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...

Papilin in development; a pericellular protein with a homology to the ADAMTS metalloproteinases

Development (Cambridge), 2000-12, Vol.127 (24), p.5475-5485

2000

Volltextzugriff (PDF)

Vinculin gene is non-essential in Drosophila melanogaster

FEBS letters, 1997-08, Vol.413 (2), p.197-201

1997

Volltextzugriff (PDF)

Mucinoprotein is a universal constituent of stable intercellular bridges in Drosophila melanogaster germ line and somatic cells

Developmental dynamics, 1999-12, Vol.216 (4‐5), p.349-360

1999

Volltextzugriff (PDF)

Position-effect variegation in Drosophila melanogaster x chromosome inversion with a breakpoint in a satellite block and its suppression in a secondary rearrangement

Chromosoma, 1997-12, Vol.106 (8), p.520-525

1997

Volltextzugriff (PDF)

Alternative splicing of papilin and the diversity of Drosophila extracellular matrix during embryonic morphogenesis

Developmental dynamics, 2003-04, Vol.226 (4), p.634-642

2003

Volltextzugriff (PDF)

Eu-heterochromatic Rearrangements Induce Replication of Heterochromatic Sequences Normally Underreplicated in Polytene Chromosomes of Drosophila melanogaster

Genetics (Austin), 2005-12, Vol.171 (4), p.1673-1681

2005

Volltextzugriff (PDF)

Cloning of human α1-antitrypsin gene and possible aspects of its utilization

Biopolimery i kletka, 1989-03, Vol.5 (2), p.43-47

1989

Volltextzugriff (PDF)

Possibility of the expression of a cloned human erythropoietin gene in CHO cells

Biopolimery i kletka, 1989-03, Vol.5 (2), p.47-51

1989

Volltextzugriff (PDF)

Simple and complex microsatellite DNAs in the region of the Drosophila vinculin gene

Molekuliarnaia biologiia, 1998-11, Vol.32 (6), p.981

1998

Volltextzugriff (PDF)

Disruption of polytenization of DNA from the euchromatin region of the Drosophila melanogaster X-chromosome, caused by euheterochromatin restructuring

Molekuliarnaia biologiia, 1998-11, Vol.32 (6), p.992

1998

Volltextzugriff (PDF)

Several copies of angiogenin gene are present in the mammalian genome

Molekuliarnaia biologiia, 1990-05, Vol.24 (3), p.709

1990

Volltextzugriff (PDF)

Cloning of human erythropoietin gene

Molekulârnaâ genetika, mikrobiologiâ i virusologiâ, 1988-07 (7), p.26

1988

Volltextzugriff (PDF)

Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro

Human molecular genetics, 2004-07, Vol.13 (13), p.1373-1388

2004

Volltextzugriff (PDF)

Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype

The Journal of cell biology, 2016-04, Vol.213 (2), p.275-288

2016

Volltextzugriff (PDF)

Satellite cell senescence underlies myopathy in a mouse model of limb-girdle muscular dystrophy 2H

The Journal of clinical investigation, 2012-05, Vol.122 (5), p.1764-1776

2012

Volltextzugriff (PDF)

Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3

Human molecular genetics, 2012-07, Vol.21 (14), p.3193-3204

2012

Volltextzugriff (PDF)

Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle

Human molecular genetics, 2008-11, Vol.17 (21), p.3271-3280

2008

Volltextzugriff (PDF)

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by Calmodulin Protein

The Journal of biological chemistry, 2015-01, Vol.290 (2), p.996-1004

2015

Volltextzugriff (PDF)

Trim32 is a Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy Type 2H that Binds to Skeletal Muscle Myosin and Ubiquitinates Actin

Journal of molecular biology, 2005-11, Vol.354 (2), p.413-424

2005

Volltextzugriff (PDF)

Spp1 (osteopontin) promotes TGFβ processing in fibroblasts of dystrophin-deficient muscles through matrix metalloproteinases

Human molecular genetics, 2019-10, Vol.28 (20), p.3431-3442

2019

Volltextzugriff (PDF)

Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle

Human molecular genetics, 2009-09, Vol.18 (17), p.3194-3205

2009

Volltextzugriff (PDF)

Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-beta

The Journal of clinical investigation, 2009-06, Vol.119 (6), p.1583-1594

2009

Volltextzugriff (PDF)

Myostatin inhibition promotes fast fibre hypertrophy but causes loss of AMP‐activated protein kinase signalling and poor exercise tolerance in a model of limb‐girdle muscular dystrophy R1/2A

The Journal of physiology, 2020-09, Vol.598 (18), p.3927-3939

2020

Volltextzugriff (PDF)

Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin–proteasome pathway

Human molecular genetics, 2005-08, Vol.14 (15), p.2125-2134

2005

Volltextzugriff (PDF)

Calpain 3 and CaMKIIβ signaling are required to induce HSP70 necessary for adaptive muscle growth after atrophy

Human molecular genetics, 2018-05, Vol.27 (9), p.1642-1653

2018

Volltextzugriff (PDF)

1 – 25 von 71

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(58)
Mit Volltextzugriff
(51)

Publikationsform

Artikel
(69)
Buchkapitel
(2)

Sprache

Erscheinungsjahr

n.n

Thema

Animals
(34)
Life Sciences & Biomedicine
(33)
Science & Technology
(33)
Mice
(22)
Biochemistry & Molecular Biology
(21)
Humans
(18)
Calpain - Genetics
(16)
Mice, Knockout
(16)
Muscle Proteins - Genetics
(15)
Genetics & Heredity
(14)
Male
(14)
Muscular Dystrophies, Limb-Girdle - Genetics
(13)
Muscle, Skeletal - Metabolism
(10)
Calpain
(9)
Cell Biology
(9)
Muscular Dystrophy
(9)
Biological And Medical Sciences
(8)
Calpain - Metabolism
(8)
Fundamental And Applied Biological Sciences. Psychology
(8)
Muscle Proteins - Metabolism
(8)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Papilin in development; a pericellular protein with a homology to the ADAMTS metalloproteinases

Vinculin gene is non-essential in Drosophila melanogaster

Mucinoprotein is a universal constituent of stable intercellular bridges in Drosophila melanogaster germ line and somatic cells

Position-effect variegation in Drosophila melanogaster x chromosome inversion with a breakpoint in a satellite block and its suppression in a secondary rearrangement

Alternative splicing of papilin and the diversity of Drosophila extracellular matrix during embryonic morphogenesis

Eu-heterochromatic Rearrangements Induce Replication of Heterochromatic Sequences Normally Underreplicated in Polytene Chromosomes of Drosophila melanogaster

Cloning of human α1-antitrypsin gene and possible aspects of its utilization

Possibility of the expression of a cloned human erythropoietin gene in CHO cells

Simple and complex microsatellite DNAs in the region of the Drosophila vinculin gene

Disruption of polytenization of DNA from the euchromatin region of the Drosophila melanogaster X-chromosome, caused by euheterochromatin restructuring

Several copies of angiogenin gene are present in the mammalian genome

Cloning of human erythropoietin gene

Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro

Osteopontin ablation ameliorates muscular dystrophy by shifting macrophages to a pro-regenerative phenotype

Satellite cell senescence underlies myopathy in a mouse model of limb-girdle muscular dystrophy 2H

Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3

Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle

Autolytic Activation of Calpain 3 Proteinase Is Facilitated by Calmodulin Protein

Trim32 is a Ubiquitin Ligase Mutated in Limb Girdle Muscular Dystrophy Type 2H that Binds to Skeletal Muscle Myosin and Ubiquitinates Actin

Spp1 (osteopontin) promotes TGFβ processing in fibroblasts of dystrophin-deficient muscles through matrix metalloproteinases

Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle

Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-beta

Myostatin inhibition promotes fast fibre hypertrophy but causes loss of AMP‐activated protein kinase signalling and poor exercise tolerance in a model of limb‐girdle muscular dystrophy R1/2A

Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin–proteasome pathway

Calpain 3 and CaMKIIβ signaling are required to induce HSP70 necessary for adaptive muscle growth after atrophy

Suchergebnisse filtern