BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

83 related articles for article (PubMed ID: 25006195)

  • 1. Shared mutation for two childhood diseases.
    Delude CM
    J Natl Cancer Inst; 2014 Jul; 106(7):. PubMed ID: 25006195
    [No Abstract]   [Full Text] [Related]  

  • 2. ACVR1 mutations in DIPG: lessons learned from FOP.
    Taylor KR; Vinci M; Bullock AN; Jones C
    Cancer Res; 2014 Sep; 74(17):4565-70. PubMed ID: 25136070
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent activating ACVR1 mutations in diffuse intrinsic pontine glioma.
    Taylor KR; Mackay A; Truffaux N; Butterfield Y; Morozova O; Philippe C; Castel D; Grasso CS; Vinci M; Carvalho D; Carcaboso AM; de Torres C; Cruz O; Mora J; Entz-Werle N; Ingram WJ; Monje M; Hargrave D; Bullock AN; Puget S; Yip S; Jones C; Grill J
    Nat Genet; 2014 May; 46(5):457-461. PubMed ID: 24705252
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma.
    Nikbakht H; Panditharatna E; Mikael LG; Li R; Gayden T; Osmond M; Ho CY; Kambhampati M; Hwang EI; Faury D; Siu A; Papillon-Cavanagh S; Bechet D; Ligon KL; Ellezam B; Ingram WJ; Stinson C; Moore AS; Warren KE; Karamchandani J; Packer RJ; Jabado N; Majewski J; Nazarian J
    Nat Commun; 2016 Apr; 7():11185. PubMed ID: 27048880
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations of the noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP).
    Lucotte G; Lagarde JP;
    Genet Couns; 2007; 18(3):349-52. PubMed ID: 18019378
    [No Abstract]   [Full Text] [Related]  

  • 6. The H3.3 K27M mutation results in a poorer prognosis in brainstem gliomas than thalamic gliomas in adults.
    Feng J; Hao S; Pan C; Wang Y; Wu Z; Zhang J; Yan H; Zhang L; Wan H
    Hum Pathol; 2015 Nov; 46(11):1626-32. PubMed ID: 26297251
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinicopathology of diffuse intrinsic pontine glioma and its redefined genomic and epigenomic landscape.
    Panditharatna E; Yaeger K; Kilburn LB; Packer RJ; Nazarian J
    Cancer Genet; 2015; 208(7-8):367-73. PubMed ID: 26206682
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Biomedical research. Bone disease gene finally found.
    Couzin J
    Science; 2006 Apr; 312(5773):514-5. PubMed ID: 16645061
    [No Abstract]   [Full Text] [Related]  

  • 9. ACVR1 mutations and the genomic landscape of pediatric diffuse glioma.
    Zadeh G; Aldape K
    Nat Genet; 2014 May; 46(5):421-2. PubMed ID: 24769718
    [No Abstract]   [Full Text] [Related]  

  • 10. Genetics: ACVR1 mutations-a key piece in paediatric diffuse glioma.
    Villanueva MT
    Nat Rev Clin Oncol; 2014 Jun; 11(6):300. PubMed ID: 24840074
    [No Abstract]   [Full Text] [Related]  

  • 11. A Novel Mouse Model of Diffuse Intrinsic Pontine Glioma Initiated in Pax3-Expressing Cells.
    Misuraca KL; Hu G; Barton KL; Chung A; Becher OJ
    Neoplasia; 2016 Jan; 18(1):60-70. PubMed ID: 26806352
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese population.
    Guo H; Peng D; Xu M; Xue J; Lu L; Xu X; Liu Y; Xiong Z; Pan Q; Hu Z; Xia K
    Clin Dysmorphol; 2010 Oct; 19(4):206-208. PubMed ID: 20736820
    [No Abstract]   [Full Text] [Related]  

  • 13. ALK2 R206H mutation linked to fibrodysplasia ossificans progressiva confers constitutive activity to the BMP type I receptor and sensitizes mesenchymal cells to BMP-induced osteoblast differentiation and bone formation.
    van Dinther M; Visser N; de Gorter DJ; Doorn J; Goumans MJ; de Boer J; ten Dijke P
    J Bone Miner Res; 2010 Jun; 25(6):1208-15. PubMed ID: 19929436
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutational screening of ACVR1 gene in Brazilian fibrodysplasia ossificans progressiva patients.
    Carvalho DR; Navarro MM; Martins BJ; Coelho KE; Mello WD; Takata RI; Speck-Martins CE
    Clin Genet; 2010 Feb; 77(2):171-6. PubMed ID: 19796185
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular landscape of pediatric diffuse intrinsic pontine gliomas: about 22 cases.
    El Ayoubi R; Boisselier B; Rousseau A
    J Neurooncol; 2017 Sep; 134(2):465-467. PubMed ID: 28589424
    [No Abstract]   [Full Text] [Related]  

  • 16. The tale of FOP, NOGGIN and myristoylation: no data, no proof!
    Seemann P; Mundlos S
    Genet Couns; 2008; 19(3):353-5; author reply 361-3. PubMed ID: 18990992
    [No Abstract]   [Full Text] [Related]  

  • 17. Allele-specific RNA interference in FOP silencing the FOP gene.
    Lowery JW; Rosen V
    Gene Ther; 2012 Jul; 19(7):701-2. PubMed ID: 22130446
    [No Abstract]   [Full Text] [Related]  

  • 18. Lateral deviation of toes requires lateral thinking.
    Mangalore Devdas J; Campbell-Hewson Q; Friswell M; Gupta A; Featherstone T; Cooke A; DeKiewiet G; Hopper NW
    Arch Dis Child; 2009 Jan; 94(1):69. PubMed ID: 19103790
    [No Abstract]   [Full Text] [Related]  

  • 19. ACVR1 gene mutations in four Turkish patients diagnosed as fibrodysplasia ossificans progressiva.
    Eresen Yazıcıoğlu C; Karatosun V; Kızıldağ S; Ozsoylu D; Kavukçu S
    Gene; 2013 Feb; 515(2):444-6. PubMed ID: 23260810
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Moral and legal reasons for altruism in the case of brainstem biopsy in diffuse glioma.
    Wilkinson R; Harris J
    Br J Neurosurg; 2008 Oct; 22(5):617-8. PubMed ID: 19016111
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.