scispace - formally typeset
M

Minnie M. Sarwal

Researcher at University of California, San Francisco

Publications -  328
Citations -  22794

Minnie M. Sarwal is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Transplantation & Kidney transplantation. The author has an hindex of 54, co-authored 300 publications receiving 19934 citations. Previous affiliations of Minnie M. Sarwal include Cardiovascular Institute of the South & University of California, Berkeley.

Papers
More filters
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

Daniel J. Klionsky, +2522 more
- 21 Jan 2016 - 
TL;DR: In this paper, the authors present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macro-autophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy

Daniel J. Klionsky, +1287 more
- 01 Apr 2012 - 
TL;DR: These guidelines are presented for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes.
Journal ArticleDOI

Calcineurin Inhibitor Nephrotoxicity

TL;DR: The authors critically review the current evidence relating systemic blood levels of cyclosporine and tacrolimus to calcineurin inhibitor nephrotoxicity, and summarize the data suggesting that local exposure to cycloporine or tacolimus could be more important than systemic exposure.
Journal ArticleDOI

Molecular heterogeneity in acute renal allograft rejection identified by DNA microarray profiling.

TL;DR: Systematic analysis of gene-expression patterns provides a window on the biology and pathogenesis of renal allograft rejection, and reveals a striking association between dense CD20+ B-cell infiltrates and both clinical glucocorticoid resistance and graft loss.