142 related articles for article (PubMed ID: 23019412)
1. Retained heterodisomy is associated with high gene expression in hyperhaploid inflammatory leiomyosarcoma.
Nord KH; Paulsson K; Veerla S; Wejde J; Brosjö O; Mandahl N; Mertens F
Neoplasia; 2012 Sep; 14(9):807-12. PubMed ID: 23019412
[TBL] [Abstract][Full Text] [Related]
2. "Inflammatory Leiomyosarcoma" and "Histiocyte-rich Rhabdomyoblastic Tumor": a clinicopathological, immunohistochemical and genetic study of 13 cases, with a proposal for reclassification as "Inflammatory Rhabdomyoblastic Tumor".
Cloutier JM; Charville GW; Mertens F; Sukov W; Fritchie K; Perry KD; Edgar M; Rowsey RA; Folpe AL
Mod Pathol; 2021 Apr; 34(4):758-769. PubMed ID: 33318583
[TBL] [Abstract][Full Text] [Related]
3. Disease-associated patterns of disomic chromosomes in hyperhaploid neoplasms.
Mandahl N; Johansson B; Mertens F; Mitelman F
Genes Chromosomes Cancer; 2012 Jun; 51(6):536-44. PubMed ID: 22334476
[TBL] [Abstract][Full Text] [Related]
4. Case Report: A Low-grade Uterine Leiomyosarcoma Showing Multiple Genetic Aberrations Including a Bi-allelic Loss of the Retinoblastoma Gene Locus, as well as Germ-line Uniparental Disomy for Part of the Long Arm of Chromosome 22.
Holzmann C; Koczan D; Loening T; Rommel B; Bullerdiek J
Anticancer Res; 2017 May; 37(5):2233-2237. PubMed ID: 28476787
[TBL] [Abstract][Full Text] [Related]
5. Inflammatory leiomyosarcoma is a distinct tumor characterized by near-haploidization, few somatic mutations, and a primitive myogenic gene expression signature.
Arbajian E; Köster J; Vult von Steyern F; Mertens F
Mod Pathol; 2018 Jan; 31(1):93-100. PubMed ID: 28884746
[TBL] [Abstract][Full Text] [Related]
6. Inflammatory leiomyosarcoma/rhabdomyoblastic tumor: A report of two cases with novel genetic findings.
Sukhanova M; Obeidin F; Streich L; Alexiev BA
Genes Chromosomes Cancer; 2022 Nov; 61(11):653-661. PubMed ID: 35655404
[TBL] [Abstract][Full Text] [Related]
7. Uterine leiomyomata with deletions of Ip represent a distinct cytogenetic subgroup associated with unusual histologic features.
Christacos NC; Quade BJ; Dal Cin P; Morton CC
Genes Chromosomes Cancer; 2006 Mar; 45(3):304-12. PubMed ID: 16320247
[TBL] [Abstract][Full Text] [Related]
8. Clonal evolution through loss of chromosomes and subsequent polyploidization in chondrosarcoma.
Olsson L; Paulsson K; Bovée JV; Nord KH
PLoS One; 2011; 6(9):e24977. PubMed ID: 21949816
[TBL] [Abstract][Full Text] [Related]
9. [Specific loss of heterozygosity of chromosome 3p loci in soft tissue leiomyosarcoma].
Peng H; Yang GH; Bu H; Gou LX
Zhonghua Bing Li Xue Za Zhi; 2003 Apr; 32(2):124-7. PubMed ID: 12839673
[TBL] [Abstract][Full Text] [Related]
10. Molecular pathogenesis of uterine smooth muscle tumors from transcriptional profiling.
Quade BJ; Wang TY; Sornberger K; Dal Cin P; Mutter GL; Morton CC
Genes Chromosomes Cancer; 2004 Jun; 40(2):97-108. PubMed ID: 15101043
[TBL] [Abstract][Full Text] [Related]
11. [Analysis of chromosome copy number changes in leiomyosarcoma through molecular cytogenetic methods].
Otaño-Joos M; Mechtersheimer G; Ohl S; Lehnert T; Willeke F; Möller P; Otto HF; Lichter P; Joos S
Verh Dtsch Ges Pathol; 1998; 82():207-9. PubMed ID: 10095435
[TBL] [Abstract][Full Text] [Related]
12. Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.
Wang L; Fidler C; Nadig N; Giagounidis A; Della Porta MG; Malcovati L; Killick S; Gattermann N; Aul C; Boultwood J; Wainscoat JS
Haematologica; 2008 Jul; 93(7):994-1000. PubMed ID: 18508791
[TBL] [Abstract][Full Text] [Related]
13. Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis.
Bullinger L; Krönke J; Schön C; Radtke I; Urlbauer K; Botzenhardt U; Gaidzik V; Carió A; Senger C; Schlenk RF; Downing JR; Holzmann K; Döhner K; Döhner H
Leukemia; 2010 Feb; 24(2):438-49. PubMed ID: 20016533
[TBL] [Abstract][Full Text] [Related]
14. Leiomyosarcoma and malignant fibrous histiocytoma share similar allelic imbalance pattern at 9p.
Sabah M; Cummins R; Leader M; Kay E
Virchows Arch; 2005 Mar; 446(3):251-8. PubMed ID: 15731925
[TBL] [Abstract][Full Text] [Related]
15. Expression of subtype-specific group 1 leiomyosarcoma markers in a wide variety of sarcomas by gene expression analysis and immunohistochemistry.
Mills AM; Beck AH; Montgomery KD; Zhu SX; Espinosa I; Lee CH; Subramanian S; Fletcher CD; van de Rijn M; West RB
Am J Surg Pathol; 2011 Apr; 35(4):583-9. PubMed ID: 21412072
[TBL] [Abstract][Full Text] [Related]
16. Loss of heterozygosity associated with uniparental disomy in breast carcinoma.
Murthy SK; DiFrancesco LM; Ogilvie RT; Demetrick DJ
Mod Pathol; 2002 Dec; 15(12):1241-50. PubMed ID: 12481003
[TBL] [Abstract][Full Text] [Related]
17. Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome.
Choufani S; Ko JM; Lou Y; Shuman C; Fishman L; Weksberg R
Genes (Basel); 2021 Jan; 12(2):. PubMed ID: 33513760
[TBL] [Abstract][Full Text] [Related]
18. Frequent occurrence of uniparental disomy in colorectal cancer.
Andersen CL; Wiuf C; Kruhøffer M; Korsgaard M; Laurberg S; Ørntoft TF
Carcinogenesis; 2007 Jan; 28(1):38-48. PubMed ID: 16774939
[TBL] [Abstract][Full Text] [Related]
19. Mosaic maternal uniparental disomy of chromosome 15 in Prader-Willi syndrome: utility of genome-wide SNP array.
Izumi K; Santani AB; Deardorff MA; Feret HA; Tischler T; Thiel BD; Mulchandani S; Stolle CA; Spinner NB; Zackai EH; Conlin LK
Am J Med Genet A; 2013 Jan; 161A(1):166-71. PubMed ID: 23225330
[TBL] [Abstract][Full Text] [Related]
20. Differential gene expression in leiomyosarcoma.
Skubitz KM; Skubitz AP
Cancer; 2003 Sep; 98(5):1029-38. PubMed ID: 12942572
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
