitani H; Ciliberto CH; Mecham RP
    Circ Res; 2007 Aug; 101(5):523-31. PubMed ID: 17626896
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Alternative splicing and tissue-specific elastin misassembly act as biological modifiers of human elastin gene frameshift mutations associated with dominant cutis laxa.
    Sugitani H; Hirano E; Knutsen RH; Shifren A; Wagenseil JE; Ciliberto C; Kozel BA; Urban Z; Davis EC; Broekelmann TJ; Mecham RP
    J Biol Chem; 2012 Jun; 287(26):22055-67. PubMed ID: 22573328
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mechanisms of emphysema in autosomal dominant cutis laxa.
    Hu Q; Shifren A; Sens C; Choi J; Szabo Z; Starcher BC; Knutsen RH; Shipley JM; Davis EC; Mecham RP; Urban Z
    Matrix Biol; 2010 Sep; 29(7):621-8. PubMed ID: 20600892
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Elastin: mutational spectrum in supravalvular aortic stenosis.
    Metcalfe K; Rucka AK; Smoot L; Hofstadler G; Tuzler G; McKeown P; Siu V; Rauch A; Dean J; Dennis N; Ellis I; Reardon W; Cytrynbaum C; Osborne L; Yates JR; Read AP; Donnai D; Tassabehji M
    Eur J Hum Genet; 2000 Dec; 8(12):955-63. PubMed ID: 11175284
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel elastin gene mutation resulting in an autosomal dominant form of cutis laxa.
    Rodriguez-Revenga L; Iranzo P; Badenas C; Puig S; Carrió A; Milà M
    Arch Dermatol; 2004 Sep; 140(9):1135-9. PubMed ID: 15381555
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic aspects of supravalvular aortic stenosis.
    Morris CA
    Curr Opin Cardiol; 1998 May; 13(3):214-9. PubMed ID: 9649945
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel mutations in the human elastin gene (ELN) causing isolated supravalvular aortic stenosis.
    Park S; Seo EJ; Yoo HW; Kim Y
    Int J Mol Med; 2006 Aug; 18(2):329-32. PubMed ID: 16820942
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel arterial pathology in mice and humans hemizygous for elastin.
    Li DY; Faury G; Taylor DG; Davis EC; Boyle WA; Mecham RP; Stenzel P; Boak B; Keating MT
    J Clin Invest; 1998 Nov; 102(10):1783-7. PubMed ID: 9819363
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Elastin-driven genetic diseases.
    Duque Lasio ML; Kozel BA
    Matrix Biol; 2018 Oct; 71-72():144-160. PubMed ID: 29501665
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Role of elastin in the development of vascular function. Knock-out study of the elastin gene in mice].
    Faury G
    J Soc Biol; 2001; 195(2):151-6. PubMed ID: 11723827
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Elastoderma--disease of elastin accumulation within the skin.
    Kornberg RL; Hendler SS; Oikarinen AI; Matsuoka LY; Uitto J
    N Engl J Med; 1985 Mar; 312(12):771-4. PubMed ID: 3974652
    [No Abstract]   [Full Text] [Related]  

  • 12. Bouncing back from elastin deficiency.
    Ahmad PJ; Osborne LR; Bendeck MP
    Circ Res; 2007 Aug; 101(5):439-40. PubMed ID: 17761933
    [No Abstract]   [Full Text] [Related]  

  • 13. Granulocyte macrophage colony-stimulating factor deficiency affects vascular elastin production and integrity of elastic lamellae.
    Weissen-Plenz G; Eschert H; Volker W; Sindermann JR; Beissert S; Robenek H; Scheld HH; Breithardt G
    J Vasc Res; 2008; 45(2):103-10. PubMed ID: 17934321
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Conditional knockout mice to study alternative splicing in vivo.
    Xu X; Fu XD
    Methods; 2005 Dec; 37(4):387-92. PubMed ID: 16314268
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Aortic aneurysmal disease and cutis laxa caused by defects in the elastin gene.
    Szabo Z; Crepeau MW; Mitchell AL; Stephan MJ; Puntel RA; Yin Loke K; Kirk RC; Urban Z
    J Med Genet; 2006 Mar; 43(3):255-8. PubMed ID: 16085695
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Elastin is an essential determinant of arterial morphogenesis.
    Li DY; Brooke B; Davis EC; Mecham RP; Sorensen LK; Boak BB; Eichwald E; Keating MT
    Nature; 1998 May; 393(6682):276-80. PubMed ID: 9607766
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Elastin, arterial mechanics, and cardiovascular disease.
    Cocciolone AJ; Hawes JZ; Staiculescu MC; Johnson EO; Murshed M; Wagenseil JE
    Am J Physiol Heart Circ Physiol; 2018 Aug; 315(2):H189-H205. PubMed ID: 29631368
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital heart disease: Molecular diagnostics of supravalvular aortic stenosis.
    Tassabehji M; Urban Z
    Methods Mol Med; 2006; 126():129-56. PubMed ID: 16930010
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Macrovascular changes in mice overexpressing human semicarbazide-sensitive amine oxidase in smooth muscle cells.
    Gokturk C; Sugimoto H; Blomgren B; Roomans GM; Forsberg-Nilsson K; Oreland L; Sjoquist M
    Am J Hypertens; 2007 Jul; 20(7):743-50. PubMed ID: 17586408
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cutis laxa arising from frameshift mutations in exon 30 of the elastin gene (ELN).
    Zhang MC; He L; Giro M; Yong SL; Tiller GE; Davidson JM
    J Biol Chem; 1999 Jan; 274(2):981-6. PubMed ID: 9873040
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.