An Actin-Dependent Step in Mitochondrial Fission Mediated by the ER-Associated Formin INF2

Recent advances into the understanding of mitochondrial fission

(2012) Kirstin Elgass et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Mitochondria: In Sickness and in Health

(2012) Jodi Nunnari et al.   CELL

Mutations to the Formin Homology 2 Domain of INF2 Protein Have Unexpected Effects on Actin Polymerization and Severing

(2012) Vinay Ramabhadran et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A French family with Charcot–Marie–Tooth disease related to simultaneous heterozygous MFN2 and GDAP1 mutations

(2012) Anne Vital et al.   NEUROMUSCULAR DISORDERS

Tau Promotes Neurodegeneration via DRP1 Mislocalization In Vivo

(2012) Brian DuBoff et al.   NEURON

Mitochondrial Dynamics and Apoptosis--the ER Connection

(2012) S. Hoppins et al.   SCIENCE

Mitochondrial Fission, Fusion, and Stress

(2012) R. J. Youle et al.   SCIENCE

Mitochondria in Apoptosis: Bcl-2 Family Members and Mitochondrial Dynamics

(2011) Jean-Claude Martinou et al.   DEVELOPMENTAL CELL

Differential interactions of the formins INF2, mDia1, and mDia2 with microtubules

(2011) Jeremie Gaillard et al.   MOLECULAR BIOLOGY OF THE CELL

Splice variant–specific cellular function of the formin INF2 in maintenance of Golgi architecture

(2011) Vinay Ramabhadran et al.   MOLECULAR BIOLOGY OF THE CELL

INF2Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

(2011) Olivia Boyer et al.   NEW ENGLAND JOURNAL OF MEDICINE

ER Tubules Mark Sites of Mitochondrial Division

(2011) J. R. Friedman et al.   SCIENCE

Conformational changes in Dnm1 support a contractile mechanism for mitochondrial fission

(2010) Jason A Mears et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

Role of mitofusin 2 mutations in the physiopathology of Charcot–Marie–Tooth disease type 2A

(2009) Romain Cartoni et al.   EXPERIMENTAL NEUROLOGY

Mitochondrial dynamics-fusion, fission, movement, and mitophagy-in neurodegenerative diseases

(2009) H. Chen et al.   HUMAN MOLECULAR GENETICS

INF2 is an endoplasmic reticulum-associated formin protein

(2009) E. S. Chhabra et al.   JOURNAL OF CELL SCIENCE

Role of kinesin-1 and cytoplasmic dynein in endoplasmic reticulum movement in VERO cells

(2009) M. J. Wozniak et al.   JOURNAL OF CELL SCIENCE

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

(2009) Elizabeth J Brown et al.   NATURE GENETICS