UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 39

Sortiert nach

LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis

Clinical immunology (Orlando, Fla.), 2016-07, Vol.168, p.88-93

2016

Link zum Volltext

Verfügbarkeit prüfen

Galactosyl ceramide expressed on dendritic cells can mediate HIV-1 transfer from monocyte derived dendritic cells to autologous T cells

Virology (New York, N.Y.), 2007-05, Vol.362 (1), p.67-74

2007

Link zum Volltext

Verfügbarkeit prüfen

X-linked primary immunodeficiency associated with hemizygous mutations in the moesin ( MSN ) gene

Journal of allergy and clinical immunology, 2016-12, Vol.138 (6), p.1681-1689.e8

2016

Link zum Volltext

Verfügbarkeit prüfen

Chronic granulomatous skin lesions leading to a diagnosis of TAP1 deficiency syndrome

Pediatric dermatology, 2018-11, Vol.35 (6), p.e375-e377

2018

Link zum Volltext

Verfügbarkeit prüfen

The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions

Journal of clinical immunology, 2018-07, Vol.38 (5), p.558-568

2018

Link zum Volltext

Verfügbarkeit prüfen

Expression of the HLA-C2-specific activating killer-cell Ig-like receptor KIR2DS1 on NK and T cells

Clinical immunology (Orlando, Fla.), 2010-04, Vol.135 (1), p.26-32

2010

Link zum Volltext

Verfügbarkeit prüfen

HIV-1-infected blood mononuclear cells form an integrin- and agrin-dependent viral synapse to induce efficient HIV-1 transcytosis across epithelial cell monolayer

Molecular biology of the cell, 2005-09, Vol.16 (9), p.4267-4279

2005

Link zum Volltext

Verfügbarkeit prüfen

Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation

Frontiers in immunology, 2018-04, Vol.9, p.718-718

2018

Link zum Volltext

Verfügbarkeit prüfen

Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand ( FASLG ) mutation

Journal of allergy and clinical immunology, 2013-02, Vol.131 (2), p.486-490

2013

Link zum Volltext

Verfügbarkeit prüfen

Diagnosis of autoimmune lymphoproliferative syndrome caused by FAS deficiency in adults

Haematologica (Roma), 2013-03, Vol.98 (3), p.389-392

2013

Link zum Volltext

Verfügbarkeit prüfen

Chronic granulomatous skin lesions leading to a diagnosis of TAP 1 deficiency syndrome

Pediatric dermatology, 2018-11, Vol.35 (6)

2018

Link zum Volltext

Verfügbarkeit prüfen

Autoimmune lymphoproliferative syndrome: a multifactorial disorder

Haematologica (Roma), 2010-11, Vol.95 (11), p.1805-1807

2010

Link zum Volltext

Verfügbarkeit prüfen

In Vitro Evaluation of the Apoptosis Function in Human Activated T Cells

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1557, p.33

2017

Link zum Volltext

Verfügbarkeit prüfen

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

Clinical immunology (Orlando, Fla.), 2018-03, Vol.188, p.52-57

2018

Link zum Volltext

Verfügbarkeit prüfen

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity

Blood, 2023-06, Vol.141 (22), p.2713

2023

Link zum Volltext

Verfügbarkeit prüfen

Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

The Journal of clinical investigation, 2011-01, Vol.121 (1), p.106-112

2011

Link zum Volltext

Verfügbarkeit prüfen

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity

Blood, 2023-03

2023

Link zum Volltext

Verfügbarkeit prüfen

RAS-associated lymphoproliferative disease evolves into severe juvenile myelo-monocytic leukemia

Blood, 2014-03, Vol.123 (12), p.1960-1963

2014

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 39

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(36)
Mit Volltextzugriff
(35)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(26)
Science & Technology
(26)
Humans
(23)
Life Sciences
(16)
Immunology
(15)
Male
(14)
Child, Preschool
(12)
Adolescent
(11)
Child
(11)
Mutation
(11)
Adult
(10)
Female
(10)
Hematology
(10)
Young Adult
(9)
Fas Receptor - Genetics
(8)
Allergy And Immunology
(7)
Autoimmune Lymphoproliferative Syndrome - Genetics
(7)
Infant
(7)
Middle Aged
(7)
Apoptosis
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Blood
(11)
Clinical Immunology
(4)
The Journal Of Immunology
(4)
Haematologica
(3)
Journal Of Allergy And Clinical Immunology
(3)
Blood Advances
(2)
Pediatric Dermatology
(2)
Cd95
(1)
Frontiers In Immunology
(1)
Journal Of Autoimmunity
(1)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis

Galactosyl ceramide expressed on dendritic cells can mediate HIV-1 transfer from monocyte derived dendritic cells to autologous T cells

X-linked primary immunodeficiency associated with hemizygous mutations in the moesin ( MSN ) gene

Chronic granulomatous skin lesions leading to a diagnosis of TAP1 deficiency syndrome

The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions

Expression of the HLA-C2-specific activating killer-cell Ig-like receptor KIR2DS1 on NK and T cells

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes

HIV-1-infected blood mononuclear cells form an integrin- and agrin-dependent viral synapse to induce efficient HIV-1 transcytosis across epithelial cell monolayer

Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patients

Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation

Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand ( FASLG ) mutation

Diagnosis of autoimmune lymphoproliferative syndrome caused by FAS deficiency in adults

Chronic granulomatous skin lesions leading to a diagnosis of TAP 1 deficiency syndrome

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes

FAS-L, IL-10, and double-negative CD4−CD8− TCR α/β+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

Autoimmune lymphoproliferative syndrome: a multifactorial disorder

In Vitro Evaluation of the Apoptosis Function in Human Activated T Cells

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity

Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome

Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

DOCK11 deficiency in patients with X-linked actinopathy and autoimmunity

RAS-associated lymphoproliferative disease evolves into severe juvenile myelo-monocytic leukemia

Suchergebnisse filtern