Author Correction: Structure of the core of the type III secretion system export apparatus.
Journal article
Kuhlen L. et al, (2018), Nat struct mol biol, 25
Structure of the core of the type III secretion system export apparatus.
Journal article
Kuhlen L. et al, (2018), Nat struct mol biol, 25, 583 - 590
Structural and Functional Characterization of the Bacterial Type III Secretion Export Apparatus.
Journal article
Dietsche T. et al, (2016), Plos pathog, 12
Building a secreting nanomachine: a structural overview of the T3SS.
Journal article
Abrusci P. et al, (2014), Curr opin struct biol, 25, 111 - 117
Architecture of the major component of the type III secretion system export apparatus
Journal article
Abrusci P. et al, (2013), Nature structural and molecular biology, 20, 99 - 104
Architecture of the major component of the type III secretion system export apparatus.
Journal article
Abrusci P. et al, (2013), Nat struct mol biol, 20, 99 - 104
Structures of lysenin reveal a shared evolutionary origin for pore-forming proteins and its mode of sphingomyelin recognition.
Journal article
De Colibus L. et al, (2012), Structure, 20, 1498 - 1507
Structures of lysenin reveal a shared evolutionary origin for pore-forming proteins and its mode of sphingomyelin recognition
Journal article
De Colibus L. et al, (2012), Structure, 20, 1498 - 1507
Structural insights into the control of type three secretion
Conference paper
Abrusci P. et al, (2011), European biophysics journal with biophysics letters, 40, 142 - 142
Timing is everything: the regulation of type III secretion.
Journal article
Deane JE. et al, (2010), Cell mol life sci, 67, 1065 - 1075
Terminal assembly of sarcomeric filaments by intermolecular beta-sheet formation.
Journal article
Pinotsis N. et al, (2009), Trends biochem sci, 34, 33 - 39
Erythrocyte adenylate kinase deficiency: characterization of recombinant mutant forms and relationship with nonspherocytic hemolytic anemia.
Journal article
Abrusci P. et al, (2007), Exp hematol, 35, 1182 - 1189
Two new mutations of the P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorder.
Journal article
Chiarelli LR. et al, (2006), Haematologica, 91, 1244 - 1247
Erythrocyte adenylate kinase deficiency: First in-depth biochemical characterization of the Y164C mutant enzyme causing hemolytic anemia
Conference paper
Abrusci P. et al, (2005), Blood, 106, 1004A - 1004A