检索结果 - Lockwood, Christina M.

Swab-free transport as an optimized pre-analytical workflow for SARS-COV-2 amplification 由 Greene, Dina N, Matthys, Tawna, Lockwood, Christina M

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Beyond the Blood: CSF-Derived cfDNA for Diagnosis and Characterization of CNS Tumors 由 McEwen, Abbye E., Leary, Sarah E. S., Lockwood, Christina M.

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TBIO-24. INTEGRATION OF GENETIC COUNSELING INTO MULTIDISCIPLINARY BRAIN TUMOR CLINIC IMPROVES IDENTIFICATION AND COUNSELING FOR CANCER PREDISPOSITION SYNDROMES 由 Stasi, Shannon M, Cole, Bonnie Lynn, Lockwood, Christina M, Leary, Sarah ES

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Integration of Genomic Medicine in Pathology Resident Training: A Work in Progress 由 Haspel, Richard L, Genzen, Jonathan R, Wagner, Jay, Lockwood, Christina M, Fong, Karen

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At Preeclampsia Diagnosis, Total Cell‐Free DNA Concentration is Elevated and Correlates With Disease Severity 由 Kolarova, Teodora R., Gammill, Hilary S., Nelson, J. Lee, Lockwood, Christina M., Shree, Raj

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Circulating miR-323-3p as a Biomarker of Ectopic Pregnancy 由 Zhao, Zhen, Zhao, Qiuhong, Warrick, Joshua, Lockwood, Christina M., Woodworth, Alison, Moley, Kelle H., Gronowski, Ann M.

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Recurrent EGFR alterations in NTRK3 fusion negative congenital mesoblastic nephroma 由 Lei, Li, Stohr, Bradley A., Berry, Stacey, Lockwood, Christina M., Davis, Jessica L., Rudzinski, Erin R., Kunder, Christian A.

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Impact of maternal autoimmune disease on cell-free DNA test characteristics 由 MACKINNON, Hayley J., KOLAROVA, Teodora R., KATZ, Ronit, HEDGE, Jaclynne M., VINOPAL, Elena, LOCKWOOD, Christina M., SHREE, Raj, DELANEY, Shani

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Low fetal fraction in obese women at first trimester cell-free DNA based prenatal screening is not accompanied by differences in total cell-free DNA 由 SHREE, Raj, KOLAROVA, Teodora R., MACKINNON, Hayley J., HEDGE, Jaclynne M., VINOPAL, Elena, MA, Kimberly K., LOCKWOOD, Christina M., CHANDRASEKARAN, Suchitra

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Microsatellite instability in prostate cancer by PCR or next-generation sequencing 由 Hempelmann, Jennifer A., Lockwood, Christina M., Konnick, Eric Q., Schweizer, Michael T., Antonarakis, Emmanuel S., Lotan, Tamara L., Montgomery, Bruce, Nelson, Peter S., Klemfuss, Nola, Salipante, Stephen J., Pritchard, Colin C.

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Validation and implementation of a modular targeted capture assay for the detection of clinically significant molecular oncology alterations 由 Kuo, Ayako J., Paulson, Vera A., Hempelmann, Jennifer A., Beightol, Mallory, Todhunter, Sheena, Colbert, Brice G., Salipante, Stephen J., Konnick, Eric Q., Pritchard, Colin C., Lockwood, Christina M.

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Development of an Immunoassay for the Kidney Specific Protein myo-Inositol Oxygenase, a Potential Biomarker of Acute Kidney Injury 由 Gaut, Joseph P., Crimmins, Dan L., Ohlendorf, Matt F., Lockwood, Christina M., Griest, Terry A., Brada, Nancy A., Hoshi, Masato, Sato, Bryan, Hotchkiss, Richard S., Jain, Sanjay, Ladenson, Jack H.

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Detection of Gene Rearrangements in Targeted Clinical Next-Generation Sequencing 由 Abel, Haley J., Al-Kateb, Hussam, Cottrell, Catherine E., Bredemeyer, Andrew J., Pritchard, Colin C., Grossmann, Allie H., Wallander, Michelle L., Pfeifer, John D., Lockwood, Christina M., Duncavage, Eric J.

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Histone deposition pathways determine the chromatin landscapes of H3.1 and H3.3 K27M oncohistones 由 Sarthy, Jay F, Meers, Michael P, Janssens, Derek H, Henikoff, Jorja G, Feldman, Heather, Paddison, Patrick J, Lockwood, Christina M, Vitanza, Nicholas A, Olson, James M, Ahmad, Kami, Henikoff, Steven

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Postmortem Somatic Sequencing of Tumors From Patients With Suspected Lynch Syndrome Has Clinical Utility for Surviving Relatives 由 Byers, Heather M., Jacobson, Angela, McFaddin, Andrew S., Ussakli, Cigdem H., Newlin, Anna, Stanich, Peter P., More, Stephanie, Hamblett, Amanda, Tait, Jonathan F., Shirts, Brian, Pritchard, Colin C., Konnick, Eric Q., Lockwood, Christina M.

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High-resolution profiling of human cytomegalovirus cell-free DNA in human plasma highlights its exceptionally fragmented nature 由 Peddu, Vikas, Bradley, Benjamin T., Casto, Amanda M., Shree, Raj, Colbert, Brice G., Xie, Hong, Santo, Tracy K., Huang, Meei-Li, Cheng, Edith Y., Konnick, Eric, Salipante, Stephen J., Jerome, Keith R., Lockwood, Christina M., Greninger, Alexander L.

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Comparable specimen collection from both ends of at-home mid-turbinate swabs 由 Truong, Melissa, Pfau, Brian, McDermot, Evan, Han, Peter D., Brandstetter, Elisabeth, Richardson, Matthew, Kim, Ashley E., Rieder, Mark J., Chu, Helen Y., Englund, Janet A., Nickerson, Deborah A., Shendure, Jay, Lockwood, Christina M., Konnick, Eric Q., Starita, Lea M.

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Comparable Specimen Collection from Both Ends of At-Home Midturbinate Swabs 由 Truong, Melissa, Pfau, Brian, McDermot, Evan, Han, Peter D., Brandstetter, Elisabeth, Richardson, Matthew, Kim, Ashley E., Rieder, Mark J., Chu, Helen Y., Englund, Janet A., Nickerson, Deborah A., Shendure, Jay, Lockwood, Christina M., Konnick, Eric Q., Starita, Lea M.

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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 由 Jiang, Bingcheng, Murray, Cameron, Cole, Bonnie L., Glover, J. N. Mark, Chan, Gordon K., Deschenes, Jean, Mani, Rajam S., Subedi, Sudip, Nerva, John D., Wang, Anthony C., Lockwood, Christina M., Mefford, Heather C., Leary, Sarah E. S., Ojemann, Jeffery G., Weinfeld, Michael, Ene, Chibawanye I.

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Desmoplastic Infantile Ganglioglioma/Astrocytoma (DIG/DIA) Are Distinct Entities with Frequent BRAFV600 Mutations 由 Wang, Anthony C., Jones, David T.W., Abecassis, Isaac Joshua, Cole, Bonnie L., Leary, Sarah E.S., Lockwood, Christina M., Chavez, Lukas, Capper, David, Korshunov, Andrey, Fallah, Aria, Wang, Shelly, Ene, Chibawanye, Olson, James M., Geyer, J. Russell, Holland, Eric C., Lee, Amy, Ellenbogen, Richard G., Ojemann, Jeffrey G.

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