Kaan Boztug
Kaan Boztug
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Bestätigte E-Mail-Adresse bei cemm.oeaw.ac.at - Startseite
TitelZitiert vonJahr
Inflammatory bowel disease and mutations affecting the interleukin-10 receptor
EO Glocker, D Kotlarz, K Boztug, EM Gertz, AA Schäffer, F Noyan, M Perro, ...
New England Journal of Medicine 361 (21), 2033-2045, 2009
10552009
Stem-cell gene therapy for the Wiskott–Aldrich syndrome
K Boztug, M Schmidt, A Schwarzer, PP Banerjee, IA Díez, RA Dewey, ...
New England Journal of Medicine 363 (20), 1918-1927, 2010
4662010
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)
C Klein, M Grudzien, G Appaswamy, M Germeshausen, I Sandrock, ...
Nature genetics 39 (1), 86, 2007
4252007
Gene therapy for Wiskott-Aldrich syndrome—long-term efficacy and genotoxicity
CJ Braun, K Boztug, A Paruzynski, M Witzel, A Schwarzer, M Rothe, ...
Science translational medicine 6 (227), 227ra33-227ra33, 2014
3252014
Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy
D Kotlarz, R Beier, D Murugan, J Diestelhorst, O Jensen, K Boztug, ...
Gastroenterology 143 (2), 347-355, 2012
2842012
A syndrome with congenital neutropenia and mutations in G6PC3
K Boztug, G Appaswamy, A Ashikov, AA Schäffer, U Salzer, J Diestelhorst, ...
New England Journal of Medicine 360 (1), 32-43, 2009
2522009
Interferon-independent, human immunodeficiency virus type 1 gp120-mediated induction of CXCL10/IP-10 gene expression by astrocytes in vivo and in vitro
VC Asensio, J Maier, R Milner, K Boztug, C Kincaid, M Moulard, ...
Journal of virology 75 (15), 7067-7077, 2001
1302001
Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27
E Salzer, S Daschkey, S Choo, M Gombert, E Santos-Valente, S Ginzel, ...
haematologica 98 (3), 473-478, 2013
1192013
Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2
J Jung, G Bohn, A Allroth, K Boztug, G Brandes, I Sandrock, AA Schäffer, ...
Blood 108 (1), 362-369, 2006
942006
Early-onset inflammatory bowel disease and common variable immunodeficiency–like disease caused by IL-21 deficiency
E Salzer, A Kansu, H Sic, P Májek, A Ikincioğullari, FE Dogu, ...
Journal of Allergy and Clinical Immunology 133 (6), 1651-1659. e12, 2014
862014
Leukocyte infiltration, but not neurodegeneration, in the CNS of transgenic mice with astrocyte production of the CXC chemokine ligand 10
K Boztug, MJ Carson, N Pham-Mitchell, VC Asensio, J DeMartino, ...
The Journal of Immunology 169 (3), 1505-1515, 2002
842002
Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies
CS Ma, N Wong, G Rao, DT Avery, J Torpy, T Hambridge, J Bustamante, ...
Journal of Allergy and Clinical Immunology 136 (4), 993-1006. e1, 2015
792015
B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ
E Salzer, E Santos-Valente, S Klaver, SA Ban, W Emminger, ...
Blood 121 (16), 3112-3116, 2013
792013
Development of novel efficient SIN vectors with improved safety features for Wiskott–Aldrich syndrome stem cell based gene therapy
I Avedillo Díez, D Zychlinski, EG Coci, M Galla, U Modlich, RA Dewey, ...
Molecular pharmaceutics 8 (5), 1525-1537, 2011
762011
Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency
OK Alkhairy, R Perez-Becker, GJ Driessen, H Abolhassani, ...
Journal of Allergy and Clinical Immunology 136 (3), 703-712. e10, 2015
692015
Inherited DOCK2 deficiency in patients with early-onset invasive infections
K Dobbs, C Domínguez Conde, S Zhang, S Parolini, M Audry, J Chou, ...
New England Journal of Medicine 372 (25), 2409-2422, 2015
692015
JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia
K Boztug, PM Järvinen, E Salzer, T Racek, S Mönch, W Garncarz, ...
Nature genetics 46 (9), 1021, 2014
652014
Interleukin-2-inducible T-cell kinase (ITK) deficiency-clinical and molecular aspects
S Ghosh, K Bienemann, K Boztug, A Borkhardt
Journal of clinical immunology 34 (8), 892-899, 2014
602014
G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction
BH Hayee, A Antonopoulos, EJ Murphy, FZ Rahman, G Sewell, BN Smith, ...
Glycobiology 21 (7), 914-924, 2011
592011
Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity
KL Willmann, S Klaver, F Doğu, E Santos-Valente, W Garncarz, I Bilic, ...
Nature communications 5, 5360, 2014
572014
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