BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 38013159)

  • 1. Characterization of Patient-Derived GNAQ Mutated Endothelial Cells from Capillary Malformations.
    Langbroek GB; Stor MLE; Janssen V; de Haan A; Horbach SER; Graupera M; van Noesel CJM; van der Horst CMAM; Wolkerstorfer A; Huveneers S
    J Invest Dermatol; 2024 Jun; 144(6):1378-1388.e1. PubMed ID: 38013159
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Somatic GNAQ mutation in different structures of port-wine macrocheilia.
    Ma G; Yu Z; Liu F; Wang L; Yu W; Zhu J; Gu H; Liu Y; Cai R; Lin X
    Br J Dermatol; 2018 Nov; 179(5):1109-1114. PubMed ID: 29878304
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic association of presence of a somatic GNAQ mutation with port-wine stain distribution in capillary malformation.
    Lee KT; Park JE; Eom Y; Lim HS; Ki CS; Lim SY
    Head Neck; 2019 Dec; 41(12):4143-4150. PubMed ID: 31532024
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel somatic mutation in GNAQ in a capillary malformation provides insight into molecular pathogenesis.
    Galeffi F; Snellings DA; Wetzel-Strong SE; Kastelic N; Bullock J; Gallione CJ; North PE; Marchuk DA
    Angiogenesis; 2022 Nov; 25(4):493-502. PubMed ID: 35635655
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Capillary malformation in the midline of the face: Salmon patch or port-wine stain?
    Cai R; Liu F; Cen Q; Yu W; Gong X; Liu Y; Hu X; Ma G; Lin X
    J Dermatol; 2018 Nov; 45(11):e317-e319. PubMed ID: 29722431
    [No Abstract]   [Full Text] [Related]  

  • 6. Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ.
    Shirley MD; Tang H; Gallione CJ; Baugher JD; Frelin LP; Cohen B; North PE; Marchuk DA; Comi AM; Pevsner J
    N Engl J Med; 2013 May; 368(21):1971-9. PubMed ID: 23656586
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Somatic GNAQ Mutation is Enriched in Brain Endothelial Cells in Sturge-Weber Syndrome.
    Huang L; Couto JA; Pinto A; Alexandrescu S; Madsen JR; Greene AK; Sahin M; Bischoff J
    Pediatr Neurol; 2017 Feb; 67():59-63. PubMed ID: 27919468
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Endothelial Cells from Capillary Malformations Are Enriched for Somatic GNAQ Mutations.
    Couto JA; Huang L; Vivero MP; Kamitaki N; Maclellan RA; Mulliken JB; Bischoff J; Warman ML; Greene AK
    Plast Reconstr Surg; 2016 Jan; 137(1):77e-82e. PubMed ID: 26368330
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The somatic GNAQ mutation c.548G>A (p.R183Q) is consistently found in Sturge-Weber syndrome.
    Nakashima M; Miyajima M; Sugano H; Iimura Y; Kato M; Tsurusaki Y; Miyake N; Saitsu H; Arai H; Matsumoto N
    J Hum Genet; 2014 Dec; 59(12):691-3. PubMed ID: 25374402
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MRC1 and LYVE1 expressing macrophages in vascular beds of GNAQ p.R183Q driven capillary malformations in Sturge Weber syndrome.
    Nasim S; Bichsel C; Dayneka S; Mannix R; Holm A; Vivero M; Alexandrescu S; Pinto A; Greene AK; Ingber DE; Bischoff J
    Acta Neuropathol Commun; 2024 Mar; 12(1):47. PubMed ID: 38532508
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Endothelial
    Huang L; Bichsel C; Norris AL; Thorpe J; Pevsner J; Alexandrescu S; Pinto A; Zurakowski D; Kleiman RJ; Sahin M; Greene AK; Bischoff J
    Arterioscler Thromb Vasc Biol; 2022 Jan; 42(1):e27-e43. PubMed ID: 34670408
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel GNAQ mutation(R183G) of Port-wine stains: first case in East Asia.
    Cai R; Gu H; Liu F; Wang L; Zeng X; Yu W; Zhang X; Liu Y; Ma G; Lin X
    Int J Dermatol; 2019 Mar; 58(3):e75-e77. PubMed ID: 30597540
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic Variants Associated with Port-Wine Stains.
    Frigerio A; Wright K; Wooderchak-Donahue W; Tan OT; Margraf R; Stevenson DA; Grimmer JF; Bayrak-Toydemir P
    PLoS One; 2015; 10(7):e0133158. PubMed ID: 26192947
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early-onset hypertension associated with extensive cutaneous capillary malformations harboring postzygotic variants in GNAQ and GNA11.
    Davies OMT; Ng AT; Tran J; Blumenthal S; Arkin LM; Nopper AJ; Cottrell CE; Garzon M; Siegel DH; Frieden IJ; Drolet BA
    Pediatr Dermatol; 2022 Nov; 39(6):914-919. PubMed ID: 36440997
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Association of Somatic GNAQ Mutation With Capillary Malformations in a Case of Choroidal Hemangioma.
    Bichsel CA; Goss J; Alomari M; Alexandrescu S; Robb R; Smith LE; Hochman M; Greene AK; Bischoff J
    JAMA Ophthalmol; 2019 Jan; 137(1):91-95. PubMed ID: 30422215
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A somatic missense mutation in GNAQ causes capillary malformation.
    Bichsel C; Bischoff J
    Curr Opin Hematol; 2019 May; 26(3):179-184. PubMed ID: 30870248
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A somatic GNA11 mutation is associated with extremity capillary malformation and overgrowth.
    Couto JA; Ayturk UM; Konczyk DJ; Goss JA; Huang AY; Hann S; Reeve JL; Liang MG; Bischoff J; Warman ML; Greene AK
    Angiogenesis; 2017 Aug; 20(3):303-306. PubMed ID: 28120216
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel genetic mutations in a sporadic port-wine stain.
    Lian CG; Sholl LM; Zakka LR; O TM; Liu C; Xu S; Stanek E; Garcia E; Jia Y; MacConaill LE; Murphy GF; Waner M; Mihm MC
    JAMA Dermatol; 2014 Dec; 150(12):1336-40. PubMed ID: 25188413
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The somatic GNAQ mutation (R183Q) is primarily located within the blood vessels of port wine stains.
    Tan W; Nadora DM; Gao L; Wang G; Mihm MC; Nelson JS
    J Am Acad Dermatol; 2016 Feb; 74(2):380-3. PubMed ID: 26775782
    [No Abstract]   [Full Text] [Related]  

  • 20. Computational analysis for GNAQ mutations: New insights on the molecular etiology of Sturge-Weber syndrome.
    Martins L; Giovani PA; Rebouças PD; Brasil DM; Haiter Neto F; Coletta RD; Machado RA; Puppin-Rontani RM; Nociti FH; Kantovitz KR
    J Mol Graph Model; 2017 Sep; 76():429-440. PubMed ID: 28779688
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.