• 4549 Citations
  • 36 h-Index
1983 …2019
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Personal profile

Area of Expertise

The overall goal of the Mathis Laboratory is to determine mechanisms involved in the pathogenesis of hypertension and renal injury. A strength of the lab is the study of both new and established neuro-immune mechanisms that may contribute to the development and maintenance of hypertension. Our lab utilizes the novel disease model, systemic lupus erythematosus (SLE) or lupus, to study the links between the nervous system, immune system/inflammation, and the kidney/blood pressure regulation. We are confident that studies in our lab will lead to a better understanding of both hypertension AND lupus.

Education/Academic qualification

MHA, Louisiana State University

EdD, University of Alabama

PhD Biochemistry, University of Texas Southwestern Medical Center

BS in Chemistry, Texas A & M University

Fingerprint Dive into the research topics where J. Michael Mathis is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Adenoviridae Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Genetic Therapy Medicine & Life Sciences
Breast Neoplasms Medicine & Life Sciences
Ovarian Neoplasms Medicine & Life Sciences
Cytochrome P-450 CYP11B2 Medicine & Life Sciences
Genes Medicine & Life Sciences
Thymidine Kinase Medicine & Life Sciences

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Research Output 1983 2019

Surface modification strategy based on the conjugation of NaYF 4 :5%Eu luminescent nanoprobe with organic aromatic compounds for application in bioimaging assays

da Silva Viana, R., de Mascena Costa, L. A., Leal, A. N. R., Williams, T. M., Luan, L., Zhang, G., Wang, M., Harmon, A. C., dos Anjos, J. V., Cueto, R., Filho, M. A. G., Falcão, E. H. L., Vicente, M. G. H., Junior, S. A. & Mathis, J. M., 1 Jan 2019, In : Journal of Nanoparticle Research. 21, 1, 23.

Research output: Contribution to journalArticleResearchpeer-review

Nanoprobes
Surface Modification
aromatic compounds
Aromatic compounds
Conjugation

Synthesis, Characterization, and Evaluation of Near-IR Boron Dipyrromethene Bioconjugates for Labeling of Adenocarcinomas by Selectively Targeting the Epidermal Growth Factor Receptor

Kaufman, N. E. M., Meng, Q., Griffin, K. E., Singh, S. S., Dahal, A., Zhou, Z., Fronczek, F. R., Mathis, J. M., Jois, S. D. & Vicente, M. G. H., 11 Apr 2019, In : Journal of Medicinal Chemistry. 62, 7, p. 3323-3335 13 p.

Research output: Contribution to journalArticleResearchpeer-review

leucyl-alanyl-arginyl-leucyl-leucyl-threonine
Boron
Epidermal Growth Factor Receptor
Adenocarcinoma
HT29 Cells
2 Citations (Scopus)

Synthesis and investigation of phthalocyanine-biotin conjugates

Okoth, E. A., Zhou, Z., Ongarora, B., Stutes, A., Mathis, J. M. & Vicente, M. G. H., 1 Jan 2019, In : Journal of Porphyrins and Phthalocyanines. 23, 1-2, p. 125-135 11 p.

Research output: Contribution to journalArticleResearchpeer-review

Biotin
hydrazine
Tumors
Bearings (structural)
Thiourea

Endocytic Selective Toxicity of Rhodamine 6G nanoGUMBOS in Breast Cancer Cells

Bhattarai, N., Mathis, J. M., Chen, M., Pérez, R. L., Siraj, N., Magut, P. K. S., McDonough, K., Sahasrabudhe, G. & Warner, I. M., 4 Sep 2018, In : Molecular Pharmaceutics. 15, 9, p. 3837-3845 9 p.

Research output: Contribution to journalArticleResearchpeer-review

Nanostructures
Breast Neoplasms
Endocytosis
Neoplasms
Clathrin

Oncolytic virotherapy for breast cancer treatment

O’bryan, S. M. & Mathis, J. M., 1 Jan 2018, In : Current Gene Therapy. 18, 4, p. 192-205 14 p.

Research output: Contribution to journalReview articleResearchpeer-review

Oncolytic Virotherapy
Breast Neoplasms
Oncolytic Viruses
Therapeutics
Baltimore