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...

VDAC2 Inhibits BAK Activation and Mitochondrial Apoptosis

Science (American Association for the Advancement of Science), 2003-07, Vol.301 (5632), p.513-517

2003

Volltextzugriff (PDF)

Clinical characterization of left ventricular noncompaction in children: A relatively common form of cardiomyopathy

Circulation (New York, N.Y.), 2003-11, Vol.108 (21), p.2672-2678

2003

Volltextzugriff (PDF)

Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease

Pediatrics (Evanston), 2004-10, Vol.114 (4), p.925-931

2004

Volltextzugriff (PDF)

Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation

American journal of human genetics, 2006-02, Vol.78 (2), p.303-314

2006

Volltextzugriff (PDF)

Serum Leptin Level Is a Regulator of Bone Mass

Proceedings of the National Academy of Sciences - PNAS, 2004-03, Vol.101 (9), p.3258-3263

2004

Volltextzugriff (PDF)

Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy

Circulation (New York, N.Y.), 2005-11, Vol.112 (18), p.2799-2804

2005

Volltextzugriff (PDF)

FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome

Clinical genetics, 2017-04, Vol.91 (4), p.634-639

2017

Volltextzugriff (PDF)

Mutations in the DNAH11 (Axonemal Heavy Chain Dynein type 11) Gene Cause One Form of Situs Inversus Totalis and Most Likely Primary Ciliary Dyskinesia

Proceedings of the National Academy of Sciences - PNAS, 2002-08, Vol.99 (16), p.10282-10286

2002

Volltextzugriff (PDF)

Mutations in the d-2-Hydroxyglutarate Dehydrogenase Gene Cause d-2-Hydroxyglutaric Aciduria

American journal of human genetics, 2005-02, Vol.76 (2), p.358-360

2005

Volltextzugriff (PDF)

Mitochondrial Regulation of Synaptic Plasticity in the Hippocampus

The Journal of biological chemistry, 2003-05, Vol.278 (20), p.17727-17734

2003

Volltextzugriff (PDF)

Voltage-dependent anion channel-1 (VDAC-1) contributes to ATP release and cell volume regulation in murine cells

The Journal of general physiology, 2004-11, Vol.124 (5), p.513-526

2004

Volltextzugriff (PDF)

Activation of cardiac Cdk9 represses PGC-1 and confers a predisposition to heart failure

The EMBO journal, 2004-09, Vol.23 (17), p.3559-3569

2004

Volltextzugriff (PDF)

Immotile Sperm and Infertility in Mice Lacking Mitochondrial Voltage-dependent Anion Channel Type 3

The Journal of biological chemistry, 2001-10, Vol.276 (42), p.39206-39212

2001

Volltextzugriff (PDF)

Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome

Clinical genetics, 2004-08, Vol.66 (2), p.128-136

2004

Volltextzugriff (PDF)

The Role of Mitochondrial Porins and the Permeability Transition Pore in Learning and Synaptic Plasticity

The Journal of biological chemistry, 2002-05, Vol.277 (21), p.18891-18897

2002

Volltextzugriff (PDF)

Altered Mitochondrial Sensitivity for ADP and Maintenance of Creatine-stimulated Respiration in Oxidative Striated Muscles from VDAC1-deficient Mice

The Journal of biological chemistry, 2001-01, Vol.276 (3), p.1954-1960

2001

Volltextzugriff (PDF)

Genetic Demonstration That the Plasma Membrane Maxianion Channel and Voltage-dependent Anion Channels Are Unrelated Proteins

The Journal of biological chemistry, 2006-01, Vol.281 (4), p.1897-1904

2006

Volltextzugriff (PDF)

New Insights into the Mechanism of Permeation through Large Channels

Biophysical journal, 2005-12, Vol.89 (6), p.3950-3959

2005

Volltextzugriff (PDF)

The murine voltage-dependent anion channel gene family. Conserved structure and function

The Journal of biological chemistry, 1997-07, Vol.272 (30), p.18966-18973

1997

Volltextzugriff (PDF)

Mitochondrial voltage-dependent anion channel gene family in Drosophila melanogaster: Complex patterns of evolution, genomic organization, and developmental expression

Molecular genetics and metabolism, 2005-08, Vol.85 (4), p.308-317

2005

Volltextzugriff (PDF)

Mouse VDAC isoforms expressed in yeast: channel properties and their roles in mitochondrial outer membrane permeability

The Journal of membrane biology, 1999-07, Vol.170 (2), p.89-102

1999

Volltextzugriff (PDF)

Isoform-Specific Imprinting of the Human PEG1/MEST Gene

American journal of human genetics, 2000, Vol.66 (1), p.309-312

2000

Volltextzugriff (PDF)

The Physiological Properties of a Novel Family of VDAC-Like Proteins from Drosophila melanogaster

Biophysical journal, 2004, Vol.86 (1), p.152-162

2004

Volltextzugriff (PDF)

Each mammalian mitochondrial outer membrane porin protein is dispensable: effects on cellular respiration

Biochimica et biophysica acta, 1999-10, Vol.1452 (1), p.68-78

1999

Volltextzugriff (PDF)

d-2-Hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction

Pediatric neurology, 1994-02, Vol.10 (1), p.49-53

1994

Volltextzugriff (PDF)

1 – 25 von 73

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(68)
Mit Volltextzugriff
(67)

Publikationsform

Artikel
(72)
Berichte
(1)

Sprache

Englisch
(73)

Erscheinungsjahr

n.n

Thema

Science & Technology
(63)
Life Sciences & Biomedicine
(60)
Humans
(42)
Animals
(33)
Biological And Medical Sciences
(30)
Mice
(30)
Genetics & Heredity
(29)
Male
(27)
Biochemistry & Molecular Biology
(22)
Female
(22)
Medical Sciences
(21)
Molecular Sequence Data
(18)
Voltage-Dependent Anion Channels
(17)
Base Sequence
(13)
Infant
(13)
Mutation
(11)
Amino Acid Sequence
(10)
Child, Preschool
(10)
Fundamental And Applied Biological Sciences. Psychology
(10)
Porins - Genetics
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

VDAC2 Inhibits BAK Activation and Mitochondrial Apoptosis

Clinical characterization of left ventricular noncompaction in children: A relatively common form of cardiomyopathy

Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease

Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation

Serum Leptin Level Is a Regulator of Bone Mass

Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy

FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome

Mutations in the DNAH11 (Axonemal Heavy Chain Dynein type 11) Gene Cause One Form of Situs Inversus Totalis and Most Likely Primary Ciliary Dyskinesia

Mutations in the d-2-Hydroxyglutarate Dehydrogenase Gene Cause d-2-Hydroxyglutaric Aciduria

Mitochondrial Regulation of Synaptic Plasticity in the Hippocampus

Voltage-dependent anion channel-1 (VDAC-1) contributes to ATP release and cell volume regulation in murine cells

Activation of cardiac Cdk9 represses PGC-1 and confers a predisposition to heart failure

Immotile Sperm and Infertility in Mice Lacking Mitochondrial Voltage-dependent Anion Channel Type 3

Interstitial deletion of 10p and atrial septal defect in DiGeorge 2 syndrome

The Role of Mitochondrial Porins and the Permeability Transition Pore in Learning and Synaptic Plasticity

Altered Mitochondrial Sensitivity for ADP and Maintenance of Creatine-stimulated Respiration in Oxidative Striated Muscles from VDAC1-deficient Mice

Genetic Demonstration That the Plasma Membrane Maxianion Channel and Voltage-dependent Anion Channels Are Unrelated Proteins

New Insights into the Mechanism of Permeation through Large Channels

The murine voltage-dependent anion channel gene family. Conserved structure and function

Mitochondrial voltage-dependent anion channel gene family in Drosophila melanogaster: Complex patterns of evolution, genomic organization, and developmental expression

Mouse VDAC isoforms expressed in yeast: channel properties and their roles in mitochondrial outer membrane permeability

Isoform-Specific Imprinting of the Human PEG1/MEST Gene

The Physiological Properties of a Novel Family of VDAC-Like Proteins from Drosophila melanogaster

Each mammalian mitochondrial outer membrane porin protein is dispensable: effects on cellular respiration

d-2-Hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction

Suchergebnisse filtern