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List of works by Truus E M Abbink

A novel long distance base-pairing interaction in human immunodeficiency virus type 1 RNA occludes the Gag start codon

scientific article published on 27 November 2002

A short sequence motif in the 5' leader of the HIV-1 genome modulates extended RNA dimer formation and virus replication

scientific article

Adult mouse eIF2Bε Arg191His astrocytes display a normal integrated stress response in vitro

scientific article published on 28 February 2018

Altered PLP1 splicing causes hypomyelination of early myelinating structures.

scientific article published on May 2015

An unusually mild presentation of megalencephalic leukoencephalopathy with subcortical cysts

scientific article published on 26 February 2013

Astrocytes are central in the pathomechanisms of vanishing white matter

scientific article

Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study

scientific article

Cathepsin A-related arteriopathy with strokes and leukoencephalopathy (CARASAL).

scientific article published on 24 September 2016

Childhood Ataxia with Central Nervous System Hypomyelination / Vanishing White Matter

scientific article published on 4 April 2019

Circularization of the HIV-1 RNA genome

scientific article (publication date: 2007)

DARS-associated leukoencephalopathy can mimic a steroid-responsive neuroinflammatory disorder

scientific article

DDX5 potentiates HIV-1 transcription as a co-factor of Tat

scientific article published on 30 March 2020

ESCRT-II functions by linking to ESCRT-I in human immunodeficiency virus-1 budding

scientific article published on 14 February 2020

Eight novel mutations in MLC1 from 18 Iranian patients with megalencephalic leukoencephalopathy with subcortical cysts.

scientific article published on 11 December 2014

Evidence that the endosomal sorting complex required for transport-II (ESCRT-II) is required for efficient human immunodeficiency virus-1 (HIV-1) production

scientific article published on 14 August 2015

Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathy

scientific article published on 12 March 2013

Forced selection of a human immunodeficiency virus type 1 variant that uses a non-self tRNA primer for reverse transcription: involvement of viral RNA sequences and the reverse transcriptase enzyme

scientific article

Genome sequencing in persistently unsolved white matter disorders

scientific article published on 07 January 2020

HIV-1 reverse transcription initiation: a potential target for novel antivirals?

scientific article published on 06 February 2008

HIV-1 reverse transcription: close encounters between the viral genome and a cellular tRNA.

scientific article published on January 2007

Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation

scientific article

Identification of 3 Novel Patients with CLCN2-Related Leukoencephalopathy due to CLCN2 Mutations.

scientific article published on 26 July 2017

Identification of RNA helicases in human immunodeficiency virus 1 (HIV-1) replication - a targeted small interfering RNA library screen using pseudotyped and WT HIV-1

scientific article published on 20 February 2015

Immune adaptor ADAP in T cells regulates HIV-1 transcription and cell-cell viral spread via different co-receptors

scientific article

LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance

scientific article

Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy

scientific article

Leukoencephalopathy with thalamus and brainstem involvement and high lactate 'LTBL' caused by EARS2 mutations

scientific article

Megalencephalic leukoencephalopathy with cysts: the Glialcam-null mouse model

scientific article published on 6 June 2017

Mice with megalencephalic leukoencephalopathy with cysts: a developmental angle

scientific article published on 4 December 2014

Mutations in APOPT1, encoding a mitochondrial protein, cause cavitating leukoencephalopathy with cytochrome c oxidase deficiency

scientific article

Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity.

scientific article

NUBPL mutations in patients with complex I deficiency and a distinct MRI pattern

scientific article

Novel (ovario) leukodystrophy related to AARS2 mutations

scientific article

Optimal translation initiation enables Vif-deficient human immunodeficiency virus type 1 to escape restriction by APOBEC3G.

scientific article published on 18 March 2009

Ovarioleukodystrophy: Vanishing white matter versus AARS2-related ovarioleukodystrophy

scientific article published on 22 June 2018

Proteomic and Metabolomic Analyses of Vanishing White Matter Mouse Astrocytes Reveal Deregulation of ER Functions.

scientific article published on 20 December 2017

RNA structure modulates splicing efficiency at the human immunodeficiency virus type 1 major splice donor

scientific article

Recessive ITPA mutations cause an early infantile encephalopathy

scientific article published on 29 July 2015

Release of filamentous and spherical influenza A virus is not restricted by tetherin

scientific article published on 18 January 2012

Ribosomal scanning on the 5'-untranslated region of the human immunodeficiency virus RNA genome

scientific article published on 9 March 2011

Secondary paroxysmal kinesigenic dyskinesia associated with CLCN2 gene mutation

scientific article published on 25 February 2015

Silencing of a gene encoding a protein component of the oxygen-evolving complex of photosystem II enhances virus replication in plants

scientific article published in April 2002

The HIV-1 leader RNA conformational switch regulates RNA dimerization but does not regulate mRNA translation

scientific article published on 01 June 2005

The availability of the primer activation signal (PAS) affects the efficiency of HIV-1 reverse transcription initiation.

scientific article published on 18 February 2007

UFM1 founder mutation in the Roma population causes recessive variant of H-ABC.

scientific article

Vanishing white matter: Eukaryotic initiation factor 2B model and the impact of missense mutations

scientific article published on 12 January 2021

Vanishing white matter: deregulated integrated stress response as therapy target

scientific article published on 18 July 2019