UB Paderborn / Katalog / Suche / in CDI

1 – 22 von 22

Sortiert nach

ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

Human molecular genetics, 2016-06, Vol.25 (11), p.2220-2233

2016

Link zum Volltext

Verfügbarkeit prüfen

Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation

Human molecular genetics, 2020-12, Vol.29 (24), p.3919-3934

2020

Link zum Volltext

Verfügbarkeit prüfen

Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation

Human molecular genetics, 2018-09, Vol.27 (17), p.3060-3078

2018

Link zum Volltext

Verfügbarkeit prüfen

Elevated dual specificity protein phosphatase 4 in cardiomyopathy caused by lamin A/C gene mutation is primarily ERK1/2-dependent and its depletion improves cardiac function and survival

Human molecular genetics, 2018-07, Vol.27 (13), p.2290-2305

2018

Link zum Volltext

Verfügbarkeit prüfen

Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery–Dreifuss muscular dystrophy

Human molecular genetics, 2007-08, Vol.16 (15), p.1884-1895

2007

Link zum Volltext

Verfügbarkeit prüfen

Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene

Human molecular genetics, 2017-01, Vol.26 (2), p.333-343

2017

Link zum Volltext

Verfügbarkeit prüfen

Abnormal p38α mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation

Human molecular genetics, 2012-10, Vol.21 (19), p.4325-4333

2012

Link zum Volltext

Verfügbarkeit prüfen

Abnormal p38 mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation

Human molecular genetics, 2012-10, Vol.21 (19), p.4325-4333

2012

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins

Human molecular genetics, 2009-01, Vol.18 (2), p.241-247

2009

Link zum Volltext

Verfügbarkeit prüfen

Depletion of extracellular signal-regulated kinase 1 in mice with cardiomyopathy caused by lamin A/C gene mutation partially prevents pathology before isoenzyme activation

Human molecular genetics, 2014-01, Vol.23 (1), p.1-11

2014

Link zum Volltext

Verfügbarkeit prüfen

Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene

Cardiovascular research, 2012-02, Vol.93 (2), p.311-319

2012

Link zum Volltext

Verfügbarkeit prüfen

Postnatal development of mice with combined genetic depletions of lamin A/C, emerin and lamina-associated polypeptide 1

Human molecular genetics, 2019-08, Vol.28 (15), p.2486-2500

2019

Link zum Volltext

Verfügbarkeit prüfen

Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype

Human molecular genetics, 2015-04, Vol.24 (8), p.2163-2174

2015

Link zum Volltext

Verfügbarkeit prüfen

Lamina-associated polypeptide 1 is dispensable for embryonic myogenesis but required for postnatal skeletal muscle growth

Human molecular genetics, 2017-01, Vol.26 (1), p.65-78

2017

Link zum Volltext

Verfügbarkeit prüfen

MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-β signaling

Human molecular genetics, 2005-02, Vol.14 (3), p.437-445

2005

Link zum Volltext

Verfügbarkeit prüfen

Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy

Human molecular genetics, 2006-02, Vol.15 (4), p.653-663

2006

Link zum Volltext

Verfügbarkeit prüfen

Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery–Dreifuss muscular dystrophy

Human molecular genetics, 2006-08, Vol.15 (16), p.2479-2489

2006

Link zum Volltext

Verfügbarkeit prüfen

Epidermal expression of the truncated prelamin A causing Hutchinson–Gilford progeria syndrome: effects on keratinocytes, hair and skin

Human molecular genetics, 2008-08, Vol.17 (15), p.2357-2369

2008

Link zum Volltext

Verfügbarkeit prüfen

Peroxisome Proliferator-Activated Receptor-γ C190S Mutation Causes Partial Lipodystrophy

The journal of clinical endocrinology and metabolism, 2007-06, Vol.92 (6), p.2248-2255

2007

Link zum Volltext

Verfügbarkeit prüfen

Molecular biological methods in diagnosis and treatment of liver diseases

Clinical chemistry (Baltimore, Md.), 1997-08, Vol.43 (8), p.1476-1486

Worman, Howard J

1997

Link zum Volltext

Verfügbarkeit prüfen

MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-² signaling

Human molecular genetics, 2005-02, Vol.14 (3), p.437

2005

Link zum Volltext

Verfügbarkeit prüfen

Molecular biological xxxmethods in diagnosis and treatment of liver diseases

Clinical chemistry (Baltimore, Md.), 1997-08, Vol.43 (8), p.1476-1486

Worman, Howard J

1997

Link zum Volltext

Verfügbarkeit prüfen

1 – 22 von 22

Suche als RSS-Feed

Aktive Filter

KollektionJournals@Ovid Complete

KollektionOxford Journals 2020 Medicine

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(22)
Mit Volltextzugriff
(22)

Publikationsform

Artikel
(22)

Sprache

Englisch
(22)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(19)
Science & Technology
(19)
Biochemistry & Molecular Biology
(16)
Genetics & Heredity
(16)
Humans
(16)
Animals
(15)
Mice
(15)
Lamin Type A - Genetics
(12)
Biological And Medical Sciences
(10)
Female
(9)
Male
(9)
Fundamental And Applied Biological Sciences. Psychology
(8)
Medical Sciences
(8)
Mutation
(8)
General Medicine
(7)
Genetics
(7)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(7)
Molecular And Cellular Biology
(7)
Molecular Biology
(7)
Lamin Type A - Metabolism
(6)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

Oxford University Press Journals
(22)
EZB Electronic Journals Library
(22)
RCN full-text journals@Ovid
(22)
NUS Single-Journal Subscriptions
(20)
National Council for the Social Studies Journals
(19)
MEDLINE
(18)

1 weiteren anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Menü

Weitere Dienste

Einstellungen

ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene

Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation

Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation

Elevated dual specificity protein phosphatase 4 in cardiomyopathy caused by lamin A/C gene mutation is primarily ERK1/2-dependent and its depletion improves cardiac function and survival

Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery–Dreifuss muscular dystrophy

Decreased WNT/β-catenin signalling contributes to the pathogenesis of dilated cardiomyopathy caused by mutations in the lamin a/C gene

Abnormal p38α mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation

Abnormal p38 mitogen-activated protein kinase signaling in dilated cardiomyopathy caused by lamin A/C gene mutation

Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins

Depletion of extracellular signal-regulated kinase 1 in mice with cardiomyopathy caused by lamin A/C gene mutation partially prevents pathology before isoenzyme activation

Treatment with selumetinib preserves cardiac function and improves survival in cardiomyopathy caused by mutation in the lamin A/C gene

Postnatal development of mice with combined genetic depletions of lamin A/C, emerin and lamina-associated polypeptide 1

Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype

Lamina-associated polypeptide 1 is dispensable for embryonic myogenesis but required for postnatal skeletal muscle growth

MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-β signaling

Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy

Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery–Dreifuss muscular dystrophy

Epidermal expression of the truncated prelamin A causing Hutchinson–Gilford progeria syndrome: effects on keratinocytes, hair and skin

Peroxisome Proliferator-Activated Receptor-γ C190S Mutation Causes Partial Lipodystrophy

Molecular biological methods in diagnosis and treatment of liver diseases

MAN1, an integral protein of the inner nuclear membrane, binds Smad2 and Smad3 and antagonizes transforming growth factor-² signaling

Molecular biological xxxmethods in diagnosis and treatment of liver diseases

Aktive Filter

Suchergebnisse filtern