Phagocytosis-initiated tumor hybrid cells acquire a c-Myc-mediated quasi-polarization state for immunoevasion and distant dissemination von Chou, Chih-Wei, Hung, Chia-Nung, Chiu, Cheryl Hsiang-Ling, Tan, Xi, Chen, Meizhen, Chen, Chien-Chin, Saeed, Moawiz, Hsu, Che-Wei, Liss, Michael A., Wang, Chiou-Miin, Lai, Zhao, Alvarez, Nathaniel, Osmulski, Pawel A., Gaczynska, Maria E., Lin, Li-Ling, Ortega, Veronica, Kirma, Nameer B., Xu, Kexin, Liu, Zhijie, Kumar, Addanki P., Taverna, Josephine A., Velagaleti, Gopalrao V. N., Chen, Chun-Liang, Zhang, Zhao, Huang, Tim Hui-Ming

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Oxidatively modified low‐density lipoproteins are potential mediators of proteasome inhibitor resistance in multiple myeloma von Polusani, Srikanth R., Cortez, Valerie, Esparza, Javier, Nguyen, Huynh Nga, Fan, Hongxin, Velagaleti, Gopalrao V. N., Butler, Matthew J., Kinney, Marsha C., Oyajobi, Babatunde O., Habib, Samy L., Asmis, Reto, Medina, Edward A.

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Position Effects Due to Chromosome Breakpoints that Map ∼900 Kb Upstream and ∼1.3 Mb Downstream of SOX9 in Two Patients with Campomelic Dysplasia von Velagaleti, Gopalrao V.N., Bien-Willner, Gabriel A., Northup, Jill K., Lockhart, Lillian H., Hawkins, Judy C., Jalal, Syed M., Withers, Marjorie, Lupski, James R., Stankiewicz, Pawel

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Myelodysplasia and Mast Cell Leukemia with t(9;22) von Haney, Brian R., Mendiola, Christina, Velagaleti, Gopalrao V. N., Hannah, William N., Shupe, Matthew P., Lago, Kathryn J., Ortega, Veronica

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Identification of Chromothripsis in Biopsy Using SNP-Based Microarray von Ortega, Veronica, Mendiola, Christina, Velagaleti, Gopalrao V. N.

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Is 5q deletion in de novo Acute Myelogenous Leukemia (AML) with excess blasts a surrogate marker for the cryptic t(7;21)(p22;q22)? A case report and review of literature von Johnston, Robert D., Sayedian, Farzaneh H., Mendiola, Christina, Ehman, William, Ortega, Veronica, Velagaleti, Gopalrao V.N.

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Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features von Kulharya, Anita S., Flannery, David B., Norris, Karen, Lovell, Carolyn, Levy, Brynn, Velagaleti, Gopalrao V.N.

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Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3‐month‐old with severe pediatric gastroesophageal reflux von Champaigne, Neena L., Laird, Nicole A., Northup, Jill K., Velagaleti, Gopalrao V.N.

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A case of Down syndrome with mirror-image duplication of chromosome 21 von Thi, Ha Thi Minh, Nhan, Nguyen Viet, Lindor, Noralane M., Meyer, Reid G., Rai, Ruhi, Velagaleti, Gopalrao V.N.

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A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma von Dadfarnia, Tahereh, Velagaleti, Gopalrao V.N, Carmichael, Kelly D, Eyzaguirre, Eduardo, Eltorky, Mahmoud A, Qiu, Suimin

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Fetoplacental Discrepancy with Normal Karyotype in Amniotic Fluid and Two Different Cell Lines in Placenta von Mendiola, Christina, Ortega, Veronica, Williamson, Eric, Higby, Kenneth, Velagaleti, Gopalrao V. N.

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First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficiencies von Northup, Jill K., Wain, Kären E., Hawkins, Judy C., Matalon, Reuben, Velagaleti, Gopalrao V.N.

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Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition? von Northup, Jill K., Gadre, Swarupa A., Ge, Yimin, Lockhart, Lillian H., Velagaleti, Gopalrao V. N.

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Immortalization and characterization of human myometrial cells from term-pregnant patients using a telomerase expression vector von Soloff, Melvyn S., Jeng, Yow-Jiun, Ilies, Monica, Soloff, Solweig L., Izban, Michael G., Wood, Thomas G., Panova, Neli I., Velagaleti, Gopalrao V.N., Anderson, Garland D.

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Subtelomeric rearrangements in idiopathic mental retardation von VELAGALETI, Gopalrao V. N, ROBINSON, Sally S, ROUSE, Bobby M, TONK, Vijay S, LOCKHART, Lillian H

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Cytogenetic and molecular studies of an unusual case of multiple primary alveolar rhabdomyosarcomas: Low-level chromosomal instability and reciprocal translocation t(6;11) von Wang, Zhiqin, Velagaleti, Gopalrao V.N., Eltorky, Mahmoud A., Tang, Wendell W., Hawkins, Hal K., Jones, Elizabeth A., Northup, Jill, Panova, Neli, Qiu, Suimin

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Cytogenetic abnormalities precede morphological abnormalities in developing malignant conditions: Report of 2 cases von Symons, Wendy A., Flynt, Frederick L., Mendiola, Christina, Ortega, Veronica, Higgins, Russell A., Velagaleti, Gopalrao V.N.

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A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia von Northup, Jill K, Matalon, Reuben, Lockhart, Lillian H, Hawkins, Judy C, Velagaleti, Gopalrao V.N

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Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement von Cooke, Susanna L., Northup, Jill K., Champaige, Neena L., Zinser, William, Edwards, Paul A.W., Lockhart, Lillian H., Velagaleti, Gopalrao V.N.

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Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family von Velagaleti, Gopalrao V. N., Hawkins, Judy C., Panova, Neli I., Lockhart, Lillian H.

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