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Journal Abstract Search

236 related items for PubMed ID: 32360898

  • 1. Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis.
    Cuellar A, Bala K, Di Pietro L, Barba M, Yagnik G, Liu JL, Stevens C, Hur DJ, Ingersoll RG, Justice CM, Drissi H, Kim J, Lattanzi W, Boyadjiev SA.
    Bone; 2020 Aug; 137():115395. PubMed ID: 32360898
    [Abstract] [Full Text] [Related]

  • 2. BBS9 gene in nonsyndromic craniosynostosis: Role of the primary cilium in the aberrant ossification of the suture osteogenic niche.
    Barba M, Di Pietro L, Massimi L, Geloso MC, Frassanito P, Caldarelli M, Michetti F, Della Longa S, Romitti PA, Di Rocco C, Arcovito A, Parolini O, Tamburrini G, Bernardini C, Boyadjiev SA, Lattanzi W.
    Bone; 2018 Jul; 112():58-70. PubMed ID: 29674126
    [Abstract] [Full Text] [Related]

  • 3. Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model.
    Gustafson JA, Park SS, Cunningham ML.
    PLoS One; 2019 Jul; 14(8):e0221402. PubMed ID: 31442251
    [Abstract] [Full Text] [Related]

  • 4. Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis.
    Coussens AK, Wilkinson CR, Hughes IP, Morris CP, van Daal A, Anderson PJ, Powell BC.
    BMC Genomics; 2007 Dec 12; 8():458. PubMed ID: 18076769
    [Abstract] [Full Text] [Related]

  • 5. Shaping modern human skull through epigenetic, transcriptional and post-transcriptional regulation of the RUNX2 master bone gene.
    Di Pietro L, Barba M, Palacios D, Tiberio F, Prampolini C, Baranzini M, Parolini O, Arcovito A, Lattanzi W.
    Sci Rep; 2021 Oct 29; 11(1):21316. PubMed ID: 34716352
    [Abstract] [Full Text] [Related]

  • 6. GLI1 and AXIN2 Are Distinctive Markers of Human Calvarial Mesenchymal Stromal Cells in Nonsyndromic Craniosynostosis.
    Di Pietro L, Barba M, Prampolini C, Ceccariglia S, Frassanito P, Vita A, Guadagni E, Bonvissuto D, Massimi L, Tamburrini G, Parolini O, Lattanzi W.
    Int J Mol Sci; 2020 Jun 19; 21(12):. PubMed ID: 32575385
    [Abstract] [Full Text] [Related]

  • 7. Genetic advances in craniosynostosis.
    Lattanzi W, Barba M, Di Pietro L, Boyadjiev SA.
    Am J Med Genet A; 2017 May 19; 173(5):1406-1429. PubMed ID: 28160402
    [Abstract] [Full Text] [Related]

  • 8. Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations.
    Seto ML, Hing AV, Chang J, Hu M, Kapp-Simon KA, Patel PK, Burton BK, Kane AA, Smyth MD, Hopper R, Ellenbogen RG, Stevenson K, Speltz ML, Cunningham ML.
    Am J Med Genet A; 2007 Apr 01; 143A(7):678-86. PubMed ID: 17343269
    [Abstract] [Full Text] [Related]

  • 9. ALX4 gain-of-function mutations in nonsyndromic craniosynostosis.
    Yagnik G, Ghuman A, Kim S, Stevens CG, Kimonis V, Stoler J, Sanchez-Lara PA, Bernstein JA, Naydenov C, Drissi H, Cunningham ML, Kim J, Boyadjiev SA.
    Hum Mutat; 2012 Dec 01; 33(12):1626-9. PubMed ID: 22829454
    [Abstract] [Full Text] [Related]

  • 10. Cranial suture response to stress: expression patterns of Noggin and Runx2.
    Heller JB, Gabbay JS, Wasson K, Mitchell S, Heller MM, Zuk P, Bradley JP.
    Plast Reconstr Surg; 2007 Jun 01; 119(7):2037-2045. PubMed ID: 17519698
    [Abstract] [Full Text] [Related]

  • 11. Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis.
    Mefford HC, Shafer N, Antonacci F, Tsai JM, Park SS, Hing AV, Rieder MJ, Smyth MD, Speltz ML, Eichler EE, Cunningham ML.
    Am J Med Genet A; 2010 Sep 01; 152A(9):2203-10. PubMed ID: 20683987
    [Abstract] [Full Text] [Related]

  • 12. PIN1 is a new therapeutic target of craniosynostosis.
    Shin HR, Bae HS, Kim BS, Yoon HI, Cho YD, Kim WJ, Choi KY, Lee YS, Woo KM, Baek JH, Ryoo HM.
    Hum Mol Genet; 2018 Nov 15; 27(22):3827-3839. PubMed ID: 30007339
    [Abstract] [Full Text] [Related]

  • 13. Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis.
    Justice CM, Musolf AM, Cuellar A, Lattanzi W, Simeonov E, Kaneva R, Paschall J, Cunningham M, Wilkie AOM, Wilson AF, Romitti PA, Boyadjiev SA.
    Genes (Basel); 2022 May 03; 13(5):. PubMed ID: 35627201
    [Abstract] [Full Text] [Related]

  • 14. BMP9 induces osteogenesis and adipogenesis in the immortalized human cranial suture progenitors from the patent sutures of craniosynostosis patients.
    Song D, Zhang F, Reid RR, Ye J, Wei Q, Liao J, Zou Y, Fan J, Ma C, Hu X, Qu X, Chen L, Li L, Yu Y, Yu X, Zhang Z, Zhao C, Zeng Z, Zhang R, Yan S, Wu T, Wu X, Shu Y, Lei J, Li Y, Zhang W, Wang J, Lee MJ, Wolf JM, Huang D, He TC.
    J Cell Mol Med; 2017 Nov 03; 21(11):2782-2795. PubMed ID: 28470873
    [Abstract] [Full Text] [Related]

  • 15. Craniosynostosis as a clinical and diagnostic problem: molecular pathology and genetic counseling.
    Kutkowska-Kaźmierczak A, Gos M, Obersztyn E.
    J Appl Genet; 2018 May 03; 59(2):133-147. PubMed ID: 29392564
    [Abstract] [Full Text] [Related]

  • 16. Identification of differentially expressed proteins between fused and open sutures in sagittal nonsyndromic craniosynostosis during suture development by quantitative proteomic analysis.
    Bala K, Cuellar A, Herren AW, Boyadjiev SA.
    Proteomics Clin Appl; 2021 May 03; 15(2-3):e2000031. PubMed ID: 33580899
    [Abstract] [Full Text] [Related]

  • 17. Retinoic acid enhances osteogenesis in cranial suture-derived mesenchymal cells: potential mechanisms of retinoid-induced craniosynostosis.
    James AW, Levi B, Xu Y, Carre AL, Longaker MT.
    Plast Reconstr Surg; 2010 May 03; 125(5):1352-1361. PubMed ID: 20134361
    [Abstract] [Full Text] [Related]

  • 18. Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis.
    Ye X, Guilmatre A, Reva B, Peter I, Heuzé Y, Richtsmeier JT, Fox DJ, Goedken RJ, Jabs EW, Romitti PA.
    Plast Reconstr Surg; 2016 Mar 03; 137(3):952-961. PubMed ID: 26910679
    [Abstract] [Full Text] [Related]

  • 19. New insights into the relationship between suture closure and craniofacial dysmorphology in sagittal nonsyndromic craniosynostosis.
    Heuzé Y, Boyadjiev SA, Marsh JL, Kane AA, Cherkez E, Boggan JE, Richtsmeier JT.
    J Anat; 2010 Aug 03; 217(2):85-96. PubMed ID: 20572900
    [Abstract] [Full Text] [Related]

  • 20. Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428.
    Musolf AM, Justice CM, Erdogan-Yildirim Z, Goovaerts S, Cuellar A, Shaffer JR, Marazita ML, Claes P, Weinberg SM, Li J, Senders C, Zwienenberg M, Simeonov E, Kaneva R, Roscioli T, Di Pietro L, Barba M, Lattanzi W, Cunningham ML, Romitti PA, Boyadjiev SA.
    Sci Rep; 2024 Apr 12; 14(1):8533. PubMed ID: 38609424
    [Abstract] [Full Text] [Related]

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