Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 103

1.

Humidity-Dependent Surface Structure and Hydroxide Conductance of a Model Quaternary Ammonium Anion Exchange Membrane.

Barnes AM, Liu B, Buratto SK.

Langmuir. 2019 Nov 5;35(44):14188-14193. doi: 10.1021/acs.langmuir.9b02160. Epub 2019 Oct 22.

PMID:
31596594
2.

Bruck syndrome 2 variant lacking congenital contractures and involving a novel compound heterozygous PLOD2 mutation.

Mumm S, Gottesman GS, Wenkert D, Campeau PM, Nenninger A, Huskey M, Bijanki VN, Veis DJ, Barnes AM, Marini JC, Stolina M, Zhang F, McAlister WH, Whyte MP.

Bone. 2019 Aug 28:115047. doi: 10.1016/j.bone.2019.115047. [Epub ahead of print]

PMID:
31472299
3.

Early E. casseliflavus gut colonization and outcomes of allogeneic hematopoietic cell transplantation.

Rashidi A, Ebadi M, Shields-Cutler RR, Kruziki K, Manias DA, Barnes AMT, DeFor TE, Ferrieri P, Young JH, Knights D, Blazar BR, Weisdorf DJ, Dunny GM.

PLoS One. 2019 Aug 8;14(8):e0220850. doi: 10.1371/journal.pone.0220850. eCollection 2019.

4.

COL1A1 C-propeptide mutations cause ER mislocalization of procollagen and impair C-terminal procollagen processing.

Barnes AM, Ashok A, Makareeva EN, Brusel M, Cabral WA, Weis M, Moali C, Bettler E, Eyre DR, Cassella JP, Leikin S, Hulmes DJS, Kessler E, Marini JC.

Biochim Biophys Acta Mol Basis Dis. 2019 Sep 1;1865(9):2210-2223. doi: 10.1016/j.bbadis.2019.04.018. Epub 2019 May 2.

PMID:
31055083
5.

Solid tumor screening recommendations in trisomy 18.

Farmakis SG, Barnes AM, Carey JC, Braddock SR.

Am J Med Genet A. 2019 Mar;179(3):455-466. doi: 10.1002/ajmg.a.61029. Epub 2019 Jan 13.

PMID:
30637956
6.

Widespread Lichtheimia Infection in a Patient with Extensive Burns: Opportunities for Novel Antifungal Agents.

Thielen BK, Barnes AMT, Sabin AP, Huebner B, Nelson S, Wesenberg E, Hansen GT.

Mycopathologia. 2019 Feb;184(1):121-128. doi: 10.1007/s11046-018-0281-6. Epub 2018 Jul 2.

PMID:
29967971
7.

Imaging Channel Connectivity in Nafion Using Electrostatic Force Microscopy.

Barnes AM, Buratto SK.

J Phys Chem B. 2018 Jan 25;122(3):1289-1295. doi: 10.1021/acs.jpcb.7b08230. Epub 2018 Jan 11.

PMID:
29290118
8.

A Noninvasive Rhizopus Infection With a Bladder Fungal Ball in a Patient With Poorly Controlled Diabetes Mellitus.

Barnes AMT, Crespo-Diaz RJ, Cohenour J, Kirsch JD, Arbefeville S, Ferrieri P.

Lab Med. 2017 Dec 22;49(1):75-79. doi: 10.1093/labmed/lmx060.

PMID:
29069422
9.

Restructuring of Enterococcus faecalis biofilm architecture in response to antibiotic-induced stress.

Dale JL, Nilson JL, Barnes AMT, Dunny GM.

NPJ Biofilms Microbiomes. 2017 Jun 30;3:15. doi: 10.1038/s41522-017-0023-4. eCollection 2017.

10.

Stochasticity in the enterococcal sex pheromone response revealed by quantitative analysis of transcription in single cells.

Breuer RJ, Bandyopadhyay A, O'Brien SA, Barnes AMT, Hunter RC, Hu WS, Dunny GM.

PLoS Genet. 2017 Jul 3;13(7):e1006878. doi: 10.1371/journal.pgen.1006878. eCollection 2017 Jul.

11.

P4HA1 mutations cause a unique congenital disorder of connective tissue involving tendon, bone, muscle and the eye.

Zou Y, Donkervoort S, Salo AM, Foley AR, Barnes AM, Hu Y, Makareeva E, Leach ME, Mohassel P, Dastgir J, Deardorff MA, Cohn RD, DiNonno WO, Malfait F, Lek M, Leikin S, Marini JC, Myllyharju J, Bönnemann CG.

Hum Mol Genet. 2017 Jun 15;26(12):2207-2217. doi: 10.1093/hmg/ddx110.

12.

Wilms tumor and trisomy 18: Is there an association?

Carey JC, Barnes AM.

Am J Med Genet C Semin Med Genet. 2016 Sep;172(3):307-8. doi: 10.1002/ajmg.c.31523. Epub 2016 Aug 26. Review. No abstract available.

PMID:
27566680
13.

Enterococcus faecalis readily colonizes the entire gastrointestinal tract and forms biofilms in a germ-free mouse model.

Barnes AMT, Dale JL, Chen Y, Manias DA, Greenwood Quaintance KE, Karau MK, Kashyap PC, Patel R, Wells CL, Dunny GM.

Virulence. 2017 Apr 3;8(3):282-296. doi: 10.1080/21505594.2016.1208890. Epub 2016 Aug 25.

14.

Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta.

Cabral WA, Ishikawa M, Garten M, Makareeva EN, Sargent BM, Weis M, Barnes AM, Webb EA, Shaw NJ, Ala-Kokko L, Lacbawan FL, Högler W, Leikin S, Blank PS, Zimmerberg J, Eyre DR, Yamada Y, Marini JC.

PLoS Genet. 2016 Jul 21;12(7):e1006156. doi: 10.1371/journal.pgen.1006156. eCollection 2016 Jul.

15.

Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix Mineralization.

Fratzl-Zelman N, Barnes AM, Weis M, Carter E, Hefferan TE, Perino G, Chang W, Smith PA, Roschger P, Klaushofer K, Glorieux FH, Eyre DR, Raggio C, Rauch F, Marini JC.

J Clin Endocrinol Metab. 2016 Sep;101(9):3516-25. doi: 10.1210/jc.2016-1334. Epub 2016 Jul 6.

16.

MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta.

Lindert U, Cabral WA, Ausavarat S, Tongkobpetch S, Ludin K, Barnes AM, Yeetong P, Weis M, Krabichler B, Srichomthong C, Makareeva EN, Janecke AR, Leikin S, Röthlisberger B, Rohrbach M, Kennerknecht I, Eyre DR, Suphapeetiporn K, Giunta C, Marini JC, Shotelersuk V.

Nat Commun. 2016 Jul 6;7:11920. doi: 10.1038/ncomms11920.

17.

Bone mineral properties in growing Col1a2(+/G610C) mice, an animal model of osteogenesis imperfecta.

Masci M, Wang M, Imbert L, Barnes AM, Spevak L, Lukashova L, Huang Y, Ma Y, Marini JC, Jacobsen CM, Warman ML, Boskey AL.

Bone. 2016 Jun;87:120-9. doi: 10.1016/j.bone.2016.04.011. Epub 2016 Apr 13.

18.

Investigation of Humidity Dependent Surface Morphology and Proton Conduction in Multi-Acid Side Chain Membranes by Conductive Probe Atomic Force Microscopy.

Economou NJ, Barnes AM, Wheat AJ, Schaberg MS, Hamrock SJ, Buratto SK.

J Phys Chem B. 2015 Nov 5;119(44):14280-7. doi: 10.1021/acs.jpcb.5b07255. Epub 2015 Oct 26.

PMID:
26439098
19.

Genetic Defects in TAPT1 Disrupt Ciliogenesis and Cause a Complex Lethal Osteochondrodysplasia.

Symoens S, Barnes AM, Gistelinck C, Malfait F, Guillemyn B, Steyaert W, Syx D, D'hondt S, Biervliet M, De Backer J, Witten EP, Leikin S, Makareeva E, Gillessen-Kaesbach G, Huysseune A, Vleminckx K, Willaert A, De Paepe A, Marini JC, Coucke PJ.

Am J Hum Genet. 2015 Oct 1;97(4):521-34. doi: 10.1016/j.ajhg.2015.08.009. Epub 2015 Sep 10.

20.

Evaluation of the Enterococcus faecalis Biofilm-Associated Virulence Factors AhrC and Eep in Rat Foreign Body Osteomyelitis and In Vitro Biofilm-Associated Antimicrobial Resistance.

Frank KL, Vergidis P, Brinkman CL, Greenwood Quaintance KE, Barnes AM, Mandrekar JN, Schlievert PM, Dunny GM, Patel R.

PLoS One. 2015 Jun 15;10(6):e0130187. doi: 10.1371/journal.pone.0130187. eCollection 2015.

21.

Multiple roles for Enterococcus faecalis glycosyltransferases in biofilm-associated antibiotic resistance, cell envelope integrity, and conjugative transfer.

Dale JL, Cagnazzo J, Phan CQ, Barnes AM, Dunny GM.

Antimicrob Agents Chemother. 2015 Jul;59(7):4094-105. doi: 10.1128/AAC.00344-15. Epub 2015 Apr 27.

22.

Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expression.

Reich A, Bae AS, Barnes AM, Cabral WA, Hinek A, Stimec J, Hill SC, Chitayat D, Marini JC.

J Clin Endocrinol Metab. 2015 Feb;100(2):E325-32. doi: 10.1210/jc.2014-3082. Epub 2014 Nov 11.

23.

Morphology-dependent electronic properties in cross-linked (P3HT-b-P3MT) block copolymer nanostructures.

Baghgar M, Barnes AM, Pentzer E, Wise AJ, Hammer BA, Emrick T, Dinsmore AD, Barnes MD.

ACS Nano. 2014 Aug 26;8(8):8344-9. doi: 10.1021/nn502806d. Epub 2014 Jul 14.

PMID:
25003706
24.

A novel IFITM5 mutation in severe atypical osteogenesis imperfecta type VI impairs osteoblast production of pigment epithelium-derived factor.

Farber CR, Reich A, Barnes AM, Becerra P, Rauch F, Cabral WA, Bae A, Quinlan A, Glorieux FH, Clemens TL, Marini JC.

J Bone Miner Res. 2014 Jun;29(6):1402-11.

25.

Lingual nerve neuropraxia following use of the Laryngeal Mask Airway Supreme.

Thiruvenkatarajan V, Van Wijk RM, Elhalawani I, Barnes AM.

J Clin Anesth. 2014 Feb;26(1):65-8. doi: 10.1016/j.jclinane.2013.10.003. Epub 2014 Jan 18.

PMID:
24444986
26.

Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations.

Barnes AM, Duncan G, Weis M, Paton W, Cabral WA, Mertz EL, Makareeva E, Gambello MJ, Lacbawan FL, Leikin S, Fertala A, Eyre DR, Bale SJ, Marini JC.

Hum Mutat. 2013 Sep;34(9):1279-88. doi: 10.1002/humu.22362. Epub 2013 Jul 8.

27.

Mutations in WNT1 cause different forms of bone fragility.

Keupp K, Beleggia F, Kayserili H, Barnes AM, Steiner M, Semler O, Fischer B, Yigit G, Janda CY, Becker J, Breer S, Altunoglu U, Grünhagen J, Krawitz P, Hecht J, Schinke T, Makareeva E, Lausch E, Cankaya T, Caparrós-Martín JA, Lapunzina P, Temtamy S, Aglan M, Zabel B, Eysel P, Koerber F, Leikin S, Garcia KC, Netzer C, Schönau E, Ruiz-Perez VL, Mundlos S, Amling M, Kornak U, Marini J, Wollnik B.

Am J Hum Genet. 2013 Apr 4;92(4):565-74. doi: 10.1016/j.ajhg.2013.02.010. Epub 2013 Mar 14.

28.

AhrC and Eep are biofilm infection-associated virulence factors in Enterococcus faecalis.

Frank KL, Guiton PS, Barnes AM, Manias DA, Chuang-Smith ON, Kohler PL, Spaulding AR, Hultgren SJ, Schlievert PM, Dunny GM.

Infect Immun. 2013 May;81(5):1696-708. doi: 10.1128/IAI.01210-12. Epub 2013 Mar 4.

29.

Enterococcus faecalis produces abundant extracellular structures containing DNA in the absence of cell lysis during early biofilm formation.

Barnes AM, Ballering KS, Leibman RS, Wells CL, Dunny GM.

MBio. 2012 Jul 24;3(4):e00193-12. doi: 10.1128/mBio.00193-12. Print 2012.

30.

Ultrastructure of a novel bacterial form located in Staphylococcus aureus in vitro and in vivo catheter-associated biofilms.

Hess DJ, Henry-Stanley MJ, Barnes AM, Dunny GM, Wells CL.

J Histochem Cytochem. 2012 Oct;60(10):770-6. Epub 2012 Jul 21.

31.

Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix.

Barnes AM, Cabral WA, Weis M, Makareeva E, Mertz EL, Leikin S, Eyre D, Trujillo C, Marini JC.

Hum Mutat. 2012 Nov;33(11):1589-98. doi: 10.1002/humu.22139. Epub 2012 Jul 16.

32.

Probing Inter- and Intrachain Exciton Coupling in Isolated Poly(3-hexylthiophene) Nanofibers: Effect of Solvation and Regioregularity.

Baghgar M, Labastide J, Bokel F, Dujovne I, McKenna A, Barnes AM, Pentzer E, Emrick T, Hayward R, Barnes MD.

J Phys Chem Lett. 2012 Jun 21;3(12):1674-9. doi: 10.1021/jz3005909. Epub 2012 Jun 7.

PMID:
26285727
33.

A novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfecta.

Takagi M, Ishii T, Barnes AM, Weis M, Amano N, Tanaka M, Fukuzawa R, Nishimura G, Eyre DR, Marini JC, Hasegawa T.

PLoS One. 2012;7(5):e36809. doi: 10.1371/journal.pone.0036809. Epub 2012 May 15.

34.

A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta.

Cabral WA, Barnes AM, Adeyemo A, Cushing K, Chitayat D, Porter FD, Panny SR, Gulamali-Majid F, Tishkoff SA, Rebbeck TR, Gueye SM, Bailey-Wilson JE, Brody LC, Rotimi CN, Marini JC.

Genet Med. 2012 May;14(5):543-51. doi: 10.1038/gim.2011.44. Epub 2012 Jan 26.

35.
36.

Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix.

Valli M, Barnes AM, Gallanti A, Cabral WA, Viglio S, Weis MA, Makareeva E, Eyre D, Leikin S, Antoniazzi F, Marini JC, Mottes M.

Clin Genet. 2012 Nov;82(5):453-9. doi: 10.1111/j.1399-0004.2011.01794.x. Epub 2011 Oct 19.

37.

Relation between antibiotic susceptibility and ultrastructure of Staphylococcus aureus biofilms on surgical suture.

Wells CL, Henry-Stanley MJ, Barnes AM, Dunny GM, Hess DJ.

Surg Infect (Larchmt). 2011 Aug;12(4):297-305. doi: 10.1089/sur.2010.104.

38.

New perspectives on osteogenesis imperfecta.

Forlino A, Cabral WA, Barnes AM, Marini JC.

Nat Rev Endocrinol. 2011 Jun 14;7(9):540-57. doi: 10.1038/nrendo.2011.81. Review.

39.

COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta.

Lindahl K, Barnes AM, Fratzl-Zelman N, Whyte MP, Hefferan TE, Makareeva E, Brusel M, Yaszemski MJ, Rubin CJ, Kindmark A, Roschger P, Klaushofer K, McAlister WH, Mumm S, Leikin S, Kessler E, Boskey AL, Ljunggren O, Marini JC.

Hum Mutat. 2011 Jun;32(6):598-609. doi: 10.1002/humu.21475. Epub 2011 Apr 7.

40.

Bacterial contamination of surgical suture resembles a biofilm.

Henry-Stanley MJ, Hess DJ, Barnes AM, Dunny GM, Wells CL.

Surg Infect (Larchmt). 2010 Oct;11(5):433-9. doi: 10.1089/sur.2010.006.

41.

Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding.

Barnes AM, Carter EM, Cabral WA, Weis M, Chang W, Makareeva E, Leikin S, Rotimi CN, Eyre DR, Raggio CL, Marini JC.

N Engl J Med. 2010 Feb 11;362(6):521-8. doi: 10.1056/NEJMoa0907705. Epub 2010 Jan 20.

42.

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. doi: 10.1007/s00441-009-0872-0. Epub 2009 Oct 28. Review.

43.

Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex.

Chang W, Barnes AM, Cabral WA, Bodurtha JN, Marini JC.

Hum Mol Genet. 2010 Jan 15;19(2):223-34. doi: 10.1093/hmg/ddp481. Epub 2009 Oct 21.

44.

Candidate cell and matrix interaction domains on the collagen fibril, the predominant protein of vertebrates.

Sweeney SM, Orgel JP, Fertala A, McAuliffe JD, Turner KR, Di Lullo GA, Chen S, Antipova O, Perumal S, Ala-Kokko L, Forlino A, Cabral WA, Barnes AM, Marini JC, San Antonio JD.

J Biol Chem. 2008 Jul 25;283(30):21187-97. doi: 10.1074/jbc.M709319200. Epub 2008 May 15.

45.

Development and use of an efficient system for random mariner transposon mutagenesis to identify novel genetic determinants of biofilm formation in the core Enterococcus faecalis genome.

Kristich CJ, Nguyen VT, Le T, Barnes AM, Grindle S, Dunny GM.

Appl Environ Microbiol. 2008 Jun;74(11):3377-86. doi: 10.1128/AEM.02665-07. Epub 2008 Apr 11.

46.

Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfecta.

Makareeva E, Mertz EL, Kuznetsova NV, Sutter MB, DeRidder AM, Cabral WA, Barnes AM, McBride DJ, Marini JC, Leikin S.

J Biol Chem. 2008 Feb 22;283(8):4787-98. Epub 2007 Dec 11.

47.

Components of the collagen prolyl 3-hydroxylation complex are crucial for normal bone development.

Marini JC, Cabral WA, Barnes AM, Chang W.

Cell Cycle. 2007 Jul 15;6(14):1675-81. Epub 2007 May 18. Review.

PMID:
17630507
48.

Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta.

Cabral WA, Chang W, Barnes AM, Weis M, Scott MA, Leikin S, Makareeva E, Kuznetsova NV, Rosenbaum KN, Tifft CJ, Bulas DI, Kozma C, Smith PA, Eyre DR, Marini JC.

Nat Genet. 2007 Mar;39(3):359-65. Epub 2007 Feb 4. Erratum in: Nat Genet. 2008 Jul;40(7):927.

PMID:
17277775
49.

Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.

Barnes AM, Chang W, Morello R, Cabral WA, Weis M, Eyre DR, Leikin S, Makareeva E, Kuznetsova N, Uveges TE, Ashok A, Flor AW, Mulvihill JJ, Wilson PL, Sundaram UT, Lee B, Marini JC.

N Engl J Med. 2006 Dec 28;355(26):2757-64.

50.

Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.

Marini JC, Forlino A, Cabral WA, Barnes AM, San Antonio JD, Milgrom S, Hyland JC, Körkkö J, Prockop DJ, De Paepe A, Coucke P, Symoens S, Glorieux FH, Roughley PJ, Lund AM, Kuurila-Svahn K, Hartikka H, Cohn DH, Krakow D, Mottes M, Schwarze U, Chen D, Yang K, Kuslich C, Troendle J, Dalgleish R, Byers PH.

Hum Mutat. 2007 Mar;28(3):209-21. Review.

Supplemental Content

Loading ...
Support Center