UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 259

Sortiert nach

Human mesenchymal stromal cell-secreted lactate induces M2-macrophage differentiation by metabolic reprogramming

Oncotarget, 2016-05, Vol.7 (21), p.30193-30210

2016

Link zum Volltext

Verfügbarkeit prüfen

Eculizumab in Severe Shiga-Toxin–Associated HUS

The New England journal of medicine, 2011-06, Vol.364 (26), p.2561-2563

2011

Link zum Volltext

Verfügbarkeit prüfen

Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease

Science (American Association for the Advancement of Science), 2000-04, Vol.288 (5466), p.669-672

2000

Link zum Volltext

Verfügbarkeit prüfen

Hematopoietic stem cell transplantation in hemophagocytic lymphohistiocytosis: a single-center report of 48 patients

Pediatrics (Evanston), 2006-04, Vol.117 (4), p.e743

2006

Link zum Volltext

Verfügbarkeit prüfen

Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis

Science (American Association for the Advancement of Science), 1999-12, Vol.286 (5446), p.1957-1959

1999

Link zum Volltext

Verfügbarkeit prüfen

What Is Competence?

Human resource development international, 2005-03, Vol.8 (1), p.27-46

2005

Link zum Volltext

Verfügbarkeit prüfen

Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic Encephalopathy

American journal of human genetics, 2018-10, Vol.103 (4), p.602-611

2018

Link zum Volltext

Verfügbarkeit prüfen

Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients

Pediatrics (Evanston), 2003-05, Vol.111 (5 Pt 1), p.e622

2003

Link zum Volltext

Verfügbarkeit prüfen

Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy

The New England journal of medicine, 2002-04, Vol.346 (16), p.1185-1193

2002

Link zum Volltext

Verfügbarkeit prüfen

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

Nature genetics, 2000-06, Vol.25 (2), p.173-176

2000

Link zum Volltext

Verfügbarkeit prüfen

Long-term T-cell reconstitution after hematopoietic stem-cell transplantation in primary T-cell–immunodeficient patients is associated with myeloid chimerism and possibly the primary disease phenotype

Blood, 2007-05, Vol.109 (10), p.4575-4581

2007

Link zum Volltext

Verfügbarkeit prüfen

La santé à l’épreuve des restructurations

Archives des maladies professionnelles et de l'environnement, 2020-10, Vol.81 (5), p.607-607

Le Deist, Françoise

2020

Link zum Volltext

Verfügbarkeit prüfen

Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV

European Journal of Immunology, 2006-01, Vol.36 (1), p.224-235

2006

Link zum Volltext

Verfügbarkeit prüfen

Mechanisms of CD47-induced caspase-independent cell death in normal and leukemic cells: link between phosphatidylserine exposure and cytoskeleton organization

Blood, 2002-10, Vol.100 (8), p.2882-2890

2002

Link zum Volltext

Verfügbarkeit prüfen

Impairment of Mycobacterial Immunity in Human Interleukin-12 Receptor Deficiency

Science (American Association for the Advancement of Science), 1998-05, Vol.280 (5368), p.1432-1435

1998

Link zum Volltext

Verfügbarkeit prüfen

Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common γc cytokine receptor subunit or JAK-3 deficiency

The Lancet (British edition), 2004-06, Vol.363 (9426), p.2051-2054

2004

Link zum Volltext

Verfügbarkeit prüfen

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome

Blood, 2001-05, Vol.97 (9), p.2772-2776

2001

Link zum Volltext

Verfügbarkeit prüfen

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

Nature, 2006-11, Vol.444 (7115), p.110-114

2006

Link zum Volltext

Verfügbarkeit prüfen

Limits to mobility: competence and qualifications in Europe

European journal of training and development, 2012-04, Vol.36 (2/3), p.262-285

2012

Link zum Volltext

Verfügbarkeit prüfen

Ataxia-Telangiectasia Presenting With a Novel Immunodeficiency

Pediatric neurology, 2012-05, Vol.46 (5), p.322-324

2012

Link zum Volltext

Verfügbarkeit prüfen

Severe combined immunodeficiency. A model disease for molecular immunology and therapy

Immunological reviews, 2005-02, Vol.203 (1), p.98-109

2005

Link zum Volltext

Verfügbarkeit prüfen

Consequences of Fas-Mediated Human Dendritic Cell Apoptosis Induced by Measles Virus

Journal of Virology, 2000-05, Vol.74 (9), p.4387-4393

2000

Link zum Volltext

Verfügbarkeit prüfen

Treatment of the Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (IPEX) by Allogeneic Bone Marrow Transplantation

The New England journal of medicine, 2001-06, Vol.344 (23), p.1758-1762

2001

Link zum Volltext

Verfügbarkeit prüfen

Anti–B-Cell Monoclonal Antibody Treatment of Severe Posttransplant B-Lymphoproliferative Disorder: Prognostic Factors and Long-Term Outcome

Blood, 1998-11, Vol.92 (9), p.3137-3147

1998

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 259

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(236)
Mit Volltextzugriff
(228)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(174)
Science & Technology
(169)
Life Sciences & Biomedicine
(162)
Biological And Medical Sciences
(89)
Male
(82)
Medical Sciences
(81)
Immunology
(69)
Female
(65)
Infant
(55)
Child, Preschool
(49)
Mutation
(49)
Child
(48)
T-Lymphocytes - Immunology
(39)
Immunopathology
(38)
Hematology
(37)
Immunodeficiencies. Immunoglobulinopathies
(34)
Adolescent
(33)
Immunodeficiencies
(33)
Adult
(27)
Severe Combined Immunodeficiency - Genetics
(27)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Blood
(30)
The New England Journal Of Medicine
(18)
The Journal Of Immunology
(16)
European Journal Of Immunology
(14)
M.S. Médecine Sciences
(13)
The Lancet
(11)
The Journal Of Clinical Investigation
(10)
Pediatrics
(8)
British Journal Of Haematology
(6)
Nature Genetics
(6)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Human mesenchymal stromal cell-secreted lactate induces M2-macrophage differentiation by metabolic reprogramming

Eculizumab in Severe Shiga-Toxin–Associated HUS

Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease

Hematopoietic stem cell transplantation in hemophagocytic lymphohistiocytosis: a single-center report of 48 patients

Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis

What Is Competence?

Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic Encephalopathy

Autoimmunity in Wiskott-Aldrich syndrome: risk factors, clinical features, and outcome in a single-center cohort of 55 patients

Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans

Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

Long-term T-cell reconstitution after hematopoietic stem-cell transplantation in primary T-cell–immunodeficient patients is associated with myeloid chimerism and possibly the primary disease phenotype

La santé à l’épreuve des restructurations

Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV

Mechanisms of CD47-induced caspase-independent cell death in normal and leukemic cells: link between phosphatidylserine exposure and cytoskeleton organization

Impairment of Mycobacterial Immunity in Human Interleukin-12 Receptor Deficiency

Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common γc cytokine receptor subunit or JAK-3 deficiency

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B–severe combined immune deficiency or Omenn syndrome

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

Limits to mobility: competence and qualifications in Europe

Ataxia-Telangiectasia Presenting With a Novel Immunodeficiency

Severe combined immunodeficiency. A model disease for molecular immunology and therapy

Consequences of Fas-Mediated Human Dendritic Cell Apoptosis Induced by Measles Virus

Treatment of the Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (IPEX) by Allogeneic Bone Marrow Transplantation

Anti–B-Cell Monoclonal Antibody Treatment of Severe Posttransplant B-Lymphoproliferative Disorder: Prognostic Factors and Long-Term Outcome

Suchergebnisse filtern