Disruption of thrombocyte and T lymphocyte development by a mutation in ARPC1B

Journal of Immunology

Volumn 199, Issue 12, 2017, Pages 4036-4045

  Somech, Raz ^a,b   Lev, Atar ^a,b   Lee, Yu Nee ^a,b   Simon, Amos J ^a,b   Barel, Ortal ^a,b   Schiby, Ginette ^a   Avivi, Camila ^a   Barshack, Iris ^a   Rhodes, Michele ^c   Yin, Jiejing ^c   Wang, Minshi ^c   Yang, Yibin ^c   Rhodes, Jennifer ^c   Marcus, Nufar ^a   Garty, Ben Zion ^a   Stein, Jerry ^a   Amariglio, Ninette ^a,b,d   Rechavi, Gideon ^a,b   Wiest, David L ^c   Zhang, Yong ^c  

^a TEL AVIV UNIVERSITY   (Israel)

^b SHEBA MEDICAL CENTER   (Israel)

^c FOX CHASE CANCER CENTER   (United States)

^d BAR ILAN UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN RELATED PROTEIN 2-3 COMPLEX; ARPC1B PROTEIN, HUMAN; MULTIPROTEIN COMPLEX; ZEBRAFISH PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARPC1B GENE; ARTICLE; CHILD; CONTROLLED STUDY; FRAMESHIFT MUTATION; GENE; GENE DELETION; GENE EXPRESSION; HEMATOPOIETIC CELL; HOMOZYGOSITY; HUMAN; HUMAN CELL; INFANT; MALE; NONHUMAN; PRESCHOOL CHILD; PRIORITY JOURNAL; T LYMPHOCYTE; THROMBOCYTE; WHOLE EXOME SEQUENCING; WISKOTT ALDRICH SYNDROME; ZEBRA FISH; ACTIN FILAMENT; CASE REPORT; CONSANGUINITY; DEFICIENCY; FATALITY; GENETICS; IMMUNE DEFICIENCY; LYMPHOPOIESIS; METABOLISM; PATHOLOGY; PEDIGREE; PHYSIOLOGY; POLYMERIZATION; STOP CODON; THROMBOCYTOPOIESIS; VDJ RECOMBINATION;

ACTIN CYTOSKELETON; ACTIN-RELATED PROTEIN 2-3 COMPLEX; BLOOD PLATELETS; CHILD, PRESCHOOL; CODON, NONSENSE; CONSANGUINITY; FATAL OUTCOME; FRAMESHIFT MUTATION; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT; LYMPHOPOIESIS; MALE; MULTIPROTEIN COMPLEXES; PEDIGREE; POLYMERIZATION; T-LYMPHOCYTES; THROMBOPOIESIS; V(D)J RECOMBINATION; WISKOTT-ALDRICH SYNDROME; ZEBRAFISH PROTEINS;

EID: 85038566773     PISSN: 00221767     EISSN: 15506606     Source Type: Journal    
DOI: 10.4049/jimmunol.1700460     Document Type: Article

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