These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

279 related articles for article (PubMed ID: 28475764)

  • 1. The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta.
    Gioia R; Tonelli F; Ceppi I; Biggiogera M; Leikin S; Fisher S; Tenedini E; Yorgan TA; Schinke T; Tian K; Schwartz JM; Forte F; Wagener R; Villani S; Rossi A; Forlino A
    Hum Mol Genet; 2017 Aug; 26(15):2897-2911. PubMed ID: 28475764
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cell differentiation and matrix organization are differentially affected during bone formation in osteogenesis imperfecta zebrafish models with different genetic defects impacting collagen type I structure.
    Daponte V; Tonelli F; Masiero C; Syx D; Exbrayat-Héritier C; Biggiogera M; Willaert A; Rossi A; Coucke PJ; Ruggiero F; Forlino A
    Matrix Biol; 2023 Aug; 121():105-126. PubMed ID: 37336269
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 4-Phenylbutyric acid enhances the mineralization of osteogenesis imperfecta iPSC-derived osteoblasts.
    Takeyari S; Kubota T; Ohata Y; Fujiwara M; Kitaoka T; Taga Y; Mizuno K; Ozono K
    J Biol Chem; 2021; 296():100027. PubMed ID: 33154166
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 4PBA reduces growth deficiency in osteogenesis imperfecta by enhancing transition of hypertrophic chondrocytes to osteoblasts.
    Scheiber AL; Wilkinson KJ; Suzuki A; Enomoto-Iwamoto M; Kaito T; Cheah KS; Iwamoto M; Leikin S; Otsuru S
    JCI Insight; 2022 Feb; 7(3):. PubMed ID: 34990412
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 4-PBA ameliorates cellular homeostasis in fibroblasts from osteogenesis imperfecta patients by enhancing autophagy and stimulating protein secretion.
    Besio R; Iula G; Garibaldi N; Cipolla L; Sabbioneda S; Biggiogera M; Marini JC; Rossi A; Forlino A
    Biochim Biophys Acta Mol Basis Dis; 2018 May; 1864(5 Pt A):1642-1652. PubMed ID: 29432813
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Compression Fractures and Partial Phenotype Rescue With a Low Phosphorus Diet in the
    Cotti S; Huysseune A; Larionova D; Koppe W; Forlino A; Witten PE
    Front Endocrinol (Lausanne); 2022; 13():851879. PubMed ID: 35282456
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta.
    Lindert U; Weis MA; Rai J; Seeliger F; Hausser I; Leeb T; Eyre D; Rohrbach M; Giunta C
    J Biol Chem; 2015 Jul; 290(29):17679-17689. PubMed ID: 26004778
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Crtap and p3h1 knock out zebrafish support defective collagen chaperoning as the cause of their osteogenesis imperfecta phenotype.
    Tonelli F; Cotti S; Leoni L; Besio R; Gioia R; Marchese L; Giorgetti S; Villani S; Gistelinck C; Wagener R; Kobbe B; Fiedler IAK; Larionova D; Busse B; Eyre D; Rossi A; Witten PE; Forlino A
    Matrix Biol; 2020 Aug; 90():40-60. PubMed ID: 32173581
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Bone biology: insights from osteogenesis imperfecta and related rare fragility syndromes.
    Besio R; Chow CW; Tonelli F; Marini JC; Forlino A
    FEBS J; 2019 Aug; 286(15):3033-3056. PubMed ID: 31220415
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Severely Impaired Bone Material Quality in Chihuahua Zebrafish Resembles Classical Dominant Human Osteogenesis Imperfecta.
    Fiedler IAK; Schmidt FN; Wölfel EM; Plumeyer C; Milovanovic P; Gioia R; Tonelli F; Bale HA; Jähn K; Besio R; Forlino A; Busse B
    J Bone Miner Res; 2018 Aug; 33(8):1489-1499. PubMed ID: 29665086
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta.
    Duran I; Zieba J; Csukasi F; Martin JH; Wachtell D; Barad M; Dawson B; Fafilek B; Jacobsen CM; Ambrose CG; Cohn DH; Krejci P; Lee BH; Krakow D
    J Bone Miner Res; 2022 Apr; 37(4):675-686. PubMed ID: 34997935
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Targeting cellular stress in vitro improves osteoblast homeostasis, matrix collagen content and mineralization in two murine models of osteogenesis imperfecta.
    Garibaldi N; Contento BM; Babini G; Morini J; Siciliani S; Biggiogera M; Raspanti M; Marini JC; Rossi A; Forlino A; Besio R
    Matrix Biol; 2021 Apr; 98():1-20. PubMed ID: 33798677
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processing.
    Cabral WA; Makareeva E; Colige A; Letocha AD; Ty JM; Yeowell HN; Pals G; Leikin S; Marini JC
    J Biol Chem; 2005 May; 280(19):19259-69. PubMed ID: 15728585
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel de novo mutation in COL1A1 leading to osteogenesis imperfecta confirmed by zebrafish model.
    Huang H; Liu J; Zhang G
    Clin Chim Acta; 2021 Jun; 517():133-138. PubMed ID: 33705765
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Radiographic analysis of zebrafish skeletal defects.
    Fisher S; Jagadeeswaran P; Halpern ME
    Dev Biol; 2003 Dec; 264(1):64-76. PubMed ID: 14623232
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Insight into the Pathology of a COL1A1 Signal Peptide Heterozygous Mutation Leading to Severe Osteogenesis Imperfecta.
    Lindert U; Gnoli M; Maioli M; Bedeschi MF; Sangiorgi L; Rohrbach M; Giunta C
    Calcif Tissue Int; 2018 Mar; 102(3):373-379. PubMed ID: 29101475
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutant MESD links cellular stress to type I collagen aggregation in osteogenesis imperfecta type XX.
    Ghosh DK; Udupa P; Shrikondawar AN; Bhavani GS; Shah H; Ranjan A; Girisha KM
    Matrix Biol; 2023 Jan; 115():81-106. PubMed ID: 36526215
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Endoplasmic reticulum stress is induced in growth plate hypertrophic chondrocytes in G610C mouse model of osteogenesis imperfecta.
    Scheiber AL; Guess AJ; Kaito T; Abzug JM; Enomoto-Iwamoto M; Leikin S; Iwamoto M; Otsuru S
    Biochem Biophys Res Commun; 2019 Jan; 509(1):235-240. PubMed ID: 30579604
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiexon deletions in the type I collagen COL1A2 gene in osteogenesis imperfecta type IB. Molecules containing the shortened alpha2(I) chains show differential incorporation into the bone and skin extracellular matrix.
    Mundlos S; Chan D; Weng YM; Sillence DO; Cole WG; Bateman JF
    J Biol Chem; 1996 Aug; 271(35):21068-74. PubMed ID: 8702873
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta.
    Marini JC; Cabral WA; Barnes AM
    Cell Tissue Res; 2010 Jan; 339(1):59-70. PubMed ID: 19862557
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.