BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

477 related articles for article (PubMed ID: 16085695)

  • 21. 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]  

  • 22. Autosomal dominant cutis laxa with severe lung disease: synthesis and matrix deposition of mutant tropoelastin.
    Urban Z; Gao J; Pope FM; Davis EC
    J Invest Dermatol; 2005 Jun; 124(6):1193-9. PubMed ID: 15955094
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Homozygous missense mutation in fibulin-5 in an Iranian autosomal recessive cutis laxa pedigree and associated haplotype.
    Elahi E; Kalhor R; Banihosseini SS; Torabi N; Pour-Jafari H; Houshmand M; Amini SS; Ramezani A; Loeys B
    J Invest Dermatol; 2006 Jul; 126(7):1506-9. PubMed ID: 16691202
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity.
    Hadj-Rabia S; Callewaert BL; Bourrat E; Kempers M; Plomp AS; Layet V; Bartholdi D; Renard M; De Backer J; Malfait F; Vanakker OM; Coucke PJ; De Paepe AM; Bodemer C
    Orphanet J Rare Dis; 2013 Feb; 8():36. PubMed ID: 23442826
    [TBL] [Abstract][Full Text] [Related]  

  • 25. No mutation of elastin and fibulin-5 genes in a patient with acquired cutis laxa associated with chronic urticaria.
    Sun XK; Chen JF
    Br J Dermatol; 2011 Jan; 164(1):215-7. PubMed ID: 20849517
    [No Abstract]   [Full Text] [Related]  

  • 26. 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]  

  • 27. Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa.
    Loeys B; Van Maldergem L; Mortier G; Coucke P; Gerniers S; Naeyaert JM; De Paepe A
    Hum Mol Genet; 2002 Sep; 11(18):2113-8. PubMed ID: 12189163
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Autosomal recessive cutis laxa syndrome revisited.
    Morava E; Guillard M; Lefeber DJ; Wevers RA
    Eur J Hum Genet; 2009 Sep; 17(9):1099-110. PubMed ID: 19401719
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fibulin-4: a novel gene for an autosomal recessive cutis laxa syndrome.
    Hucthagowder V; Sausgruber N; Kim KH; Angle B; Marmorstein LY; Urban Z
    Am J Hum Genet; 2006 Jun; 78(6):1075-80. PubMed ID: 16685658
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Elastin production and degradation in cutis laxa acquisita.
    Fornieri C; Quaglino D; Lungarella G; Cavarra E; Tiozzo R; Giro MG; Canciani M; Davidson JM; Ronchetti IP
    J Invest Dermatol; 1994 Oct; 103(4):583-8. PubMed ID: 7930686
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Altered TGFbeta signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency.
    Renard M; Holm T; Veith R; Callewaert BL; Adès LC; Baspinar O; Pickart A; Dasouki M; Hoyer J; Rauch A; Trapane P; Earing MG; Coucke PJ; Sakai LY; Dietz HC; De Paepe AM; Loeys BL
    Eur J Hum Genet; 2010 Aug; 18(8):895-901. PubMed ID: 20389311
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of a de novo mutation of the elastin gene by targeted exome sequencing in autosomal dominant cutis laxa.
    Makino T; Terada Y; Mizawa M; Hirono K; Adachi Y; Aoki S; Kubo A; Shimizu T
    Clin Exp Dermatol; 2022 Oct; 47(10):1895-1897. PubMed ID: 36002914
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa.
    Dasouki M; Markova D; Garola R; Sasaki T; Charbonneau NL; Sakai LY; Chu ML
    Am J Med Genet A; 2007 Nov; 143A(22):2635-41. PubMed ID: 17937443
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cutis laxa in hereditary gelsolin amyloidosis.
    Kiuru-Enari S; Keski-Oja J; Haltia M
    Br J Dermatol; 2005 Feb; 152(2):250-7. PubMed ID: 15727635
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Autosomal recessive form of congenital cutis laxa: more than the clinical appearance.
    Andiran N; Sarikayalar F; Saraçlar M; Cağlar M
    Pediatr Dermatol; 2002; 19(5):412-4. PubMed ID: 12383097
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Autosomal dominant cutis laxa and critical stenosis of the left main coronary artery in a 21-year-old female with an intronic mutation in the elastin gene.
    Krarup NT; Hvidbjerg M; Zaremba T; Sommerlund M; Christensen MK
    Am J Med Genet A; 2023 Apr; 191(4):1059-1064. PubMed ID: 36541930
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Cutis laxa. Classification, clinical aspects and molecular defects].
    Mensing H; Krieg T; Meigel W; Braun-Falco O
    Hautarzt; 1984 Oct; 35(10):506-11. PubMed ID: 6500933
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families.
    McKenzie F; Mina K; Callewaert B; Beyens A; Dickinson JE; Jevon G; Papadimitriou J; Diness BR; Steensberg JN; Ek J; Baynam G
    Clin Genet; 2021 Aug; 100(2):168-175. PubMed ID: 33866545
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Abnormalities of fibrillin in acquired cutis laxa.
    Lebwohl MG; Schwartz E; Jacobs L; Lebwohl M; Sakai L; Fleischmajer R
    J Am Acad Dermatol; 1994 Jun; 30(6):950-4. PubMed ID: 8188885
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 24.