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Pediatric Sarcomas: The Next Generation of Molecular Studies
by
Parham, David M.
, Giannikopoulos, Petros
in
Biopsy
/ Bone cancer
/ Brain cancer
/ Cancer therapies
/ Cell cycle
/ Chemotherapy
/ Children
/ Chromosomes
/ CRISPR
/ Epigenetics
/ Ewings sarcoma
/ Gene expression
/ Genomics
/ Laboratories
/ Medical prognosis
/ Metastases
/ Metastasis
/ Mutation
/ Oncology
/ Pediatrics
/ Radiation
/ Review
/ Transcription factors
/ Tumors
2022
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Pediatric Sarcomas: The Next Generation of Molecular Studies
by
Parham, David M.
, Giannikopoulos, Petros
in
Biopsy
/ Bone cancer
/ Brain cancer
/ Cancer therapies
/ Cell cycle
/ Chemotherapy
/ Children
/ Chromosomes
/ CRISPR
/ Epigenetics
/ Ewings sarcoma
/ Gene expression
/ Genomics
/ Laboratories
/ Medical prognosis
/ Metastases
/ Metastasis
/ Mutation
/ Oncology
/ Pediatrics
/ Radiation
/ Review
/ Transcription factors
/ Tumors
2022
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Do you wish to request the book?
Pediatric Sarcomas: The Next Generation of Molecular Studies
by
Parham, David M.
, Giannikopoulos, Petros
in
Biopsy
/ Bone cancer
/ Brain cancer
/ Cancer therapies
/ Cell cycle
/ Chemotherapy
/ Children
/ Chromosomes
/ CRISPR
/ Epigenetics
/ Ewings sarcoma
/ Gene expression
/ Genomics
/ Laboratories
/ Medical prognosis
/ Metastases
/ Metastasis
/ Mutation
/ Oncology
/ Pediatrics
/ Radiation
/ Review
/ Transcription factors
/ Tumors
2022
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Pediatric Sarcomas: The Next Generation of Molecular Studies
Journal Article
Pediatric Sarcomas: The Next Generation of Molecular Studies
2022
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Overview
Pediatric sarcomas constitute one of the largest groups of childhood cancers, following hematopoietic, neural, and renal lesions. Partly because of their diversity, they continue to offer challenges in diagnosis and treatment. In spite of the diagnostic, nosologic, and therapeutic gains made with genetic technology, newer means for investigation are needed. This article reviews emerging technology being used to study human neoplasia and how these methods might be applicable to pediatric sarcomas. Methods reviewed include single cell RNA sequencing (scRNAseq), spatial multi-omics, high-throughput functional genomics, and clustered regularly interspersed short palindromic sequence-Cas9 (CRISPR-Cas9) technology. In spite of these advances, the field continues to be challenged by a dearth of properly annotated materials, particularly from recurrences and metastases and pre- and post-treatment samples.
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