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Items: 15

1.

Establishment of a murine culture system for modeling the temporal progression of cranial and trunk neural crest cell differentiation.

Replogle MR, Sreevidya VS, Lee VM, Laiosa MD, Svoboda KR, Udvadia AJ.

Dis Model Mech. 2018 Nov 8. pii: dmm.035097. doi: 10.1242/dmm.035097. [Epub ahead of print]

2.

Functional Assays of Hematopoietic Stem Cells in Toxicology Research.

Laiosa MD.

Methods Mol Biol. 2018;1803:317-333. doi: 10.1007/978-1-4939-8549-4_19.

PMID:
29882147
3.

Effects of Developmental Activation of the Aryl Hydrocarbon Receptor by 2,3,7,8-Tetrachlorodibenzo-p-dioxin on Long-term Self-renewal of Murine Hematopoietic Stem Cells.

Laiosa MD, Tate ER, Ahrenhoerster LS, Chen Y, Wang D.

Environ Health Perspect. 2016 Jul;124(7):957-65. doi: 10.1289/ehp.1509820. Epub 2015 Oct 23.

4.

Fetal Hematopoietic Stem Cells Are the Canaries in the Coal Mine That Portend Later Life Immune Deficiency.

Laiosa MD, Tate ER.

Endocrinology. 2015 Oct;156(10):3458-65. doi: 10.1210/en.2015-1347. Epub 2015 Aug 4. Review.

5.

Developmental exposure to 2,3,7,8 tetrachlorodibenzo-p-dioxin attenuates later-life Notch1-mediated T cell development and leukemogenesis.

Ahrenhoerster LS, Leuthner TC, Tate ER, Lakatos PA, Laiosa MD.

Toxicol Appl Pharmacol. 2015 Mar 1;283(2):99-108. doi: 10.1016/j.taap.2014.12.017. Epub 2015 Jan 10.

6.

Developmental exposure to 2,3,7,8 tetrachlorodibenzo-p-dioxin attenuates capacity of hematopoietic stem cells to undergo lymphocyte differentiation.

Ahrenhoerster LS, Tate ER, Lakatos PA, Wang X, Laiosa MD.

Toxicol Appl Pharmacol. 2014 Jun 1;277(2):172-82. doi: 10.1016/j.taap.2014.03.020. Epub 2014 Apr 4.

7.

Immunotoxicology: fifty years of global scientific progress.

McKarns SC, Kerkvliet NI, Dean JH, Bonn MB, Cohen MD, Franko J, Laiosa MD, Lawrence BP, Luebke RW, Luster MI, Miller PG, Palmer RK, Pfau JC, Raman P, Regal JF, Rodgers KE, Schondelmeyer RS, Zhang X, Burns-Naas LA.

J Immunotoxicol. 2012 Oct-Dec;9(4):339-40. doi: 10.3109/1547691X.2012.658530. Epub 2012 Oct 19.

PMID:
23078377
8.

Cell individuality: the bistable gene expression of the type III secretion system in Dickeya dadantii 3937.

Zeng Q, Laiosa MD, Steeber DA, Biddle EM, Peng Q, Yang CH.

Mol Plant Microbe Interact. 2012 Jan;25(1):37-47. doi: 10.1094/MPMI-05-11-0105.

9.

Identification of stage-specific gene modulation during early thymocyte development by whole-genome profiling analysis after aryl hydrocarbon receptor activation.

Laiosa MD, Mills JH, Lai ZW, Singh KP, Middleton FA, Gasiewicz TA, Silverstone AE.

Mol Pharmacol. 2010 May;77(5):773-83. doi: 10.1124/mol.109.062497. Epub 2010 Feb 16.

10.

Reduction of myeloid suppressor cell derived nitric oxide provides a mechanistic basis of lead enhancement of alloreactive CD4(+) T cell proliferation.

Farrer DG, Hueber S, Laiosa MD, Eckles KG, McCabe MJ Jr.

Toxicol Appl Pharmacol. 2008 Jun 1;229(2):135-45. doi: 10.1016/j.taap.2007.12.011. Epub 2008 Apr 22.

11.

Exposure to inorganic mercury in vivo attenuates extrinsic apoptotic signaling in Staphylococcal aureus enterotoxin B stimulated T-cells.

Laiosa MD, Eckles KG, Langdon M, Rosenspire AJ, McCabe MJ Jr.

Toxicol Appl Pharmacol. 2007 Dec 15;225(3):238-50. Epub 2007 Jun 19.

12.

Low and nontoxic inorganic mercury burdens attenuate BCR-mediated signal transduction.

McCabe MJ Jr, Laiosa MD, Li L, Menard SL, Mattingly RR, Rosenspire AJ.

Toxicol Sci. 2007 Oct;99(2):512-21. Epub 2007 Jul 26.

PMID:
17656488
13.

Cell proliferation arrest within intrathymic lymphocyte progenitor cells causes thymic atrophy mediated by the aryl hydrocarbon receptor.

Laiosa MD, Wyman A, Murante FG, Fiore NC, Staples JE, Gasiewicz TA, Silverstone AE.

J Immunol. 2003 Nov 1;171(9):4582-91.

14.

2,3,7,8-tetrachlorodibenzo-p-dioxin causes alterations in lymphocyte development and thymic atrophy in hemopoietic chimeras generated from mice deficient in ARNT2.

Laiosa MD, Lai ZW, Thurmond TS, Fiore NC, DeRossi C, Holdener BC, Gasiewicz TA, Silverstone AE.

Toxicol Sci. 2002 Sep;69(1):117-24.

PMID:
12215665
15.

Mouse fzd4 maps within a region of chromosome 7 important for thymus and cardiac development.

DeRossi C, Laiosa MD, Silverstone AE, Holdener BC.

Genesis. 2000 Jun;27(2):64-75.

PMID:
10890980

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