scispace - formally typeset
J

Jerzy Lasota

Researcher at Thomas Jefferson University

Publications -  10
Citations -  329

Jerzy Lasota is an academic researcher from Thomas Jefferson University. The author has contributed to research in topics: Gene mapping & Loss of heterozygosity. The author has an hindex of 8, co-authored 10 publications receiving 318 citations. Previous affiliations of Jerzy Lasota include University of Helsinki & Harvard University.

Papers
More filters
Journal Article

Loss of Heterozygosity at the Familial RCC t(3;8) Locus in Most Clear Cell Renal Carcinomas

TL;DR: There may be another gene in the vicinity of the 3p14.2 break of the familial RCC-associated translocation, t(3;8)(p 14.2;q24), which has been hypothesized to affect expression of an RCC suppressor gene or oncogene in the majority of clear cell RCCs.
Journal ArticleDOI

True histiocytic lymphoma of small intestine. Analysis of two S-100 protein-positive cases with features of interdigitating reticulum cell sarcoma.

TL;DR: Results indicate the tumors are true histiocytic lymphomas, which have immunophenotypic features of both ordinary histiocytes and interdigitating reticulum cells.
Journal ArticleDOI

Cytokeratin-positive large-cell lymphomas of B-cell lineage. A study of five phenotypically unusual cases verified by polymerase chain reaction.

TL;DR: It is shown that some B-cell lymphomas can have unusual and confusing immunophenotypes, including keratin positivity and leukocyte antigen negativity, and use of PCR-based molecular genetic demonstration of clonal immunoglobulin heavychain gene rearrangement is helpful in establishing the correct diagnosis in such cases.
Journal Article

Detailed Genetic and Physical Map of the 3p Chromosome Region Surrounding the Familial Renal Cell Carcinoma Chromosome Translocation, t(3;8)(p14.2;q24.1)

TL;DR: A panel of rodent-human hybrids carrying portions of 3p, including a hybrid carrying the derivative 8 (der(8)(8pter-->8q24.1::3p14.2-->3pter)) from the RCC family, have been characterized using 3p anchor probes and cytogenetic methods, and a large number of genetically mapped probes were mapped into seven physical intervals between 3p12 and 3pter defined by the hybrid panel.