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Items: 1 to 20 of 21

1.

Proteomic profiling of extracellular vesicles released from vascular smooth muscle cells during initiation of phosphate-induced mineralization.

Chaudhary SC, Khalid S, Smethurst V, Monier D, Mobley J, Huet A, Conway JF, Napierala D.

Connect Tissue Res. 2018 Dec;59(sup1):55-61. doi: 10.1080/03008207.2018.1444759.

PMID:
29471680
2.

Phosphate induces formation of matrix vesicles during odontoblast-initiated mineralization in vitro.

Chaudhary SC, Kuzynski M, Bottini M, Beniash E, Dokland T, Mobley CG, Yadav MC, Poliard A, Kellermann O, Millán JL, Napierala D.

Matrix Biol. 2016 May-Jul;52-54:284-300. doi: 10.1016/j.matbio.2016.02.003. Epub 2016 Feb 13.

3.

Dspp-independent Effects of Transgenic Trps1 Overexpression on Dentin Formation.

Mobley CG, Kuzynski M, Zhang H, Jani P, Qin C, Napierala D.

J Dent Res. 2015 Aug;94(8):1128-34. doi: 10.1177/0022034515586709. Epub 2015 May 21.

4.

The growth and aggressive behavior of human osteosarcoma is regulated by a CaMKII-controlled autocrine VEGF signaling mechanism.

Daft PG, Yang Y, Napierala D, Zayzafoon M.

PLoS One. 2015 Apr 10;10(4):e0121568. doi: 10.1371/journal.pone.0121568. eCollection 2015.

5.

Specificity protein 7 is not essential for tooth morphogenesis.

Clarke JC, Bae JM, Adhami M, Rashid H, Chen H, Napierala D, Gutierrez SE, Sinha K, Crombrugghe Bd, Javed A.

Connect Tissue Res. 2014 Aug;55 Suppl 1:88-91. doi: 10.3109/03008207.2014.923874.

6.

Dual role of the Trps1 transcription factor in dentin mineralization.

Kuzynski M, Goss M, Bottini M, Yadav MC, Mobley C, Winters T, Poliard A, Kellermann O, Lee B, Millan JL, Napierala D.

J Biol Chem. 2014 Oct 3;289(40):27481-93. doi: 10.1074/jbc.M114.550129. Epub 2014 Aug 15.

7.

Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues.

Homan EP, Lietman C, Grafe I, Lennington J, Morello R, Napierala D, Jiang MM, Munivez EM, Dawson B, Bertin TK, Chen Y, Lua R, Lichtarge O, Hicks J, Weis MA, Eyre D, Lee BH.

PLoS Genet. 2014 Jan;10(1):e1004121. doi: 10.1371/journal.pgen.1004121. Epub 2014 Jan 23. Erratum in: PLoS Genet. 2014 Jun;10(6):e1004473.

8.

Transcriptional repression of the Dspp gene leads to dentinogenesis imperfecta phenotype in Col1a1-Trps1 transgenic mice.

Napierala D, Sun Y, Maciejewska I, Bertin TK, Dawson B, D'Souza R, Qin C, Lee B.

J Bone Miner Res. 2012 Aug;27(8):1735-45. doi: 10.1002/jbmr.1636.

9.

Runx2 contributes to murine Col10a1 gene regulation through direct interaction with its cis-enhancer.

Li F, Lu Y, Ding M, Napierala D, Abbassi S, Chen Y, Duan X, Wang S, Lee B, Zheng Q.

J Bone Miner Res. 2011 Dec;26(12):2899-910. doi: 10.1002/jbmr.504.

10.

Mutations in SERPINF1 cause osteogenesis imperfecta type VI.

Homan EP, Rauch F, Grafe I, Lietman C, Doll JA, Dawson B, Bertin T, Napierala D, Morello R, Gibbs R, White L, Miki R, Cohn DH, Crawford S, Travers R, Glorieux FH, Lee B.

J Bone Miner Res. 2011 Dec;26(12):2798-803. doi: 10.1002/jbmr.487.

11.

Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome.

Kelley BP, Malfait F, Bonafe L, Baldridge D, Homan E, Symoens S, Willaert A, Elcioglu N, Van Maldergem L, Verellen-Dumoulin C, Gillerot Y, Napierala D, Krakow D, Beighton P, Superti-Furga A, De Paepe A, Lee B.

J Bone Miner Res. 2011 Mar;26(3):666-72. doi: 10.1002/jbmr.250.

12.

Localization of the cis-enhancer element for mouse type X collagen expression in hypertrophic chondrocytes in vivo.

Zheng Q, Keller B, Zhou G, Napierala D, Chen Y, Zabel B, Parker AE, Lee B.

J Bone Miner Res. 2009 Jun;24(6):1022-32. doi: 10.1359/jbmr.081249.

13.

Tricho-rhino-phalangeal syndrome with supernumerary teeth.

Kantaputra P, Miletich I, Lüdecke HJ, Suzuki EY, Praphanphoj V, Shivdasani R, Wuelling M, Vortkamp A, Napierala D, Sharpe PT.

J Dent Res. 2008 Nov;87(11):1027-31.

PMID:
18946009
14.

Uncoupling of chondrocyte differentiation and perichondrial mineralization underlies the skeletal dysplasia in tricho-rhino-phalangeal syndrome.

Napierala D, Sam K, Morello R, Zheng Q, Munivez E, Shivdasani RA, Lee B.

Hum Mol Genet. 2008 Jul 15;17(14):2244-54. doi: 10.1093/hmg/ddn125. Epub 2008 Apr 17.

15.

De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.

Purandare SM, Mendoza-Londono R, Yatsenko SA, Napierala D, Scott DA, Sibai T, Casas K, Wilson P, Lee J, Muneer R, Leonard JC, Ramji FG, Lachman R, Li S, Stankiewicz P, Lee B, Mulvihill JJ.

Am J Med Genet A. 2008 Feb 15;146A(4):453-8. doi: 10.1002/ajmg.a.31750.

16.

The presence of germ line mosaicism in cleidocranial dysplasia.

Pal T, Napierala D, Becker TA, Loscalzo M, Baldridge D, Lee B, Sutphen R.

Clin Genet. 2007 Jun;71(6):589-91.

PMID:
17539909
17.

Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation.

Napierala D, Garcia-Rojas X, Sam K, Wakui K, Chen C, Mendoza-Londono R, Zhou G, Zheng Q, Lee B.

Mol Genet Metab. 2005 Sep-Oct;86(1-2):257-68.

PMID:
16140555
18.

Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.

Mendoza-Londono R, Lammer E, Watson R, Harper J, Hatamochi A, Hatamochi-Hayashi S, Napierala D, Hermanns P, Collins S, Roa BB, Hedge MR, Wakui K, Nguyen D, Stockton DW, Lee B.

Am J Hum Genet. 2005 Jul;77(1):161-8. Epub 2005 May 27.

19.

Crane-Heise syndrome: a second familial case report with elaboration of phenotype.

Zand DJ, Carpentieri D, Huff D, Medne L, Napierala D, Lee B, Zackai E.

Am J Med Genet A. 2003 Apr 30;118A(3):223-8.

PMID:
12673651
20.

Mosaicism in tuberous sclerosis as a potential cause of the failure of molecular diagnosis.

Kwiatkowska J, Wigowska-Sowinska J, Napierala D, Slomski R, Kwiatkowski DJ.

N Engl J Med. 1999 Mar 4;340(9):703-7. No abstract available.

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