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Items: 1 to 50 of 124

1.

Homologs of the LapD-LapG c-di-GMP Effector System Control Biofilm Formation by Bordetella bronchiseptica.

Ambrosis N, Boyd CD, O Toole GA, Fernández J, Sisti F.

PLoS One. 2016 Jul 5;11(7):e0158752. doi: 10.1371/journal.pone.0158752. eCollection 2016.

2.

Diagnostic utility of aquaporin-4 in the analysis of active demyelinating lesions.

Popescu BF, Guo Y, Jentoft ME, Parisi JE, Lennon VA, Pittock SJ, Weinshenker BG, Wingerchuk DM, Giannini C, Metz I, Brück W, Shuster EA, Carter J, Boyd CD, Clardy SL, Cohen BA, Lucchinetti CF.

Neurology. 2015 Jan 13;84(2):148-58. doi: 10.1212/WNL.0000000000001126. Epub 2014 Dec 10.

3.

Mechanistic insight into the conserved allosteric regulation of periplasmic proteolysis by the signaling molecule cyclic-di-GMP.

Chatterjee D, Cooley RB, Boyd CD, Mehl RA, O'Toole GA, Sondermann H.

Elife. 2014 Sep 2;3:e03650. doi: 10.7554/eLife.03650.

4.

Visuoperception test predicts pathologic diagnosis of Alzheimer disease in corticobasal syndrome.

Boyd CD, Tierney M, Wassermann EM, Spina S, Oblak AL, Ghetti B, Grafman J, Huey E.

Neurology. 2014 Aug 5;83(6):510-9. doi: 10.1212/WNL.0000000000000667. Epub 2014 Jul 2.

5.

Structural features of the Pseudomonas fluorescens biofilm adhesin LapA required for LapG-dependent cleavage, biofilm formation, and cell surface localization.

Boyd CD, Smith TJ, El-Kirat-Chatel S, Newell PD, Dufrêne YF, O'Toole GA.

J Bacteriol. 2014 Aug;196(15):2775-88. doi: 10.1128/JB.01629-14. Epub 2014 May 16.

6.

Hydrocephalus in neuromyelitis optica.

Clardy SL, Lucchinetti CF, Krecke KN, Lennon VA, O'Toole O, Weinshenker BG, Boyd CD, Krieger S, McGraw C, Guo Y, Pittock SJ.

Neurology. 2014 May 20;82(20):1841-3. doi: 10.1212/WNL.0000000000000428. Epub 2014 Apr 23. No abstract available.

7.

Single-cell and single-molecule analysis deciphers the localization, adhesion, and mechanics of the biofilm adhesin LapA.

El-Kirat-Chatel S, Beaussart A, Boyd CD, O'Toole GA, Dufrêne YF.

ACS Chem Biol. 2014 Feb 21;9(2):485-94. doi: 10.1021/cb400794e. Epub 2013 Dec 6.

8.

Single-molecule analysis of Pseudomonas fluorescens footprints.

El-Kirat-Chatel S, Boyd CD, O'Toole GA, Dufrêne YF.

ACS Nano. 2014 Feb 25;8(2):1690-8. doi: 10.1021/nn4060489. Epub 2014 Jan 23.

9.

Treatment of Alzheimer's Disease: Current Management and Experimental Therapeutics.

Honig LS, Boyd CD.

Curr Transl Geriatr Exp Gerontol Rep. 2013 Sep;2(3):174-181.

10.

Atomic force and super-resolution microscopy support a role for LapA as a cell-surface biofilm adhesin of Pseudomonas fluorescens.

Ivanov IE, Boyd CD, Newell PD, Schwartz ME, Turnbull L, Johnson MS, Whitchurch CB, O'Toole GA, Camesano TA.

Res Microbiol. 2012 Nov-Dec;163(9-10):685-91. doi: 10.1016/j.resmic.2012.10.001. Epub 2012 Oct 9.

11.

Second messenger regulation of biofilm formation: breakthroughs in understanding c-di-GMP effector systems.

Boyd CD, O'Toole GA.

Annu Rev Cell Dev Biol. 2012;28:439-62. doi: 10.1146/annurev-cellbio-101011-155705. Review.

12.

LapG, required for modulating biofilm formation by Pseudomonas fluorescens Pf0-1, is a calcium-dependent protease.

Boyd CD, Chatterjee D, Sondermann H, O'Toole GA.

J Bacteriol. 2012 Aug;194(16):4406-14. doi: 10.1128/JB.00642-12. Epub 2012 Jun 15.

13.

Structural characterization of a conserved, calcium-dependent periplasmic protease from Legionella pneumophila.

Chatterjee D, Boyd CD, O'Toole GA, Sondermann H.

J Bacteriol. 2012 Aug;194(16):4415-25. doi: 10.1128/JB.00640-12. Epub 2012 Jun 15.

14.

A c-di-GMP effector system controls cell adhesion by inside-out signaling and surface protein cleavage.

Newell PD, Boyd CD, Sondermann H, O'Toole GA.

PLoS Biol. 2011 Feb 1;9(2):e1000587. doi: 10.1371/journal.pbio.1000587.

15.

A novel fibrotic disorder associated with increased dermal fibroblast proliferation and downregulation of genes of the microfibrillar network.

Szauter KM, Ordas A, Laxer RM, Pope E, Wherrett D, Alman B, Mink M, Boyd CD, Csiszar K, Hinek A.

Br J Dermatol. 2010 Nov;163(5):1102-15. doi: 10.1111/j.1365-2133.2010.09911.x.

PMID:
20560960
16.

Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations.

Smith MJ, Boyd CD, MacCollin MM, Plotkin SR.

Clin Genet. 2009 May;75(5):501-2. doi: 10.1111/j.1399-0004.2009.01156.x. Epub 2009 Mar 23. No abstract available.

PMID:
19320657
17.

A cell stress signaling model of fetal hemoglobin induction: what doesn't kill red blood cells may make them stronger.

Mabaera R, West RJ, Conine SJ, Macari ER, Boyd CD, Engman CA, Lowrey CH.

Exp Hematol. 2008 Sep;36(9):1057-72. doi: 10.1016/j.exphem.2008.06.014. Review.

PMID:
18718415
18.

Lysyl oxidase in development, aging and pathologies of the skin.

Szauter KM, Cao T, Boyd CD, Csiszar K.

Pathol Biol (Paris). 2005 Sep;53(7):448-56.

PMID:
16085123
20.

Analysis of ABCC6 (MRP6) in normal human tissues.

Beck K, Hayashi K, Dang K, Hayashi M, Boyd CD.

Histochem Cell Biol. 2005 Jun;123(4-5):517-28. Epub 2005 May 12.

PMID:
15889270
22.

The dMRP/CG6214 gene of Drosophila is evolutionarily and functionally related to the human multidrug resistance-associated protein family.

Tarnay JN, Szeri F, Iliás A, Annilo T, Sung C, Le Saux O, Váradi A, Dean M, Boyd CD, Robinow S.

Insect Mol Biol. 2004 Oct;13(5):539-48.

PMID:
15373810
23.

The distribution of Abcc6 in normal mouse tissues suggests multiple functions for this ABC transporter.

Beck K, Hayashi K, Nishiguchi B, Le Saux O, Hayashi M, Boyd CD.

J Histochem Cytochem. 2003 Jul;51(7):887-902.

PMID:
12810839
24.

Evidence for a founder effect for pseudoxanthoma elasticum in the Afrikaner population of South Africa.

Le Saux O, Beck K, Sachsinger C, Treiber C, Göring HH, Curry K, Johnson EW, Bercovitch L, Marais AS, Terry SF, Viljoen DL, Boyd CD.

Hum Genet. 2002 Oct;111(4-5):331-8. Epub 2002 Sep 7.

PMID:
12384774
25.

A serial analysis of gene expression in sun-damaged human skin.

Urschitz J, Iobst S, Urban Z, Granda C, Souza KA, Lupp C, Schilling K, Scott I, Csiszar K, Boyd CD.

J Invest Dermatol. 2002 Jul;119(1):3-13.

26.

Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndrome.

Urbán Z, Riazi S, Seidl TL, Katahira J, Smoot LB, Chitayat D, Boyd CD, Hinek A.

Am J Hum Genet. 2002 Jul;71(1):30-44. Epub 2002 May 6.

27.

Loss of ATP-dependent transport activity in pseudoxanthoma elasticum-associated mutants of human ABCC6 (MRP6).

Iliás A, Urbán Z, Seidl TL, Le Saux O, Sinkó E, Boyd CD, Sarkadi B, Váradi A.

J Biol Chem. 2002 May 10;277(19):16860-7. Epub 2002 Mar 5.

28.

Somatic mutations of the lysyl oxidase gene on chromosome 5q23.1 in colorectal tumors.

Csiszar K, Fong SF, Ujfalusi A, Krawetz SA, Salvati EP, Mackenzie JW, Boyd CD.

Int J Cancer. 2002 Feb 10;97(5):636-42.

29.

Researching the biology of PXE: partnering in the process.

Terry SF, Boyd CD.

Am J Med Genet. 2001 Fall;106(3):177-84.

PMID:
11778977
30.

Supravalvular aortic stenosis: genetic and molecular dissection of a complex mutation in the elastin gene.

Urbán Z, Zhang J, Davis EC, Maeda GK, Kumar A, Stalker H, Belmont JW, Boyd CD, Wallace MR.

Hum Genet. 2001 Nov;109(5):512-20. Epub 2001 Oct 13.

PMID:
11735026
31.

A spectrum of ABCC6 mutations is responsible for pseudoxanthoma elasticum.

Le Saux O, Beck K, Sachsinger C, Silvestri C, Treiber C, Göring HH, Johnson EW, De Paepe A, Pope FM, Pasquali-Ronchetti I, Bercovitch L, Marais AS, Viljoen DL, Terry SF, Boyd CD.

Am J Hum Genet. 2001 Oct;69(4):749-64. Epub 2001 Aug 31. Erratum in: Am J Hum Genet 2001 Dec;69(6):1413. Am J Hum Genet 2002 Aug;71(2):448.

33.

Hyperglycemia enhances DNA fragmentation after transient cerebral ischemia.

Li PA, Rasquinha I, He QP, Siesjö BK, Csiszár K, Boyd CD, MacManus JP.

J Cereb Blood Flow Metab. 2001 May;21(5):568-76.

PMID:
11333367
34.

A quantitative evaluation of SAGE.

Stollberg J, Urschitz J, Urban Z, Boyd CD.

Genome Res. 2000 Aug;10(8):1241-8.

35.

Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay.

Urbán Z, Michels VV, Thibodeau SN, Davis EC, Bonnefont JP, Munnich A, Eyskens B, Gewillig M, Devriendt K, Boyd CD.

Hum Genet. 2000 Jun;106(6):577-88.

PMID:
10942104
36.

Elastic-fiber pathologies: primary defects in assembly-and secondary disorders in transport and delivery.

Urbán Z, Boyd CD.

Am J Hum Genet. 2000 Jul;67(1):4-7. Epub 2000 Jun 6. No abstract available.

37.

Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum.

Le Saux O, Urban Z, Tschuch C, Csiszar K, Bacchelli B, Quaglino D, Pasquali-Ronchetti I, Pope FM, Richards A, Terry S, Bercovitch L, de Paepe A, Boyd CD.

Nat Genet. 2000 Jun;25(2):223-7.

PMID:
10835642
38.

Elastin gene deletions in Williams syndrome patients result in altered deposition of elastic fibers in skin and a subclinical dermal phenotype.

Urbán Z, Peyrol S, Plauchu H, Zabot MT, Lebwohl M, Schilling K, Green M, Boyd CD, Csiszár K.

Pediatr Dermatol. 2000 Jan-Feb;17(1):12-20.

PMID:
10720981
39.

Identification of heterozygote carriers in families with a recessive form of pseudoxanthoma elasticum (PXE).

Bacchelli B, Quaglino D, Gheduzzi D, Taparelli F, Boraldi F, Trolli B, Le Saux O, Boyd CD, Ronchetti IP.

Mod Pathol. 1999 Dec;12(12):1112-23.

PMID:
10619263
40.

Novel trisaccharide fatty acid ester identified from the fruits of Morinda citrifolia (Noni).

Wang M, Kikuzaki H, Csiszar K, Boyd CD, Maunakea A, Fong SF, Ghai G, Rosen RT, Nakatani N, Ho CT.

J Agric Food Chem. 1999 Dec;47(12):4880-2.

PMID:
10606546
41.

Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16.

Le Saux O, Urban Z, Göring HH, Csiszar K, Pope FM, Richards A, Pasquali-Ronchetti I, Terry S, Bercovitch L, Lebwohl MG, Breuning M, van den Berg P, Kornet L, Doggett N, Ott J, de Jong PT, Bergen AA, Boyd CD.

Genomics. 1999 Nov 15;62(1):1-10. Erratum in: Genomics 2000 Feb 1;63(3):439.

PMID:
10585762
42.

Sequential loss of two neighboring exons of the tropoelastin gene during primate evolution.

Szabó Z, Levi-Minzi SA, Christiano AM, Struminger C, Stoneking M, Batzer MA, Boyd CD.

J Mol Evol. 1999 Nov;49(5):664-71.

PMID:
10552047
43.

The LOXL2 gene encodes a new lysyl oxidase-like protein and is expressed at high levels in reproductive tissues.

Jourdan-Le Saux C, Tronecker H, Bogic L, Bryant-Greenwood GD, Boyd CD, Csiszar K.

J Biol Chem. 1999 Apr 30;274(18):12939-44.

44.

Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcripts.

Urbán Z, Michels VV, Thibodeau SN, Donis-Keller H, Csiszár K, Boyd CD.

Hum Genet. 1999 Feb;104(2):135-42.

PMID:
10190324
45.

Altered bladder function in transgenic mice expressing rat elastin.

Lemack GE, Szabo Z, Urban Z, Boyd CD, Csiszar K, Vaughan ED Jr, Felsen D.

Neurourol Urodyn. 1999;18(1):55-68.

PMID:
10090127
46.

Coexpression of the lysyl oxidase-like gene (LOXL) and the gene encoding type III procollagen in induced liver fibrosis.

Kim Y, Peyrol S, So CK, Boyd CD, Csiszar K.

J Cell Biochem. 1999 Feb 1;72(2):181-8.

PMID:
10022501
47.

A gene-dosage PCR method for the detection of elastin gene deletions in patients with Williams syndrome.

del Rio T, Urbán Z, Csiszár K, Boyd CD.

Clin Genet. 1998 Aug;54(2):129-35.

PMID:
9761391
48.

The human lysyl oxidase-related gene (LOXL2) maps between markers D8S280 and D8S278 on chromosome 8p21.2-p21.3.

Jourdan-Le Saux C, Le Saux O, Donlon T, Boyd CD, Csiszar K.

Genomics. 1998 Jul 15;51(2):305-7. No abstract available.

PMID:
9722957
49.

In vitro translation of messenger RNA in a wheat germ extract cell-free system.

Olliver L, Grobler-Rabie A, Boyd CD.

Methods Mol Biol. 1998;86:229-33. No abstract available.

PMID:
9664474
50.

In vitro translation of messenger RNA in a rabbit reticulocyte lysate cell-free system.

Olliver L, Boyd CD.

Methods Mol Biol. 1998;86:221-7. No abstract available.

PMID:
9664473

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