Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Emile de Meijer"'
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 9, Iss 4, Pp 987-991 (2019)
Parasitoid insects are important model systems for a multitude of biological research topics and widely used as biological control agents against insect pests. While the parasitoid lifestyle has evolved numerous times in different insect groups, rese
Externí odkaz:
https://doaj.org/article/dea9c575e70b46578d30f8207d844c9c
Autor:
Ken Kraaijeveld, Vicencio Oostra, Maartje Liefting, Bregje Wertheim, Emile de Meijer, Jacintha Ellers
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-15 (2018)
Abstract Background Selection acts on the phenotype, yet only the genotype is inherited. While both the phenotypic and genotypic response to short-term selection can be measured, the link between these is a major unsolved problem in evolutionary biol
Externí odkaz:
https://doaj.org/article/27dfaca9c7d24486ab93393a1ae5d132
Autor:
Cornelis L. Harteveld, Stefan J. White, Emile de Meijer, Henk P. J. Buermans, Quint P Hottentot
Publikováno v:
International Journal of Laboratory Hematology, 43(6), 1628-1634. WILEY
Introduction The high-sequence homology of the α-globin-gene cluster is responsible for microhomology-mediated recombination events during meiosis, resulting in a high density of deletion breakpoints within a 10 kb region. Commonly used deletion det
Autor:
Quint P, Hottentot, Emile, de Meijer, Henk P J, Buermans, Stefan J, White, Cornelis L, Harteveld
Publikováno v:
International journal of laboratory hematology. 43(6)
The high-sequence homology of the α-globin-gene cluster is responsible for microhomology-mediated recombination events during meiosis, resulting in a high density of deletion breakpoints within a 10 kb region. Commonly used deletion detection method
Autor:
Peter de Knijff, Emile de Meijer, Rosemarie H M J M Kroon, Henk P. J. Buermans, Vered Raz, Rick H. de Leeuw, Dominique Garnier, Baziel G.M. van Engelen, Corinne G.C. Horlings
Publikováno v:
European Journal of Human Genetics, 27, 3, pp. 400-407
European Journal of Human Genetics
European Journal of Human Genetics, 27(3), 400-407. NATURE PUBLISHING GROUP
European Journal of Human Genetics, 27, 400-407
European Journal of Human Genetics
European Journal of Human Genetics, 27(3), 400-407. NATURE PUBLISHING GROUP
European Journal of Human Genetics, 27, 400-407
Short tandem repeats (STRs) are scattered throughout the human genome. Some STRs, like trinucleotide repeat expansion (TRE) variants, cause hereditable disorders. Unambiguous molecular diagnostics of TRE disorders is hampered by current technical lim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e57edf60a5792cbf9ebd466a64efa109
https://hdl.handle.net/1887/122255
https://hdl.handle.net/1887/122255
Autor:
Emile de Meijer, Pieter van de Putte, Claude Backendorf, David F. Fischer, Murielle W.J. Sark
Publikováno v:
Journal of Biological Chemistry. 273:24683-24692
The 173-base pair proximal promoter of SPRR1A is necessary and sufficient for regulated expression in primary keratinocytes induced to differentiate either by increasing extracellular calcium or by 12-O-tetradecanoylphorbol-13-acetate (TPA) treatment
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 209