Erratum: Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect (Nature Communications (2014) 5:4746 (doi: 10.1038/ncomms5746));Megakaryocyte-specific Profilin1-deficiency alters microtubule stability and causes a Wiskott-Aldrich syndrome-like platelet defect

Nature Communications

Volumn 5, Issue , 2014, Pages

  Bender, Markus ^a,b   Stritt, Simon ^a   Nurden, Paquita ^a,c   Van Eeuwijk, Judith M M ^a   Zieger, Barbara ^d   Kentouche, Karim ^e   Schulze, Harald ^a   Morbach, Henner ^a   Stegner, David ^a   Heinze, Katrin ^a   Dütting, Sebastian ^a   Gupta, Shuchi ^a   Witke, Walter ^f   Falet, Hervé ^b   Fischer, Alain ^g   Hartwig, John H ^b   Nieswandt, Bernhard ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c Ctr Geriatrie Ctr Hosp Univ B   (France)

^d UNIVERSITY OF FREIBURG   (Germany)

^e FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

^f UNIVERSITY OF BONN   (Germany)

^g HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; PHOSPHATIDYLINOSITIDE; PROFILIN; PROFILIN 1; PROTEIN WIP; UNCLASSIFIED DRUG; WISKOTT ALDRICH SYNDROME PROTEIN; CYTOSKELETON PROTEIN; PFN1 PROTEIN, MOUSE; SIGNAL PEPTIDE; WAS PROTEIN, HUMAN; WIPF1 PROTEIN, HUMAN;

DISABILITY; GENE EXPRESSION; IMMUNE RESPONSE; MUTATION; PROTEIN; RODENT;

ANIMAL CELL; ARTICLE; BONE MARROW; CONTROLLED STUDY; ECZEMA; FEMALE; GENE MUTATION; IMMUNE DEFICIENCY; MALE; MEGAKARYOCYTE; MICROTUBULE; MOUSE; MUTATOR GENE; NONHUMAN; THROMBOCYTE ANOMALY; THROMBOCYTE RELEASE REACTION; THROMBOCYTOPENIA; WAS GENE; WISKOTT ALDRICH SYNDROME; ADOLESCENT; ANIMAL; CASE REPORT; CHILD; DEFICIENCY; GENE EXPRESSION REGULATION; GENETICS; HEMATOPOIESIS; HUMAN; INFANT; METABOLISM; MUTATION; PATHOLOGY; PRESCHOOL CHILD; SIGNAL TRANSDUCTION; THROMBOCYTE;

MUS;

ADOLESCENT; ANIMALS; BLOOD PLATELETS; BONE MARROW; CHILD; CHILD, PRESCHOOL; CYTOSKELETAL PROTEINS; GENE EXPRESSION REGULATION; HEMATOPOIESIS; HUMANS; INFANT; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MEGAKARYOCYTES; MICE; MICROTUBULES; MUTATION; PROFILINS; SIGNAL TRANSDUCTION; WISKOTT-ALDRICH SYNDROME; WISKOTT-ALDRICH SYNDROME PROTEIN;

EID: 84920935863     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms7507     Document Type: Erratum

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