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...

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Brain (London, England : 1878), 2014-08, Vol.137 (Pt 8), p.2329-2345

2014

Volltextzugriff (PDF)

Author Correction: TDP-43 and PINK1 mediate CHCHD10S59L mutation–induced defects in Drosophila and in vitro

Nature communications, 2021-05, Vol.12 (1), p.3165-3165, Article 3165

2021

Volltextzugriff (PDF)

CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability

Brain (London, England : 1878), 2022-10, Vol.145 (10), p.3415-3430

2022

Volltextzugriff (PDF)

TDP-43 and PINK1 mediate CHCHD10S59L mutation–induced defects in Drosophila and in vitro

Nature communications, 2021-03, Vol.12 (1), Article 1924

2021

Volltextzugriff (PDF)

NDUFS6 related Leigh syndrome: a case report and review of the literature

Journal of human genetics, 2019-07, Vol.64 (7), p.637-645

2019

Volltextzugriff (PDF)

A Survey of Autoencoder Algorithms to Pave the Diagnosis of Rare Diseases

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10891

2021

Volltextzugriff (PDF)

Neurologic features and genotype-phenotype correlation in Wolfram syndrome

Annals of neurology, 2011-03, Vol.69 (3), p.501-508

2011

Volltextzugriff (PDF)

HIV-1 TAR RNA: the target of molecular interactions between the virus and its host

Current HIV research, 2005-01, Vol.3 (1), p.61-71

2005

Volltextzugriff (PDF)

Petite Integration Factor 1 (PIF1) helicase deficiency increases weight gain in Western diet-fed female mice without increased inflammatory markers or decreased glucose clearance

PloS one, 2019-05, Vol.14 (5), p.e0203101-e0203101

2019

Volltextzugriff (PDF)

Multi-Omics Approaches to Improve Mitochondrial Disease Diagnosis: Challenges, Advances, and Perspectives

Frontiers in molecular biosciences, 2020-11, Vol.7, p.590842

2020

Volltextzugriff (PDF)

Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases

BMC medical genetics, 2018-04, Vol.19 (1), p.57-57, Article 57

2018

Volltextzugriff (PDF)

Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice

Mitochondrion, 2016-09, Vol.30, p.126-137

2016

Volltextzugriff (PDF)

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse

Acta neuropathologica, 2019-07, Vol.138 (1), p.123-145

2019

Volltextzugriff (PDF)

TRBP Control of PACT-Induced Phosphorylation of Protein Kinase R Is Reversed by Stress

Molecular and Cellular Biology, 2009-01, Vol.29 (1), p.254-265

2009

Volltextzugriff (PDF)

A novel variant m.8561C>T in the overlapping region of MT-ATP6 and MT-ATP8 in a child with early-onset severe neurological signs

Molecular genetics and metabolism reports, 2019-12, Vol.21, p.100543-100543, Article 100543

2019

Volltextzugriff (PDF)

Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes

Biological research, 2016-01, Vol.49 (4), p.4-4, Article 4

2016

Volltextzugriff (PDF)

Small Interfering RNAs against the TAR RNA Binding Protein, TRBP, a Dicer Cofactor, Inhibit Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression and Viral Production

Journal of Virology, 2007-05, Vol.81 (10), p.5121-5131

2007

Volltextzugriff (PDF)

Low TRBP Levels Support an Innate Human Immunodeficiency Virus Type 1 Resistance in Astrocytes by Enhancing the PKR Antiviral Response

Journal of Virology, 2005-10, Vol.79 (20), p.12763-12772

2005

Volltextzugriff (PDF)

Astrocyte infection by HIV-1: mechanisms of restricted virus replication, and role in the pathogenesis of HIV-1-associated dementia

Current HIV research, 2003-10, Vol.1 (4), p.463-473

2003

Volltextzugriff (PDF)

Two Dimerization Domains in the Trans-activation Response RNA-binding Protein (TRBP) Individually Reverse the Protein Kinase R Inhibition of HIV-1 Long Terminal Repeat Expression

The Journal of biological chemistry, 2001-09, Vol.276 (36), p.33899-33905

2001

Volltextzugriff (PDF)

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

Brain (London, England : 1878), 2012-01, Vol.135 (1), p.23-34

2012

Volltextzugriff (PDF)

ABEILLE: a novel method for ABerrant Expression Identification empLoying machine LEarning from RNA-sequencing data

Bioinformatics (Oxford, England), 2022-10, Vol.38 (20), p.4754-4761

2022

Volltextzugriff (PDF)

1 – 25 von 100

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(94)
Mit Volltextzugriff
(96)

Publikationsform

Artikel
(99)
Berichte
(1)

Sprache

Englisch
(98)
Französisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

Author Correction: TDP-43 and PINK1 mediate CHCHD10S59L mutation–induced defects in Drosophila and in vitro

CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability

TDP-43 and PINK1 mediate CHCHD10S59L mutation–induced defects in Drosophila and in vitro

NDUFS6 related Leigh syndrome: a case report and review of the literature

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases

CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis

A Survey of Autoencoder Algorithms to Pave the Diagnosis of Rare Diseases

Neurologic features and genotype-phenotype correlation in Wolfram syndrome

Improved detection of mitochondrial DNA instability in mitochondrial genome maintenance disorders

HIV-1 TAR RNA: the target of molecular interactions between the virus and its host

Petite Integration Factor 1 (PIF1) helicase deficiency increases weight gain in Western diet-fed female mice without increased inflammatory markers or decreased glucose clearance

Multi-Omics Approaches to Improve Mitochondrial Disease Diagnosis: Challenges, Advances, and Perspectives

Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases

Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse

TRBP Control of PACT-Induced Phosphorylation of Protein Kinase R Is Reversed by Stress

A novel variant m.8561C>T in the overlapping region of MT-ATP6 and MT-ATP8 in a child with early-onset severe neurological signs

Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes

Small Interfering RNAs against the TAR RNA Binding Protein, TRBP, a Dicer Cofactor, Inhibit Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression and Viral Production

Low TRBP Levels Support an Innate Human Immunodeficiency Virus Type 1 Resistance in Astrocytes by Enhancing the PKR Antiviral Response

Astrocyte infection by HIV-1: mechanisms of restricted virus replication, and role in the pathogenesis of HIV-1-associated dementia

Two Dimerization Domains in the Trans-activation Response RNA-binding Protein (TRBP) Individually Reverse the Protein Kinase R Inhibition of HIV-1 Long Terminal Repeat Expression

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

ABEILLE: a novel method for ABerrant Expression Identification empLoying machine LEarning from RNA-sequencing data

Suchergebnisse filtern