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Indistinguishable genomic profiles and shared prognostic markers in undifferentiated pleomorphic sarcoma and leiomyosarcoma: different sides of a single coin?
43/43 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
5 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 43 checked references that resolve
resolves10.1200/JCO.2001.19.12.3045
Clinicopathologic Re-Evaluation of 100 Malignant Fibrous Histiocytomas: Prognostic Relevance of Subclassification
resolves10.1016/S0140-6736(02)08270-3
Molecular characterisation of soft tissue tumours: a gene expression study
resolves10.1016/S0002-9440(10)63696-6
Classification and Subtype Prediction of Adult Soft Tissue Sarcoma by Functional Genomics
resolves10.1186/1471-2164-8-73
Diagnostic and prognostic gene expression signatures in 177 soft tissue sarcomas: hypoxia-induced transcription profile signifies metastatic potential
resolves10.1038/modpathol.3800794
Gene expression analysis of soft tissue sarcomas: characterization and reclassification of malignant fibrous histiocytoma
resolves10.1038/labinvest.3780229
Leiomyosarcomas and Most Malignant Fibrous Histiocytomas Share Very Similar Comparative Genomic Hybridization Imbalances: An Analysis of a Series of 27 Leiomyosarcomas
resolves10.1016/S0165-4608(02)00614-3
A subgroup of malignant fibrous histiocytomas is associated with genetic changes similar to those of well-differentiated liposarcomas
resolves10.1136/jcp.2005.034942
Cytogenetic analysis of myxoid liposarcoma and myxofibrosarcoma by array-based comparative genomic hybridisation
resolves10.1038/sj.onc.1209693
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays
resolves10.1136/jcp.56.9.666
Expression of smooth muscle markers in so called malignant fibrous histiocytomas
resolves10.1097/00000478-200208000-00001
Practical Application of Molecular Genetic Testing as an Aid to the Surgical Pathologic Diagnosis of Sarcomas
resolves10.1080/01913120801897141
Contribution of Cytogenetics to the Management of Poorly Differentiated Sarcomas
resolves10.1002/ijc.21475
Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma
resolves10.1186/gb-2002-3-8-software0003
BioArray Software Environment (BASE): a platform for comprehensive management and analysis of microarray data
resolves10.1073/pnas.0402932101
High-resolution characterization of the pancreatic adenocarcinoma genome
resolves10.1093/nar/30.4.e15
Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation
resolves10.2307/2530299
Nomograms for Calculating the Number of Patients Needed for a Clinical Trial with Survival as an Endpoint
resolves10.1038/sj.onc.1209985
Using array-comparative genomic hybridization to define molecular portraits of primary breast cancers
resolves10.1016/S0165-4608(99)00114-4
Comparative Cytogenetic Study of Spindle Cell and Pleomorphic Leiomyosarcomas of Soft Tissues
resolves10.1002/(SICI)1098-2264(199805)22:1<16::AID-GCC3>3.0.CO;2-A
Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: A report of the CHAMP study group
resolves10.1002/gcc.1118
Characterization of chromosome aberrations associated with soft‐tissue leiomyosarcomas by twenty‐four‐color karyotyping and comparative genomic hybridization analysis
resolves10.1002/(SICI)1098-2744(199708)19:4<273::AID-MC9>3.0.CO;2-D
Analysis of genetic alterations in uterine leiomyomas and leiomyosarcomas by comparative genomic hybridization
resolves10.1016/S0165-4608(00)00225-9
Molecular Cytogenetic Analysis of Uterine Leiomyoma and Leiomyosarcoma by Comparative Genomic Hybridization
resolves10.1016/S0165-4608(98)00227-1
Loss of Chromosome 13 is the Most Frequent Genomic Imbalance in Malignant Fibrous Histiocytomas
resolves10.1038/modpathol.2008.84
Fluorescence in situ hybridization for MDM2 gene amplification as a diagnostic tool in lipomatous neoplasms
resolves10.1002/path.1579
Inflammatory malignant fibrous histiocytomas and dedifferentiated liposarcomas: histological review, genomic profile, and <i>MDM2</i> and <i>CDK4</i> status favour a single entity
resolves10.1093/jnci/86.17.1297
MDM2 Gene Amplification and Transcript Levels in Human Sarcomas: Relationship to TP53 Gene Status
resolves10.1016/j.cancergencyto.2004.11.009
Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: leiomyosarcoma
resolves10.1038/sj.bjc.6600766
Molecular classification of synovial sarcomas, leiomyosarcomas and malignant fibrous histiocytomas by gene expression profiling
resolves10.1007/s11999-008-0330-4
Global Protein-expression Analysis of Bone and Soft Tissue Sarcomas
resolves10.1002/pmic.200600196
Proteomic signatures corresponding to histological classification and grading of soft‐tissue sarcomas
resolves10.1002/cncr.23160
The bone morphogenetic protein pathway is active in human colon adenomas and inactivated in colorectal cancer
resolves10.1038/sj.onc.1207675
Involvement of cadherins 7 and 20 in mouse embryogenesis and melanocyte transformation
The 5 references without a DOI — listed, not checked
no DOI — not checked10.1038/labinvest.2009.18_bib2
no DOI — not checkedMicroarray-based copy number and expression profiling in dedifferentiated and pleomorphic liposarcoma
no DOI — not checkedCGH-Plotter: MATLAB toolbox for CGH-data analysis
no DOI — not checkedLoss of chromosome 13q is a frequently acquired event in genetic progression of soft tissue sarcomas in the abdominal cavity
no DOI — not checkedThe RB1 gene is the target of chromosome 13 deletions in malignant fibrous histiocytoma
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