Výsledky vyhledávání - "Kim Vancampenhout"

Akademický článek

A bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome.

Autor: Kim Vancampenhout, Ben Caljon, Claudia Spits, Katrien Stouffs, An Jonckheere, Linda De Meirleir, Willy Lissens, Arnaud Vanlander, Joél Smet, Boel De Paepe, Rudy Van Coster, Sara Seneca

Publikováno v: PLoS ONE, Vol 9, Iss 11, p e112950 (2014)

The advent of massive parallel sequencing (MPS) has revolutionized the field of human molecular genetics, including the diagnostic study of mitochondrial (mt) DNA dysfunction. The analysis of the complete mitochondrial genome using MPS platforms is n

Externí odkaz: https://doaj.org/article/084d91aa6c5742289cd80d0e88be09ce

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Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells

Autor: Ben Caljon, Claudia Spits, Luca Gianaroli, Joke Mertens, Sara Seneca, Kim Vancampenhout, Karen Sermon, Filippo Zambelli, Thierry Voet, Daniel Brown, Dorien Daneels, Sonia Van Dooren

Publikováno v: European journal of human genetics : EJHG. 25(11)

Massive parallel sequencing (MPS) can accurately quantify mitochondrial DNA (mtDNA) single nucleotide variants (SNVs), but no MPS methods are currently validated to simultaneously and accurately establish the breakpoints and frequency of large deleti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e70ac45fd021e21e4aebb88a3771323
https://pubmed.ncbi.nlm.nih.gov/28832570

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Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

Autor: Kim Vancampenhout, Joél Smet, Katrien Stouffs, Arnaud Vanlander, Linda De Meirleir, Rudy Van Coster, Sara Seneca, Willy Lissens, An I. Jonckheere, Boel De Paepe

Publikováno v: Vrije Universiteit Brussel

Next-generation sequencing (NGS), an innovative sequencing technology that enables the successful analysis of numerous gene sequences in a massive parallel sequencing approach, has revolutionized the field of molecular biology. Although NGS was intro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce4de94e12e28a7fb22439ed95b17bf0
https://doi.org/10.1038/ejhg.2014.49

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High molecular diversity in the rhodopsin gene in closely related goby fishes: A role for visual pigments in adaptive speciation?

Autor: Tine Huyse, Filip Volckaert, Maarten Larmuseau, Kim Vancampenhout, Jeroen Van Houdt

Publikováno v: Molecular Phylogenetics and Evolution. 55:689-698

The spectral tuning mechanism of visual pigments is an excellent model to elucidate the mechanisms of adaptive evolution and the importance of selection as an evolutionary force. Therefore, we use a phylogenetic approach to determine whether there is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d65c421bf2c96eaefedd151b3e365198
https://doi.org/10.1016/j.ympev.2009.10.007

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Differential modes of selection on the rhodopsin gene in coastal Baltic and North Sea populations of the sand goby, Pomatoschistus minutus

Autor: Joost A. M. Raeymaekers, Filip Volckaert, Maarten Larmuseau, Jeroen Van Houdt, Kim Vancampenhout

Publikováno v: Molecular Ecology. 19:2256-2268

An excellent model to elucidate the mechanisms and importance of evolution in the marine environment is the spectral tuning mechanism of the visual pigment in vertebrates. In the sand goby Pomatoschistus minutus (Teleostei; Gobiidae), a distribution-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9ab6e72a70682e23ccfdb3f53242acdc
https://doi.org/10.1111/j.1365-294x.2010.04643.x

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Differential modes of selection on the rhodopsin gene in coastal Baltic and North Sea populations of the sand goby, Pomatoschistus minutus

Autor: Maarten H D, Larmuseau, Kim, Vancampenhout, Joost A M, Raeymaekers, Jeroen K J, Van Houdt, Filip A M, Volckaert

Publikováno v: Molecular ecology. 19(11)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::75902e9231d008d02f412062fedc166d
https://pubmed.ncbi.nlm.nih.gov/20444083

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A Bumpy Ride on the Diagnostic Bench of Massive Parallel Sequencing, the Case of the Mitochondrial Genome

Autor: Boel De Paepe, Sara Seneca, Linda De Meirleir, Arnaud Vanlander, Kim Vancampenhout, Joél Smet, Ben Caljon, Claudia Spits, Willy Lissens, Rudy Van Coster, Katrien Stouffs, An I. Jonckheere

Publikováno v: PLoS ONE
Vrije Universiteit Brussel
PLOS ONE
PLoS ONE, Vol 9, Iss 11, p e112950 (2014)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa64059222030d45b108695b5632325a
https://doi.org/10.1371/journal.pone.0112950

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Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene

Autor: François-Guillaume Debray, Sara Seneca, Gonce, M., Kim Vancampenhout, Boemer, F., Laurent Weekers, Joel Smet, Rudy Van Coster

Publikováno v: Vrije Universiteit Brussel

Cytochrome c oxidase (COX) deficiency is one of the most common respiratory chain deficiencies. A woman was presented at the age of 18 y with acute loss of consciousness, non-convulsive status epilepticus, slow neurological deterioration, transient c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ac1a98ed5c8ba490087cd27b9c3b1103
https://researchportal.vub.be/en/publications/71da4e93-0bb0-4638-8712-2b7caa2078f2

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