INF2Mutations in Charcot–Marie–Tooth Disease with Glomerulopathy

Mutations in INF2 Are a Major Cause of Autosomal Dominant Focal Segmental Glomerulosclerosis

(2011) O. Boyer et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2)

(2011) H. Sun et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Formin INF2 regulates MAL-mediated transport of Lck to the plasma membrane of human T lymphocytes

(2010) L. Andres-Delgado et al.   BLOOD

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

(2010) H. Skre   CLINICAL GENETICS

The Formin INF2 Regulates Basolateral-to-Apical Transcytosis and Lumen Formation in Association with Cdc42 and MAL2

(2010) Ricardo Madrid et al.   DEVELOPMENTAL CELL

Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy

(2010) James R. Lupski et al.   NEW ENGLAND JOURNAL OF MEDICINE

Charcot–Marie–Tooth disease

(2009) Kinga Szigeti et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology

(2009) E. Machuca et al.   HUMAN MOLECULAR GENETICS

INF2 is an endoplasmic reticulum-associated formin protein

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

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

(2009) Elizabeth J Brown et al.   NATURE GENETICS

Unleashing formins to remodel the actin and microtubule cytoskeletons

(2009) Melissa A. Chesarone et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY