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...

NF-κB: At the Borders of Autoimmunity and Inflammation

Frontiers in immunology, 2021-08, Vol.12, p.716469-716469

2021

Volltextzugriff (PDF)

FAS and RAS related Apoptosis defects: From autoimmunity to leukemia

Immunological reviews, 2019-01, Vol.287 (1), p.50-61

2019

Volltextzugriff (PDF)

Paediatric‐onset Evans syndrome: Breaking away from refractory immune thrombocytopenia

British journal of haematology, 2023-10, Vol.203 (1), p.28-35

2023

Volltextzugriff (PDF)

Impaired type I interferon activity and inflammatory responses in severe COVID-19 patients

Science (American Association for the Advancement of Science), 2020-08, Vol.369 (6504), p.718-724

2020

Volltextzugriff (PDF)

PD-L1 is expressed on human activated naive effector CD4+ T cells. Regulation by dendritic cells and regulatory CD4+ T cells

PloS one, 2021-11, Vol.16 (11), p.e0260206-e0260206

2021

Volltextzugriff (PDF)

RASopathies: From germline mutations to somatic and multigenic diseases

Biomedical Journal, 2021-08, Vol.44 (4), p.422-432

2021

Volltextzugriff (PDF)

Regulation of the acetylcholine/α7nAChR anti-inflammatory pathway in COVID-19 patients

Scientific reports, 2021-06, Vol.11 (1), p.11886-11886, Article 11886

2021

Volltextzugriff (PDF)

Autoimmunity by haploinsufficiency

Science (American Association for the Advancement of Science), 2014-09, Vol.345 (6204), p.1560-1561

2014

Volltextzugriff (PDF)

Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy ( TMEM173 Mutation)

Chest, 2016-09, Vol.150 (3), p.e65-e71

2016

Volltextzugriff (PDF)

Efficacy of Gene Therapy for X-Linked Severe Combined Immunodeficiency

The New England journal of medicine, 2010-07, Vol.363 (4), p.355-364

2010

Volltextzugriff (PDF)

Severe combined immunodeficiency in stimulator of interferon genes (STING) V154M/wild-type mice

Journal of allergy and clinical immunology, 2019-02, Vol.143 (2), p.712-725.e5

2019

Volltextzugriff (PDF)

The genetic landscape of the FAS pathway deficiencies

Biomedical Journal, 2021-08, Vol.44 (4), p.388-399

2021

Volltextzugriff (PDF)

Monitoring Disease Activity in Systemic Lupus Erythematosus With Single‐Molecule Array Digital Enzyme‐Linked Immunosorbent Assay Quantification of Serum Interferon‐α

Arthritis & rheumatology (Hoboken, N.J.), 2019-05, Vol.71 (5), p.756-765

2019

Volltextzugriff (PDF)

Platelet activation in critically ill COVID-19 patients

Annals of intensive care, 2021-07, Vol.11 (1), p.113-113, Article 113

2021

Volltextzugriff (PDF)

Long-term assessment of haematological recovery following somatic genetic rescue in a MYSM1-deficient patient: Implications for in vivo gene therapy

British journal of haematology, 2024-09

2024

Volltextzugriff (PDF)

Efficacy of Ruxolitinib Therapy in a Patient With Severe Enterocolitis Associated With a STAT3 Gain-of-Function Mutation

Gastroenterology (New York, N.Y. 1943), 2019-03, Vol.156 (4), p.1206-1210.e1

2019

Volltextzugriff (PDF)

Severe Food Allergy as a Variant of IPEX Syndrome Caused by a Deletion in a Noncoding Region of the FOXP3 Gene

Gastroenterology (New York, N.Y. 1943), 2007-05, Vol.132 (5), p.1705-1717

2007

Volltextzugriff (PDF)

Biological functions of extracellular vesicles from mammalian cells

Biomedical Journal, 2024-10, Vol.47 (5), p.100788, Article 100788

2024

Volltextzugriff (PDF)

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

Proceedings of the National Academy of Sciences - PNAS, 2011-07, Vol.108 (28), p.11554-11559

2011

Volltextzugriff (PDF)

Casitas B-lineage lymphoma Gene Mutation Ocular Phenotype

International journal of molecular sciences, 2022-07, Vol.23 (14), p.7868

2022

Volltextzugriff (PDF)

Generation of an iPSC line (IMAGINi011-A) from a patient carrying a STING mutation

Stem cell research, 2021-01, Vol.50, p.102107-102107, Article 102107

2021

Volltextzugriff (PDF)

Are RASopathies new monogenic predisposing conditions to the development of systemic lupus erythematosus? Case report and systematic review of the literature

Seminars in arthritis and rheumatism, 2013-10, Vol.43 (2), p.217-219

2013

Volltextzugriff (PDF)

Study of the potential role of CASPASE-10 mutations in the development of autoimmune lymphoproliferative syndrome

Cell death & disease, 2024-05, Vol.15 (5), p.315-315, Article 315

2024

Volltextzugriff (PDF)

1 – 25 von 278

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(265)
Mit Volltextzugriff
(251)

Publikationsform

Sprache

Englisch
(267)
Französisch
(11)

Erscheinungsjahr

n.n

Thema

Science & Technology
(202)
Humans
(170)
Life Sciences & Biomedicine
(158)
Immunology
(107)
Life Sciences
(100)
Male
(94)
Female
(84)
Mutation
(69)
Child
(56)
Adult
(49)
Lymphocytes
(46)
Child, Preschool
(45)
Patients
(45)
Multidisciplinary Sciences
(44)
Science & Technology - Other Topics
(44)
Adolescent
(39)
Autoimmune Diseases
(37)
Apoptosis
(36)
Autoimmunity
(36)
Hematology
(36)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

NF-κB: At the Borders of Autoimmunity and Inflammation

FAS and RAS related Apoptosis defects: From autoimmunity to leukemia

Paediatric‐onset Evans syndrome: Breaking away from refractory immune thrombocytopenia

Impaired type I interferon activity and inflammatory responses in severe COVID-19 patients

PD-L1 is expressed on human activated naive effector CD4+ T cells. Regulation by dendritic cells and regulatory CD4+ T cells

RASopathies: From germline mutations to somatic and multigenic diseases

Regulation of the acetylcholine/α7nAChR anti-inflammatory pathway in COVID-19 patients

Autoimmunity by haploinsufficiency

Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy ( TMEM173 Mutation)

Efficacy of Gene Therapy for X-Linked Severe Combined Immunodeficiency

Severe combined immunodeficiency in stimulator of interferon genes (STING) V154M/wild-type mice

The genetic landscape of the FAS pathway deficiencies

Monitoring Disease Activity in Systemic Lupus Erythematosus With Single‐Molecule Array Digital Enzyme‐Linked Immunosorbent Assay Quantification of Serum Interferon‐α

Platelet activation in critically ill COVID-19 patients

Long-term assessment of haematological recovery following somatic genetic rescue in a MYSM1-deficient patient: Implications for in vivo gene therapy

Efficacy of Ruxolitinib Therapy in a Patient With Severe Enterocolitis Associated With a STAT3 Gain-of-Function Mutation

Severe Food Allergy as a Variant of IPEX Syndrome Caused by a Deletion in a Noncoding Region of the FOXP3 Gene

Biological functions of extracellular vesicles from mammalian cells

Long term follow-up of pediatric-onset Evans syndrome: broad immunopathological manifestations and high treatment burden

NBEAL2 deficiency in humans leads to low CTLA-4 expression in activated conventional T cells

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

Casitas B-lineage lymphoma Gene Mutation Ocular Phenotype

Generation of an iPSC line (IMAGINi011-A) from a patient carrying a STING mutation

Are RASopathies new monogenic predisposing conditions to the development of systemic lupus erythematosus? Case report and systematic review of the literature

Study of the potential role of CASPASE-10 mutations in the development of autoimmune lymphoproliferative syndrome

Suchergebnisse filtern