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...

Mutation-specific Fabry disease patient-derived cell model to evaluate the amenability to chaperone therapy

Journal of medical genetics, 2019-08, Vol.56 (8), p.548-556

2019

Volltextzugriff (PDF)

Comparative analysis of SEC61A1 mutant R236C in two patient-derived cellular platforms

Scientific reports, 2024-04, Vol.14 (1), p.9506-9506, Article 9506

2024

Volltextzugriff (PDF)

ATP7B knockout disturbs copper and lipid metabolism in Caco-2 cells

PloS one, 2020-03, Vol.15 (3), p.e0230025-e0230025

2020

Volltextzugriff (PDF)

Antibody Response to SARS-CoV-2 Membrane Protein in Patients of the Acute and Convalescent Phase of COVID-19

Frontiers in immunology, 2021-08, Vol.12, p.679841-679841

2021

Volltextzugriff (PDF)

CRISPR/Cas9-mediated correction of mutated copper transporter ATP7B

PloS one, 2020-09, Vol.15 (9), p.e0239411-e0239411

2020

Volltextzugriff (PDF)

Combined transgene immortalized urothelial cells capable of reprogramming and hepatic differentiation

Biochemistry and biophysics reports, 2022-09, Vol.31, p.101308-101308, Article 101308

2022

Volltextzugriff (PDF)

In Vitro and In Vivo Effects of SerpinA1 on the Modulation of Transthyretin Proteolysis

International journal of molecular sciences, 2021-08, Vol.22 (17), p.9488

2021

Volltextzugriff (PDF)

Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell lines

World journal of gastroenterology : WJG, 2016-04, Vol.22 (16), p.4109-4119

2016

Volltextzugriff (PDF)

Evaluation of Therapeutic Oligonucleotides for Familial Amyloid Polyneuropathy in Patient-Derived Hepatocyte-Like Cells

PloS one, 2016-09, Vol.11 (9), p.e0161455-e0161455

2016

Volltextzugriff (PDF)

Spatial investigation of the elemental distribution in Wilson’s disease liver after d-penicillamine treatment by LA-ICP-MS

Journal of trace elements in medicine and biology, 2017-12, Vol.44, p.26-31

2017

Volltextzugriff (PDF)

Neue Therapieoptionen für die hereditäre Transthyretin-Amyloidose

Deutsche medizinische Wochenschrift, 2019-10, Vol.144 (20), p.1438-1443

2019

Volltextzugriff (PDF)

Dietary copper triggers onset of fulminant hepatitis in the Long-Evans cinnamon rat model

World journal of gastroenterology : WJG, 2012-10, Vol.18 (39), p.5542-5550

Siaj, Ramsi

2012

Volltextzugriff (PDF)

Repeated transplantation of hepatocytes prevents fulminant hepatitis in a rat model of Wilson's disease

Liver transplantation, 2012-02, Vol.18 (2), p.248-259

2012

Volltextzugriff (PDF)

Functional Characterization of Novel ATP7B Variants for Diagnosis of Wilson Disease

Frontiers in pediatrics, 2018-04, Vol.6, p.106-106

2018

Volltextzugriff (PDF)

THU-272 - CRISPR/Cas9-mediated gene correction of Wilson disease H1069Q mutation in an iPS cell model

Journal of hepatology, 2023-06, Vol.78, p.S957-S958

2023

Volltextzugriff (PDF)

CRISPR/Cas9-mediated gene correction of Wilson disease H1069Q mutation in an iPS cell model

Journal of hepatology, 2023-06, Vol.78, p.S957-S958

2023

Volltextzugriff (PDF)

THU-271 - Immortalized patient-derived cell models for analysis of liver disease

Journal of hepatology, 2023-06, Vol.78, p.S957-S957

2023

Volltextzugriff (PDF)

Immortalized patient-derived cell models for analysis of liver disease

Journal of hepatology, 2023-06, Vol.78, p.S957

2023

Volltextzugriff (PDF)

Activation of Autophagy, Observed in Liver Tissues From Patients With Wilson Disease and From ATP7B-Deficient Animals, Protects Hepatocytes From Copper-Induced Apoptosis

Gastroenterology (New York, N.Y. 1943), 2019-03, Vol.156 (4), p.1173-1189.e5

2019

Volltextzugriff (PDF)

Human bone marrow stromal cells inhibit allogeneic T-cell responses by indoleamine 2,3-dioxygenase–mediated tryptophan degradation

Blood, 2004-06, Vol.103 (12), p.4619-4621

2004

Volltextzugriff (PDF)

Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial

Neurology, 2012-08, Vol.79 (8), p.785-792

2012

Volltextzugriff (PDF)

Angiotensin II type 1 receptor blockers increase tolerance of cells to copper and cisplatin

Microbial cell, 2014-10, Vol.1 (11), p.352-364

2014

Volltextzugriff (PDF)

Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy

The Egyptian journal of medical human genetics, 2014-07, Vol.15 (3), p.235-240

2014

Volltextzugriff (PDF)

A SEC61A1 variant is associated with autosomal dominant polycystic liver disease

Liver international, 2023-02, Vol.43 (2), p.401-412

2023

Volltextzugriff (PDF)

Current approaches for treatment of hereditary transthyretin amyloidosis (ATTR)

Deutsche medizinische Wochenschrift (1946), 2019-10, Vol.144 (20), p.1438

2019

Volltextzugriff (PDF)

1 – 25 von 68

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(64)
Mit Volltextzugriff
(56)

Publikationsform

Artikel
(68)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(49)
Life Sciences & Biomedicine
(44)
Humans
(33)
Animals
(19)
Biological And Medical Sciences
(15)
Virology
(12)
Copper
(11)
Biochemistry & Molecular Biology
(10)
Female
(10)
Fundamental And Applied Biological Sciences. Psychology
(10)
Gastroenterology & Hepatology
(10)
Mutation
(10)
Male
(9)
Molecular Sequence Data
(9)
Mice
(8)
Microbiology
(8)
Wilson's Disease
(8)
Base Sequence
(7)
Cell Line
(6)
Liver
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Mutation-specific Fabry disease patient-derived cell model to evaluate the amenability to chaperone therapy

Comparative analysis of SEC61A1 mutant R236C in two patient-derived cellular platforms

ATP7B knockout disturbs copper and lipid metabolism in Caco-2 cells

Antibody Response to SARS-CoV-2 Membrane Protein in Patients of the Acute and Convalescent Phase of COVID-19

CRISPR/Cas9-mediated correction of mutated copper transporter ATP7B

Combined transgene immortalized urothelial cells capable of reprogramming and hepatic differentiation

In Vitro and In Vivo Effects of SerpinA1 on the Modulation of Transthyretin Proteolysis

Functional analysis and drug response to zinc and D-penicillamine in stable ATP7B mutant hepatic cell lines

Evaluation of Therapeutic Oligonucleotides for Familial Amyloid Polyneuropathy in Patient-Derived Hepatocyte-Like Cells

Spatial investigation of the elemental distribution in Wilson’s disease liver after d-penicillamine treatment by LA-ICP-MS

Neue Therapieoptionen für die hereditäre Transthyretin-Amyloidose

Dietary copper triggers onset of fulminant hepatitis in the Long-Evans cinnamon rat model

Repeated transplantation of hepatocytes prevents fulminant hepatitis in a rat model of Wilson's disease

Functional Characterization of Novel ATP7B Variants for Diagnosis of Wilson Disease

THU-272 - CRISPR/Cas9-mediated gene correction of Wilson disease H1069Q mutation in an iPS cell model

CRISPR/Cas9-mediated gene correction of Wilson disease H1069Q mutation in an iPS cell model

THU-271 - Immortalized patient-derived cell models for analysis of liver disease

Immortalized patient-derived cell models for analysis of liver disease

Activation of Autophagy, Observed in Liver Tissues From Patients With Wilson Disease and From ATP7B-Deficient Animals, Protects Hepatocytes From Copper-Induced Apoptosis

Human bone marrow stromal cells inhibit allogeneic T-cell responses by indoleamine 2,3-dioxygenase–mediated tryptophan degradation

Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial

Angiotensin II type 1 receptor blockers increase tolerance of cells to copper and cisplatin

Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy

A SEC61A1 variant is associated with autosomal dominant polycystic liver disease

Current approaches for treatment of hereditary transthyretin amyloidosis (ATTR)

Suchergebnisse filtern