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Items: 33

1.

tp53-dependent and independent signaling underlies the pathogenesis and possible prevention of Acrofacial Dysostosis - Cincinnati type.

Watt KEN, Neben CL, Hall S, Merrill AE, Trainor PA.

Hum Mol Genet. 2018 May 10. doi: 10.1093/hmg/ddy172. [Epub ahead of print]

PMID:
29750247
2.

FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination.

Neben CL, Tuzon CT, Mao X, Lay FD, Merrill AE.

Hum Mol Genet. 2017 Sep 1;26(17):3253-3270. doi: 10.1093/hmg/ddx209.

PMID:
28595297
3.

Pseudohypophosphatemia associated with high-dose liposomal amphotericin B therapy.

Mays JA, Greene DN, Poon A, Merrill AE.

Clin Biochem. 2017 Nov;50(16-17):967-971. doi: 10.1016/j.clinbiochem.2017.05.016. Epub 2017 May 31.

PMID:
28578095
4.

Signaling networks in joint development.

Salva JE, Merrill AE.

Dev Dyn. 2017 Apr;246(4):262-274. doi: 10.1002/dvdy.24472. Epub 2016 Dec 29. Review.

5.

Ribosome biogenesis is dynamically regulated during osteoblast differentiation.

Neben CL, Lay FD, Mao X, Tuzon CT, Merrill AE.

Gene. 2017 May 15;612:29-35. doi: 10.1016/j.gene.2016.11.010. Epub 2016 Nov 12.

6.

The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome.

Noack Watt KE, Achilleos A, Neben CL, Merrill AE, Trainor PA.

PLoS Genet. 2016 Jul 22;12(7):e1006187. doi: 10.1371/journal.pgen.1006187. eCollection 2016 Jul.

7.

NeuCode Proteomics Reveals Bap1 Regulation of Metabolism.

Baughman JM, Rose CM, Kolumam G, Webster JD, Wilkerson EM, Merrill AE, Rhoads TW, Noubade R, Katavolos P, Lesch J, Stapleton DS, Rabaglia ME, Schueler KL, Asuncion R, Domeyer M, Zavala-Solorio J, Reich M, DeVoss J, Keller MP, Attie AD, Hebert AS, Westphall MS, Coon JJ, Kirkpatrick DS, Dey A.

Cell Rep. 2016 Jul 12;16(2):583-595. doi: 10.1016/j.celrep.2016.05.096. Epub 2016 Jun 30.

8.

Modeling craniofacial and skeletal congenital birth defects to advance therapies.

Neben CL, Roberts RR, Dipple KM, Merrill AE, Klein OD.

Hum Mol Genet. 2016 Oct 1;25(R2):R86-R93. Epub 2016 Jun 26. Review.

9.

Method-to-method variability in urine albumin measurements.

Merrill AE, Khan J, Dickerson JA, Holmes DT, Harris NS, Greene DN.

Clin Chim Acta. 2016 Sep 1;460:114-9. doi: 10.1016/j.cca.2016.06.015. Epub 2016 Jun 15.

PMID:
27315746
10.

Clinical and radiographic delineation of Bent Bone Dysplasia-FGFR2 type or Bent Bone Dysplasia with Distinctive Clavicles and Angel-shaped Phalanges.

Krakow D, Cohn DH, Wilcox WR, Noh GJ, Raffel LJ, Sarukhanov A, Ivanova MH, Danielpour M, Grange DK, Elliott AM, Bernstein JA, Rimoin DL, Merrill AE, Lachman RS.

Am J Med Genet A. 2016 Oct;170(10):2652-61. doi: 10.1002/ajmg.a.37772. Epub 2016 May 30.

11.

TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions.

Zieba J, Forlenza KN, Khatra JS, Sarukhanov A, Duran I, Rigueur D, Lyons KM, Cohn DH, Merrill AE, Krakow D.

PLoS Genet. 2016 Mar 28;12(3):e1005936. doi: 10.1371/journal.pgen.1005936. eCollection 2016 Mar.

12.

Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders.

Neben CL, Merrill AE.

Curr Top Dev Biol. 2015;115:493-542. doi: 10.1016/bs.ctdb.2015.09.005. Epub 2015 Oct 23. Review.

PMID:
26589936
13.

NeuCode Labeling in Nematodes: Proteomic and Phosphoproteomic Impact of Ascaroside Treatment in Caenorhabditis elegans.

Rhoads TW, Prasad A, Kwiecien NW, Merrill AE, Zawack K, Westphall MS, Schroeder FC, Kimble J, Coon JJ.

Mol Cell Proteomics. 2015 Nov;14(11):2922-35. doi: 10.1074/mcp.M115.049684. Epub 2015 Sep 21.

14.

A calibration routine for efficient ETD in large-scale proteomics.

Rose CM, Rush MJ, Riley NM, Merrill AE, Kwiecien NW, Holden DD, Mullen C, Westphall MS, Coon JJ.

J Am Soc Mass Spectrom. 2015 Nov;26(11):1848-57. doi: 10.1007/s13361-015-1183-1. Epub 2015 Jun 26.

15.

Proteome sequencing goes deep.

Richards AL, Merrill AE, Coon JJ.

Curr Opin Chem Biol. 2015 Feb;24:11-7. doi: 10.1016/j.cbpa.2014.10.017. Epub 2014 Nov 8. Review.

16.

Pathway connectivity and signaling coordination in the yeast stress-activated signaling network.

Chasman D, Ho YH, Berry DB, Nemec CM, MacGilvray ME, Hose J, Merrill AE, Lee MV, Will JL, Coon JJ, Ansari AZ, Craven M, Gasch AP.

Mol Syst Biol. 2014 Nov 19;10:759. doi: 10.15252/msb.20145120.

17.

NeuCode labels for relative protein quantification.

Merrill AE, Hebert AS, MacGilvray ME, Rose CM, Bailey DJ, Bradley JC, Wood WW, El Masri M, Westphall MS, Gasch AP, Coon JJ.

Mol Cell Proteomics. 2014 Sep;13(9):2503-12. doi: 10.1074/mcp.M114.040287. Epub 2014 Jun 17.

18.

Bent bone dysplasia syndrome reveals nucleolar activity for FGFR2 in ribosomal DNA transcription.

Neben CL, Idoni B, Salva JE, Tuzon CT, Rice JC, Krakow D, Merrill AE.

Hum Mol Genet. 2014 Nov 1;23(21):5659-71. doi: 10.1093/hmg/ddu282. Epub 2014 Jun 6.

19.

Neutron-encoded mass signatures for quantitative top-down proteomics.

Rhoads TW, Rose CM, Bailey DJ, Riley NM, Molden RC, Nestler AJ, Merrill AE, Smith LM, Hebert AS, Westphall MS, Pagliarini DJ, Garcia BA, Coon JJ.

Anal Chem. 2014 Mar 4;86(5):2314-9. doi: 10.1021/ac403579s. Epub 2014 Feb 19.

20.

Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders.

Trainor PA, Merrill AE.

Biochim Biophys Acta. 2014 Jun;1842(6):769-78. doi: 10.1016/j.bbadis.2013.11.010. Epub 2013 Nov 16. Review.

21.

Neutron-encoded protein quantification by peptide carbamylation.

Ulbrich A, Merrill AE, Hebert AS, Westphall MS, Keller MP, Attie AD, Coon JJ.

J Am Soc Mass Spectrom. 2014 Jan;25(1):6-9. doi: 10.1007/s13361-013-0765-z. Epub 2013 Oct 29.

22.

Amine-reactive neutron-encoded labels for highly plexed proteomic quantitation.

Hebert AS, Merrill AE, Stefely JA, Bailey DJ, Wenger CD, Westphall MS, Pagliarini DJ, Coon JJ.

Mol Cell Proteomics. 2013 Nov;12(11):3360-9. doi: 10.1074/mcp.M113.032011. Epub 2013 Jul 23.

23.

Quantifying proteomes and their post-translational modifications by stable isotope label-based mass spectrometry.

Merrill AE, Coon JJ.

Curr Opin Chem Biol. 2013 Oct;17(5):779-86. doi: 10.1016/j.cbpa.2013.06.011. Epub 2013 Jul 5. Review.

24.

Neutron encoded labeling for peptide identification.

Rose CM, Merrill AE, Bailey DJ, Hebert AS, Westphall MS, Coon JJ.

Anal Chem. 2013 May 21;85(10):5129-37. doi: 10.1021/ac400476w. Epub 2013 May 2.

25.

Neutron-encoded mass signatures for multiplexed proteome quantification.

Hebert AS, Merrill AE, Bailey DJ, Still AJ, Westphall MS, Strieter ER, Pagliarini DJ, Coon JJ.

Nat Methods. 2013 Apr;10(4):332-4. doi: 10.1038/nmeth.2378. Epub 2013 Feb 24.

26.

Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling.

Merrill AE, Sarukhanov A, Krejci P, Idoni B, Camacho N, Estrada KD, Lyons KM, Deixler H, Robinson H, Chitayat D, Curry CJ, Lachman RS, Wilcox WR, Krakow D.

Am J Hum Genet. 2012 Mar 9;90(3):550-7. doi: 10.1016/j.ajhg.2012.02.005. Epub 2012 Mar 1.

27.

Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.

Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, Aktas D, Alikasifoglu M, Tuncbilek E, Orhan D, Bakar FT, Zabel B, Superti-Furga A, Bruckner-Tuderman L, Curry CJ, Pyott S, Byers PH, Eyre DR, Baldridge D, Lee B, Merrill AE, Davis EC, Cohn DH, Akarsu N, Krakow D.

Am J Hum Genet. 2010 Apr 9;86(4):551-9. doi: 10.1016/j.ajhg.2010.02.022. Epub 2010 Apr 1. Erratum in: Am J Hum Genet. 2010 Oct 8;87(4):572-3.

28.

Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome.

Merrill AE, Merriman B, Farrington-Rock C, Camacho N, Sebald ET, Funari VA, Schibler MJ, Firestein MH, Cohn ZA, Priore MA, Thompson AK, Rimoin DL, Nelson SF, Cohn DH, Krakow D.

Am J Hum Genet. 2009 Apr;84(4):542-9. doi: 10.1016/j.ajhg.2009.03.015.

29.

Mesenchyme-dependent BMP signaling directs the timing of mandibular osteogenesis.

Merrill AE, Eames BF, Weston SJ, Heath T, Schneider RA.

Development. 2008 Apr;135(7):1223-34. doi: 10.1242/dev.015933. Epub 2008 Feb 20.

30.

Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis.

Merrill AE, Bochukova EG, Brugger SM, Ishii M, Pilz DT, Wall SA, Lyons KM, Wilkie AO, Maxson RE Jr.

Hum Mol Genet. 2006 Apr 15;15(8):1319-28. Epub 2006 Mar 15.

PMID:
16540516
31.

A phylogenetically conserved cis-regulatory module in the Msx2 promoter is sufficient for BMP-dependent transcription in murine and Drosophila embryos.

Brugger SM, Merrill AE, Torres-Vazquez J, Wu N, Ting MC, Cho JY, Dobias SL, Yi SE, Lyons K, Bell JR, Arora K, Warrior R, Maxson R.

Development. 2004 Oct;131(20):5153-65.

32.

Msx2 and Twist cooperatively control the development of the neural crest-derived skeletogenic mesenchyme of the murine skull vault.

Ishii M, Merrill AE, Chan YS, Gitelman I, Rice DP, Sucov HM, Maxson RE Jr.

Development. 2003 Dec;130(24):6131-42.

33.

Msx2 is an immediate downstream effector of Pax3 in the development of the murine cardiac neural crest.

Kwang SJ, Brugger SM, Lazik A, Merrill AE, Wu LY, Liu YH, Ishii M, Sangiorgi FO, Rauchman M, Sucov HM, Maas RL, Maxson RE Jr.

Development. 2002 Jan;129(2):527-38.

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