E-LIB Suche - Ergebnisse für: Oostra, Anneke B.

1

Warsaw Breakage Syndrome associated DDX11 helicase resolves..:

van Schie, Janne J. M. ; Faramarz, Atiq ; Balk, Jesper A....
Nature Communications. 11 (2020) 1 - p. , 2020

Link: https://doi.org/10.1038/..

2

Non-redundant roles in sister chromatid cohesion of the DNA..:

Faramarz, Atiq ; Balk, Jesper A. ; van Schie, Janne J. M....
PLOS ONE. 15 (2020) 1 - p. e0220348 , 2020

Link: https://doi.org/10.1371/..

3

HSF2BP negatively regulates homologous recombination in DNA..:

Zelensky, Alex N ; Kanaar, Roland ; Knipscheer, Puck...
Nucleic Acids Research. 48 (2020) 5 - p. 2442-2456 , 2020

Link: https://doi.org/10.1093/..

4

The iron-sulfur cluster assembly network component NARFL is..:

Corbin, Monique V. ; Rockx, Davy A.P. ; Oostra, Anneke B...
Free Radical Biology and Medicine. 89 (2015) - p. 863-872 , 2015

Link: https://doi.org/10.1016/..

5

A novel Fanconi anaemia subtype associated with a dominant-..:

Ameziane, Najim ; May, Patrick ; Haitjema, Anneke...
Nature Communications. 6 (2015) 1 - p. , 2015

Link: https://doi.org/10.1038/..

6

Sensitivity to chromosomal breakage as risk factor in young..:

Braakhuis, Boudewijn J. M. ; Nieuwint, Aggie W. M. ; Oostra, Anneke B....
Journal of Oral Pathology & Medicine. 45 (2015) 3 - p. 189-192 , 2015

Link: https://doi.org/10.1111/..

7

Defective sister chromatid cohesion is synthetically lethal..:

de Lange, Job ; Faramarz, Atiq ; Oostra, Anneke B....
Nature Communications. 6 (2015) 1 - p. , 2015

Link: https://doi.org/10.1038/..

8

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis:

Oostra, Anneke B. ; Nieuwint, Aggie W. M. ; Joenje, Hans.
Anemia. 2012 (2012) - p. 1-9 , 2012

Link: https://doi.org/10.1155/..

9

A Ubiquitin-Binding Protein, FAAP20, Links RNF8-Mediated Ub..:

Yan, Zhijiang ; Guo, Rong ; Paramasivam, Manikandan...
Molecular Cell. 47 (2012) 1 - p. 61-75 , 2012

Link: https://doi.org/10.1016/..

10

SLX4, a coordinator of structure-specific endonucleases, is..:

Stoepker, Chantal ; Hain, Karolina ; Schuster, Beatrice...
Nature Genetics. 43 (2011) 2 - p. 138-141 , 2011

Link: https://doi.org/10.1038/..

11

Evidence for complete epistasis of null mutations in murine..:

van de Vrugt, Henri J. ; Koomen, Mireille ; Bakker, Sietske...
DNA Repair. 10 (2011) 12 - p. 1252-1261 , 2011

Link: https://doi.org/10.1016/..

12

Fancf‐deficient mice are prone to develop ovarian tumours:

Bakker, Sietske T ; van de Vrugt, Henri J ; Visser, Jenny A...
The Journal of Pathology. 226 (2011) 1 - p. 28-39 , 2011

Link: https://doi.org/10.1002/..

13

Warsaw breakage syndrome, a cohesinopathy associated with m..:

, In: American journal of human genetics / American Society of Human Genetics

Lelij, Petra van der ; Chrzanowska, Krystyna H. ; Godthelp, Barbara C..... (2010) 2 - p. 262-266

Copies: Zentrale: z hbi 820 jc/81; Zentrale:Magazin Zs fb 2581

14

Diagnostic Overlap between Fanconi Anemia and the Cohesinop..:

van der Lelij, Petra ; Oostra, Anneke B. ; Rooimans, Martin A...
Anemia. 2010 (2010) - p. 1-7 , 2010

Link: https://doi.org/10.1155/..

15

Fancm-deficient mice reveal unique features of Fanconi anem..:

Bakker, Sietske T. ; van de Vrugt, Henri J. ; Rooimans, Martin A....
Human Molecular Genetics. 18 (2009) 18 - p. 3484-3495 , 2009

Link: https://doi.org/10.1093/..