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...

Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria

Molecular biology of the cell, 2017-03, Vol.28 (5), p.600-612

2017

Volltextzugriff (PDF)

Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia

Brain (London, England : 1878), 2016-11, Vol.139 (11), p.2877-2890

2016

Volltextzugriff (PDF)

C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

Nature genetics, 2007-09, Vol.39 (9), p.1068-1070

2007

Volltextzugriff (PDF)

Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue

Communications biology, 2022-09, Vol.5 (1), p.989-989, Article 989

2022

Volltextzugriff (PDF)

Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis

Science (American Association for the Advancement of Science), 2004-06, Vol.304 (5676), p.1509-1513

2004

Volltextzugriff (PDF)

Rapid development of Purkinje cell excitability, functional cerebellar circuit, and afferent sensory input to cerebellum in zebrafish

Frontiers in neural circuits, 2014-12, Vol.8, p.147-147

2014

Volltextzugriff (PDF)

Enhancement of fermentative volatile fatty acids production from waste activated sludge by combining sodium dodecylbenzene sulfonate and low-thermal pretreatment

Bioresource technology, 2020-07, Vol.308, p.123291-123291, Article 123291

2020

Volltextzugriff (PDF)

Overview of key operation factors and strategies for improving fermentative volatile fatty acid production and product regulation from sewage sludge

Journal of environmental sciences (China), 2020-01, Vol.87, p.93-111

2020

Volltextzugriff (PDF)

Episodic ataxias

Handbook of Clinical Neurology, 2018, Vol.155, p.205-215

2018

Volltextzugriff (PDF)

Factors influencing resorcinol–formaldehyde–latex‐coated continuous basalt fiber cord/rubber interfacial fatigue behavior: Loading direction and RFL formula

Journal of applied polymer science, 2018-08, Vol.135 (32), p.n/a

2018

Volltextzugriff (PDF)

Effects of coupling agents on the properties of an NR/SBR matrix and its adhesion to continuous basalt fiber cords

Journal of applied polymer science, 2019-02, Vol.136 (8), p.n/a

2019

Volltextzugriff (PDF)

Effects of heat and moisture on characteristics, tensile properties of RFL‐coated rayon cords, and their adhesion with NR/SBR matrix

Journal of applied polymer science, 2017-12, Vol.134 (48), p.n/a

2017

Volltextzugriff (PDF)

Structure and adhesive properties of the RFL‐coated continuous basalt fiber cord/rubber interface

Journal of applied polymer science, 2017-01, Vol.134 (1), p.np-n/a

2017

Volltextzugriff (PDF)

Static and dynamic adhesive properties between continuous basalt fibre cords and NR/SBR matrix tackified by p-octylphenolic resins

International journal of adhesion and adhesives, 2018-10, Vol.85, p.1-7

2018

Volltextzugriff (PDF)

Mechanical and tribological performance of chopped basalt fiber/acrylonitrile–butadiene rubber composites

Polymer composites, 2019-02, Vol.40 (2), p.630-637

2019

Volltextzugriff (PDF)

Nonconsensus intronic mutations cause episodic ataxia

Annals of neurology, 2005-01, Vol.57 (1), p.131-135

2005

Volltextzugriff (PDF)

Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

Brain (London, England : 1878), 2022-09, Vol.145 (9), p.3308-3327

2022

Volltextzugriff (PDF)

Episodic ataxias

Handbook of Clinical Neurology, 2018, Vol.148, p.521-529

2018

Volltextzugriff (PDF)

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake

Archives of neurology (Chicago), 2009-01, Vol.66 (1), p.97

2009

Volltextzugriff (PDF)

Disruption of RNA Processing in Pontocerebellar Hypoplasia with Spinal Muscular Atrophy (PCH1B) (P05.047)

Neurology, 2013-02, Vol.80 (7_supplement)

2013

Volltextzugriff (PDF)

Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling

Science advances, 2022-01, Vol.8 (3), p.eabl5613

2022

Volltextzugriff (PDF)

Large Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2

Frontiers in neurology, 2011, Vol.2, p.51-51

2011

Volltextzugriff (PDF)

Evidence of crustal ＇channel flow＇ in the eastern margin of Tibetan Plateau from MT measurements

Chinese science bulletin, 2008-06, Vol.53 (12), p.1887-1893

2008

Volltextzugriff (PDF)

1 – 25 von 106

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(81)
Mit Volltextzugriff
(93)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(69)
Life Sciences & Biomedicine
(32)
Physical Sciences
(31)
Humans
(20)
Technology
(17)
Chemistry
(16)
Materials Science
(13)
Engineering
(10)
Science & Technology - Other Topics
(10)
Neurosciences
(9)
Physics
(9)
Animals
(8)
Female
(8)
Male
(8)
Adult
(7)
Chemistry, Organic
(7)
Materials Science, Multidisciplinary
(7)
Catalysis
(6)
Chemistry, Multidisciplinary
(6)
Mutation
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Diagnostic utility of transcriptome sequencing for rare Mendelian diseases

Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria

Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia

Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration

C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

Single nuclei transcriptomics of muscle reveals intra-muscular cell dynamics linked to dystrophin loss and rescue

Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis

Rapid development of Purkinje cell excitability, functional cerebellar circuit, and afferent sensory input to cerebellum in zebrafish

Enhancement of fermentative volatile fatty acids production from waste activated sludge by combining sodium dodecylbenzene sulfonate and low-thermal pretreatment

Overview of key operation factors and strategies for improving fermentative volatile fatty acid production and product regulation from sewage sludge

Episodic ataxias

Factors influencing resorcinol–formaldehyde–latex‐coated continuous basalt fiber cord/rubber interfacial fatigue behavior: Loading direction and RFL formula

Effects of coupling agents on the properties of an NR/SBR matrix and its adhesion to continuous basalt fiber cords

Effects of heat and moisture on characteristics, tensile properties of RFL‐coated rayon cords, and their adhesion with NR/SBR matrix

Structure and adhesive properties of the RFL‐coated continuous basalt fiber cord/rubber interface

Static and dynamic adhesive properties between continuous basalt fibre cords and NR/SBR matrix tackified by p-octylphenolic resins

Mechanical and tribological performance of chopped basalt fiber/acrylonitrile–butadiene rubber composites

Nonconsensus intronic mutations cause episodic ataxia

Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes

Episodic ataxias

Episodic ataxia associated with EAAT1 mutation C186S affecting glutamate reuptake

Disruption of RNA Processing in Pontocerebellar Hypoplasia with Spinal Muscular Atrophy (PCH1B) (P05.047)

Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling

Large Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2

Evidence of crustal ＇channel flow＇ in the eastern margin of Tibetan Plateau from MT measurements

Suchergebnisse filtern