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Ivana Novak

Researcher at University of Split

Publications -  22
Citations -  8578

Ivana Novak is an academic researcher from University of Split. The author has contributed to research in topics: Autophagy & Mitophagy. The author has an hindex of 17, co-authored 19 publications receiving 7157 citations. Previous affiliations of Ivana Novak include University of Canterbury & Karolinska Institutet.

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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.
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A role for ubiquitin in selective autophagy.

TL;DR: The hypothesis that ubiquitin represents a selective degradation signal suitable for targeting various types of cargo, ranging from protein aggregates to membrane-bound organelles and microbes, is explored.
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Nix is a selective autophagy receptor for mitochondrial clearance

TL;DR: Nix functions as an autophagy receptor, which mediates mitochondrial clearance after mitochondrial damage and during erythrocyte differentiation, and ablation of the Nix:LC3/GABARAP interaction retards mitochondrial clearance in maturing murine reticulocytes.
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Modulation of Serines 17 and 24 in the LC3-interacting Region of Bnip3 Determines Pro-survival Mitophagy versus Apoptosis

TL;DR: It is demonstrated that enhancing Bnip3-Atg8 interactions via phosphorylation-mimicked LIR mutations increased mitochondrial sequestration, lysosomal delivery, and degradation, and Importantly, mitochondria were targeted by mitophagy prior to cytochrome c release, resulting in reduced cellular cytochrom c release capacity.
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Two novel proteins recruited by synaptonemal complex protein 1 (SYCP1) are at the centre of meiosis

TL;DR: Two new proteins, SYCE1 and CESC1, interact with the transverse filament protein SYCP1, and their localisation to the central element of the mammalian synaptonemal complex appears to depend on recruitment bySYCP1.