J
Jeffrey B. Hodgin
Researcher at University of Michigan
Publications - 70
Citations - 4532
Jeffrey B. Hodgin is an academic researcher from University of Michigan. The author has contributed to research in topics: Kidney disease & Kidney. The author has an hindex of 26, co-authored 70 publications receiving 3331 citations. Previous affiliations of Jeffrey B. Hodgin include Columbia University.
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Journal ArticleDOI
Netting Neutrophils Induce Endothelial Damage, Infiltrate Tissues, and Expose Immunostimulatory Molecules in Systemic Lupus Erythematosus
Eneida C. Villanueva,Srilakshmi Yalavarthi,Celine C. Berthier,Jeffrey B. Hodgin,Ritika Khandpur,Andrew M. Lin,Cory J. Rubin,Wenpu Zhao,Stephen H. Olsen,Matthew W. Klinker,David Shealy,Michael F. Denny,Joel Plumas,Joel Plumas,Laurence Chaperot,Laurence Chaperot,Matthias Kretzler,Allen T. Bruce,Mariana J. Kaplan +18 more
TL;DR: The results expand the potential pathogenic roles of aberrant lupus neutrophils and suggest that dysregulation of NET formation and its subsequent responses may play a prominent deleterious role.
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Peptidylarginine deiminase inhibition is immunomodulatory and vasculoprotective in murine lupus
Jason S. Knight,Wenpu Zhao,Wei Luo,Venkataraman Subramanian,Alexander A. O’Dell,Srilakshmi Yalavarthi,Jeffrey B. Hodgin,Daniel T. Eitzman,Paul R. Thompson,Mariana J. Kaplan +9 more
TL;DR: It is suggested that PAD inhibition can modulate phenotypes crucial for lupus pathogenesis and disease activity and may represent an important strategy for mitigating cardiovascular risk in lupu patients.
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Peptidylarginine deiminase inhibition disrupts NET formation and protects against kidney, skin and vascular disease in lupus-prone MRL/lpr mice
Jason S. Knight,Venkataraman Subramanian,Alexander A. O’Dell,Srilakshmi Yalavarthi,Wenpu Zhao,Carolyne K. Smith,Jeffrey B. Hodgin,Paul R. Thompson,Mariana J. Kaplan +8 more
TL;DR: It is demonstrated that peptidylarginine deiminase (PAD) inhibition reduces NET formation and protects against lupus-related vascular damage in the New Zealand Mixed model of l upus.
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Defining cell-type specificity at the transcriptional level in human disease.
Wenjun Ju,Casey S. Greene,Casey S. Greene,Felix Eichinger,Viji Nair,Jeffrey B. Hodgin,Markus Bitzer,Young-suk Lee,Qian Zhu,Masami Kehata,Min Li,Song Jiang,Maria Pia Rastaldi,Clemens D. Cohen,Olga G. Troyanskaya,Matthias Kretzler +15 more
TL;DR: The first genome-scale method to identify genes with cell-lineage-specific expression, even in lineages not separable by experimental microdissection is developed, which identified genes implicated as causal in hereditary glomerular disease and involved in molecular pathways of acquired and chronic renal diseases.
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An endoplasmic reticulum stress-regulated lncRNA hosting a microRNA megacluster induces early features of diabetic nephropathy.
Mitsuo Kato,Mei Wang,Zhuo Chen,Kirti Bhatt,Hyung Jung Oh,Linda Lanting,Supriya Deshpande,Ye Jia,Jennifer Y. Lai,Christopher L. O’Connor,YiFan Wu,Jeffrey B. Hodgin,Robert G. Nelson,Markus Bitzer,Rama Natarajan +14 more
TL;DR: It is shown that a megacluster of nearly 40 microRNAs and their host long non-coding RNA transcript (lnc-MGC) are coordinately increased in the glomeruli of mouse models of DN, and mesangial cells treated with transforming growth factor-β1 (TGF- β1) or high glucose.