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Showing 1–16 of 16 results

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Research | 13 February 2019
Primary malignant melanoma of esophagus: clinicopathologic characterization of 20 cases including molecular genetic profiling of 15 tumors
- Jerzy Lasota
- , Artur Kowalik
- , Anna Felisiak-Golabek
- , Sebastian Zięba
- , Piotr Waloszczyk
- , Marek Masiuk
- , Jaroslaw Wejman
- , Justyna Szumilo
- & Markku Miettinen
Modern Pathology 32 , 957–966

Rights & permissionsfor article Primary malignant melanoma of esophagus: clinicopathologic characterization of 20 cases including molecular genetic profiling of 15 tumors . Opens in a new window.
Research | 4 November 2016
Clinicopathologic profile, immunophenotype, and genotype of CD274 (PD-L1)-positive colorectal carcinomas
Modern Pathology 30 , 278–285

Rights & permissionsfor article Clinicopathologic profile, immunophenotype, and genotype of CD274 (PD-L1)-positive colorectal carcinomas . Opens in a new window.
Research | 28 November 2014
Nuclear expression and gain-of-function β-catenin mutation in glomangiopericytoma (sinonasal-type hemangiopericytoma): insight into pathogenesis and a diagnostic marker
Modern Pathology 28 , 715–720

Rights & permissionsfor article Nuclear expression and gain-of-function β-catenin mutation in glomangiopericytoma (sinonasal-type hemangiopericytoma): insight into pathogenesis and a diagnostic marker . Opens in a new window.
Research | 22 January 2016
Frequency and clinicopathologic profile of PIK3CA mutant GISTs: molecular genetic study of 529 cases
Modern Pathology 29 , 275–282

Rights & permissionsfor article Frequency and clinicopathologic profile of PIK3CA mutant GISTs: molecular genetic study of 529 cases . Opens in a new window.
Research | 24 May 2013
No KRAS mutations found in gastrointestinal stromal tumors (GISTs): molecular genetic study of 514 cases
- Jerzy Lasota
- , Liqiang Xi
- , Tiffany Coates
- , RaShonda Dennis
- , Moses O Evbuomwan
- , Zeng-Feng Wang
- , Mark Raffeld
- & Markku Miettinen
Modern Pathology 26 , 1488–1491

Rights & permissionsfor article No KRAS mutations found in gastrointestinal stromal tumors (GISTs): molecular genetic study of 514 cases . Opens in a new window.
6 December 2004
Loss of heterozygosity on chromosome 22q in gastrointestinal stromal tumors (GISTs): a study on 50 cases
Laboratory Investigation 85 , 237–247

Rights & permissionsfor article Loss of heterozygosity on chromosome 22q in gastrointestinal stromal tumors (GISTs): a study on 50 cases . Opens in a new window.
Research | 15 May 2009
Gain-of-function PDGFRA mutations, earlier reported in gastrointestinal stromal tumors, are common in small intestinal inflammatory fibroid polyps. A study of 60 cases
Modern Pathology 22 , 1049–1056

Rights & permissionsfor article Gain-of-function PDGFRA mutations, earlier reported in gastrointestinal stromal tumors, are common in small intestinal inflammatory fibroid polyps. A study of 60 cases . Opens in a new window.
Research | 1 September 2003
Evaluation of NF2 and NF1 Tumor Suppressor Genes in Distinctive Gastrointestinal Nerve Sheath Tumors Traditionally Diagnosed as Benign Schwannomas: A Study of 20 Cases
Laboratory Investigation 83 , 1361–1371

Rights & permissionsfor article Evaluation of NF2 and NF1 Tumor Suppressor Genes in Distinctive Gastrointestinal Nerve Sheath Tumors Traditionally Diagnosed as Benign Schwannomas: A Study of 20 Cases . Opens in a new window.
17 May 2004
A great majority of GISTs with PDGFRA mutations represent gastric tumors of low or no malignant potential
Laboratory Investigation 84 , 874–883

Rights & permissionsfor article A great majority of GISTs with PDGFRA mutations represent gastric tumors of low or no malignant potential . Opens in a new window.
Research | 1 May 2000
KIT Expression in Angiosarcomas and Fetal Endothelial Cells: Lack of Mutations of Exon 11 and Exon 17 of C-kit
Modern Pathology 13 , 536–541

Rights & permissionsfor article KIT Expression in Angiosarcomas and Fetal Endothelial Cells: Lack of Mutations of Exon 11 and Exon 17 of C-kit . Opens in a new window.
Research | 1 February 2008
Clinicopathologic profile of gastrointestinal stromal tumors (GISTs) with primary KIT exon 13 or exon 17 mutations: a multicenter study on 54 cases
Modern Pathology 21 , 476–484

Rights & permissionsfor article Clinicopathologic profile of gastrointestinal stromal tumors (GISTs) with primary KIT exon 13 or exon 17 mutations: a multicenter study on 54 cases . Opens in a new window.
24 October 2005
GISTs with PDGFRA exon 14 mutations represent subset of clinically favorable gastric tumors with epithelioid morphology
Laboratory Investigation 86 , 94–100

Rights & permissionsfor article GISTs with PDGFRA exon 14 mutations represent subset of clinically favorable gastric tumors with epithelioid morphology . Opens in a new window.
Research | 15 January 2010
Carbonic anhydrase II. A novel biomarker for gastrointestinal stromal tumors
- Seppo Parkkila
- , Jerzy Lasota
- , Jonathan A Fletcher
- , Wen-bin Ou
- , Antti J Kivelä
- , Kyösti Nuorva
- , Anna-Kaisa Parkkila
- , Jyrki Ollikainen
- , William S Sly
- , Abdul Waheed
- , Silvia Pastorekova
- , Jaromir Pastorek
- , Jorma Isola
- & Markku Miettinen
Modern Pathology 23 , 743–750

Rights & permissionsfor article Carbonic anhydrase II. A novel biomarker for gastrointestinal stromal tumors . Opens in a new window.
Research | 1 July 2002
Complex Genetic Alterations in Gastrointestinal Stromal Tumors with Autonomic Nerve Differentiation
- Maria Debiec-Rychter
- , Patrick Pauwels
- , Jerzy Lasota
- , Sabine Franke
- , Rita De Vos
- , Ivo de Wever
- , Anne Hagemeijer
- & Raf Sciot
Modern Pathology 15 , 692–698

Rights & permissionsfor article Complex Genetic Alterations in Gastrointestinal Stromal Tumors with Autonomic Nerve Differentiation . Opens in a new window.
Research | 1 December 2003
Gastrointestinal Stromal Tumors with Internal Tandem Duplications in 3′ End of KIT Juxtamembrane Domain Occur Predominantly in Stomach and Generally Seem to Have a Favorable Course
Modern Pathology 16 , 1257–1264

Rights & permissionsfor article Gastrointestinal Stromal Tumors with Internal Tandem Duplications in 3′ End of KIT Juxtamembrane Domain Occur Predominantly in Stomach and Generally Seem to Have a Favorable Course . Opens in a new window.
16 July 2007
Presence of homozygous KIT exon 11 mutations is strongly associated with malignant clinical behavior in gastrointestinal stromal tumors
- Jerzy Lasota
- , Anna Jerzak vel Dobosz
- , Bartosz Wasag
- , Agnieszka Wozniak
- , Ewa Kraszewska
- , Wanda Michej
- , Konrad Ptaszynski
- , Piotr Rutkowski
- , Maarit Sarlomo-Rikala
- , Sonja E Steigen
- , Regine Schneider-Stock
- , Jerzy Stachura
- , Maria Chosia
- , Gabriel Ogun
- , Wlodzimierz Ruka
- , Janusz A Siedlecki
- & Markku Miettinen
Laboratory Investigation 87 , 1029–1041

Rights & permissionsfor article Presence of homozygous KIT exon 11 mutations is strongly associated with malignant clinical behavior in gastrointestinal stromal tumors . Opens in a new window.

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