Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Jonathan C. Neumann"'
Autor:
Palanikumar Manoharan, Jerry B. Lingrel, Joshua E. Basford, Robyn Pilcher-Roberts, David Y. Hui, Jonathan C. Neumann
Publikováno v:
Journal of Biological Chemistry. 289:31638-31646
Previous studies have shown that the myeloid-specific deficiency of the transcription factor Krüppel-like factor 2 (KLF2) accelerates atherosclerosis in hypercholesterolemic Ldlr(-/-) mice due to the enhanced adhesion of myeloid cells to activated e
Autor:
Jerry B. Lingrel, Valerie M. Lasko, Tara N. Rindler, Michelle L. Nieman, Jonathan C. Neumann, John N. Lorenz, Iva Dostanic
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 301:H1396-H1404
The α2-isoform of Na,K-ATPase (α2) is thought to play a role in blood pressure regulation, but the specific cell type(s) involved have not been identified. Therefore, it is important to study the role of the α2in individual cell types in the cardi
Autor:
Anil G. Menon, Kyle T. O'Connor, Brad D. Wagner, Maureen A. Sartor, Saikumar Karyala, Paranthaman SenthamaraiKannan, Jonathan C. Neumann, Paul Succop, Mario Medvedovic, James Philip Klyza
Publikováno v:
Physiological Genomics. 43:317-324
The mechanisms for provisioning maternal resources to offspring in placental mammals involve complex interactions between maternally regulated and fetally regulated gene networks in the placenta, a tissue that is derived from the zygote and therefore
Autor:
Roy L. Sutliff, Anastasia Andringa, Jonathan C. Neumann, Marian L. Miller, Gail J. Pyne, Gary E. Shull, Gbolahan Okunade, Thomas Doetschman, Kyle T. O'Connor, Richard J. Paul, Vikram Prasad, Daniel A. Miller
Publikováno v:
Journal of Biological Chemistry. 279:33742-33750
The relative importance of plasma membrane Ca2+-ATPase (PMCA) 1 and PMCA4 was assessed in mice carrying null mutations in their genes (Atp2b1 and Atp2b4). Loss of both copies of the gene encoding PMCA1 caused embryolethality, whereas heterozygous mut
Publikováno v:
Handbook of ATPases: Biochemistry, Cell Biology, Pathophysiology
Autor:
Alison Woo, Jerry B. Lingrel, Iva Dostanic, Jonathan C. Neumann, Kyle T. O'Connor, Suiwen He, Paul F. James, Amy E. Moseley, Marc Cougnon
Publikováno v:
Annals of the New York Academy of Sciences. 986:354-359
The Na,K-ATPase is composed of two subunits, alpha and beta, and each subunit consists of multiple isoforms. In the case of alpha, four isoforms, alpha1, alpha2, alpha3, and alpha4 are present in mammalian cells. The distribution of these isoforms is
Autor:
Jonathan C. Neumann, A. Kumar, John N. Lorenz, John J. Duffy, L. Close, J. L. Lessard, Jeffrey Robbins, Thomas Doetschman, B. A. O’Toole, Gregory P. Boivin, K. Crawford, Sharon A. Pawlowski, M. Madison
Publikováno v:
Proceedings of the National Academy of Sciences. 94:4406-4411
The muscle actins in higher vertebrates display highly conserved amino acid sequences, yet they show distinct expression patterns. Thus, cardiac α-actin, skeletal α-actin, vascular smooth muscle α-actin, and enteric smooth muscle γ-actin comprise
Publikováno v:
Nucleic Acids Research. 22:4748-4755
The Na,K-ATPase is an integral plasma membrane protein consisting of alpha and beta subunits, each of which has discrete isoforms expressed in a tissue-specific manner. Of the three functional alpha isoform genes, the one encoding the alpha 3 isoform
Autor:
Tara N, Rindler, Iva, Dostanic, Valerie M, Lasko, Michelle L, Nieman, Jonathan C, Neumann, John N, Lorenz, Jerry B, Lingrel
Publikováno v:
American journal of physiology. Heart and circulatory physiology. 301(4)
The α(2)-isoform of Na,K-ATPase (α(2)) is thought to play a role in blood pressure regulation, but the specific cell type(s) involved have not been identified. Therefore, it is important to study the role of the α(2) in individual cell types in th
Autor:
Iva Dostanic, Ingrid L. Grupp, Jonathan C. Neumann, John N. Lorenz, Maqsood A. Wani, Jo El J. Schultz, Jerry B. Lingrel
Publikováno v:
The Journal of biological chemistry. 278(52)
Inhibition of Na,K-ATPase activity by cardiac glycosides is believed to be the major mechanism by which this class of drugs increases heart contractility. However, direct evidence demonstrating this is lacking. Furthermore it is unknown which specifi