Výsledky vyhledávání - "Anneke B, Oostra"

Akademický článek

Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2.

Autor: Atiq Faramarz, Jesper A Balk, Janne J M van Schie, Anneke B Oostra, Cherien A Ghandour, Martin A Rooimans, Rob M F Wolthuis, Job de Lange

Publikováno v: PLoS ONE, Vol 15, Iss 1, p e0220348 (2020)

In a process linked to DNA replication, duplicated chromosomes are entrapped in large, circular cohesin complexes and functional sister chromatid cohesion (SCC) is established by acetylation of the SMC3 cohesin subunit. Roberts Syndrome (RBS) and War

Externí odkaz: https://doaj.org/article/70c181c7128843c4bada5b22ebd8f2ca

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Supplemetal Material and Methods, Figure 1-7 and Table 1 from Defects in the Fanconi Anemia Pathway and Chromatid Cohesion in Head and Neck Cancer

Autor: Ruud H. Brakenhoff, Stephan M. Feller, Hans Joenje, Bauke Ylstra, Jesper A. Balk, Ralf Dietrich, Arjen Brink, Saskia E. van Mil, Martin A. Rooimans, Anneke B. Oostra, Irsan E. Kooi, Petra van der Lelij, Najim Ameziane, Chantal Stoepker

Supplemental Material and Methods. Supplemental Figure S1. Cell cycle analysis in FA and sporadic HNSCC cell lines upon ICL treatment. Supplemental Figure S2. FANCM protein expression is absent in FaDu cells. Supplemental Figure S3. Overview of possi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3787e8371329b3552a21a7e7c61e5949
https://doi.org/10.1158/0008-5472.22405466

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HSF2BP negatively regulates homologous recombination in DNA interstrand crosslink repair

Autor: Puck Knipscheer, Nicole S. Verkaik, Anneke B. Oostra, Roland Kanaar, Koichi Sato, Josephine C. Dorsman, Alex N. Zelensky, Inger Brandsma, Sari E. van Rossum-Fikkert, Dik C. van Gent

Publikováno v: Sato, K, Brandsma, I, van Rossum-Fikkert, S E, Verkaik, N, Oostra, A B, Dorsman, J C, van Gent, D C, Knipscheer, P, Kanaar, R & Zelensky, A N 2020, ' HSF2BP negatively regulates homologous recombination in DNA interstrand crosslink repair ', Nucleic Acids Research, vol. 48, no. 5, pp. 2442-2456 . https://doi.org/10.1093/nar/gkz1219
Nucleic Acids Research, 48(5), 2442-2456. Oxford University Press
Nucleic Acids Research, 48, 2442-2456. Oxford University Press
Nucleic Acids Research

The tumor suppressor BRCA2 is essential for homologous recombination (HR), replication fork stability and DNA interstrand crosslink (ICL) repair in vertebrates. We show that ectopic production of HSF2BP, a BRCA2-interacting protein required for meiot

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91546f48a230b80eb1d8f85f40395d9a
https://doi.org/10.1093/nar/gkz1219

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Biallelic

Autor: Sara, Carvalhal, Ingrid, Bader, Martin A, Rooimans, Anneke B, Oostra, Jesper A, Balk, René G, Feichtinger, Christine, Beichler, Michael R, Speicher, Johanna M, van Hagen, Quinten, Waisfisz, Mieke, van Haelst, Martijn, Bruijn, Alexandra, Tavares, Johannes A, Mayr, Rob M F, Wolthuis, Raquel A, Oliveira, Job, de Lange

Publikováno v: Science Advances

Budding uninhibited by benzimidazoles (BUB1) contributes to multiple mitotic processes. Here, we describe the first two patients with biallelic BUB1 germline mutations, who both display microcephaly, intellectual disability, and several patient-speci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f78dfdf066237826698f3c845e9c86b3
https://pubmed.ncbi.nlm.nih.gov/35044816

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Akademický článek

Identification of the Fanconi Anemia Complementation Group I Gene, FANCI

Autor: Josephine C. Dorsman, Marieke Levitus, Davy Rockx, Martin A. Rooimans, Anneke B. Oostra, Anneke Haitjema, Sietske T. Bakker, Jûrgen Steltenpool, Dezsö Schuler, Sheila Mohan, Detlev Schindler, Fré Arwert, Gerard Pals, Christopher G. Mathew, Quinten Waisfisz, Johan P. de Winter, Hans Joenje

Publikováno v: Cellular Oncology, Vol 29, Iss 3, Pp 211-218 (2007)

To identify the gene underlying Fanconi anemia (FA) complementation group I we studied informative FA-I families by a genome-wide linkage analysis, which resulted in 4 candidate regions together encompassing 351 genes. Candidates were selected via bi

Externí odkaz: https://doaj.org/article/1d446edcb77d4052afe9b566c074090a

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WAPL-Dependent Repair of Damaged DNA Replication Forks Underlies Oncogene-Induced Loss of Sister Chromatid Cohesion

Autor: Bente Benedict, Hein te Riele, Anneke B. Oostra, Janne J. M. van Schie, Rob M. F. Wolthuis, Jesper A. Balk, Job de Lange

Publikováno v: Developmental Cell, 52(6), 683-698.e7. Cell Press
Benedict, B, van Schie, J J M, Oostra, A B, Balk, J A, Wolthuis, R M F, Riele, H T & de Lange, J 2020, ' WAPL-Dependent Repair of Damaged DNA Replication Forks Underlies Oncogene-Induced Loss of Sister Chromatid Cohesion ', Developmental Cell, vol. 52, no. 6, pp. 683-698.e7 . https://doi.org/10.1016/j.devcel.2020.01.024
Developmental cell, 52(6), 683-698.e7. Cell Press

Summary Premature loss of sister chromatid cohesion at metaphase is a diagnostic marker for different cohesinopathies. Here, we report that metaphase spreads of many cancer cell lines also show premature loss of sister chromatid cohesion. Cohesion lo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c192ac2928199eade74f6e1f8dd1387a
https://research.vumc.nl/en/publications/7e131367-b0d7-44c9-be9c-eaa2cefff403

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Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2

Autor: Anneke B. Oostra, Jesper A. Balk, Cherien A. Ghandour, Rob M. F. Wolthuis, Job de Lange, Atiq Faramarz, Martin A. Rooimans, Janne J. M. van Schie

Publikováno v: PLoS ONE, 15(1):e0220348. Public Library of Science
PLoS ONE, Vol 15, Iss 1, p e0220348 (2020)
Faramarz, A, Balk, J A, van Schie, J J M, Oostra, A B, Ghandour, C A, Rooimans, M A, Wolthuis, R M F & de Lange, J 2020, ' Non-redundant roles in sister chromatid cohesion of the DNA helicase DDX11 and the SMC3 acetyl transferases ESCO1 and ESCO2 ', PLoS ONE, vol. 15, no. 1, e0220348, pp. e0220348 . https://doi.org/10.1371/journal.pone.0220348
PLoS ONE

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64c2656aa59e74c81bcf9a92bdd88143
https://research.vumc.nl/en/publications/ecd743ae-f239-4fe2-a504-4286627096d4

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Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion

Autor: Najim Ameziane, Francesca M. Pisani, Erika Cantelli, Joanna L Parish, Job de Lange, Atiq Faramarz, Marjon van Slegtenhorst, Ingeborg Barišić, Jesper A. Balk, Grant S. Stewart, Martin A. Rooimans, Janne J. M. van Schie, Rob M. F. Wolthuis, Katja Dumic, Hein te Riele, Karin E. M. Diderich, Cynthia de Almeida Estéves, Anneke B. Oostra, Mohammad Mahtab

Publikováno v: Nature communications 11 (2020): 4287–4305. doi:10.1038/s41467-020-18066-8
info:cnr-pdr/source/autori:van Schie J.J.M.; Faramarz A.; Balk J.A.; Stewart G.S.; Cantelli E.; Oostra A.B.; Rooimans M.A.; Parish J.L.; de Almeida Esteves C.; Dumic K.; Barisic I.; Diderich K.E.M.; van Slegtenhorst M.A.; Mahtab M.; Pisani F.M.; te Riele H.; Ameziane N.; Wolthuis R.M.F.; de Lange J./titolo:Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion/doi:10.1038%2Fs41467-020-18066-8/rivista:Nature communications/anno:2020/pagina_da:4287/pagina_a:4305/intervallo_pagine:4287–4305/volume:11
Nature Communications, 11(1):4287. Nature Publishing Group
Nature Communications
Nature communications, 11(1):4287. Nature Publishing Group
Nature Communications, 11(1):4287. Nature Publishing Group UK
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
van Schie, J J M, Faramarz, A, Balk, J A, Stewart, G S, Cantelli, E, Oostra, A B, Rooimans, M A, Parish, J L, de Almeida Estéves, C, Dumic, K, Barisic, I, Diderich, K E M, van Slegtenhorst, M A, Mahtab, M, Pisani, F M, Te Riele, H, Ameziane, N, Wolthuis, R M F & de Lange, J 2020, ' Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion ', Nature Communications, vol. 11, no. 1, 4287, pp. 4287 . https://doi.org/10.1038/s41467-020-18066-8

Warsaw Breakage Syndrome (WABS) is a rare disorder related to cohesinopathies and Fanconi anemia, caused by bi-allelic mutations in DDX11. Here, we report multiple compound heterozygous WABS cases, each displaying destabilized DDX11 protein and resid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d2904393f00b9ed4fde7c1c05a3cda8

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Akademický článek

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

Autor: Anneke B. Oostra, Aggie W. M. Nieuwint, Hans Joenje, Johan P. de Winter

Publikováno v: Anemia, Vol 2012 (2012)

Fanconi anemia (FA) is a rare inherited syndrome with diverse clinical symptoms including developmental defects, short stature, bone marrow failure, and a high risk of malignancies. Fifteen genetic subtypes have been distinguished so far. The mode of

Externí odkaz: https://doaj.org/article/f64d2709500c4622afcda90ac7b52874

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