Christopher F Bennett
Overview
Explore the profile of Christopher F Bennett including associated specialties, affiliations and a list of published articles.
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Articles
24
Citations
2536
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Recent Articles
1.
Latorre-Muro P, Vitale T, Ravichandran M, Zhang K, Palozzi J, Bennett C, et al.
Nat Cell Biol
. 2025 Jan;
27(1):130-140.
PMID: 39753947
Outer mitochondrial membrane (OMM) proteins communicate with the cytosol and other organelles, including the endoplasmic reticulum. This communication is important in thermogenic adipocytes to increase the energy expenditure that controls...
2.
Shin Y, Latorre-Muro P, Djurabekova A, Zdorevskyi O, Bennett C, Burger N, et al.
Cell
. 2024 Oct;
187(23):6584-6598.e17.
PMID: 39395414
In response to cold, mammals activate brown fat for respiratory-dependent thermogenesis reliant on the electron transport chain. Yet, the structural basis of respiratory complex adaptation upon cold exposure remains elusive....
3.
Shin Y, Latorre-Muro P, Djurabekova A, Zdorevskyi O, Bennett C, Burger N, et al.
bioRxiv
. 2024 Jan;
PMID: 38293190
In response to cold, mammals activate brown fat for respiratory-dependent thermogenesis reliant on the electron transport chain (1, 2). Yet, the structural basis of respiratory complex adaptation to cold remains...
4.
Ronayne C, Jackson T, Bennett C, Perry E, Kantorovic N, Puigserver P
EMBO Rep
. 2023 Oct;
24(12):e57228.
PMID: 37818824
Mitochondrial diseases are a group of disorders defined by defects in oxidative phosphorylation caused by nuclear- or mitochondrial-encoded gene mutations. A main cellular phenotype of mitochondrial disease mutations is redox...
5.
Sohn J, Mutlu B, Latorre-Muro P, Liang J, Bennett C, Sharabi K, et al.
Cell Metab
. 2023 Jul;
35(8):1356-1372.e5.
PMID: 37473754
Liver mitochondria undergo architectural remodeling that maintains energy homeostasis in response to feeding and fasting. However, the specific components and molecular mechanisms driving these changes and their impact on energy...
6.
Ronayne C, Bennett C, Perry E, Kantorovich N, Puigserver P
bioRxiv
. 2023 Mar;
PMID: 36945631
Mitochondrial diseases are a group of disorders defined by defects in oxidative phosphorylation caused by nuclear- or mitochondrial-encoded gene mutations. A main cellular phenotype of mitochondrial disease mutations are redox...
7.
Bennett C, Latorre-Muro P, Puigserver P
Nat Rev Mol Cell Biol
. 2022 Jul;
23(12):817-835.
PMID: 35804199
Mitochondrial energetic adaptations encompass a plethora of conserved processes that maintain cell and organismal fitness and survival in the changing environment by adjusting the respiratory capacity of mitochondria. These mitochondrial...
8.
Bennett C, Ronayne C, Puigserver P
FEBS J
. 2021 Sep;
289(22):6969-6993.
PMID: 34510753
Mitochondrial dysfunction is increasingly appreciated as a central contributor to human disease. Oxidative metabolism at the mitochondrial respiratory chain produces ATP and is intricately tied to redox homeostasis and biosynthetic...
9.
Bennett C, OMalley K, Perry E, Balsa E, Latorre-Muro P, Riley C, et al.
Nat Chem Biol
. 2021 Mar;
17(6):703-710.
PMID: 33723432
The protein complexes of the mitochondrial electron transport chain exist in isolation and in higher order assemblies termed supercomplexes (SCs) or respirasomes (SC I+III+IV). The association of complexes I, III...
10.
Latorre-Muro P, OMalley K, Bennett C, Perry E, Balsa E, Tavares C, et al.
Cell Metab
. 2021 Feb;
33(3):598-614.e7.
PMID: 33592173
The architecture of cristae provides a spatial mitochondrial organization that contains functional respiratory complexes. Several protein components including OPA1 and MICOS complex subunits organize cristae structure, but upstream regulatory mechanisms...