Gert C Scheper
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Explore the profile of Gert C Scheper including associated specialties, affiliations and a list of published articles.
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52
Citations
1841
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Recent Articles
1.
Tang K, Vasani S, Menezes L, Taheri T, Walsh L, Hughes B, et al.
Cancer Sci
. 2020 Jul;
111(10):3854-3861.
PMID: 32713038
Given that oropharyngeal squamous cell carcinoma (OPSCC) have now surpassed cervical cancer as the most common human papillomavirus (HPV)-driven cancer, there is an interest in developing non-invasive predictive biomarkers to...
2.
Tang K, Menezes L, Baeten K, Walsh L, Whitfield B, Batstone M, et al.
Biomolecules
. 2020 Feb;
10(2).
PMID: 32028653
The role of human papillomavirus type 16 (HPV16) in oral potentially malignant disorders (OPMD) and oral cavity carcinoma (OC) is still under debate. We investigated HPV16 prevalence in unstimulated saliva,...
3.
Dooves S, Bugiani M, Postma N, Polder E, Land N, Horan S, et al.
J Clin Invest
. 2016 Mar;
126(4):1512-24.
PMID: 26974157
Vanishing white matter (VWM) is a fatal leukodystrophy that is caused by mutations in genes encoding subunits of eukaryotic translation initiation factor 2B (eIF2B). Disease onset and severity are codetermined...
4.
Dubey M, Bugiani M, Ridder M, Postma N, Brouwers E, Polder E, et al.
Ann Neurol
. 2014 Nov;
77(1):114-31.
PMID: 25382142
Objective: Megalencephalic leukoencephalopathy with cysts (MLC) is a genetic disease characterized by infantile onset white matter edema and delayed onset neurological deterioration. Loss of MLC1 function causes MLC. MLC1 is...
5.
van Berge L, Hamilton E, Linnankivi T, Uziel G, Steenweg M, Isohanni P, et al.
Brain
. 2014 Feb;
137(Pt 4):1019-29.
PMID: 24566671
Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation is a disorder caused by recessive mutations in the gene DARS2, which encodes mitochondrial aspartyl-tRNA synthetase. Recent observations indicate that...
6.
Schwenzer H, Scheper G, Zorn N, Moulinier L, Gaudry A, Leize E, et al.
Biochimie
. 2013 Oct;
100:18-26.
PMID: 24120687
Mammalian mitochondrial aminoacyl-tRNA synthetases are nuclear-encoded enzymes that are essential for mitochondrial protein synthesis. Due to an endosymbiotic origin of the mitochondria, many of them share structural domains with homologous...
7.
de Almeida R, Fogli A, Gaillard M, Scheper G, Boesflug-Tanguy O, Pavitt G
PLoS One
. 2013 Jan;
8(1):e53958.
PMID: 23335982
Recessive inherited mutations in any of five subunits of the general protein synthesis factor eIF2B are responsible for a white mater neurodegenerative disease with a large clinical spectrum. The classical...
8.
van Berge L, Kevenaar J, Polder E, Gaudry A, Florentz C, Sissler M, et al.
Biochem J
. 2012 Dec;
450(2):345-50.
PMID: 23216004
The autosomal recessive white matter disorder LBSL (leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation) is caused by mutations in DARS2, coding for mtAspRS (mitochondrial aspartyl-tRNA synthetase)....
9.
Valalik I, van der Knaap M, Scheper G, Jobbagy A, Liptai Z, Csokay A
Parkinsonism Relat Disord
. 2012 May;
18(9):1048-50.
PMID: 22632853
No abstract available.
10.
van Berge L, Dooves S, van Berkel C, Polder E, van der Knaap M, Scheper G
Biochem J
. 2011 Oct;
441(3):955-62.
PMID: 22023289
LBSL (leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation) is an autosomal recessive white matter disorder with slowly progressive cerebellar ataxia, spasticity and dorsal column dysfunction. Magnetic...