Works matching AU Biswas, Kajal

Results: 34
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    BRCA2-DSS1 interaction is dispensable for RAD51 recruitment at replication-induced and meiotic DNA double strand breaks.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29409-y
    By:
    • Mishra, Arun Prakash;
    • Hartford, Suzanne A.;
    • Sahu, Sounak;
    • Klarmann, Kimberly;
    • Chittela, Rajani Kant;
    • Biswas, Kajal;
    • Jeon, Albert B.;
    • Martin, Betty K.;
    • Burkett, Sandra;
    • Southon, Eileen;
    • Reid, Susan;
    • Albaugh, Mary E.;
    • Karim, Baktiar;
    • Tessarollo, Lino;
    • Keller, Jonathan R.;
    • Sharan, Shyam K.
    Publication type:
    Article
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    Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies.

    Published in:
    Nature Communications, 2016, v. 7, n. 8, p. 12425, doi. 10.1038/ncomms12425
    By:
    • Ding, Xia;
    • Chaudhuri, Arnab Ray;
    • Callen, Elsa;
    • Pang, Yan;
    • Biswas, Kajal;
    • Klarmann, Kimberly D.;
    • Martin, Betty K.;
    • Burkett, Sandra;
    • Cleveland, Linda;
    • Stauffer, Stacey;
    • Sullivan, Teresa;
    • Dewan, Aashish;
    • Marks, Hanna;
    • Tubbs, Anthony T.;
    • Wong, Nancy;
    • Buehler, Eugen;
    • Akagi, Keiko;
    • Martin, Scott E.;
    • Keller, Jonathan R.;
    • Nussenzweig, André
    Publication type:
    Article
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    Saturation genome editing of 11 codons and exon 13 of BRCA2 coupled with chemotherapeutic drug response accurately determines pathogenicity of variants.

    Published in:
    PLoS Genetics, 2023, v. 19, n. 9, p. 1, doi. 10.1371/journal.pgen.1010940
    By:
    • Sahu, Sounak;
    • Sullivan, Teresa L.;
    • Mitrophanov, Alexander Y.;
    • Galloux, Mélissa;
    • Nousome, Darryl;
    • Southon, Eileen;
    • Caylor, Dylan;
    • Mishra, Arun Prakash;
    • Evans, Christine N.;
    • Clapp, Michelle E.;
    • Burkett, Sandra;
    • Malys, Tyler;
    • Chari, Raj;
    • Biswas, Kajal;
    • Sharan, Shyam K.
    Publication type:
    Article
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    Rare germline variants in PALB2 and BRCA2 in familial and sporadic chordoma.

    Published in:
    Human Mutation, 2022, v. 43, n. 10, p. 1396, doi. 10.1002/humu.24427
    By:
    • Xia, Bing;
    • Biswas, Kajal;
    • Foo, Tzeh K.;
    • Gomes, Thiago T.;
    • Riedel‐Topper, Maximilian;
    • Southon, Eileen;
    • Kang, Zhihua;
    • Huo, Yanying;
    • Reid, Susan;
    • Stauffer, Stacey;
    • Zhou, Weiyin;
    • Zhu, Bin;
    • Koka, Hela;
    • Yepes, Sally;
    • Brodie, Seth A.;
    • Jones, Kristine;
    • Vogt, Aurelie;
    • Carter, Brian;
    • Freedman, Neal D.;
    • Hicks, Belynda
    Publication type:
    Article
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    Epidemiological and ES cell‐based functional evaluation of BRCA2 variants identified in families with breast cancer.

    Published in:
    Human Mutation, 2021, v. 42, n. 2, p. 200, doi. 10.1002/humu.24154
    By:
    • Sullivan, Teresa;
    • Thirthagiri, Eswary;
    • Chong, Chan‐Eng;
    • Stauffer, Stacey;
    • Reid, Susan;
    • Southon, Eileen;
    • Hassan, Tiara;
    • Ravichandran, Aravind;
    • Wijaya, Eldarina;
    • Lim, Joanna;
    • Taib, Nur Aishah Mohd;
    • Fadzli, Farhana;
    • Yip, Cheng Har;
    • Hartman, Mikael;
    • Li, Jingmei;
    • Dam, Rob M.;
    • North, Susan L.;
    • Das, Ranabir;
    • Easton, Douglas F.;
    • Biswas, Kajal
    Publication type:
    Article
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    BRCA2 minor transcript lacking exons 4-7 supports viability in mice and may account for survival of humans with a pathogenic biallelic mutation.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 10, p. 1934, doi. 10.1093/hmg/ddw066
    By:
    • Thirthagiri, Eswary;
    • Klarmann, Kimberly D.;
    • Shukla, Anil K.;
    • Southon, Eileen;
    • Biswas, Kajal;
    • Martin, Betty K.;
    • North, Susan Lynn;
    • Magidson, Valentin;
    • Burkett, Sandra;
    • Haines, Diana C.;
    • Noer, Kathleen;
    • Matthai, Roberta;
    • Tessarollo, Lino;
    • Loncarek, Jadranka;
    • Keller, Jonathan R.;
    • Sharan, Shyam K.
    Publication type:
    Article
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    Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assay.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 18, p. 3993, doi. 10.1093/hmg/dds222
    By:
    • Biswas, Kajal;
    • Das, Ranabir;
    • Eggington, Julie M.;
    • Qiao, Huanyu;
    • North, Susan L.;
    • Stauffer, Stacey;
    • Burkett, Sandra S.;
    • Martin, Betty K.;
    • Southon, Eileen;
    • Sizemore, Scott C.;
    • Pruss, Dmitry;
    • Bowles, Karla R.;
    • Roa, Benjamin B.;
    • Hunter, Neil;
    • Tessarollo, Lino;
    • Wenstrup, Richard J.;
    • Byrd, R. Andrew;
    • Sharan, Shyam K.
    Publication type:
    Article
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    A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicing.

    Published in:
    Cell Death & Disease, 2021, v. 12, n. 9, p. 1, doi. 10.1038/s41419-021-04130-8
    By:
    • Biswas, Kajal;
    • Couillard, Martin;
    • Cavallone, Luca;
    • Burkett, Sandra;
    • Stauffer, Stacey;
    • Martin, Betty K.;
    • Southon, Eileen;
    • Reid, Susan;
    • Plona, Teri M.;
    • Baugher, Ryan N.;
    • Mellott, Stephanie D.;
    • Pike, Kristen M.;
    • Albaugh, Mary E.;
    • Maedler-Kron, Chelsea;
    • Hamel, Nancy;
    • Tessarollo, Lino;
    • Marcus, Victoria;
    • Foulkes, William D.;
    • Sharan, Shyam K.
    Publication type:
    Article