UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Size-dependent anti-inflammatory activity of a peptide-gold nanoparticle hybrid in vitro and in a mouse model of acute lung injury

Acta biomaterialia, 2019-02, Vol.85, p.203-217

2019

Volltextzugriff (PDF)

Germline CBM-opathies: From immunodeficiency to atopy

Journal of allergy and clinical immunology, 2019-05, Vol.143 (5), p.1661-1673

2019

Volltextzugriff (PDF)

The CBM-opathies-A Rapidly Expanding Spectrum of Human Inborn Errors of Immunity Caused by Mutations in the CARD11-BCL10-MALT1 Complex

Frontiers in immunology, 2018-09, Vol.9, p.2078-2078

2018

Volltextzugriff (PDF)

Inborn errors of immunity manifesting as atopic disorders

Journal of allergy and clinical immunology, 2021-11, Vol.148 (5), p.1130-1139

2021

Volltextzugriff (PDF)

MALT1-Dependent Cleavage of HOIL1 Modulates Canonical NF-κB Signaling and Inflammatory Responsiveness

Frontiers in immunology, 2021-10, Vol.12, p.749794-749794

2021

Volltextzugriff (PDF)

A Novel Germline Heterozygous BCL11B Variant Causing Severe Atopic Disease and Immune Dysregulation

Frontiers in immunology, 2021-11, Vol.12, p.788278

2021

Volltextzugriff (PDF)

Integrating knowledge of protein sequence with protein function for the prediction and validation of new MALT1 substrates

Computational and structural biotechnology journal, 2022-01, Vol.20, p.4717-4732

2022

Volltextzugriff (PDF)

Human MALT1 deficiency and predisposition to infections

Current opinion in immunology, 2021-10, Vol.72, p.1-12

2021

Volltextzugriff (PDF)

Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report

BMC pediatrics, 2021-01, Vol.21 (1), p.45-45, Article 45

2021

Volltextzugriff (PDF)

Fetal Hemoglobin Regulation in Beta-Thalassemia

Hematology/oncology clinics of North America, 2023-04, Vol.37 (2), p.301-312

2023

Volltextzugriff (PDF)

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

The Journal of experimental medicine, 2023-05, Vol.220 (5)

2023

Volltextzugriff (PDF)

Limitations of Qdot labelling compared to directly-conjugated probes for single particle tracking of B cell receptor mobility

Scientific reports, 2017-09, Vol.7 (1), p.11379-13, Article 11379

2017

Volltextzugriff (PDF)

Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiency

Journal of allergy and clinical immunology, 2021-12, Vol.148 (6), p.1559-1574.e13

2021

Volltextzugriff (PDF)

Monogenic immune disorders and severe atopic disease

Nature genetics, 2017-08, Vol.49 (8), p.1162-1163

2017

Volltextzugriff (PDF)

Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancy

Blood, 2022-10, Vol.140 (17), p.1858-1874

2022

Volltextzugriff (PDF)

Homozygous RMRP Promoter Duplications Cause Severely Reduced Transcript Abundance and SCID Associated with Cartilage Hair Hypoplasia

Journal of clinical immunology, 2023-08, Vol.43 (6), p.1139-1142

2023

Volltextzugriff (PDF)

Autosomal Recessive Inflammatory Skin Disease Caused by a Novel Biallelic Loss-of-Function Variant in CARD11

Journal of clinical immunology, 2023-05, Vol.43 (4), p.709-713

2023

Volltextzugriff (PDF)

Real-time 3D stabilization of a super-resolution microscope using an electrically tunable lens

Optics express, 2016-10, Vol.24 (20), p.22959-22970

2016

Volltextzugriff (PDF)

The importance of functional validation after next‐generation sequencing: evaluation of a novel CARD11 variant

Pediatric allergy and immunology, 2018-09, Vol.29 (6), p.663-668

2018

Volltextzugriff (PDF)

Mutational landscape influences immunotherapy outcomes among patients with non-small-cell lung cancer with human leukocyte antigen supertype B44

Nature cancer, 2020-12, Vol.1 (12), p.1167-1175

2020

Volltextzugriff (PDF)

Combination therapy with proteasome inhibitors and TLR agonists enhances tumour cell death and IL-1β production

Cell death & disease, 2018-02, Vol.9 (2), p.162-13, Article 162

2018

Volltextzugriff (PDF)

Effect of Ag content on the microstructure development of Sn-Ag-Cu interconnects

Journal of materials science. Materials in electronics, 2006-03, Vol.17 (3), p.171-188

2006

Volltextzugriff (PDF)

Clinical IRAK4 deficiency caused by homozygosity for the novel IRAK4 (c.1049delG, p.Gly350Glufs15) variant

Cold Spring Harbor molecular case studies, 2020-06, Vol.6 (3), p.a005298

2020

Volltextzugriff (PDF)

Marginal zone B cells have higher basal BCR signaling that correlates with altered mobility and spatial organization of IgM-BCRs

The Journal of immunology (1950), 2021-05, Vol.206 (1_Supplement), p.63-63.16

2021

Volltextzugriff (PDF)

Solid-liquid reactions: The effect of Cu content on Sn-Ag-Cu interconnects

JOM (1989), 2005-06, Vol.57 (6), p.30-35

2005

Volltextzugriff (PDF)

1 – 25 von 252

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(222)
Mit Volltextzugriff
(218)

Publikationsform

Sprache

Englisch
(251)
Französisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Size-dependent anti-inflammatory activity of a peptide-gold nanoparticle hybrid in vitro and in a mouse model of acute lung injury

Germline CBM-opathies: From immunodeficiency to atopy

The CBM-opathies-A Rapidly Expanding Spectrum of Human Inborn Errors of Immunity Caused by Mutations in the CARD11-BCL10-MALT1 Complex

Inborn errors of immunity manifesting as atopic disorders

MALT1-Dependent Cleavage of HOIL1 Modulates Canonical NF-κB Signaling and Inflammatory Responsiveness

A Novel Germline Heterozygous BCL11B Variant Causing Severe Atopic Disease and Immune Dysregulation

Integrating knowledge of protein sequence with protein function for the prediction and validation of new MALT1 substrates

Human MALT1 deficiency and predisposition to infections

Idiopathic splenomegaly in childhood and the spectrum of RAS-associated lymphoproliferative disease: a case report

Fetal Hemoglobin Regulation in Beta-Thalassemia

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Limitations of Qdot labelling compared to directly-conjugated probes for single particle tracking of B cell receptor mobility

Mechanistic understanding of the combined immunodeficiency in complete human CARD11 deficiency

Monogenic immune disorders and severe atopic disease

Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancy

Homozygous RMRP Promoter Duplications Cause Severely Reduced Transcript Abundance and SCID Associated with Cartilage Hair Hypoplasia

Autosomal Recessive Inflammatory Skin Disease Caused by a Novel Biallelic Loss-of-Function Variant in CARD11

Real-time 3D stabilization of a super-resolution microscope using an electrically tunable lens

The importance of functional validation after next‐generation sequencing: evaluation of a novel CARD11 variant

Mutational landscape influences immunotherapy outcomes among patients with non-small-cell lung cancer with human leukocyte antigen supertype B44

Combination therapy with proteasome inhibitors and TLR agonists enhances tumour cell death and IL-1β production

Effect of Ag content on the microstructure development of Sn-Ag-Cu interconnects

Clinical IRAK4 deficiency caused by homozygosity for the novel IRAK4 (c.1049delG, p.Gly350Glufs15) variant

Marginal zone B cells have higher basal BCR signaling that correlates with altered mobility and spatial organization of IgM-BCRs

Solid-liquid reactions: The effect of Cu content on Sn-Ag-Cu interconnects

Suchergebnisse filtern