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...

An ELISA for quantifying GPIHBP1 autoantibodies and making a diagnosis of the GPIHBP1 autoantibody syndrome

Clinica chimica acta, 2018-12, Vol.487, p.174-178

2018

Volltextzugriff (PDF)

Multimerization of Glycosylphosphatidylinositol-anchored High Density Lipoprotein-binding Protein 1 (GPIHBP1) and Familial Chylomicronemia from a Serine-to-Cysteine Substitution in GPIHBP1 Ly6 Domain

The Journal of biological chemistry, 2014-07, Vol.289 (28), p.19491-19499

2014

Volltextzugriff (PDF)

Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia

Journal of lipid research, 2010-06, Vol.51 (6), p.1535-1545

2010

Volltextzugriff (PDF)

GPIHBP1 autoantibody syndrome during interferon β1a treatment

Journal of clinical lipidology, 2019-01, Vol.13 (1), p.62-69

2019

Volltextzugriff (PDF)

Chylomicronemia From GPIHBP1 Autoantibodies Successfully Treated With Rituximab: A Case Report

Annals of internal medicine, 2020-11, Vol.173 (9), p.764-765

2020

Volltextzugriff (PDF)

Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase

Arteriosclerosis, thrombosis, and vascular biology, 2009-06, Vol.29 (6), p.956-962

2009

Volltextzugriff (PDF)

GPIHBP1 autoantibodies in a patient with unexplained chylomicronemia

Journal of clinical lipidology, 2017-07, Vol.11 (4), p.964-971

2017

Volltextzugriff (PDF)

Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia

The New England journal of medicine, 2017-04, Vol.376 (17), p.1647-1658

2017

Volltextzugriff (PDF)

Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46)

The New England journal of medicine, 1989-06, Vol.320 (24), p.1604-1610

1989

Volltextzugriff (PDF)

Relationship of apolipoprotein E phenotypes to hypocholesterolemia

The American journal of medicine, 1993-11, Vol.95 (5), p.480-488

1993

Volltextzugriff (PDF)

Phenotypes of apolipoprotein B and apolipoprotein E after liver transplantation

The Journal of clinical investigation, 1991-07, Vol.88 (1), p.270-281

1991

Volltextzugriff (PDF)

Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B(B-31): a unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins

The Journal of clinical investigation, 1990-03, Vol.85 (3), p.933-942

1990

Volltextzugriff (PDF)

Familial Defective Apolipoprotein B-100: Enhanced Binding of Monoclonal Antibody MB47 to Abnormal Low Density Lipoproteins

Proceedings of the National Academy of Sciences - PNAS, 1988-12, Vol.85 (24), p.9758-9762

1988

Volltextzugriff (PDF)

A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia

The Journal of clinical investigation, 1991-05, Vol.87 (5), p.1748-1754

1991

Volltextzugriff (PDF)

Detection of two apolipoprotein B species (apoB c and apoB g) by a monoclonal antibody

Atherosclerosis, 1987-06, Vol.65 (3), p.247-256

1987

Volltextzugriff (PDF)

Trial of Early, Goal-Directed Resuscitation for Septic Shock

The New England journal of medicine, 2015-04, Vol.372 (14), p.1301-1311

2015

Volltextzugriff (PDF)

Maribavir prophylaxis for prevention of cytomegalovirus disease in recipients of allogeneic stem-cell transplants: a phase 3, double-blind, placebo-controlled, randomised trial

The Lancet infectious diseases, 2011-04, Vol.11 (4), p.284-292

2011

Volltextzugriff (PDF)

Ozanimod as Induction and Maintenance Therapy for Ulcerative Colitis

The New England journal of medicine, 2021-09, Vol.385 (14), p.1280-1291

2021

Volltextzugriff (PDF)

n−3 Fatty Acid Supplementation for the Treatment of Dry Eye Disease

The New England journal of medicine, 2018-05, Vol.378 (18), p.1681-1690

2018

Volltextzugriff (PDF)

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

Nature communications, 2015-08, Vol.6 (1), p.7502-7502, Article 7502

2015

Volltextzugriff (PDF)

Accuracy of Digital Breast Tomosynthesis for Depicting Breast Cancer Subgroups in a UK Retrospective Reading Study (TOMMY Trial)

Radiology, 2015-12, Vol.277 (3), p.697-706

2015

Volltextzugriff (PDF)

Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study

Journal of clinical oncology, 2012-03, Vol.30 (9), p.958-964

2012

Volltextzugriff (PDF)

Body-mass index and all-cause mortality: individual-participant-data meta-analysis of 239 prospective studies in four continents

The Lancet (British edition), 2016-08, Vol.388 (10046), p.776-786

2016

Volltextzugriff (PDF)

Microbial Composition of the Human Nasopharynx Varies According to Influenza Virus Type and Vaccination Status

mBio, 2019-07, Vol.10 (4)

2019

Volltextzugriff (PDF)

Improved blood pressure control associated with a large-scale hypertension program

JAMA : the journal of the American Medical Association, 2013-08, Vol.310 (7), p.699

2013

Volltextzugriff (PDF)

1 – 25 von 251

Suche als RSS-Feed

Aktive Filter

ThemaAdult

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(236)
Mit Volltextzugriff
(201)

Publikationsform

Artikel
(251)

Sprache

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

An ELISA for quantifying GPIHBP1 autoantibodies and making a diagnosis of the GPIHBP1 autoantibody syndrome

Multimerization of Glycosylphosphatidylinositol-anchored High Density Lipoprotein-binding Protein 1 (GPIHBP1) and Familial Chylomicronemia from a Serine-to-Cysteine Substitution in GPIHBP1 Ly6 Domain

Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia

GPIHBP1 autoantibody syndrome during interferon β1a treatment

Chylomicronemia From GPIHBP1 Autoantibodies Successfully Treated With Rituximab: A Case Report

Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase

GPIHBP1 autoantibodies in a patient with unexplained chylomicronemia

Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia

Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46)

Relationship of apolipoprotein E phenotypes to hypocholesterolemia

Phenotypes of apolipoprotein B and apolipoprotein E after liver transplantation

Familial hypobetalipoproteinemia caused by a mutation in the apolipoprotein B gene that results in a truncated species of apolipoprotein B(B-31): a unique mutation that helps to define the portion of the apolipoprotein B molecule required for the formation of buoyant, triglyceride-rich lipoproteins

Familial Defective Apolipoprotein B-100: Enhanced Binding of Monoclonal Antibody MB47 to Abnormal Low Density Lipoproteins

A truncated species of apolipoprotein B (B67) in a kindred with familial hypobetalipoproteinemia

Detection of two apolipoprotein B species (apoB c and apoB g) by a monoclonal antibody

Trial of Early, Goal-Directed Resuscitation for Septic Shock

Maribavir prophylaxis for prevention of cytomegalovirus disease in recipients of allogeneic stem-cell transplants: a phase 3, double-blind, placebo-controlled, randomised trial

Ozanimod as Induction and Maintenance Therapy for Ulcerative Colitis

n−3 Fatty Acid Supplementation for the Treatment of Dry Eye Disease

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

Accuracy of Digital Breast Tomosynthesis for Depicting Breast Cancer Subgroups in a UK Retrospective Reading Study (TOMMY Trial)

Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study

Body-mass index and all-cause mortality: individual-participant-data meta-analysis of 239 prospective studies in four continents

Microbial Composition of the Human Nasopharynx Varies According to Influenza Virus Type and Vaccination Status

Improved blood pressure control associated with a large-scale hypertension program

Aktive Filter

Suchergebnisse filtern