UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...

Enhanced antibody half-life improves in vivo activity

Nature biotechnology, 2010-02, Vol.28 (2), p.157-159

2010

Link zum Volltext

Verfügbarkeit prüfen

CD8⁺ T regulatory cells express the Ly49 Class I MHC receptor and are defective in autoimmune prone B6-Yaa mice

Proceedings of the National Academy of Sciences - PNAS, 2011-02, Vol.108 (5), p.2010-2015

2011

Link zum Volltext

Verfügbarkeit prüfen

Functional analysis of Collagen 17a1: A genetic modifier of junctional epidermolysis bullosa in mice

PloS one, 2023-10, Vol.18 (10), p.e0292456-e0292456

2023

Link zum Volltext

Verfügbarkeit prüfen

critical role for IL-21 receptor signaling in the pathogenesis of systemic lupus erythematosus in BXSB-Yaa mice

Proceedings of the National Academy of Sciences - PNAS, 2009-02, Vol.106 (5), p.1518-1523

2009

Link zum Volltext

Verfügbarkeit prüfen

Dystonin modifiers of junctional epidermolysis bullosa and models of epidermolysis bullosa simplex without dystonia musculorum

PloS one, 2023-10, Vol.18 (10), p.e0293218-e0293218

2023

Link zum Volltext

Verfügbarkeit prüfen

Enhanced half-life of genetically engineered human IgG1 antibodies in a humanized FcRn mouse model: potential application in humorally mediated autoimmune disease

International immunology, 2006-12, Vol.18 (12), p.1759-1769

2006

Link zum Volltext

Verfügbarkeit prüfen

IL-21 is a double-edged sword in the systemic lupus erythematosus-like disease of BXSB.Yaa mice

The Journal of immunology (1950), 2013-11, Vol.191 (9), p.4581-4588

2013

Link zum Volltext

Verfügbarkeit prüfen

Human FcRn transgenic mice for pharmacokinetic evaluation of therapeutic antibodies

Methods in molecular biology (Clifton, N.J.), 2010-01, Vol.602, p.93

2010

Link zum Volltext

Verfügbarkeit prüfen

Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in Dystonia musculorum mice

Disease models & mechanisms, 2020-05, Vol.13 (5)

2020

Link zum Volltext

Verfügbarkeit prüfen

The MHC Class I-Like IgG Receptor Controls Perinatal IgG Transport, IgG Homeostasis, and Fate of IgG-Fc-Coupled Drugs

The Journal of immunology (1950), 2003-04, Vol.170 (7), p.3528-3533

2003

Link zum Volltext

Verfügbarkeit prüfen

Interleukin 6 Accelerates Mortality by Promoting the Progression of the Systemic Lupus Erythematosus-Like Disease of BXSB.Yaa Mice

PloS one, 2016-04, Vol.11 (4), p.e0153059-e0153059

2016

Link zum Volltext

Verfügbarkeit prüfen

Molecular identification of collagen 17a1 as a major genetic modifier of laminin gamma 2 mutation-induced junctional epidermolysis bullosa in mice

PLoS genetics, 2014-02, Vol.10 (2), p.e1004068-e1004068

2014

Link zum Volltext

Verfügbarkeit prüfen

Precocious Interleukin 21 Expression in Naive Mice Identifies a Natural Helper Cell Population in Autoimmune Disease

Cell reports (Cambridge), 2017-10, Vol.21 (1), p.208-221

2017

Link zum Volltext

Verfügbarkeit prüfen

Coronary artery disease from isolated non-H2-determined incompatibilities in transplanted mouse hearts

Transplantation, 2011-04, Vol.91 (8), p.847

2011

Link zum Volltext

Verfügbarkeit prüfen

Seven naturally variant loci serve as genetic modifiers of Lamc2jeb induced non-Herlitz junctional Epidermolysis Bullosa in mice

PloS one, 2023-07, Vol.18 (7), p.e0288263-e0288263

2023

Link zum Volltext

Verfügbarkeit prüfen

Phenotypic differences in intermediate generalized junctional epidermolysis bullosa with homozygous LAMC2 mutation and a potential genetic modifier

Journal of the European Academy of Dermatology and Venereology, 2024-02

2024

Link zum Volltext

Verfügbarkeit prüfen

A mouse model of heritable cerebrovascular disease

PloS one, 2010-12, Vol.5 (12), p.e15327-e15327

2010

Link zum Volltext

Verfügbarkeit prüfen

Human FcRn Transgenic Mice for Pharmacokinetic Evaluation of Therapeutic Antibodies

Methods in molecular biology (Clifton, N.J.), 2016-01, Vol.1438, p.103

2016

Link zum Volltext

Verfügbarkeit prüfen

Structural variant in mitochondrial-associated gene (MRPL3) induces adult-onset neurodegeneration with memory impairment in the mouse

The Journal of neuroscience, 2020-06, Vol.40 (23), p.4576-4585

2020

Link zum Volltext

Verfügbarkeit prüfen

Albumin-deficient mouse models for studying metabolism of human albumin and pharmacokinetics of albumin-based drugs

mAbs, 2015-03, Vol.7 (2), p.344-351

2015

Link zum Volltext

Verfügbarkeit prüfen

A single-amino-acid variant of the H60 CD8 epitope generates specific immunity with diverse TCR recruitment

Molecules and Cells, 2012, 33(4), , pp.393-399

2012

Link zum Volltext

Verfügbarkeit prüfen

IL-21–Driven Neoplasms in SJL Mice Mimic Some Key Features of Human Angioimmunoblastic T-Cell Lymphoma

The American journal of pathology, 2015-11, Vol.185 (11), p.3102-3114

2015

Link zum Volltext

Verfügbarkeit prüfen

Quantitative Analysis of the Immune Response to Mouse Non-MHC Transplantation Antigens In Vivo: The H60 Histocompatibility Antigen Dominates Over All Others

The Journal of immunology (1950), 2001-04, Vol.166 (7), p.4370-4379

2001

Link zum Volltext

Verfügbarkeit prüfen

Enhancing the efficacy of glycolytic blockade in cancer cells via RAD51 inhibition

Cancer biology & therapy, 2019-02, Vol.20 (2), p.169-182

2019

Link zum Volltext

Verfügbarkeit prüfen

Minor genomic differences between related B6 and B10 mice affect severity of schistosome infection by governing the mode of dendritic cell activation

European journal of immunology, 2015-08, Vol.45 (8), p.2312-2323

2015

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 71

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(67)
Mit Volltextzugriff
(60)

Publikationsform

Artikel
(65)
Reviews
(5)
Bücher
(1)

Sprache

Englisch
(71)
Japanisch
(13)

Erscheinungsjahr

n.n

Thema

Science & Technology
(44)
Life Sciences & Biomedicine
(37)
Mice
(32)
Animals
(31)
Humans
(18)
Female
(16)
Mice, Inbred C57bl
(16)
Immunology
(14)
Male
(14)
Mice, Transgenic
(9)
Mutation
(8)
Multidisciplinary Sciences
(7)
Proteins
(7)
Rodents
(7)
Science & Technology - Other Topics
(7)
Cd8-Positive T-Lymphocytes - Immunology
(6)
Disease Models, Animal
(6)
Genes
(6)
Minor Histocompatibility Antigens - Immunology
(6)
Biological And Medical Sciences
(5)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Enhanced antibody half-life improves in vivo activity

CD8⁺ T regulatory cells express the Ly49 Class I MHC receptor and are defective in autoimmune prone B6-Yaa mice

Functional analysis of Collagen 17a1: A genetic modifier of junctional epidermolysis bullosa in mice

critical role for IL-21 receptor signaling in the pathogenesis of systemic lupus erythematosus in BXSB-Yaa mice

Dystonin modifiers of junctional epidermolysis bullosa and models of epidermolysis bullosa simplex without dystonia musculorum

Enhanced half-life of genetically engineered human IgG1 antibodies in a humanized FcRn mouse model: potential application in humorally mediated autoimmune disease

IL-21 is a double-edged sword in the systemic lupus erythematosus-like disease of BXSB.Yaa mice

Human FcRn transgenic mice for pharmacokinetic evaluation of therapeutic antibodies

Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in Dystonia musculorum mice

The MHC Class I-Like IgG Receptor Controls Perinatal IgG Transport, IgG Homeostasis, and Fate of IgG-Fc-Coupled Drugs

Interleukin 6 Accelerates Mortality by Promoting the Progression of the Systemic Lupus Erythematosus-Like Disease of BXSB.Yaa Mice

Molecular identification of collagen 17a1 as a major genetic modifier of laminin gamma 2 mutation-induced junctional epidermolysis bullosa in mice

Precocious Interleukin 21 Expression in Naive Mice Identifies a Natural Helper Cell Population in Autoimmune Disease

Coronary artery disease from isolated non-H2-determined incompatibilities in transplanted mouse hearts

Seven naturally variant loci serve as genetic modifiers of Lamc2jeb induced non-Herlitz junctional Epidermolysis Bullosa in mice

Phenotypic differences in intermediate generalized junctional epidermolysis bullosa with homozygous LAMC2 mutation and a potential genetic modifier

A mouse model of heritable cerebrovascular disease

Human FcRn Transgenic Mice for Pharmacokinetic Evaluation of Therapeutic Antibodies

Structural variant in mitochondrial-associated gene (MRPL3) induces adult-onset neurodegeneration with memory impairment in the mouse

Albumin-deficient mouse models for studying metabolism of human albumin and pharmacokinetics of albumin-based drugs

A single-amino-acid variant of the H60 CD8 epitope generates specific immunity with diverse TCR recruitment

IL-21–Driven Neoplasms in SJL Mice Mimic Some Key Features of Human Angioimmunoblastic T-Cell Lymphoma

Quantitative Analysis of the Immune Response to Mouse Non-MHC Transplantation Antigens In Vivo: The H60 Histocompatibility Antigen Dominates Over All Others

Enhancing the efficacy of glycolytic blockade in cancer cells via RAD51 inhibition

Minor genomic differences between related B6 and B10 mice affect severity of schistosome infection by governing the mode of dendritic cell activation

Suchergebnisse filtern