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...

Pharmacology, Pharmacokinetics and Pharmacodynamics of Eculizumab, and Possibilities for an Individualized Approach to Eculizumab

Clinical pharmacokinetics, 2019-07, Vol.58 (7), p.859-874

2019

Volltextzugriff (PDF)

Implications of genetic variation in the complement system in age-related macular degeneration

Progress in retinal and eye research, 2021-09, Vol.84, p.100952-100952, Article 100952

2021

Volltextzugriff (PDF)

Assembly factor Omp85 recognizes its outer membrane protein substrates by a species-specific C-terminal motif

PLoS biology, 2006-11, Vol.4 (11), p.e377-e377

2006

Volltextzugriff (PDF)

Editorial: Complement and Immunotherapeutics

Frontiers in immunology, 2021-02, Vol.12, p.663459-663459

2021

Volltextzugriff (PDF)

Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy

The Journal of immunology (1950), 2018-04, Vol.200 (7), p.2464-2478

2018

Volltextzugriff (PDF)

Effect of rare coding variants in the CFI gene on Factor I expression levels

Human molecular genetics, 2020-08, Vol.29 (14), p.2313-2324

2020

Volltextzugriff (PDF)

The β-Barrel Outer Membrane Protein Assembly Complex of Neisseria meningitidis

Journal of Bacteriology, 2009-11, Vol.191 (22), p.7074-7085

2009

Volltextzugriff (PDF)

Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome

Frontiers in immunology, 2022-01, Vol.12, p.789897-789897

2022

Volltextzugriff (PDF)

Regulators of complement activity mediate inhibitory mechanisms through a common C3b-binding mode

The EMBO journal, 2016-05, Vol.35 (10), p.1133-1149

2016

Volltextzugriff (PDF)

Species-specificity of the BamA component of the bacterial outer membrane protein-assembly machinery

PloS one, 2013-12, Vol.8 (12), p.e85799-e85799

2013

Volltextzugriff (PDF)

Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene

Human molecular genetics, 2022-02, Vol.31 (3), p.455-470

2022

Volltextzugriff (PDF)

Safety and effectiveness of restrictive eculizumab treatment in atypical haemolytic uremic syndrome

Nephrology, dialysis, transplantation, 2018-04, Vol.33 (4), p.635-645

2018

Volltextzugriff (PDF)

Challenges in diagnostic testing of nephritic factors

Frontiers in immunology, 2022-11, Vol.13, p.1036136-1036136

2022

Volltextzugriff (PDF)

Role of the Periplasmic Chaperones Skp, SurA, and DegQ in Outer Membrane Protein Biogenesis in Neisseria meningitidis

Journal of Bacteriology, 2011-04, Vol.193 (7), p.1612-1621

2011

Volltextzugriff (PDF)

Case Report: Variable Pharmacokinetic Profile of Eculizumab in an aHUS Patient

Frontiers in immunology, 2021-01, Vol.11, p.612706

2021

Volltextzugriff (PDF)

The Role of Properdin in C5 Convertase Activity and C5b-9 Formation in the Complement Alternative Pathway

The Journal of immunology (1950), 2021-11, Vol.207 (10), p.2465-2472

2021

Volltextzugriff (PDF)

Placental passage of eculizumab and complement blockade in a newborn

Kidney international, 2019-04, Vol.95 (4), p.996-996

2019

Volltextzugriff (PDF)

Placental disposition of eculizumab, C5 and C5‐eculizumab in two pregnancies of a woman with paroxysmal nocturnal haemoglobinuria

British journal of clinical pharmacology, 2021-04, Vol.87 (4), p.2128-2131

2021

Volltextzugriff (PDF)

Heme as Possible Contributing Factor in the Evolvement of Shiga-Toxin Escherichia coli Induced Hemolytic-Uremic Syndrome

Frontiers in immunology, 2020-12, Vol.11, p.547406-547406

2020

Volltextzugriff (PDF)

Different Aspects of Classical Pathway Overactivation in Patients With C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis

Frontiers in immunology, 2021-08, Vol.12, p.715704-715704

2021

Volltextzugriff (PDF)

Proposal for individualized dosing of eculizumab in atypical haemolytic uraemic syndrome: patient friendly and cost-effective

Nephrology, dialysis, transplantation, 2023-02, Vol.38 (2), p.362-371

2023

Volltextzugriff (PDF)

Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene

Journal of human genetics, 2012-07, Vol.57 (7), p.459-464

2012

Volltextzugriff (PDF)

Analysis of rare variants in the C3 gene in patients with age-related macular degeneration

PloS one, 2014-04, Vol.9 (4), p.e94165

2014

Volltextzugriff (PDF)

Overactivity of Alternative Pathway Convertases in Patients With Complement-Mediated Renal Diseases

Frontiers in immunology, 2018-04, Vol.9 (APR), p.612-612

2018

Volltextzugriff (PDF)

Sensitive, reliable and easy-performed laboratory monitoring of eculizumab therapy in atypical hemolytic uremic syndrome

Clinical immunology (Orlando, Fla.), 2015-10, Vol.160 (2), p.237-243

2015

Volltextzugriff (PDF)

1 – 25 von 68

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(65)
Mit Volltextzugriff
(63)

Publikationsform

Artikel
(67)
Buchkapitel
(1)

Sprache

Englisch
(67)
Russisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Pharmacology, Pharmacokinetics and Pharmacodynamics of Eculizumab, and Possibilities for an Individualized Approach to Eculizumab

Implications of genetic variation in the complement system in age-related macular degeneration

Assembly factor Omp85 recognizes its outer membrane protein substrates by a species-specific C-terminal motif

Editorial: Complement and Immunotherapeutics

Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy

Effect of rare coding variants in the CFI gene on Factor I expression levels

The β-Barrel Outer Membrane Protein Assembly Complex of Neisseria meningitidis

Functional Analysis of Variants in Complement Factor I Identified in Age-Related Macular Degeneration and Atypical Hemolytic Uremic Syndrome

Regulators of complement activity mediate inhibitory mechanisms through a common C3b-binding mode

Species-specificity of the BamA component of the bacterial outer membrane protein-assembly machinery

Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene

Safety and effectiveness of restrictive eculizumab treatment in atypical haemolytic uremic syndrome

Challenges in diagnostic testing of nephritic factors

Role of the Periplasmic Chaperones Skp, SurA, and DegQ in Outer Membrane Protein Biogenesis in Neisseria meningitidis

Case Report: Variable Pharmacokinetic Profile of Eculizumab in an aHUS Patient

The Role of Properdin in C5 Convertase Activity and C5b-9 Formation in the Complement Alternative Pathway

Placental passage of eculizumab and complement blockade in a newborn

Placental disposition of eculizumab, C5 and C5‐eculizumab in two pregnancies of a woman with paroxysmal nocturnal haemoglobinuria

Heme as Possible Contributing Factor in the Evolvement of Shiga-Toxin Escherichia coli Induced Hemolytic-Uremic Syndrome

Different Aspects of Classical Pathway Overactivation in Patients With C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative Glomerulonephritis

Proposal for individualized dosing of eculizumab in atypical haemolytic uraemic syndrome: patient friendly and cost-effective

Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene

Analysis of rare variants in the C3 gene in patients with age-related macular degeneration

Overactivity of Alternative Pathway Convertases in Patients With Complement-Mediated Renal Diseases

Sensitive, reliable and easy-performed laboratory monitoring of eculizumab therapy in atypical hemolytic uremic syndrome

Suchergebnisse filtern