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...

Accessorizing and anchoring the LINC complex for multifunctionality

The Journal of cell biology, 2015-01, Vol.208 (1), p.11-22

2015

Volltextzugriff (PDF)

Prelamin A and ZMPSTE24 in premature and physiological aging

Nucleus (Austin, Tex.), 2023-12, Vol.14 (1), p.2270345-2270345

2023

Volltextzugriff (PDF)

Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene

Circulation (New York, N.Y.), 2011-01, Vol.123 (1), p.53-61

2011

Volltextzugriff (PDF)

Laminopathies and the long strange trip from basic cell biology to therapy

The Journal of clinical investigation, 2009-07, Vol.119 (7), p.1825-1836

2009

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Temsirolimus activates autophagy and ameliorates cardiomyopathy caused by lamin A/C gene mutation

Science translational medicine, 2012-07, Vol.4 (144), p.144ra102

2012

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movement

The Journal of cell biology, 2017-03, Vol.216 (3), p.657-674

2017

Volltextzugriff (PDF)

Apoptosis-induced translocation of nesprin-2 from the nuclear envelope to mitochondria is associated with mitochondrial dysfunction

Nucleus (Austin, Tex.), 2024-12, Vol.15 (1), p.2413501

2024

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy

The Journal of clinical investigation, 2007-05, Vol.117 (5), p.1282-1293

2007

Volltextzugriff (PDF)

Long live lamins

The Journal of cell biology, 2024-01, Vol.223 (1), p.1

2024

Volltextzugriff (PDF)

Jaundice in patients with COVID‐19

JGH open, 2021-10, Vol.5 (10), p.1166-1171

2021

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Permanently Farnesylated Prelamin A, Progeria, and Atherosclerosis

Circulation (New York, N.Y.), 2018-07, Vol.138 (3), p.283-286

2018

Volltextzugriff (PDF)

Emery-Dreifuss muscular dystrophy: focal point nuclear envelope

Current opinion in neurology, 2019-10, Vol.32 (5), p.728-734

2019

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Nuclear envelope-localized torsinA-LAP1 complex regulates hepatic VLDL secretion and steatosis

The Journal of clinical investigation, 2019-11, Vol.129 (11), p.4885-4900

2019

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Pathogenic mutations in genes encoding nuclear envelope proteins and defective nucleocytoplasmic connections

Experimental Biology and Medicine, 2019-11, Vol.244 (15), p.1333-1344

2019

Volltextzugriff (PDF)

Localization and phosphorylation of HP1 proteins during the cell cycle in mammalian cells

Chromosoma, 1999-08, Vol.108 (4), p.220-234

1999

Volltextzugriff (PDF)

mTOR Inhibition Prolongs Survival and Has Beneficial Effects on Heart Function After Onset of Lamin A/C Gene Mutation Cardiomyopathy in Mice

Circulation. Heart failure, 2024-04, Vol.17 (4)

2024

Volltextzugriff (PDF)

“Laminopathies”: A wide spectrum of human diseases

Experimental cell research, 2007-06, Vol.313 (10), p.2121-2133

2007

Volltextzugriff (PDF)

1 – 25 von 82

Suche als RSS-Feed

Aktive Filter

KollektionWiley Online Library Full Collection 2018

KollektionJournals@Ovid Complete

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(82)
Mit Volltextzugriff
(72)

Publikationsform

Artikel
(82)

Sprache

Englisch
(82)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(73)
Science & Technology
(73)
Humans
(54)
Animals
(43)
Mice
(31)
Lamin Type A - Genetics
(27)
Cell Biology
(23)
Biochemistry & Molecular Biology
(21)
Biological And Medical Sciences
(21)
Genetics & Heredity
(21)
Mutation
(21)
Male
(20)
Proteins
(20)
Female
(16)
Medical Sciences
(16)
Nuclear Envelope - Metabolism
(15)
Lamin Type A - Metabolism
(14)
Nuclear Envelope
(12)
Fundamental And Applied Biological Sciences. Psychology
(11)
Lamin
(11)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Accessorizing and anchoring the LINC complex for multifunctionality

Prelamin A and ZMPSTE24 in premature and physiological aging

Mitogen-Activated Protein Kinase Inhibitors Improve Heart Function and Prevent Fibrosis in Cardiomyopathy Caused by Mutation in Lamin A/C Gene

Laminopathies and the long strange trip from basic cell biology to therapy

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

Temsirolimus activates autophagy and ameliorates cardiomyopathy caused by lamin A/C gene mutation

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

TorsinA controls TAN line assembly and the retrograde flow of dorsal perinuclear actin cables during rearward nuclear movement

Apoptosis-induced translocation of nesprin-2 from the nuclear envelope to mitochondria is associated with mitochondrial dysfunction

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 pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy

Long live lamins

Jaundice in patients with COVID‐19

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

Permanently Farnesylated Prelamin A, Progeria, and Atherosclerosis

Emery-Dreifuss muscular dystrophy: focal point nuclear envelope

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

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

Nuclear envelope-localized torsinA-LAP1 complex regulates hepatic VLDL secretion and steatosis

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

Pathogenic mutations in genes encoding nuclear envelope proteins and defective nucleocytoplasmic connections

Localization and phosphorylation of HP1 proteins during the cell cycle in mammalian cells

mTOR Inhibition Prolongs Survival and Has Beneficial Effects on Heart Function After Onset of Lamin A/C Gene Mutation Cardiomyopathy in Mice

“Laminopathies”: A wide spectrum of human diseases

Aktive Filter

Suchergebnisse filtern