Using Recombineering to Generate Point Mutations: galK-Based Positive-Negative Selection Method

Por Biswas, Kajal, Stauffer, Stacey, Sharan, Shyam K.
Publicado no Methods Mol Biol (2012)

Using Recombineering to Generate Point Mutations: Oligonucleotide-based “Hit & Fix” Method

Por Chang, Suhwan, Stauffer, Stacey, Sharan, Shyam K.
Publicado no Methods Mol Biol (2012)

Bypass of Premature Stop Codons and Generation of Functional BRCA2 by Exon Skipping

Por Stauffer, Stacey, Biswas, Kajal, Sharan, Shyam K.
Publicado no J Hum Genet (2020)

Expression of human BRCA1 variants in mouse ES cells allows functional analysis of BRCA1 mutations

Por Chang, Suhwan, Biswas, Kajal, Martin, Betty K., Stauffer, Stacey, Sharan, Shyam K.
Publicado em 2009

The Arf GTPase-activating protein ASAP1 regulates the actin cytoskeleton

Por Randazzo, Paul A., Andrade, Josefa, Miura, Koichi, Brown, Megan T., Long, Ya-Qiu, Stauffer, Stacey, Roller, Peter, Cooper, Jonathan A.
Publicado em 2000

Functional evaluation of five BRCA2 unclassified variants identified in a Sri Lankan cohort with inherited cancer syndromes using a mouse embryonic stem cell-based assay

Por Sirisena, Nirmala, Biswas, Kajal, Sullivan, Teresa, Stauffer, Stacey, Cleveland, Linda, Southon, Eileen, Dissanayake, Vajira H. W., Sharan, Shyam K.
Publicado no Breast Cancer Res (2020)

A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell–based assay

Por Biswas, Kajal, Das, Ranabir, Alter, Blanche P., Kuznetsov, Sergey G., Stauffer, Stacey, North, Susan L., Burkett, Sandra, Brody, Lawrence C., Meyer, Stefan, Byrd, R. Andrew, Sharan, Shyam K.
Publicado em 2011

Functional redundancy of exon 12 of BRCA2 revealed by a comprehensive analysis of the c.6853A>G p.I2285V variant

Por Li, Lili, Biswas, Kajal, Habib, Laura Anne, Kuznetsov, Sergey G., Hamel, Nancy, Kirchhoff, Tomas, Wong, Nora, Armel, Susan, Chong, George, Narod, Steven A., Claes, Kathleen, Offit, Kenneth, Robson, Mark E, Stauffer, Stacey, Sharan, Shyam K., Foulkes, William D.
Publicado em 2009

Functional evaluation of BRCA2 variants mapping to the PALB2-binding and C-terminal DNA-binding domains using a mouse ES cell-based assay

Por 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.
Publicado em 2012

Synthetic viability by BRCA2 and PARP1/ARTD1 deficiencies

Por 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, Sharan, Shyam K.
Publicado no Nat Commun (2016)

Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption

Por Meyer, Stefan, Stevens, Adam, Paredes, Roberto, Schneider, Marion, Walker, Michael J, Williamson, Andrew J K, Gonzalez-Sanchez, Maria-Belen, Smetsers, Stephanie, Dalal, Vineet, Teng, Hsiang Ying, White, Daniel J, Taylor, Sam, Muter, Joanne, Pierce, Andrew, de Leonibus, Chiara, Rockx, Davy A P, Rooimans, Martin A, Spooncer, Elaine, Stauffer, Stacey, Biswas, Kajal, Godthelp, Barbara, Dorsman, Josephine, Clayton, Peter E, Sharan, Shyam K, Whetton, Anthony D
Publicado no Cell Death Dis (2017)