Lymphogranuloma venereum variant L2b-specific polymerase chain reaction: insertion used to close an epidemiological gap

Autor: Sander Ouburg, A. Lombardi, Daniel Goldenberger, F. Dutly, Arnold Catsburg, Roel Heijmans, Stephan P. Verweij, Servaas A. Morré, Reno Frei

Publikováno v: Verweij, S P W, Catsburg, A, Ouburg, S, Lombardi, A, Heijmans, R, Dutlay, F, Frei, R & Morre, S A 2011, ' Lymphogranuloma venereum variant L2b-specific polymerase chain reaction: insertion used to close an epidemiological gap. ', Clinical Microbiology and Infection, vol. 17, no. 11, pp. 1727-1730 . https://doi.org/10.1111/j.1469-0691.2011.03481.x
Clinical Microbiology and Infection, 17(11), 1727-1730

The management of the ongoing lymphogranuloma venereum epidemic in industrialized Western countries caused by Chlamydia trachomatis variant L2b still needs improvements in diagnosis, therapy and prevention. We therefore developed the first rapid C. t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a623dd5b8dfb5ba321174731d6dd48d
https://hdl.handle.net/1871/36332

Neurons and astrocytes influence the development of purified o-2a progenitor cells

Autor: F. Dutly, Martin E. Schwab

Publikováno v: Glia. 4:559-571

To investigate the possible role of neurons and astrocytes for oligodendrocyte development we prepared a pure population of precursor cells positive for the precursor marker GD3 with the help of fluorescence-activated cell sorting (FACS). Large numbe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff42e7e93f69853ca760eb07a5c74f1a
https://doi.org/10.1002/glia.440040603

Analysis of 721 Chlamydia trachomatis-positive urogenital specimens from men and women using LGV L2-specific real-time PCR assay

Autor: Daniel Goldenberger, M Gebhardt, F Dutly

Publikováno v: Weekly releases (1997–2007). 11

The epidemic of rectal lymphogranuloma venereum among men who have sex with men in western Europe and other parts of the world is ongoing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::038939ef653afded62530daedd757e85
https://doi.org/10.2807/esw.11.42.03064-en

Seven cases of Wiedmann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11

Autor: F, Dutly, A, Baumer, H, Kayserili, M, Yüksel-Apak, T, Zerova, G, Hebisch, A, Schinzel

Publikováno v: American journal of medical genetics. 79(5)

Genomic imprinting of chromosome arm 11p is involved in the Wiedemann-Beckwith syndrome (WBS). About 20% of patients with sporadic WBS have paternal uniparental disomy (UPD) of 11p. Mitotic recombination at the 11p region has been suggested to be res

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::491451e54ae61527a0dd6bf5c0437a7f
https://pubmed.ncbi.nlm.nih.gov/9779800

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