Skip navigation
Skip navigation

Browsing by Author Enders, Anselm

Or enter first few letters:  
Showing results 1 to 20 of 29
01_Enders_A_Severe_Form_of_Human_2006.pdf.jpg

A Severe Form of Human Combined Immunodeficiency Due to Mutations in DNA Ligase IV

Author(s)Enders, Anselm; Fisch, Paul; Schwarz, Klaus, et al
TypeJournal article
Date Published2006
Date Created-

ATP11C is critical for the internalization of phosphatidylserine and differentiation of B lymphocytes

Author(s)Yabas, Mehmet; Teh, Charis; Frankenreiter, Sandra, et al
TypeJournal article
Date Published2011
Date Created-
BergmannetalBcellsurvival,surfaceBCR2013.pdf.jpg

B cell survival, surface BCR and BAFFR expression, CD74 metabolism, and CD8-dendritic cells require the intramembrane endopeptidase SPPL2A

Author(s)Bergmann, Hannes; Yabas, Mehmet; Short, Alanna, et al
TypeJournal article
Date Published14-Jan-2013
Date Created-

Comparison of predicted and actual consequences of missense mutations

Author(s)Miosge, Lisa; Field, Matthew; Sontani, Yovina, et al
TypeJournal article
Date Published2015
Date Created-
1-s2.0-S0091674912026383-main.pdf.jpg

Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects.

Author(s)Stepensky, Polina; Keller, Baerbel; Buchta, Mary, et al
TypeJournal article
Date PublishedFeb-2013
Date Created-
Blood.pdf.jpg

DOCK8 is critical for the survival and function of NKT cells

Author(s)Crawford, Greg; Enders, Anselm; Gileadi, Uzi, et al
TypeJournal article
Date Published19-Sep-2013
Date Created-

Dock8 mutations cripple B cell immunological synapses, germinal centers and long-lived antibody production

Author(s)Randall, Katrina; Lambe, Teresa; Johnson, Andy L, et al
TypeJournal article
Date Published2009
Date Created-

Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome

Author(s)Rensing-Ehl, A.; Pannicke, Ulrich; Zimmermann, S.-Y., et al
TypeJournal article
Date Published2015
Date Created-
Teh et al Heterozygous mis-sense mutations in Prkcb 2013.pdf.jpg

Heterozygous mis-sense mutations in Prkcb as a critical determinant of anti-polysaccharide antibody formation

Author(s)Teh, C E; Horikawa, K; Arnold, C N, et al
TypeJournal article
Date PublishedJun-2013
Date Created-

Identification of phenotypically and functionally heterogeneous mouse mucosal-associated invariant t cells using MR1 tetramers

Author(s)Rahimpour, Azad; Koay, Hui Fern; Enders, Anselm, et al
TypeJournal article
Date Published2015
Date Created-

Lethal hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type II

Author(s)Enders, Anselm; Zieger, Barbra; Schwarz, Klaus, et al
TypeJournal article
Date Published2006
Date Created-

Loss of the pro-apoptotic BH3-only Bcl-2 family member Bim inhibits BCR stimulation-induced apoptosis and deletion of autoreactive B cells

Author(s)Enders, Anselm; Bouillet, Philippe; Puthalakath, Hamsa, et al
TypeJournal article
Date Published2003
Date Created-
01_Andrews_Massively_parallel_sequencing_2012.pdf.jpg

Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models

Author(s)Andrews, Thomas Daniel; Whittle, Belinda; Field, Matthew, et al
TypeJournal article
Date Published2012
Date Created-
Yabas et al Mice deficient in the putative 2014.pdf.jpg

Mice deficient in the putative phospholipid flippase ATP11C exhibit altered erythrocyte shape, anemia, and reduced erythrocyte life span

Author(s)Yabas, Mehmet; Coupland, Lucy A; Cromer, Deborah, et al
TypeJournal article
Date Published4-Jun-2014
Date Created-
01_Theodoratos_Mouse_strains_with_point_2010.pdf.jpg

Mouse strains with point mutations in TAP1 and TAP2

Author(s)Theodoratos, Angelo; Whittle, Belinda; Enders, Anselm, et al
TypeJournal article
Date Published2010
Date Created-

Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency

Author(s)Fuchs, Sebastian; Rensing-Ehl, A.; Pannicke, Ulrich, et al
TypeJournal article
Date Published2015
Date Created-
Daley et al Rasgrp1 mutation increases 2013.pdf.jpg

Rasgrp1 mutation increases naïve T-cell CD44 expression and drives mTOR-dependent accumulation of Helios+ T cells and autoantibodies

Author(s)Daley, Stephen R; Coakley, Kristen M; Hu, Daniel Y, et al
TypeJournal article
Date Published12-Dec-2013
Date Created-

Reduced memory B cells in patients with hyper IgE syndrome

Author(s)Speckmann, Carsten; Enders, Anselm; Woellner, C., et al
TypeJournal article
Date Published2008
Date Created-
01_Field_Reducing_the_search_space_for_2015.pdf.jpg

Reducing the search space for causal genetic variants with VASP

Author(s)Field, Matthew; Cho, Eun; Cook, Matthew, et al
TypeJournal article
Date Published2015
Date Created-

Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome

Author(s)Jessen, B; Maul-Pavicic, A.; Ufheil, H, et al
TypeJournal article
Date Published2011
Date Created-

Updated:  12 April 2016/ Responsible Officer:  University Librarian/ Page Contact:  Library Systems & Web Coordinator