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Journal Articles

Circulating B-Cell Precursor Cells As Potential Diagnostic and Therapeutic Biomarker in Patients with WHIM Syndrome

Ulrich Salzer, Christoph B. Geier, Maryssa Ellison, Melis Yilmaz, Caroline von Spee-Mayer, Carsten Speckmann, Stephan Ehl, Olaf Neth, Ana Pilar Garcia Garcia, Angela Deya Martinez, Laia Alsina, Katja Sockel, Catharina Schuetz, David E. Potts, Boglarka Ujhazi, Krisztian Csomos, Jolan E. Walter, Klaus Warnatz

Blood (2022) 140 (Supplement 1): 2626–2627.

https://doi.org/10.1182/blood-2022-159190

Published: 2022

Journal Articles

Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiency

Blood (2020) 135 (17): 1452–1457.

https://doi.org/10.1182/blood.2019003855

Published: 2020

Includes: Supplemental data

Journal Articles

A novel disease-causing synonymous exonic mutation in GATA2 affecting RNA splicing

Claudia Wehr, Katja Grotius, Silvia Casadei, Dorothee Bleckmann, Sebastian F. N. Bode, Björn C. Frye, Maximilian Seidl, Suleyman Gulsuner, Mary-Claire King, Mary-Beth Percival, Colin C. Pritchard, Tom Walsh, David Wu, Siobán Keel, Ulrich Salzer

Blood (2018) 132 (11): 1211–1215.

https://doi.org/10.1182/blood-2018-03-837336

Published: 2018

Includes: Supplemental data

Journal Articles

A Novel Mutation Causing GATA2 Haploinsufficiency Activates a Cryptic Splice Site in Exon 3

Claudia Wehr, Katja Grotius, Dorothee Bleckmann, Emilia J Kozyra, Sebastian Bode, Björn C Frye, Marcin W. Wlodarski, MD PhD, Maximilian Seidl, Ulrich Salzer

Blood (2017) 130 (Supplement 1): 2467.

https://doi.org/10.1182/blood.V130.Suppl_1.2467.2467

Published: 2017

Journal Articles

Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations

Blood (2017) 130 (Supplement 1): 2449.

https://doi.org/10.1182/blood.V130.Suppl_1.2449.2449

Published: 2017

Journal Articles

Recipient Dendritic Cells Are Regulated By MiR-146a during Acute GvHD

Natalie Stickel, MSc, Kathrin Hanke, MSc, Martin Köhler, MSc, Gabriele Prinz, Dietmar Pfeifer, Annette Schmitt-Graeff, MD, Tilman Brummer, PhD, Juergen Finke, MD, Justus Duyster, MD PhD, Ulrich Salzer, MD, Robert Zeiser, MD

Blood (2015) 126 (23): 146.

https://doi.org/10.1182/blood.V126.23.146.146

Published: 2015

Journal Articles

Somatic Genetic and Epigenetic Architecture of Myelodysplastic Syndromes Arising from GATA2 Deficiency

Victor Bengt Pastor Loyola, MSc, Shinsuke Hirabayashi, MD, Sandra Pohl, PhD, Emilia J Kozyra, MSc, Albert Catala, MD, Barbara De Moerloose, MD PhD, Michael Dworzak, MD, Henrik Hasle, MD, Riccardo Masetti, MD, Markus Schmugge, MD, Owen Smith, Jan Starý, MD, Marek Ussowicz, MD, Marry M. van den Heuvel-Eibrink, MD PhD, Ester Mejstrikova, MD PhD, Ulrich Salzer, MD, Michael Lübbert, MD, Daniel Heudobler, MD, David Betts, MD, Jose Cervera, MD, Gudrun Göhring, MD, Oskar A. Haas, Olga Haus, MD, Kyra Michalova, PhD DSc, Francesco Pasquali, MD, Joelle Tchinda, MD, Nadine van Roy, MD, Brigitte Schlegelberger, MD Prof., H. Berna Beverloo, PhD, Peter Noellke, MSc, Ayami Yoshimi, MD, Franco Locatelli, Prof, MD PhD, Brigitte Strahm, MD, Jaroslaw P. Maciejewski, MD PhD, Michael Rehli, PhD, Charlotte M Niemeyer, Prof, MD, Marcin W Wlodarski, MD

Blood (2015) 126 (23): 299.

https://doi.org/10.1182/blood.V126.23.299.299

Published: 2015

Journal Articles

Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome

Anne Rensing-Ehl, Ulrich Pannicke, Stefanie-Yvonne Zimmermann, Myriam Ricarda Lorenz, Benedicte Neven, Ilka Fuchs, Ulrich Salzer, Carsten Speckmann, Anne Strauss, Eberhard Maaβ, Benedicte Collet, Anselm Enders, Remi Favier, Marie Christine Alessi, Frederic Rieux-Laucat, Barbara Zieger, Klaus Schwarz, Stephan Ehl

Blood (2015) 126 (16): 1967–1969.

https://doi.org/10.1182/blood-2015-06-654145

Published: 2015

Journal Articles

MiR-146a Regulates the TRAF6/TNF-Axis in Donor T Cells during Graft-Versus-Host Disease

Natalie Stickel, MS, Gabriele Prinz, Dietmar Pfeifer, PhD, Annette Schmitt-Graeff, MD, Marie Follo, PhD, Jürgen Finke, Justus Duyster, MD, Ulrich Salzer, MD, Robert Zeiser

Blood (2014) 124 (21): 843.

https://doi.org/10.1182/blood.V124.21.843.843

Published: 2014

Journal Articles

MiR-146a regulates the TRAF6/TNF-axis in donor T cells during GVHD

Natalie Stickel, Gabriele Prinz, Dietmar Pfeifer, Peter Hasselblatt, Annette Schmitt-Graeff, Marie Follo, Robert Thimme, Jürgen Finke, Justus Duyster, Ulrich Salzer, Robert Zeiser

Blood (2014) 124 (16): 2586–2595.

https://doi.org/10.1182/blood-2014-04-569046

Published: 2014

Includes: Supplemental data

Journal Articles

T and B lymphocyte abnormalities in bone marrow biopsies of common variable immunodeficiency

Manuella L. Gomes Ochtrop, Sigune Goldacker, Annette M. May, Marta Rizzi, Ruth Draeger, Dieter Hauschke, Claudia Stehfest, Klaus Warnatz, Heike Goebel, Katja Technau-Ihling, Martin Werner, Ulrich Salzer, Hermann Eibel, Michael Schlesier, Hans Hartmut Peter

Blood (2011) 118 (2): 309–318.

https://doi.org/10.1182/blood-2010-11-321695

Published: 2011

Includes: Supplemental data

Journal Articles

Severe Early-Onset Inflammatory Bowel Disease Caused by IL10 Receptor Deficiency Can Be Cured by Allogeneic Hematopoietic Stem Cell Transplantation.

Blood (2009) 114 (22): 713.

https://doi.org/10.1182/blood.V114.22.713.713

Published: 2009

Journal Articles

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Blood (2009) 113 (9): 1967–1976.

https://doi.org/10.1182/blood-2008-02-141937

Published: 2009

Includes: Supplemental data

Journal Articles

A Novel Clinical Syndrome Associating Severe Congenital Neutropenia and Complex Developmental Aberrations Caused by Deficiency of G6PC3

Blood (2008) 112 (11): 5.

https://doi.org/10.1182/blood.V112.11.5.5

Published: 2008

Journal Articles

Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency

Klaus Warnatz, Lukas Bossaller, Ulrich Salzer, Andrea Skrabl-Baumgartner, Wolfgang Schwinger, Mirjam van der Burg, Jacques J. M. van Dongen, Marzena Orlowska-Volk, Rolf Knoth, Anne Durandy, Ruth Draeger, Michael Schlesier, Hans Hartmut Peter, Bodo Grimbacher

Blood (2006) 107 (8): 3045–3052.

https://doi.org/10.1182/blood-2005-07-2955

Published: 2006

Includes: Supplemental data

Journal Articles

Stomatin is a major lipid-raft component of platelet α granules

Mario Mairhofer, Marianne Steiner, Wilhelm Mosgoeller, Rainer Prohaska, Ulrich Salzer

Blood (2002) 100 (3): 897–904.

https://doi.org/10.1182/blood.V100.3.897

Published: 2002

Journal Articles

Ca ++ -dependent vesicle release from erythrocytes involves stomatin-specific lipid rafts, synexin (annexin VII), and sorcin

Ulrich Salzer, Peter Hinterdorfer, Ursula Hunger, Cordula Borken, Rainer Prohaska

Blood (2002) 99 (7): 2569–2577.

https://doi.org/10.1182/blood.V99.7.2569

Published: 2002

Journal Articles

Stomatin, flotillin-1, and flotillin-2 are major integral proteins of erythrocyte lipid rafts

Ulrich Salzer, Rainer Prohaska

Blood (2001) 97 (4): 1141–1143.

https://doi.org/10.1182/blood.V97.4.1141

Published: 2001

Journal Articles

Polytrauma induces increased expression of pyruvate kinase in neutrophils

Rudolf Oehler, Gertrude Weingartmann, Nicole Manhart, Ulrich Salzer, Michael Meissner, Werner Schlegel, Andreas Spittler, Michael Bergmann, Daniela Kandioler, Christiane Oismüller, Heidi M. Struse, Erich Roth

Blood (2000) 95 (3): 1086–1092.

https://doi.org/10.1182/blood.V95.3.1086.003k09_1086_1092

Published: 2000

NARROW

Circulating B-Cell Precursor Cells As Potential Diagnostic and Therapeutic Biomarker in Patients with WHIM Syndrome

Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiency

A novel disease-causing synonymous exonic mutation in GATA2 affecting RNA splicing

A Novel Mutation Causing GATA2 Haploinsufficiency Activates a Cryptic Splice Site in Exon 3

Systematic Assessment of GATA2 Genetic Variation Reveals the Presence of Novel Disease-Causing Synonymous Exonic Mutations

Recipient Dendritic Cells Are Regulated By MiR-146a during Acute GvHD

Somatic Genetic and Epigenetic Architecture of Myelodysplastic Syndromes Arising from GATA2 Deficiency

Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome

MiR-146a Regulates the TRAF6/TNF-Axis in Donor T Cells during Graft-Versus-Host Disease

MiR-146a regulates the TRAF6/TNF-axis in donor T cells during GVHD

T and B lymphocyte abnormalities in bone marrow biopsies of common variable immunodeficiency

Severe Early-Onset Inflammatory Bowel Disease Caused by IL10 Receptor Deficiency Can Be Cured by Allogeneic Hematopoietic Stem Cell Transplantation.

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

A Novel Clinical Syndrome Associating Severe Congenital Neutropenia and Complex Developmental Aberrations Caused by Deficiency of G6PC3

Human ICOS deficiency abrogates the germinal center reaction and provides a monogenic model for common variable immunodeficiency

Stomatin is a major lipid-raft component of platelet α granules

Ca ++ -dependent vesicle release from erythrocytes involves stomatin-specific lipid rafts, synexin (annexin VII), and sorcin

Stomatin, flotillin-1, and flotillin-2 are major integral proteins of erythrocyte lipid rafts

Polytrauma induces increased expression of pyruvate kinase in neutrophils

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American Society of Hematology

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ASH Publications

American Society of Hematology

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