BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

188 related articles for article (PubMed ID: 34570228)

  • 1. A dominant-negative SOX18 mutant disrupts multiple regulatory layers essential to transcription factor activity.
    McCann AJ; Lou J; Moustaqil M; Graus MS; Blum A; Fontaine F; Liu H; Luu W; Rudolffi-Soto P; Koopman P; Sierecki E; Gambin Y; Meunier FA; Liu Z; Hinde E; Francois M
    Nucleic Acids Res; 2021 Nov; 49(19):10931-10955. PubMed ID: 34570228
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Further delineation of the SOX18-related Hypotrichosis, Lymphedema, Telangiectasia syndrome (HTLS).
    Valenzuela I; Fernández-Alvarez P; Plaja A; Ariceta G; Sabaté-Rotés A; García-Arumí E; Vendrell T; Tizzano E
    Eur J Med Genet; 2018 May; 61(5):269-272. PubMed ID: 29307792
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Vascular defects in a mouse model of hypotrichosis-lymphedema-telangiectasia syndrome indicate a role for SOX18 in blood vessel maturation.
    Downes M; François M; Ferguson C; Parton RG; Koopman P
    Hum Mol Genet; 2009 Aug; 18(15):2839-50. PubMed ID: 19429912
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel autosomal dominant mutation in SOX18 resulting in a fatal case of hypotrichosis-lymphedema-telangiectasia syndrome.
    Wangberg H; Wigby K; Jones MC
    Am J Med Genet A; 2018 Dec; 176(12):2824-2828. PubMed ID: 30549413
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.
    Wünnemann F; Kokta V; Leclerc S; Thibeault M; McCuaig C; Hatami A; Stheneur C; Grenier JC; Awadalla P; Mitchell GA; Andelfinger G; Preuss C
    Can J Cardiol; 2016 Jan; 32(1):135.e1-7. PubMed ID: 26148450
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia.
    Irrthum A; Devriendt K; Chitayat D; Matthijs G; Glade C; Steijlen PM; Fryns JP; Van Steensel MA; Vikkula M
    Am J Hum Genet; 2003 Jun; 72(6):1470-8. PubMed ID: 12740761
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene.
    Moalem S; Brouillard P; Kuypers D; Legius E; Harvey E; Taylor G; Francois M; Vikkula M; Chitayat D
    Clin Genet; 2015 Apr; 87(4):378-82. PubMed ID: 24697860
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Arap3 is dysregulated in a mouse model of hypotrichosis-lymphedema-telangiectasia and regulates lymphatic vascular development.
    Kartopawiro J; Bower NI; Karnezis T; Kazenwadel J; Betterman KL; Lesieur E; Koltowska K; Astin J; Crosier P; Vermeren S; Achen MG; Stacker SA; Smith KA; Harvey NL; François M; Hogan BM
    Hum Mol Genet; 2014 Mar; 23(5):1286-97. PubMed ID: 24163130
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sox7 and Sox17 are strain-specific modifiers of the lymphangiogenic defects caused by Sox18 dysfunction in mice.
    Hosking B; François M; Wilhelm D; Orsenigo F; Caprini A; Svingen T; Tutt D; Davidson T; Browne C; Dejana E; Koopman P
    Development; 2009 Jul; 136(14):2385-91. PubMed ID: 19515696
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypotrichosis-lymphedema-telangiectasia syndrome: Report of ileal atresia associated with a SOX18 de novo pathogenic variant and review of the phenotypic spectrum.
    Coulie R; Niyazov DM; Gambello MJ; Fastré E; Brouillard P; Vikkula M
    Am J Med Genet A; 2021 Jul; 185(7):2153-2159. PubMed ID: 33851505
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Expanding the clinical spectrum of SOX18-related Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome.
    Dailey C; Oshodi RB; Boull C; Aggarwal A
    Eur J Med Genet; 2022 Nov; 65(11):104607. PubMed ID: 36096470
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis-lymphedema-telangiectasia syndrome by Whole Exome Sequencing.
    Bastaki F; Mohamed M; Nair P; Saif F; Tawfiq N; Al-Ali MT; Brandau O; Hamzeh AR
    Mol Cell Probes; 2016 Feb; 30(1):18-21. PubMed ID: 26631803
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The VCAM-1 gene that encodes the vascular cell adhesion molecule is a target of the Sry-related high mobility group box gene, Sox18.
    Hosking BM; Wang SC; Downes M; Koopman P; Muscat GE
    J Biol Chem; 2004 Feb; 279(7):5314-22. PubMed ID: 14634005
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sox18 induces development of the lymphatic vasculature in mice.
    François M; Caprini A; Hosking B; Orsenigo F; Wilhelm D; Browne C; Paavonen K; Karnezis T; Shayan R; Downes M; Davidson T; Tutt D; Cheah KS; Stacker SA; Muscat GE; Achen MG; Dejana E; Koopman P
    Nature; 2008 Dec; 456(7222):643-7. PubMed ID: 18931657
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Construction and functional analysis of novel dominant-negative mutant of human SOX18 protein.
    Milivojevic M; Petrovic I; Kovacevic-Grujicic N; Popovic J; Mojsin M; Stevanovic M
    Biochemistry (Mosc); 2013 Nov; 78(11):1287-92. PubMed ID: 24460943
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Sox18 and Sox7 play redundant roles in vascular development.
    Cermenati S; Moleri S; Cimbro S; Corti P; Del Giacco L; Amodeo R; Dejana E; Koopman P; Cotelli F; Beltrame M
    Blood; 2008 Mar; 111(5):2657-66. PubMed ID: 18094332
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sox18 genetically interacts with VegfC to regulate lymphangiogenesis in zebrafish.
    Cermenati S; Moleri S; Neyt C; Bresciani E; Carra S; Grassini DR; Omini A; Goi M; Cotelli F; François M; Hogan BM; Beltrame M
    Arterioscler Thromb Vasc Biol; 2013 Jun; 33(6):1238-47. PubMed ID: 23520166
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sox18 mutations in the ragged mouse alleles ragged-like and opossum.
    James K; Hosking B; Gardner J; Muscat GE; Koopman P
    Genesis; 2003 May; 36(1):1-6. PubMed ID: 12748961
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytoplasmic plaque formation in hemidesmosome development is dependent on SoxF transcription factor function.
    Oommen S; Francois M; Kawasaki M; Murrell M; Kawasaki K; Porntaveetus T; Ghafoor S; Young NJ; Okamatsu Y; McGrath J; Koopman P; Sharpe PT; Ohazama A
    PLoS One; 2012; 7(9):e43857. PubMed ID: 22962592
    [TBL] [Abstract][Full Text] [Related]  

  • 20. R-propranolol is a small molecule inhibitor of the SOX18 transcription factor in a rare vascular syndrome and hemangioma.
    Overman J; Fontaine F; Wylie-Sears J; Moustaqil M; Huang L; Meurer M; Chiang IK; Lesieur E; Patel J; Zuegg J; Pasquier E; Sierecki E; Gambin Y; Hamdan M; Khosrotehrani K; Andelfinger G; Bischoff J; Francois M
    Elife; 2019 Jul; 8():. PubMed ID: 31358114
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.