Search Results - "NELSON, Marilu"

Identification of a Novel, Recurrent SLC44A1-PRKCA Fusion in Papillary Glioneuronal Tumor by Bridge, Julia A., Liu, Xiao-qiong, Sumegi, Janos, Nelson, Marilu, Reyes, Christine, Bruch, Leslie A., Rosenblum, Marc, Puccioni, Mark J., Bowdino, Bradley S., McComb, Rodney D.

“…Mixed neuronal‐glial tumors are rare and challenging to subclassify. One recently recognized variant, papillary glioneuronal tumor (PGNT), is characterized by…”
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Pericytoma with t(7;12) and ACTB-GLI1 fusion arising in bone by Bridge, Julia A., MD, Sanders, Kyle, MD, Huang, Dali, MD, Nelson, Marilu, MS, Neff, James R., MD, Muirhead, David, MSA, Walker, Craig, MD, Seemayer, Thomas A., MD, Sumegi, Janos, MD, PhD

“…Summary Cytogenetic analysis of a primary bone neoplasm with pericytic features in a 67-year-old man revealed a t(7;12)(p22;q13) among other karyotypic…”
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Alveolar rhabdomyosarcoma of the head and neck region in older adults: genetic characterization and a review of the literature by Yasuda, Taketoshi, MD, Perry, Kyle D., MD, Nelson, Marilu, BS, CLsp(CGMG), Bui, Marilyn M., MD, Nasir, Aejaz, MD, Goldschmidt, Robert, MD, Gnepp, Douglas R., MD, Bridge, Julia A., MD

“…Summary Alveolar rhabdomyosarcoma is remarkably rare in adults older than 45 years. Initial immunoprofiling of a small cell neoplasm of the head and neck…”
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Papillary tumor of the pineal region with synchronous suprasellar focus and novel cytogenetic features by Mobley, Bret C., MD, Kumar, Manoj, MD, Sanger, Warren G., PhD, Nelson, Marilu, MS, Nickols, Hilary H., MD, PhD, Chambless, Lola B., MD, Gokden, Murat, MD

“…Summary Papillary tumor of the pineal region (PTPR) is an uncommon neoplasm with variable biologic behavior. Cytogenetic and molecular diagnostic studies are…”
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Lymphoma Cytogenetics by Dave, Bhavana J., PhD, Nelson, Marilu, MS, CG, MB (ASCP), Sanger, Warren G., PhD

“…Lymphomas are a heterogeneous group of neoplasms with distinct morphologic, immunologic, and cytogenetic characteristics. Overlapping morphologic and…”
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Gene targeting in adult rhesus macaque fibroblasts by Meehan, Daniel T, Zink, Mary Ann, Mahlen, Melissa, Nelson, Marilu, Sanger, Warren G, Mitalipov, Shoukhrat M, Wolf, Don P, Ouellette, Michel M, Norgren, Jr, Robert B

“…Gene targeting in nonhuman primates has the potential to produce critical animal models for translational studies related to human diseases. Successful gene…”
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Renal cell carcinoma with novel VCL–ALK fusion: new representative of ALK-associated tumor spectrum by Debelenko, Larisa V, Raimondi, Susana C, Daw, Najat, Shivakumar, Bangalore R, Huang, Dali, Nelson, Marilu, Bridge, Julia A

“…Renal cell carcinoma represents a model for contemporary classification of solid tumors; however, unusual and unclassifiable cases exist and are not rare in…”
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A novel t(4;22)(q31;q12) produces an EWSR1–SMARCA5 fusion in extraskeletal Ewing sarcoma/primitive neuroectodermal tumor by Sumegi, Janos, Nishio, Jun, Nelson, Marilu, Frayer, Robert W, Perry, Deborah, Bridge, Julia A

“…Over 90% of Ewing sarcoma/primitive neuroectodermal tumors (PNETs) feature an 11;22 translocation leading to an EWSR1–FLI1 fusion. Less commonly, a member of…”
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The recurrent TUBB3 Gly98Ser substitution is the first described to inconsistently result in CFEOM3 by Smith, Scott C., Olney, Ann Haskins, Beavers, Angela, Spaulding, Joanna, Nelson, Marilu, Nielsen, Shelly, Sanmann, Jennifer N.

“…Missense variants in TUBB3 have historically been associated with either congenital fibrosis of the extraocular muscles type 3 (CFEOM3) or malformations of…”
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C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipoma by Huang, Dali, Sumegi, Janos, Dal Cin, Paola, Reith, John D., Yasuda, Taketoshi, Nelson, Marilu, Muirhead, David, Bridge, Julia A.

“…Chondroid lipoma, a rare benign adipose tissue tumor, may histologically resemble myxoid liposarcoma or extraskeletal myxoid chondrosarcoma, but is genetically…”
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Characterization of a variant SYT-SSX1 synovial sarcoma fusion transcript by Safar, A, Wickert, R, Nelson, M, Neff, J R, Bridge, J A

“…Synovial sarcoma is characterized cytogenetically by an X;18 translocation [t (X;18) (p11;q11)] that results in the fusion of the SYT gene from chromosome 18…”
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An increased frequency of 13q deletions detected by fluorescence in situ hybridization and its impact on survival in children and adolescents with Burkitt lymphoma: results from the Children’s Oncology Group study CCG‐5961 by Nelson, Marilu, Perkins, Sherrie L., Dave, Bhavana J., Coccia, Peter F., Bridge, Julia A., Lyden, Elizabeth R., Heerema, Nyla A., Lones, Mark A., Harrison, Lauren, Cairo, Mitchell S., Sanger, Warren G.

“…Summary Burkitt lymphoma (BL), an aggressive B‐cell malignancy, is often curable with short intensive treatment regiments. Nearly all BLs contain…”
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Cytogenetic abnormalities and clinical correlations in peripheral T‐cell lymphoma by Nelson, Marilu, Horsman, Douglas E., Weisenburger, Dennis D., Gascoyne, Randy D., Dave, Bhavana J., Loberiza, Fausto R., Ludkovski, Olga, Savage, Kerry J., Armitage, James O., Sanger, Warren G.

“…Summary Cytogenetic correlations among most types of peripheral T‐cell lymphoma (PTCL) have not been very informative to date. This study aimed to identify…”
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Breast Cancer and Non-Hodgkin Lymphoma in a Young Male with Cowden Syndrome: Male with Cowden Syndrome Presents with Lymphoma and Breast Cancer by Hagelstrom, Robert Tanner, Ford, James, Reiser, Gwendolyn M., Nelson, Marilu, Pickering, Diane L., Althof, Pamela A., Sanger, Warren G., Coccia, Peter F.

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Breast Cancer and Non-Hodgkin Lymphoma in a Young Male with Cowden Syndrome by Hagelstrom, Robert Tanner, Ford, James, Reiser, Gwendolyn M., Nelson, Marilu, Pickering, Diane L., Althof, Pamela A., Sanger, Warren G., Coccia, Peter F.

“…Male breast cancer (MBC) is unusual, especially in young adults. Most cases of MBC as a secondary malignancy relate to the previous treatment with ionizing…”
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40 - Apparent Lack of Segregation of a Pathogenic Nonsense PALB2 Variant in a Family With a Strong History of Cancer by Carstens, Julie M., Reiser, Gwen, Nelson, Marilu, Williamson, Janet E., Rief, Emily J., Roberts, Evan M., Scott, Karissa M., Bishay, Dani L., Dave, Bhavana J., Sanmann, Jennifer N.

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Cytogenetic abnormalities in follicular dendritic cell sarcoma: report of two cases and literature review by Perry, Anamarija M, Nelson, Marilu, Sanger, Warren G, Bridge, Julia A, Greiner, Timothy C

“…The identification of chromosomal abnormalities in many hematopoietic and mesenchymal neoplasms has contributed significantly to classification systems…”
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Translocation T(12;17)(Q24.1;Q21) as the Sole Anomaly in a Nasal Chondromesenchymal Hamartoma Arising in a Patient with Pleuropulmonary Blastoma by Behery, Radwa El, Bedrnicek, Jiri, Lazenby, Audrey, Nelson, Marilu, Grove, Jennifer, Huang, Dali, Smith, Russell, Bridge, Julia A.

“…The identification of recurrent chromosomal abnormalities in benign and malignant mesenchymal neoplasms has provided important pathogenetic insight as well as…”
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Chromosome 6 abnormalities are recurrent in synovial chondromatosis by Buddingh, Emilie P, Krallman, Pamela, Neff, James R, Nelson, Marilu, Liu, Jian, Bridge, Julia A

“…Synovial chondromatosis, a lesion composed of multiple nodules of cartilage involving articular or tendon sheath synovial membranes, has traditionally been…”
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Lymphoma Cytogenetics: Clinical Cytogenetics by DAVE, Bhavana J, NELSON, Marilu, SANGER, Warren G

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