Page 1 | Search Results | Blood | American Society of Hematology

1-7 of 7

Sort by

Sort Order Select

Journal Articles

LAMTOR2 Is Dispensable for T Cell Receptor-Mediated Signaling of Thymocytes but Controls Medullary Thymic Epithelial Cells

Lina Wendeler, MSc, Lukas A Huber, MD, Christoph Klein, MD PhD, Daniel Kotlarz, MD PhD

Blood (2018) 132 (Supplement 1): 1122.

https://doi.org/10.1182/blood-2018-99-119645

Published: 2018

Journal Articles

Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency

Alberto Prandini, Valentina Salvi, Francesca Colombo, Daniele Moratto, Luisa Lorenzi, William Vermi, Maria Antonia De Francesco, Lucia Dora Notarangelo, Fulvio Porta, Alessandro Plebani, Fabio Facchetti, Silvano Sozzani, Raffaele Badolato

Blood (2016) 127 (26): 3382–3386.

https://doi.org/10.1182/blood-2015-06-650689

Published: 2016

Includes: Supplemental data

Journal Articles

LAMTOR2 Regulates Stem Cell Maintenance and Acts in Lineage Choice By Modulating Cytokine Receptor-Mediated Signaling

Daniel Kotlarz, MD, Gudrun Brandes, PhD, Schwarzer Adrian, MD PhD, Glage Silke, MD, Büsche Guntram, MD, Pfeifer Dietmar, PhD, Lukas A Huber, MD, Christoph Klein, MD PhD

Blood (2014) 124 (21): 249.

https://doi.org/10.1182/blood.V124.21.249.249

Published: 2014

Journal Articles

Whole Exome Sequencing Identifies Novel Lyst-Missense Mutations In Incomplete Childhood Chediak-Higashi-Syndrome Presenting As Hemphagocytic Lymphohistiocytosis (HLH)

Joachim Kunz, MD, Tobias Rausch, PhD, Obul R Bandapalli, PhD, Adrian M Stuetz, PhD, Johann Greil, MD, Ingrid Hausser, MD, Jan Korbel, PhD, Andreas E Kulozik, MD, PhD

Blood (2013) 122 (21): 3479.

https://doi.org/10.1182/blood.V122.21.3479.3479

Published: 2013

Journal Articles

Innate immunity defects in Hermansky-Pudlak type 2 syndrome

Stefania Fontana, Silvia Parolini, William Vermi, Sarah Booth, Federico Gallo, Marta Donini, Marzia Benassi, Francesca Gentili, Daniela Ferrari, Lucia D. Notarangelo, Patrizia Cavadini, Emanuela Marcenaro, Stefano Dusi, Marco Cassatella, Fabio Facchetti, Gillian M. Griffiths, Alessandro Moretta, Luigi D. Notarangelo, Raffaele Badolato

Blood (2006) 107 (12): 4857–4864.

https://doi.org/10.1182/blood-2005-11-4398

Published: 2006

Journal Articles

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients

Gaël Ménasché, Jérôme Feldmann, Anne Houdusse, Catherine Desaymard, Alain Fischer, Bruno Goud, Geneviève de Saint Basile

Blood (2003) 101 (7): 2736–2742.

https://doi.org/10.1182/blood-2002-09-2789

Published: 2003

Journal Articles

Kappa-Chain Deficiency

George M. Bernier, M.D., J. Richard Gunderman, M.D., Frederick B. Ruymann, LTC MC

Blood (1972) 40 (6): 795–805.

https://doi.org/10.1182/blood.V40.6.795.795

Published: 1972

NARROW

LAMTOR2 Is Dispensable for T Cell Receptor-Mediated Signaling of Thymocytes but Controls Medullary Thymic Epithelial Cells

Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency

LAMTOR2 Regulates Stem Cell Maintenance and Acts in Lineage Choice By Modulating Cytokine Receptor-Mediated Signaling

Whole Exome Sequencing Identifies Novel Lyst-Missense Mutations In Incomplete Childhood Chediak-Higashi-Syndrome Presenting As Hemphagocytic Lymphohistiocytosis (HLH)

Innate immunity defects in Hermansky-Pudlak type 2 syndrome

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients

Kappa-Chain Deficiency

Email alerts

ASH Publications

American Society of Hematology

LAMTOR2 Is Dispensable for T Cell Receptor-Mediated Signaling of Thymocytes but Controls Medullary Thymic Epithelial Cells

Impairment of dendritic cell functions in patients with adaptor protein-3 complex deficiency

LAMTOR2 Regulates Stem Cell Maintenance and Acts in Lineage Choice By Modulating Cytokine Receptor-Mediated Signaling

Whole Exome Sequencing Identifies Novel Lyst-Missense Mutations In Incomplete Childhood Chediak-Higashi-Syndrome Presenting As Hemphagocytic Lymphohistiocytosis (HLH)

Innate immunity defects in Hermansky-Pudlak type 2 syndrome

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients

Kappa-Chain Deficiency

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only