A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination von Wang, Anderson T., Kim, Taeho, Wagner, John E., Conti, Brooke A., Lach, Francis P., Huang, Athena L., Molina, Henrik, Sanborn, Erica M., Zierhut, Heather, Cornes, Belinda K., Abhyankar, Avinash, Sougnez, Carrie, Gabriel, Stacey B., Auerbach, Arleen D., Kowalczykowski, Stephen C., Smogorzewska, Agata

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Mutations of the SLX4 gene in Fanconi anemia von Smogorzewska, Agata, Kim, Yonghwan, Lach, Francis P, Desetty, Rohini, Hanenberg, Helmut, Auerbach, Arleen D

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Distinct roles of BRCA2 in replication fork protection in response to hydroxyurea and DNA interstrand cross-links von Rickman, Kimberly A., Noonan, Raymond J., Lach, Francis P., Sridhar, Sunandini, Wang, Anderson T., Abhyankar, Avinash, Huang, Athena, Kelly, Michael, Auerbach, Arleen D., Smogorzewska, Agata

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Regulation of multiple DNA repair pathways by the Fanconi anemia protein SLX4 von Kim, Yonghwan, Spitz, Gabriella S., Veturi, Uma, Lach, Francis P., Auerbach, Arleen D., Smogorzewska, Agata

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Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer von Seal, Sheila, Barker, Karen, Ariffin, Hany, Rahman, Nazneen, Hanks, Sandra, Hanenberg, Helmut, Reid, Sarah, Freund, Marcel, Kelly, Patrick, Auerbach, Arleen D, Wurm, Melanie, Tischkowitz, Marc, Batish, Sat Dev, Mathew, Christopher G, Yetgin, Sevgi, Neveling, Kornelia, Lach, Francis P, Schindler, Detlev, Kalb, Reinhard, Neitzel, Heidemarie

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Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia von Rickman, Kimberly A., Lach, Francis P., Abhyankar, Avinash, Donovan, Frank X., Sanborn, Erica M., Kennedy, Jennifer A., Sougnez, Carrie, Gabriel, Stacey B., Elemento, Olivier, Chandrasekharappa, Settara C., Schindler, Detlev, Auerbach, Arleen D., Smogorzewska, Agata

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FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway von Ali, Abdullah Mahmood, Pradhan, Arun, Singh, Thiyam Ramsingh, Du, Changhu, Li, Jie, Wahengbam, Kebola, Grassman, Elke, Auerbach, Arleen D., Pang, Qishen, Meetei, Amom Ruhikanta

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A 20-year perspective on the International Fanconi Anemia Registry (IFAR) von Kutler, David I., Singh, Bhuvanesh, Satagopan, Jaya, Batish, Sat Dev, Berwick, Marianne, Giampietro, Philip F., Hanenberg, Helmut, Auerbach, Arleen D.

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Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia von Chandrasekharappa, Settara C., Lach, Francis P., Kimble, Danielle C., Kamat, Aparna, Teer, Jamie K., Donovan, Frank X., Flynn, Elizabeth, Sen, Shurjo K., Thongthip, Supawat, Sanborn, Erica, Smogorzewska, Agata, Auerbach, Arleen D., Ostrander, Elaine A., NISC Comparative Sequencing Program

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The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia von Levran, Orna, Milton, Kelly L, Henry, Rashida T, Neveling, Kornelia, Ott, Jurg, Attwooll, Claire, Rio, Paula, Schindler, Detlev, Petrini, John, Batish, Sat Dev, Auerbach, Arleen D, Velleuer, Eunike, Kalb, Reinhard, Barral, Sandra, Hanenberg, Helmut

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Unrelated donor bone marrow transplantation for the treatment of Fanconi anemia von Wagner, John E., Eapen, Mary, MacMillan, Margaret L., Harris, Richard E., Pasquini, Ricardo, Boulad, Farid, Zhang, Mei-Jie, Auerbach, Arleen D.

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Correct mRNA Processing at a Mutant TT Splice Donor in FANCC Ameliorates the Clinical Phenotype in Patients and Is Enhanced by Delivery of Suppressor U1 snRNAs von Hartmann, Linda, Neveling, Kornelia, Borkens, Stephanie, Schneider, Hildegard, Freund, Marcel, Grassman, Elke, Theiss, Stephan, Wawer, Angela, Burdach, Stefan, Auerbach, Arleen D., Schindler, Detlev, Hanenberg, Helmut, Schaal, Heiner

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Diagnosis of Fanconi Anemia by Diepoxybutane Analysis von Auerbach, Arleen D.

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Comprehensive Analysis of Pathogenic Deletion Variants in Fanconi Anemia Genes von Flynn, Elizabeth K., Kamat, Aparna, Lach, Francis P., Donovan, Frank X., Kimble, Danielle C., Narisu, Narisu, Sanborn, Erica, Boulad, Farid, Davies, Stella M., Gillio III, Alfred P., Harris, Richard E., MacMillan, Margaret L., Wagner, John E., Smogorzewska, Agata, Auerbach, Arleen D., Ostrander, Elaine A., Chandrasekharappa, Settara C.

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FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway von Ling, Chen, Ishiai, Masamichi, Ali, Abdullah Mahmood, Medhurst, Annette L, Neveling, Kornelia, Kalb, Reinhard, Yan, Zhijiang, Xue, Yutong, Oostra, Anneke B, Auerbach, Arleen D, Hoatlin, Maureen E, Schindler, Detlev, Joenje, Hans, de Winter, Johan P, Takata, Minoru, Meetei, Amom Ruhikanta, Wang, Weidong

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Stem Cell Collection and Gene Transfer in Fanconi Anemia von Kelly, Patrick F, Radtke, Susan, Kalle, Christof von, Balcik, Brenden, Bohn, Kimberley, Mueller, Robin, Schuesler, Todd, Haren, Moira, Reeves, Lilith, Cancelas, Jose A, Leemhuis, Thomas, Harris, Richard, Auerbach, Arleen D, Smith, Franklin O, Davies, Stella M, Williams, David A

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Genetic heterogeneity among fanconi anemia heterozygotes and risk of cancer von BERWICK, Marianne, SATAGOPAN, Jaya M, DEV BATISH, Sat, MORALES, José, SCHINDLER, Detlev, HANENBERG, Helmut, HROMAS, Robert, LEVRAN, Orna, AUERBACH, Arleen D, BEN-PORAT, Leah, CARLSON, Ann, MAH, Katherine, HENRY, Rashida, DIOTTI, Raffaella, MILTON, Kelly, PUJARA, Kanan, LANDERS, Tom

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Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer von Webster, Andrew L. H., Sanders, Mathijs A., Patel, Krupa, Dietrich, Ralf, Noonan, Raymond J., Lach, Francis P., White, Ryan R., Goldfarb, Audrey, Hadi, Kevin, Edwards, Matthew M., Donovan, Frank X., Hoogenboezem, Remco M., Jung, Moonjung, Sridhar, Sunandini, Wiley, Tom F., Fedrigo, Olivier, Tian, Huasong, Rosiene, Joel, Heineman, Thomas, Kennedy, Jennifer A., Bean, Lorenzo, Rosti, Rasim O., Tryon, Rebecca, Gonzalez, Ashlyn-Maree, Rosenberg, Allana, Luo, Ji-Dung, Carroll, Thomas S., Shroff, Sanjana, Beaumont, Michael, Velleuer, Eunike, Rastatter, Jeff C., Wells, Susanne I., Surrallés, Jordi, Bagby, Grover, MacMillan, Margaret L., Wagner, John E., Cancio, Maria, Boulad, Farid, Scognamiglio, Theresa, Vaughan, Roger, Beaumont, Kristin G., Koren, Amnon, Imielinski, Marcin, Chandrasekharappa, Settara C., Auerbach, Arleen D., Singh, Bhuvanesh, Kutler, David I., Campbell, Peter J., Smogorzewska, Agata

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Successful engraftment without radiation after fludarabine-based regimen in Fanconi anemia patients undergoing genotypically identical donor hematopoietic cell transplantation von Tan, Poh-Lin, Wagner, John E., Auerbach, Arleen D., DeFor, Todd E., Slungaard, Arne, MacMillan, Margaret L.

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Natural history and management of Fanconi anemia patients with head and neck cancer: A 10-year follow-up von Kutler, David I., Patel, Krupa R., Auerbach, Arleen D., Kennedy, Jennifer, Lach, Francis P., Sanborn, Erica, Cohen, Marc A., Kuhel, William I., Smogorzewska, Agata

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