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...

Metabolic Syndrome, Dyslipidemia and Regulation of Lipoprotein Metabolism

Current diabetes reviews, 2018-01, Vol.14 (5), p.427-433

2018

Volltextzugriff (PDF)

ATP-Binding Cassette Protein ABCC10 Deficiency Prevents Diet-Induced Obesity but Not Atherosclerosis in Mice

International journal of molecular sciences, 2022-11, Vol.23 (22), p.13813

2022

Volltextzugriff (PDF)

High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots

Frontiers in immunology, 2018-04, Vol.9, p.782-782

2018

Volltextzugriff (PDF)

Lipid Raft Integrity and Cellular Cholesterol Homeostasis Are Critical for SARS-CoV-2 Entry into Cells

Nutrients, 2022-08, Vol.14 (16), p.3417

2022

Volltextzugriff (PDF)

Inhibition of RORγT Skews TCRα Gene Rearrangement and Limits T Cell Repertoire Diversity

Cell reports (Cambridge), 2016-12, Vol.17 (12), p.3206-3218

2016

Volltextzugriff (PDF)

In DOCK8 deficiency donor cell engraftment post–genoidentical hematopoietic stem cell transplantation is possible without conditioning

Journal of allergy and clinical immunology, 2013-04, Vol.131 (4), p.1244-1245

2013

Volltextzugriff (PDF)

Genetic and clinical characteristics of pediatric patients with familial hemophagocytic lymphohistiocytosis

Blood Research, 2021, 56(2), , pp.86-101

2021

Volltextzugriff (PDF)

Role for rearranged variable gene segments in directing secondary T cell receptor α recombination

Proceedings of the National Academy of Sciences - PNAS, 2007-01, Vol.104 (3), p.903-907

2007

Volltextzugriff (PDF)

C5 Complement Deficiency in a Saudi Family, Molecular Characterization of Mutation and Literature Review

Journal of clinical immunology, 2013-05, Vol.33 (4), p.871-875

2013

Volltextzugriff (PDF)

Grave aortic aneurysmal dilatation in DOCK8 deficiency

Modern rheumatology, 2014-07, Vol.24 (4), p.690-693

2014

Volltextzugriff (PDF)

Molecular typing of MRSA isolates by spa and PFGE

Journal of King Saud University. Science, 2019-10, Vol.31 (4), p.999-1004

2019

Volltextzugriff (PDF)

Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases

Journal of allergy and clinical immunology, 2016-06, Vol.137 (6), p.1780-1787

2016

Volltextzugriff (PDF)

Specification of Vδ and Vα usage by Tcra/Tcrd locus V gene segment promoters

The Journal of immunology (1950), 2015-01, Vol.194 (2), p.790-794

2015

Volltextzugriff (PDF)

Specification of Vδ and Vα usage by Tcra/Tcrd locus V gene segment promoters1,2

The Journal of immunology (1950), 2014-12, Vol.194 (2), p.790-794

2014

Volltextzugriff (PDF)

Hematopoietic stem cell transplantation corrects WIP deficiency

Journal of allergy and clinical immunology, 2017-03, Vol.139 (3), p.1039-1040.e4

2017

Volltextzugriff (PDF)

Regulation of T cell receptor α gene assembly by a complex hierarchy of germline J α promoters

Nature immunology, 2005-05, Vol.6 (5), p.481-489

2005

Volltextzugriff (PDF)

Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients

Journal of clinical immunology, 2013, Vol.33 (1), p.55-67

2013

Volltextzugriff (PDF)

Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2019-03, Vol.7 (3), p.848-855

2019

Volltextzugriff (PDF)

In DOCKS deficiency donor cell engraftment post―genoidentical hematopoietic stem cell transplantation is possible without conditioning

Journal of allergy and clinical immunology, 2013, Vol.131 (4), p.1244-1245

2013

Volltextzugriff (PDF)

Clinical, Immunological, and Molecular Characterization of Hyper-IgM Syndrome Due to CD40 Deficiency in Eleven Patients

Journal of clinical immunology, 2013-11, Vol.33 (8), p.1325-1335

2013

Volltextzugriff (PDF)

Regulation of Intestinal Cholesterol Absorption: A Disease Perspective

Advances in biological chemistry, 2017, Vol.7 (1), p.60-75

2017

Volltextzugriff (PDF)

Regulation of T cell receptor alpha gene assembly by a complex hierarchy of germline J promoters

Nature immunology, 2005-05, Vol.6 (5), p.481-489

2005

Volltextzugriff (PDF)

Regulation of TCR delta and alpha repertoires by local and long-distance control of variable gene segment chromatin structure

The Journal of experimental medicine, 2005-08, Vol.202 (4), p.467-472

2005

Volltextzugriff (PDF)

Novel mutation in DOCK8-HIES with severe phenotype and successful transplantation

Clinical immunology (Orlando, Fla.), 2017-05, Vol.178, p.39-44

2017

Volltextzugriff (PDF)

Loss of NHEJ1 Protein Due to a Novel Splice Site Mutation in a Family Presenting with Combined Immunodeficiency, Microcephaly, and Growth Retardation and Literature Review

Journal of clinical immunology, 2017-08, Vol.37 (6), p.575-581

2017

Volltextzugriff (PDF)

1 – 25 von 54

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(48)
Mit Volltextzugriff
(51)

Publikationsform

Artikel
(51)
Berichte
(3)

Sprache

Englisch
(54)

Erscheinungsjahr

n.n

Thema

Science & Technology
(30)
Life Sciences & Biomedicine
(28)
Immunology
(21)
Humans
(19)
Animals
(13)
Mice
(12)
Male
(11)
Child
(8)
Female
(8)
Adolescent
(6)
Child, Preschool
(6)
Receptors, Antigen, T-Cell, Alpha-Beta - Genetics
(6)
Hematopoietic Stem Cell Transplantation
(5)
Immunodeficiency
(5)
Immunologic Deficiency Syndromes - Genetics
(5)
Mutation
(5)
Allergy
(4)
Allergy And Immunology
(4)
Biological And Medical Sciences
(4)
Biomedical And Life Sciences
(4)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Metabolic Syndrome, Dyslipidemia and Regulation of Lipoprotein Metabolism

ATP-Binding Cassette Protein ABCC10 Deficiency Prevents Diet-Induced Obesity but Not Atherosclerosis in Mice

High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots

Lipid Raft Integrity and Cellular Cholesterol Homeostasis Are Critical for SARS-CoV-2 Entry into Cells

Inhibition of RORγT Skews TCRα Gene Rearrangement and Limits T Cell Repertoire Diversity

In DOCK8 deficiency donor cell engraftment post–genoidentical hematopoietic stem cell transplantation is possible without conditioning

Genetic and clinical characteristics of pediatric patients with familial hemophagocytic lymphohistiocytosis

Role for rearranged variable gene segments in directing secondary T cell receptor α recombination

C5 Complement Deficiency in a Saudi Family, Molecular Characterization of Mutation and Literature Review

Grave aortic aneurysmal dilatation in DOCK8 deficiency

Molecular typing of MRSA isolates by spa and PFGE

Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases

Specification of Vδ and Vα usage by Tcra/Tcrd locus V gene segment promoters

Specification of Vδ and Vα usage by Tcra/Tcrd locus V gene segment promoters1,2

Hematopoietic stem cell transplantation corrects WIP deficiency

Regulation of T cell receptor α gene assembly by a complex hierarchy of germline J α promoters

Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients

Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency

In DOCKS deficiency donor cell engraftment post―genoidentical hematopoietic stem cell transplantation is possible without conditioning

Clinical, Immunological, and Molecular Characterization of Hyper-IgM Syndrome Due to CD40 Deficiency in Eleven Patients

Regulation of Intestinal Cholesterol Absorption: A Disease Perspective

Regulation of T cell receptor alpha gene assembly by a complex hierarchy of germline J promoters

Regulation of TCR delta and alpha repertoires by local and long-distance control of variable gene segment chromatin structure

Novel mutation in DOCK8-HIES with severe phenotype and successful transplantation

Loss of NHEJ1 Protein Due to a Novel Splice Site Mutation in a Family Presenting with Combined Immunodeficiency, Microcephaly, and Growth Retardation and Literature Review

Suchergebnisse filtern