Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ankie Koeken"'
Autor:
Alphons H. Temmink, Paul R.M. van Hattum, Nils E. van 't Veer, Christa M. Cobbaert, Maureen A. ter Laak, Ankie Koeken
Publikováno v:
Pediatric Neurology. 43:159-162
Ten out of 100 children treated for attention deficit hyperactivity disorder with standard doses of atomoxetine were selected by a neurologist for cytochrome P450 2D6 and cytochrome P450 2C19 genotyping, based on late response (>9 weeks) and adverse
Autor:
Enevold Falsen, Herman Goossens, Wim Quint, Peter Vandamme, Ankie Koeken, Jolanda Koopmans, Marjan van Esbroeck, Johan C. Kuijpers M.D., Alex van Belkum
Publikováno v:
Molecular and cellular probes
The nucleotide sequence of the region between the 16S and 23S rRNA genes of the facultative anaerobic bacterium Gardnerella vaginalis has been determined, together with the 5' proximal 500 nucleotides of the 23S rRNA gene. Regions suited for the deve
Autor:
Anton A M Ermens, Brigitte C M Haberkorn, Ankie Koeken, Christa M. Cobbaert, Coen van Guldener
Publikováno v:
Clinical chemistry and laboratory medicine. 50(1)
Background: Adult-type hypolactasia is caused by genetic lactase non-persistence. It is the most common cause of lactose intolerance, which results in gastrointestinal symptoms after ingestion of dairy products. Currently, lactose intolerance is inve
Publikováno v:
Clinical Chemistry and Laboratory Medicine. 40
Comparative analysis of the hemochromatosis-associated mutations C282Y, H63D and S65C in the HFE gene in 51 patients using three different methods is reported. One PCR-RFLP method was based on general primers, whereas another employed mutation-specif
Autor:
Ankie Koeken, H. Goossens, H. P. Endtz, H. Stegeman, A. van Belkum, B. A. J. Giesendorf, Hubert G. M. Niesters, Wim Quint
Publikováno v:
Scopus-Elsevier
Journal of medical microbiology, 40(2), 141-147
Journal of medical microbiology
Journal of medical microbiology, 40(2), 141-147
Journal of medical microbiology
The applicability of polymerase chain reaction (PCR)-mediated DNA typing, with primers complementary to dispersed repetitive DNA sequences and arbitrarily chosen DNA motifs, to study the epidemiology of campylobacter infection was evaluated. With a s
Publikováno v:
Clinical Chemistry. 53:1715-1715
Hemochromatosis is an autosomal recessive disorder of iron metabolism affecting 0.2%–0.5% of white populations. Approximately 90% of affected individuals are homozygous for the C282Y mutation, but the H63D and S65C mutations are also of interest. V
Autor:
W. G. V. Quint, M. H. C. Henkens, A. van Belkum, Herman Goossens, J. van der Plas, H. Stegeman, B. A. J. Giesendorf, Ankie Koeken, Hubert G. M. Niesters
Publikováno v:
Scopus-Elsevier
Journal of clinical microbiology
Journal of Clinical Microbiology, 31(6), 1541-1546. AMER SOC MICROBIOLOGY
Journal of clinical microbiology
Journal of Clinical Microbiology, 31(6), 1541-1546. AMER SOC MICROBIOLOGY
The application of polymerase chain reaction (PCR) fingerprinting assays enables discrimination between species and strains of microorganisms. PCR primers aiming at arbitrary sequences in combination with primers directed against the repetitive extra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66373276d6030383e79c49d7954c13b9
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027204781&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027204781&partnerID=MN8TOARS