Výsledky vyhledávání - "Jacqueline R, Batanian"

Akademický článek

Papillary Thyroid Cancer in Struma Testis with Malignant Transformation in the Lung Associated with Trisomy 17 Successfully Treated with Total Thyroidectomy and Radioiodine Ablation

Autor: Shadi Barakat, Jamie Odem, Jacqueline R. Batanian, Shahzad Raza, Uzma Z. Khan

Publikováno v: Case Reports in Oncology, Vol 7, Iss 3, Pp 751-757 (2014)

Background: Struma testis is a rare entity, and there are only few reports on the malignant transformation of a testicular teratoma to papillary thyroid carcinoma in the literature. In this report, we describe the malignant transformation of struma t

Externí odkaz: https://doaj.org/article/57920eaa3049419492fb4ae13021c865

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A novel aberration ofCOL1A1‐PDGFBfusion as an insertion in chromosome 15 in one case of dermatofibrosarcoma protuberans involving a rare location

Autor: Alexander Daoud, Jessica A. Kozel, Jacqueline R. Batanian, Christopher R Cunningham, Jordan B. Slutsky, Reena Varade

Publikováno v: Journal of Cutaneous Pathology. 48:285-289

Dermatofibrosarcoma protuberans (DFSP) is a rare sarcoma of the skin arising from the dermis. Its location is most commonly presented on the trunk of middle-aged adults and rarely on the face. The characteristic genetic aberration in the form of a re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ab6cce7fa912104861322187044fc254
https://doi.org/10.1111/cup.13770

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A novel translocation t(10;17)(p13;q11.2) harboring two cryptic deletions identified by array‐CGH and characterized by SUZ12 overexpression in a patient with chronic thrombocytosis

Autor: Jacqueline R. Batanian, Wendy N. Erber, Jacques A J Malherbe

Publikováno v: Genes, Chromosomes and Cancer. 59:661-666

No specific translocation is associated with myeloproliferative neoplasms (MPNs). However, an interstitial deletion involving subband 17q11.2 which includes the NF1 gene, although rare, is a recurrent aberration in several myeloid disorders including

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dd62fb5c1b8b5c60370304c05ac40f69
https://doi.org/10.1002/gcc.22881

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A Novel Variant Rearrangement of the Rare Aberration dic(17;20)(p11.2;q11.2) Characterized by Array-CGH as an Insertion in a Patient with Myelodysplastic Syndrome of Multilineage Dysplasia (MDS-MLD)

Autor: Vasiliki Grammatopoulou, Jianhui Yao, Maryna A Vazmitsel, Jacqueline R. Batanian

Publikováno v: Cytogenetic and Genome Research. 160:22-28

We report on a novel variant of the dicentric chromosome 17;20 (dic (17;20)(p11.2;q11.2) in a patient with de novo myelodysplastic syndrome (MDS). Based on FISH and array-CGH, the variant turns out to be an insertion of chromosome 17 (17p11.2-telomer

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8869a2c7e307dcf06280cff88c982153
https://doi.org/10.1159/000506030

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Narrowing down the Common Cytogenetic Deletion 14q to a 5.6-Mb Critical Region in 1p/19q Codeletion Oligodendroglioma-Relapsed Patients Points to Two Potential Relapse-Related Genes: SEL1L and STON2

Autor: Miguel A. Guzman, Tao Zhang, Jacqueline R. Batanian

Publikováno v: Cytogenetic and Genome Research. 160:316-320

Based on a literature review and our database, we report on the smallest 14q deletion identified in a brain tumor characterized by 1p/19q codeletion low-grade oligodendroglioma. In 2013, array-comparative genomic hybridization of the brain tumor reve

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::23bbe4c2bb982727affa7d87af07e404
https://doi.org/10.1159/000509020

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Three Novel Aberrations Involving PLAG1 Leading to Lipoblastoma in Three Different Patients: High Amplification, Partial Deletion, and a Unique Complex Rearrangement

Autor: Miguel A. Guzman, Guoliang Wang, Jacqueline R. Batanian

Publikováno v: Cytogenetic and Genome Research. 159:81-87

Lipoblastoma is a rare benign neoplasm with overlapping histology with other lipomatous tumors. Genetic aberrations including translocations of 8q and splitting of the PLAG1 probe leading to “promoter swapping” and gains of chromosome 8 or PLAG1

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a9dbcad0eca99d9e1925d95d891c9c3f
https://doi.org/10.1159/000503158

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A Novel t(10;22) Translocation Harboring an IGL Gene Deletion in a CLL Patient Transforming to B-PLL with 1q Gain

Autor: Lei, Sun, Vinit V, Patil, Nathan, Wilgus, Jianhui, Yao, Jacqueline R, Batanian

Publikováno v: Journal of the Association of Genetic Technologists. 46(2)

We report on a rare case of B-cell prolymphocytic leukemia (B-PLL) in a patient with a history of chronic lymphocytic leukemia (CLL) that showed a novel translocation t(10;22)(q21;q11.22) and an interstitial deletion of 11q14.1-q23.3 in 2017. The chr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::49dde220756f3b0657324f1fb9d6a548
https://pubmed.ncbi.nlm.nih.gov/32526732

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