Ram P Naikawadi
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Explore the profile of Ram P Naikawadi including associated specialties, affiliations and a list of published articles.
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13
Citations
2338
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Recent Articles
1.
Wilson C, Mertens T, Shivshankar P, Bi W, Collum S, Wareing N, et al.
JCI Insight
. 2022 Apr;
7(10).
PMID: 35420997
Idiopathic pulmonary fibrosis (IPF) is a fatal disease with limited treatment options. The role of the developmental transcription factor Sine oculis homeobox homolog 1 (SIX1) in the pathophysiology of lung...
2.
Arora S, Thompson P, Wang Y, Bhattacharyya A, Apostolopoulou H, Hatano R, et al.
Med
. 2021 Oct;
2(8):938-950.
PMID: 34617070
Background: The failure of immune surveillance to remove senescent cells drive age-related diseases. Here, we target an endogenous immune surveillance mechanism that can promote elimination of senescent cells and reverse...
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4.
Baluk P, Naikawadi R, Kim S, Rodriguez F, Choi D, Hong Y, et al.
Am J Pathol
. 2020 Oct;
190(12):2355-2375.
PMID: 33039355
Despite many reports about pulmonary blood vessels in lung fibrosis, the contribution of lymphatics to fibrosis is unknown. We examined the mechanism and consequences of lymphatic remodeling in mice with...
5.
Naikawadi R, Green G, Jones K, Achtar-Zadeh N, Mieleszko J, Arnould I, et al.
Am J Respir Cell Mol Biol
. 2020 Jun;
63(4):490-501.
PMID: 32551854
Telomere dysfunction is associated with multiple fibrotic lung processes, including chronic lung allograft dysfunction (CLAD)-the major limitation to long-term survival following lung transplantation. Although shorter donor telomere lengths are associated...
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7.
Aran D, Looney A, Liu L, Wu E, Fong V, Hsu A, et al.
Nat Immunol
. 2019 Jan;
20(2):163-172.
PMID: 30643263
Tissue fibrosis is a major cause of mortality that results from the deposition of matrix proteins by an activated mesenchyme. Macrophages accumulate in fibrosis, but the role of specific subgroups...
8.
Van Dyken S, Liang H, Naikawadi R, Woodruff P, Wolters P, Erle D, et al.
Cell
. 2017 Apr;
169(3):497-509.e13.
PMID: 28431248
The environmentally widespread polysaccharide chitin is degraded and recycled by ubiquitous bacterial and fungal chitinases. Although vertebrates express active chitinases from evolutionarily conserved loci, their role in mammalian physiology is...
9.
Naikawadi R, Disayabutr S, Mallavia B, Donne M, Green G, La J, et al.
JCI Insight
. 2016 Oct;
1(14):e86704.
PMID: 27699234
Telomeres are short in type II alveolar epithelial cells (AECs) of patients with idiopathic pulmonary fibrosis (IPF). Whether dysfunctional telomeres contribute directly to development of lung fibrosis remains unknown. The...
10.
Disayabutr S, Kim E, Cha S, Green G, Naikawadi R, Jones K, et al.
PLoS One
. 2016 Jul;
11(6):e0158367.
PMID: 27362652
Pathologic features of idiopathic pulmonary fibrosis (IPF) include genetic predisposition, activation of the unfolded protein response, telomere attrition, and cellular senescence. The mechanisms leading to alveolar epithelial cell (AEC) senescence...