BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

376 related articles for article (PubMed ID: 26966495)

  • 1. Fibrodysplasia ossificans progressiva with minor unilateral hallux anomaly in a sporadic case from Northern Tanzania with the common ACVR1c.617G>A mutation.
    Saleh M; Commandeur J; Bocciardi R; Kinabo G; Hamel B
    Pan Afr Med J; 2015; 22():299. PubMed ID: 26966495
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Early diagnosis of fibrodysplasia ossificans progressiva.
    Kaplan FS; Xu M; Glaser DL; Collins F; Connor M; Kitterman J; Sillence D; Zackai E; Ravitsky V; Zasloff M; Ganguly A; Shore EM
    Pediatrics; 2008 May; 121(5):e1295-300. PubMed ID: 18450872
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Classical and atypical Fibrodysplasia Ossificans Progressiva in India.
    Madhuri V; Santhanam M; Sugumar LK; Rajagopal K; Chilbule SK
    Ann Hum Genet; 2015 Jul; 79(4):245-52. PubMed ID: 26058333
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The congenital great toe malformation of fibrodysplasia ossificans progressiva? - A close call.
    Towler OW; Shore EM; Xu M; Bamford A; Anderson I; Pignolo RJ; Kaplan FS
    Eur J Med Genet; 2017 Jul; 60(7):399-402. PubMed ID: 28473268
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressiva.
    Nakajima M; Haga N; Takikawa K; Manabe N; Nishimura G; Ikegawa S
    J Hum Genet; 2007; 52(5):473-475. PubMed ID: 17351709
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Difficult diagnosis and genetic analysis of fibrodysplasia ossificans progressiva: a case report.
    Tian S; Zhu J; Lu Y
    BMC Med Genet; 2018 Feb; 19(1):30. PubMed ID: 29482508
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fibrodysplasia ossificans progressiva: clinical and genetic aspects.
    Pignolo RJ; Shore EM; Kaplan FS
    Orphanet J Rare Dis; 2011 Dec; 6():80. PubMed ID: 22133093
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo 617G-A nucleotide mutation in the ACVR1 gene in a Taiwanese patient with fibrodysplasia ossificans progressiva.
    Lin GT; Chang HW; Liu CS; Huang PJ; Wang HC; Cheng YM
    J Hum Genet; 2006; 51(12):1083-1086. PubMed ID: 17077940
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.
    Kaplan FS; Xu M; Seemann P; Connor JM; Glaser DL; Carroll L; Delai P; Fastnacht-Urban E; Forman SJ; Gillessen-Kaesbach G; Hoover-Fong J; Köster B; Pauli RM; Reardon W; Zaidi SA; Zasloff M; Morhart R; Mundlos S; Groppe J; Shore EM
    Hum Mutat; 2009 Mar; 30(3):379-90. PubMed ID: 19085907
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and molecular characterisation of two siblings with fibrodysplasia ossificans progressiva, from the Colombian Pacific coast (South America).
    Pachajoa H; Botero AF
    BMJ Case Rep; 2015 Jun; 2015():. PubMed ID: 26055602
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Atypical fibrodysplasia ossificans progressiva diagnosed by whole-exome sequencing.
    Liu H; Sawyer SL; Gos M; Grynspan D; Issa K; Ramphal R; Rotaru C; ; Majewski J; Boycott KM; Graham G; Bromwich M
    Am J Med Genet A; 2015 Jun; 167(6):1337-41. PubMed ID: 25899773
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fibrodysplasia ossificans progressiva in a newborn with cardiac involvement.
    Marseglia L; D'Angelo G; Manti S; Manganaro A; Calabrò MP; Salpietro C; Gitto E
    Pediatr Int; 2015 Aug; 57(4):719-21. PubMed ID: 25809395
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Morpholino-Mediated Exon Skipping Targeting Human ACVR1/ALK2 for Fibrodysplasia Ossificans Progressiva.
    Maruyama R; Yokota T
    Methods Mol Biol; 2018; 1828():497-502. PubMed ID: 30171563
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rarely occurring mutation of ACVR1 gene in Moroccan patient with fibrodysplasia ossificans progressiva.
    Ratbi I; Bocciardi R; Regragui A; Ravazzolo R; Sefiani A
    Clin Rheumatol; 2010 Jan; 29(1):119-21. PubMed ID: 19795179
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fibrodysplasia ossificans progressiva (FOP): watch the great toes!
    Kartal-Kaess M; Shore EM; Xu M; Schwering L; Uhl M; Korinthenberg R; Niemeyer C; Kaplan FS; Lauten M
    Eur J Pediatr; 2010 Nov; 169(11):1417-21. PubMed ID: 20577760
    [TBL] [Abstract][Full Text] [Related]  

  • 16. BMP signaling and skeletal development in fibrodysplasia ossificans progressiva (FOP).
    Towler OW; Shore EM
    Dev Dyn; 2022 Jan; 251(1):164-177. PubMed ID: 34133058
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients.
    Lucotte G; Houzet A; Hubans C; Lagarde JP; Lenoir G
    Genet Couns; 2009; 20(1):53-62. PubMed ID: 19400542
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1.
    Whyte MP; Wenkert D; Demertzis JL; DiCarlo EF; Westenberg E; Mumm S
    J Bone Miner Res; 2012 Mar; 27(3):729-37. PubMed ID: 22131272
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational analysis of the ACVR1 gene in Italian patients affected with fibrodysplasia ossificans progressiva: confirmations and advancements.
    Bocciardi R; Bordo D; Di Duca M; Di Rocco M; Ravazzolo R
    Eur J Hum Genet; 2009 Mar; 17(3):311-8. PubMed ID: 18830232
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Confirmation of the recurrent ACVR1 617G>A mutation in South Africans with fibrodysplasia ossificans progressiva.
    Dandara C; Scott C; Urban M; Fieggen K; Arendse R; Beighton P
    S Afr Med J; 2012 May; 102(7):631-3. PubMed ID: 22748444
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.