S. Hoppins

发表

A mitochondrial-focused genetic interaction map reveals a scaffold-like complex required for inner membrane organization in mitochondria

Benedikt Westermann, Jonathan S. Weissman, Maya Schuldiner, 2011, The Journal of cell biology.

Tim50, a novel component of the TIM23 preprotein translocase of mitochondria

H. Prokisch, C. Kozany, D. Mokranjac, 2003, The EMBO journal.

Mitochondrial Dynamics and Apoptosis—the ER Connection

J. Nunnari, S. Hoppins, 2012, Science.

Uniform nomenclature for the mitochondrial contact site and cristae organizing system

Sang Ki Park, Susan S. Taylor, J. Weissman, 2014, The Journal of cell biology.

Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion

Rachel M. Devay, H. Stahlberg, J. Nunnari, 2009, The Journal of cell biology.

Alternative Splicing Gives Rise to Different Isoforms of the Neurospora crassa Tob55 Protein That Vary in Their Ability to Insert β-Barrel Proteins Into the Outer Mitochondrial Membrane

W. Neupert, F. Nargang, D. Rapaport, 2007, Genetics.

A catalytic domain variant of mitofusin requiring a wildtype paralog for function uncouples mitochondrial outer-membrane tethering and fusion

S. Hoppins, E. Engelhart, 2019, The Journal of Biological Chemistry.

Cell-Free Analysis of Mitochondrial Fusion by Fluorescence Microscopy.

N. B. Samanas, S. Hoppins, N. Samanas, 2020, Methods in molecular biology.

Aberrant Drp1‐mediated mitochondrial division presents in humans with variable outcomes

Sharyn A. Lincoln, I. Glass, M. Tarnopolsky, 2018, Human molecular genetics.

The regulation of mitochondrial dynamics.

S. Hoppins, 2014, Current opinion in cell biology.

In vitro and in vivo assays for mitochondrial fission and fusion.

J. Mears, L. Lackner, S. Hoppins, 2020, Methods in cell biology.

A dominant negative mitofusin causes mitochondrial perinuclear clusters because of aberrant tethering

S. Hoppins, Stephanie R. Sloat, 2022, Life Science Alliance.

Mitochondrial fusion defects caused by CMT2A disease-associated variants of Mfn2

N. B. Samanas, S. Hoppins, E. Engelhart, 2019 .

Identification of a mitofusin specificity region that confers unique activities to Mfn1 and Mfn2

S. Hoppins, SR Sloat, BN Whitley, 2019, bioRxiv.

The molecular mechanism of mitochondrial fusion.

J. Nunnari, S. Hoppins, 2009, Biochimica et biophysica acta.

Mitochondrial dynamics and their potential as a therapeutic target.

S. Hoppins, E. Engelhart, B. N. Whitley, 2019, Mitochondrion.

Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A

M. Bamshad, P. Byers, A. Stergachis, 2023, bioRxiv.

Cutting Edge: Glycolytic Metabolism and Mitochondrial Metabolism Are Uncoupled in Antigen-Activated CD8+ Recent Thymic Emigrants

P. Fink, S. Hoppins, Cody A. Cunningham, 2018, The Journal of Immunology.

The Tim8-Tim13 Complex of Neurospora crassa Functions in the Assembly of Proteins into Both Mitochondrial Membranes*

F. Nargang, S. Hoppins, Frank E Nargang, 2004, Journal of Biological Chemistry.

Mitochondrial outer and inner membrane fusion requires a modified carrier protein

J. McCaffery, J. Nunnari, Cheng Song, 2009, The Journal of cell biology.

The soluble form of Bax regulates mitochondrial fusion via MFN2 homotypic complexes.

Soojay Banerjee, R. Youle, J. McCaffery, 2011, Molecular cell.

Defective nucleotide-dependent assembly and membrane fusion in Mfn2 CMT2A variants improved by Bax

S. Hoppins, E. Engelhart, N. Samanas, 2020, Life Science Alliance.

Mfn2 requires Hinge 1 integrity for efficient nucleotide-dependent assembly and membrane fusion

S. Hoppins, E. Engelhart, N. Samanas, 2019, bioRxiv.

Uniform nomenclature for the mitochondrial contact site and cristae organizing system

Sang Ki Park, Susan S. Taylor, J. Weissman, 2014, Journal of Cell Biology.