The Fanconi Anemia Pathway of Genomic Maintenance

Por Levitus, Marieke, Joenje, Hans, de Winter, Johan P.
Publicado no Cell Oncol (2006)

Learning from a paradox: recent insights into Fanconi anaemia through studying mouse models

Por Bakker, Sietske T., de Winter, Johan P., te Riele, Hein
Publicado em 2013

Analysis of baseline and cisplatin-inducible gene expression in Fanconi anemia cells using oligonucleotide-based microarrays

Por Waisfisz, Quinten, Miyazato, Akira, de Winter, Johan P, Liu, Johnson M, Joenje, Hans
Publicado em 2002

Diagnosis of Fanconi Anemia: Chromosomal Breakage Analysis

Por Oostra, Anneke B., Nieuwint, Aggie W. M., Joenje, Hans, de Winter, Johan P.
Publicado em 2012

Biochemical Characterization of Warsaw Breakage Syndrome Helicase

Por Wu, Yuliang, Sommers, Joshua A., Khan, Irfan, de Winter, Johan P., Brosh, Robert M.
Publicado em 2012

Diagnostic Overlap between Fanconi Anemia and the Cohesinopathies: Roberts Syndrome and Warsaw Breakage Syndrome

Por van der Lelij, Petra, Oostra, Anneke B., Rooimans, Martin A., Joenje, Hans, de Winter, Johan P.
Publicado em 2010

Diagnosis of Fanconi Anemia: Mutation Analysis by Multiplex Ligation-Dependent Probe Amplification and PCR-Based Sanger Sequencing

Por Gille, Johan J. P., Floor, Karijn, Kerkhoven, Lianne, Ameziane, Najim, Joenje, Hans, de Winter, Johan P.
Publicado em 2012

Loss of expression of FANCD2 protein in sporadic and hereditary breast cancer

Por van der Groep, Petra, Hoelzel, Michael, Buerger, Horst, Joenje, Hans, de Winter, Johan P., van Diest, Paul J.
Publicado em 2007

A Protein Prioritization Approach Tailored for the FA/BRCA Pathway

Por Haitjema, Anneke, Brandt, Bernd W., Ameziane, Najim, May, Patrick, Heringa, Jaap, de Winter, Johan P., Joenje, Hans, Dorsman, Josephine C.
Publicado em 2013

Correction: A Protein Prioritization Approach Tailored for the FA/BRCA Pathway

Por Haitjema, Anneke, Brandt, Bernd W., Ameziane, Najim, May, Patrick, Heringa, Jaap, de Winter, Johan P., Joenje, Hans, Dorsman, Josephine C.
Publicado em 2013

The DNA Translocase FANCM/MHF Promotes Replication Traverse of DNA Interstrand Crosslinks

Por Huang, Jing, Liu, Shuo, Bellani, Marina, Thazhathveetil, Arun Kalliat, Ling, Chen, de Winter, Johan P., Wang, Yinsheng, Wang, Weidong, Seidman, Michael M.
Publicado em 2013

Recruitment of Fanconi Anemia and Breast Cancer Proteins to DNA Damage Sites is differentially Governed by Replication

Por Shen, Xi, Do, Huong, Li, Yongjian, Chung, Woo-Hyun, Tomasz, Maria, de Winter, Johan P., Xia, Bing, Elledge, Stephen J., Wang, Weidong, Li, Lei
Publicado em 2009

Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChlR1

Por van der Lelij, Petra, Chrzanowska, Krystyna H., Godthelp, Barbara C., Rooimans, Martin A., Oostra, Anneke B., Stumm, Markus, Zdzienicka, Małgorzata Z., Joenje, Hans, de Winter, Johan P.
Publicado em 2010

Diagnosis of Fanconi Anemia: Mutation Analysis by Next-Generation Sequencing

Por Ameziane, Najim, Sie, Daoud, Dentro, Stefan, Ariyurek, Yavuz, Kerkhoven, Lianne, Joenje, Hans, Dorsman, Josephine C., Ylstra, Bauke, Gille, Johan J. P., Sistermans, Erik A., de Winter, Johan P.
Publicado em 2012

A novel splice site mutation in the non-coding region of BRCA2: Implications for Fanconi anemia and familial breast cancer diagnostics

Por Bakker, Janine L., Thirthagiri, Eswary, van Mil, Saskia E., Adank, Muriel A., Ikeda, Hideyuki, Verheul, Henk M. W., Meijers-Heijboer, Hanne, de Winter, Johan P., Sharan, Shyam K., Waisfisz, Quinten
Publicado em 2014

Evidence for subcomplexes in the Fanconi anemia pathway

Por Medhurst, Annette L., Laghmani, El Houari, Steltenpool, Jurgen, Ferrer, Miriam, Fontaine, Chantal, de Groot, Jan, Rooimans, Martin A., Scheper, Rik J., Meetei, Amom Ruhikanta, Wang, Weidong, Joenje, Hans, de Winter, Johan P.
Publicado em 2006

Coregulation of FANCA and BRCA1 in human cells

Por Haitjema, Anneke, Mol, Berber M, Kooi, Irsan E, Massink, Maarten PG, Jørgensen, Jens AL, Rockx, Davy AP, Rooimans, Martin A, de Winter, Johan P, Meijers-Heijboer, Hanne, Joenje, Hans, Dorsman, Josephine C
Publicado em 2014

A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA

Por Waisfisz, Quinten, de Winter, Johan P., Kruyt, Frank A. E., de Groot, Jan, van der Weel, Laura, Dijkmans, Lonneke M., Zhi, Yu, Arwert, Fré, Scheper, Rik J., Youssoufian, Hagop, Hoatlin, Maureen E., Joenje, Hans
Publicado em 1999

A Human Orthologue of Archaeal DNA Repair Protein Hef is Defective in Fanconi Anemia Complementation Group M

Por Meetei, Amom Ruhikanta, Medhurst, Annette L., Ling, Chen, Xue, Yutong, Singh, Thiyam Ramsing, Bier, Patrick, Steltenpool, Jurgen, Stone, Stacie, Dokal, Inderjeet, Mathew, Christopher G., Hoatlin, Maureen, Joenje, Hans, de Winter, Johan P., Wang, Weidong
Publicado em 2005

The Cellular Phenotype of Roberts Syndrome Fibroblasts as Revealed by Ectopic Expression of ESCO2

Por van der Lelij, Petra, Godthelp, Barbara C., van Zon, Wouter, van Gosliga, Djoke, Oostra, Anneke B., Steltenpool, Jûrgen, de Groot, Jan, Scheper, Rik J., Wolthuis, Rob M., Waisfisz, Quinten, Darroudi, Firouz, Joenje, Hans, de Winter, Johan P.
Publicado em 2009