Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bas, de Wolf"'
Autor:
Marijke P. Baltissen, Sandra Hanks, Eelco C. Tromer, Shawn Yost, Bas de Wolf, Geert J.P.L. Kops, Michiel Vermeulen, Philippe Piloquet, Bertrand Isidor, Ali Oghabian, Jolien J. E. van Hooff, Berend Snel, Esther C.H. Uijttewaal, Nazneen Rahman, Jens Verbeeren, Laura E van Rooijen, Lisa van Voorthuijsen, Maureen V. Akinyi, Mikko J. Frilander
Publikováno v:
EMBO Journal
EMBO Journal, 40(14), 1. Nature Publishing Group
EMBO Journal, 40(14). Nature Publishing Group
The EMBO Journal
EMBO Journal, 40(14), 1. Nature Publishing Group
EMBO Journal, 40(14). Nature Publishing Group
The EMBO Journal
Aneuploidy is the leading cause of miscarriage and congenital birth defects, and a hallmark of cancer. Despite this strong association with human disease, the genetic causes of aneuploidy remain largely unknown. Through exome sequencing of patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97d7b40146969ea51a965e5d52d5c292
https://dspace.library.uu.nl/handle/1874/414082
https://dspace.library.uu.nl/handle/1874/414082
Autor:
Bas de Wolf
Mosaic Variegated Aneuploidy (MVA) is a rare developmental disorder characterized by a clinically heterogeneous phenotype and the presence of mosaic aneuploidies (predominantly trisomies and monosomies of mostly random chromosomes). These aneuploid c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca79c2ae9ff82a450afaea58cb4fdf45
https://hdl.handle.net/1874/399871
https://hdl.handle.net/1874/399871
Autor:
Anna Zachariou, Esther Uijttewaal, Shawn Yost, Richarda M. de Voer, Susan Picton, Bas de Wolf, Anna Elliott, Chiara Marcozzi, Sarah F. Smithson, Gunnar Houge, Elise Ruark, Sandra Hanks, Emma Ramsay, Harriet Wylie, Jonathon Pines, Sheila Seal, Nazneen Rahman, Matthew Clarke, Banafsheh Etemad, Geert J. P. L. Kops, Audrey Smith
Publikováno v:
Nature Genetics, 49, 7, pp. 1148-1151
Nature Genetics, 49, 1148-1151
Nature Genetics, 49(7), 1148-1151. Nature Publishing Group
Nature Genetics, 49, 1148-1151
Nature Genetics, 49(7), 1148-1151. Nature Publishing Group
Through exome sequencing, we identified six individuals with biallelic loss-of-function mutations in TRIP13. All six developed Wilms tumor. Constitutional mosaic aneuploidies, microcephaly, developmental delay and seizures, which are features of mosa
Autor:
Bas, de Wolf, Geert J P L, Kops
Publikováno v:
Advances in experimental medicine and biology. 1002
The cell cycle culminates in mitosis with the purpose of dividing the cell's DNA content equally over two daughter cells. Error-free segregation relies on correct connections between chromosomes and spindle microtubules. Kinetochores are complex mult
Autor:
Bas de Wolf, Geert J. P. L. Kops
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783319571256
Cell Division Machinery and Disease, 1002, 69. Springer
Cell Division Machinery and Disease, 1002, 69. Springer
The cell cycle culminates in mitosis with the purpose of dividing the cell’s DNA content equally over two daughter cells. Error-free segregation relies on correct connections between chromosomes and spindle microtubules. Kinetochores are complex mu