Search Results - "Lockwood, Christina M."
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Pan-Trk Immunohistochemistry Identifies NTRK Rearrangements in Pediatric Mesenchymal Tumors
Published in The American journal of surgical pathology (01-07-2018)“…Activating neurotrophic receptor kinase (NTRK) fusions define certain pediatric mesenchymal tumors, including infantile fibrosarcoma and cellular mesoblastic…”
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Expanding the Spectrum of Pediatric NTRK-rearranged Mesenchymal Tumors
Published in The American journal of surgical pathology (01-04-2019)“…Pediatric mesenchymal tumors harboring variant NTRK fusions (ETV6-negative) are being increasingly described; however, the histologic and clinical features of…”
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Variability in, variability out: best practice recommendations to standardize pre-analytical variables in the detection of circulating and tissue microRNAs
Published in Clinical chemistry and laboratory medicine (01-05-2017)“…microRNAs (miRNAs) hold promise as biomarkers for a variety of disease processes and for determining cell differentiation. These short RNA species are robust,…”
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Infantile NTRK-associated Mesenchymal Tumors
Published in Pediatric and developmental pathology (01-01-2018)“…Pediatric fibroblastic/myofibroblastic lesions are a relatively common group of tumors with varying morphologies, for which the molecular mechanisms are…”
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T-cell clonality assessment by next-generation sequencing improves detection sensitivity in mycosis fungoides
Published in Journal of the American Academy of Dermatology (01-08-2015)“…Background T-cell receptor (TCR) clonality assessment is a principal diagnostic test in the management of mycosis fungoides (MF). However, current polymerase…”
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Histone deposition pathways determine the chromatin landscapes of H3.1 and H3.3 K27M oncohistones
Published in eLife (09-09-2020)“…Lysine 27-to-methionine (K27M) mutations in the H3.1 or H3.3 histone genes are characteristic of pediatric diffuse midline gliomas (DMGs). These oncohistone…”
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Beyond the Blood: CSF-Derived cfDNA for Diagnosis and Characterization of CNS Tumors
Published in Frontiers in cell and developmental biology (18-02-2020)“…Genetic data are rapidly becoming part of tumor classification and are integral to prognosis and predicting response to therapy. Current molecular tumor…”
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Genomic surveillance of SARS-CoV-2 Omicron variants on a university campus
Published in Nature communications (06-09-2022)“…Novel variants continue to emerge in the SARS-CoV-2 pandemic. University testing programs may provide timely epidemiologic and genomic surveillance data to…”
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At Preeclampsia Diagnosis, Total Cell‐Free DNA Concentration is Elevated and Correlates With Disease Severity
Published in Journal of the American Heart Association (03-08-2021)“…Background Placental derived cell‐free DNA (cfDNA), widely utilized for prenatal screening, may serve as a biomarker for preeclampsia. To determine whether…”
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Detection of FLT3 Internal Tandem Duplication in Targeted, Short-Read-Length, Next-Generation Sequencing Data
Published in The Journal of molecular diagnostics : JMD (2013)“…A recurrent somatic mutation frequently found in cytogenetically normal acute myeloid leukemia (AML) is internal tandem duplication (ITD) in the fms-related…”
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Circulating MicroRNA miR-323-3p as a Biomarker of Ectopic Pregnancy
Published in Clinical chemistry (Baltimore, Md.) (01-05-2012)“…The use of serum human chorionic gonadotropin (hCG) and progesterone to identify patients with ectopic pregnancy (EP) has been shown to have poor clinical…”
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Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program
Published in Genome medicine (28-03-2022)“…The All of Us Research Program (AoURP, "the program") is an initiative, sponsored by the National Institutes of Health (NIH), that aims to enroll one million…”
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Microsatellite instability in prostate cancer by PCR or next-generation sequencing
Published in Journal for immunotherapy of cancer (17-04-2018)“…Microsatellite instability (MSI) is now being used as a sole biomarker to guide immunotherapy treatment for men with advanced prostate cancer. Yet current…”
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Mutations of the DNA repair gene PNKP in a patient with microcephaly, seizures, and developmental delay (MCSZ) presenting with a high-grade brain tumor
Published in Scientific reports (30-03-2022)“…Polynucleotide Kinase-Phosphatase (PNKP) is a bifunctional enzyme that possesses both DNA 3′-phosphatase and DNA 5′-kinase activities, which are required for…”
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Looking beyond year 1 in the molecular era of pediatric brain tumor diagnosis: confirmatory testing of germline variants found on tumor sequencing
Published in Frontiers in oncology (06-03-2024)“…Somatic molecular profiling of pediatric brain tumors aids with the diagnosis and treatment of patients with a variety of high- and low-grade central nervous…”
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Validation and implementation of a modular targeted capture assay for the detection of clinically significant molecular oncology alterations
Published in Practical laboratory medicine (01-03-2020)“…The rapid discovery of clinically significant genetic variants has translated to next-generation sequencing assays becoming out-of-date by the time they are…”
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Detection of Gene Rearrangements in Targeted Clinical Next-Generation Sequencing
Published in The Journal of molecular diagnostics : JMD (01-07-2014)“…The identification of recurrent gene rearrangements in the clinical laboratory is the cornerstone for risk stratification and treatment decisions in many…”
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Clarification of Information in "Navigating Next-Generation Sequencing Laboratory Developed Tests: A Critical Look at Proficiency Testing, US Food and Drug Administration Regulations, and Clinical Laboratory Performance Tests"
Published in Archives of pathology & laboratory medicine (1976) (01-05-2024)Get full text
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The “SEED” Study: The Feasibility of Selecting Patient-Specific Biologically Targeted Therapy with Sorafenib, Everolimus, Erlotinib or Dasatinib for Pediatric and Young Adult Patients with Recurrent or Refractory Brain Tumors
Published in Frontiers in bioscience (Landmark. Print) (12-07-2022)“…BACKGROUNDPediatric brain tumors are the leading cause of cancer death in children and represent a variety of diseases and molecular subtypes. This study…”
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Recurrent EGFR alterations in NTRK3 fusion negative congenital mesoblastic nephroma
Published in Practical laboratory medicine (01-08-2020)“…To identify oncogenic driver mutations in congenital mesoblastic nephroma (CMN) cases lacking ETV6-NTRK3 fusion and discuss their diagnostic value. The…”
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