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Parashar, Deepak, Geethadevi, Anjali, Mittal, Sonam, McAlarnen, Lindsey A, George, Jasmine, Kadamberi, Ishaque P, Gupta, Prachi, Uyar, Denise S, Hopp, Elizabeth E, Drendel, Holli, Bishop, Erin A, Bradley, William H, Bone, Kathleen M, Rader, Janet S, Pradeep, Sunila, Chaluvally-Raghavan, Pradeep
Published in Cancers (01.02.2022)
Published in Cancers (01.02.2022)
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STAT1 is phosphorylated and downregulated by the oncogenic tyrosine kinase NPM-ALK in ALK-positive anaplastic large-cell lymphoma
Wu, Chengsheng, Molavi, Ommoleila, Zhang, Haifeng, Gupta, Nidhi, Alshareef, Abdulraheem, Bone, Kathleen M., Gopal, Keshav, Wu, Fang, Lewis, Jamie T., Douglas, Donna N., Kneteman, Norman M., Lai, Raymond
Published in Blood (16.07.2015)
Published in Blood (16.07.2015)
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Identification of two novel phenotypically distinct breast cancer cell subsets based on Sox2 transcription activity
Wu, Fang, Zhang, Jingdong, Wang, Peng, Ye, Xiaoxia, Jung, Karen, Bone, Kathleen M., Pearson, Joel D., Ingham, Robert J., McMullen, Todd P., Ma, Yupo, Lai, Raymond
Published in Cellular signalling (01.11.2012)
Published in Cellular signalling (01.11.2012)
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Correction: Parashar et al. Patient-Derived Ovarian Cancer Spheroids Rely on PI3K-AKT Signaling Addiction for Cancer Stemness and Chemoresistance. Cancers 2022, 14 , 958
Parashar, Deepak, Geethadevi, Anjali, Mittal, Sonam, McAlarnen, Lindsey A, George, Jasmine, Kadamberi, Ishaque P, Gupta, Prachi, Uyar, Denise S, Hopp, Elizabeth E, Drendel, Holli, Bishop, Erin A, Bradley, William H, Bone, Kathleen M, Rader, Janet S, Pradeep, Sunila, Chaluvally-Raghavan, Pradeep
Published in Cancers (16.05.2022)
Published in Cancers (16.05.2022)
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Detection of chromosomal alteration after infusion of gene-edited allogeneic CAR T cells
Sasu, Barbra J., Opiteck, Gregory J., Gopalakrishnan, Suhasni, Kaimal, Vivek, Furmanak, Tom, Huang, David, Goswami, Angshumala, He, Ying, Chen, Jiamin, Nguyen, Anh, Balakumaran, Arun, Shah, Nirav N., Hamadani, Mehdi, Bone, Kathleen M., Prashad, Sacha, Bowen, Michael A., Pertel, Thomas, Embree, Heather D., Gidwani, Shalini G., Chang, David, Moore, Alison, Leonard, Mark, Amado, Rafael G.
Published in Molecular therapy (01.03.2023)
Published in Molecular therapy (01.03.2023)
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A multicenter analysis of individuals with a 47,XXY/46,XX karyotype
Guess, Tiffany, Wheeler, Ferrin C., Yenamandra, Ashwini, Schilit, Samantha L.P., Anderson, Hannah S., Bone, Kathleen M., Carstens, Billie, Conlin, Laura, Dulik, Matthew C., Dupont, Barbra R., Fanning, Elizabeth, Gardner, Juli-Anne, Haag, Mary, Hilton, Benjamin A., Johnson, Jill, Kogan, Jillene, Murry, Jacyln, Polonis, Katarzyna, Quigley, Denise I., Repnikova, Elena A., Rowsey, Ross A., Spinner, Nancy, Stoeker, Mikayla, Thurston, Virginia, Wiley, Margaret, Zhang, Lei
Published in Genetics in medicine (01.10.2024)
Published in Genetics in medicine (01.10.2024)
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Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns‐like phenotype
Bone, Kathleen M., Chernos, Judy E., Perrier, Renee, Innes, A. Micheil, Bernier, Francois P., McLeod, Ross, Thomas, Mary Ann
Published in Prenatal diagnosis (01.06.2017)
Published in Prenatal diagnosis (01.06.2017)
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Fusion Tyrosine Kinase NPM-ALK Deregulates MSH2 and Suppresses DNA Mismatch Repair Function Novel Insights into a Potent Oncoprotein
YOUNG, Leah C, BONE, Kathleen M, LAI, Raymond, PENG WANG, FANG WU, ADAM, Benjamin A, HEGAZY, Samar, GELEBART, Pascal, HOLOVATI, Jelena, LIANG LI, ANDREW, Susan E
Published in The American journal of pathology (01.07.2011)
Published in The American journal of pathology (01.07.2011)
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Fusion Tyrosine Kinase NPM-ALK Deregulates MSH2 and Suppresses DNA Mismatch Repair Function
Young, Leah C, Bone, Kathleen M, Wang, Peng, Wu, Fang, Adam, Benjamin A, Hegazy, Samar, Gelebart, Pascal, Holovati, Jelena, Li, Liang, Andrew, Susan E, Lai, Raymond
Published in The American journal of pathology (2011)
Published in The American journal of pathology (2011)
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Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype: Prenatal diagnosis of mosaic trisomy 1q
Bone, Kathleen M., Chernos, Judy E., Perrier, Renee, Innes, A. Micheil, Bernier, Francois P., McLeod, Ross, Thomas, Mary Ann
Published in Prenatal diagnosis (01.06.2017)
Published in Prenatal diagnosis (01.06.2017)
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