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المؤلفون: Calixto-Hope G Lucas, Christian J Davidson, Mouied Alashari, Angelica R Putnam, Nicholas S Whipple, Carol S Bruggers, Joe S Mendez, Samuel H Cheshier, Jeffrey B Walker, Biswarathan Ramani, Cathryn R Cadwell, Daniel V Sullivan, Rufei Lu, Kanish Mirchia, Jessica Van Ziffle, Patrick Devine, Ezequiel Goldschmidt, Shawn L Hervey-Jumper, Nalin Gupta, Nancy Ann Oberheim Bush, David R Raleigh, Andrew Bollen, Tarik Tihan, Melike Pekmezci, David A Solomon, Joanna J Phillips, Arie Perry
المصدر: J Neuropathol Exp Neurol
Journal of neuropathology and experimental neurology, vol 81, iss 8مصطلحات موضوعية: Adult, Male, Proto-Oncogene Proteins B-raf, Adolescent, Molecular neuropathology, Clinical Sciences, Intratumoral heterogeneity, Astrocytoma, Pathology and Forensic Medicine, Clonal Evolution, Cellular and Molecular Neuroscience, Young Adult, Rare Diseases, Genetics, Humans, Collision tumor, Pleomorphic xanthoastrocytoma, Cyclin-Dependent Kinase Inhibitor p16, Cancer, Ganglioglioma, Sequence Deletion, Neurology & Neurosurgery, Brain Neoplasms, Precision medicine, Human Genome, Homozygote, Neurooncology, Neurosciences, High-Throughput Nucleotide Sequencing, General Medicine, Original Articles, DNA, Neurology, Mutation, Female, Neurology (clinical), Biotechnology
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ad0b321c7b4d9dbc6bc0a4c5593793eTest
https://europepmc.org/articles/PMC9297094Test/ -
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المؤلفون: Stephanie Hilz, Joseph F. Costello, Rong Li, Joanna J. Phillips, James P. Grenert, Tarik Tihan, Arie Perry, Megan K. Dishop, Elizabeth Alva, Carol S. Bruggers, Biswarathan Ramani, Peter P. Sun, Nalin Gupta, Julieann C. Lee, Shipra Garg, Cynthia Wetmore, Cathryn R. Cadwell, Gregory Moes, Corey Raffel, Patrick Devine, Mitchel S. Berger, Nancy Ann Oberheim Bush, Edward F. Chang, Courtney Onodera, Emily A. Sloan, Steve Braunstein, Jeffrey W. Hofmann, Cassie Kline, Anu Banerjee, David A. Solomon, Jessica Van Ziffle, Mouied Alashari, Melike Pekmezci, Rohit Gupta, John Y.H. Kim, Alyssa Reddy, Andrew W. Bollen, Susan M. Chang
المصدر: Acta neuropathologica, vol 139, iss 5
Acta Neuropatholمصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Clinical Sciences, Article, Pathology and Forensic Medicine, Li-Fraumeni Syndrome, Young Adult, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, medicine, Humans, Genetic Predisposition to Disease, Theology, Child, Preschool, Germ-Line Mutation, Neurology & Neurosurgery, Philosophy, Neurosciences, Glioma, medicine.disease, 030104 developmental biology, Li–Fraumeni syndrome, Child, Preschool, Female, Neurology (clinical), Tumor Suppressor Protein p53, 030217 neurology & neurosurgery
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f423d386df65743cc259399840c239aTest
https://doi.org/10.1007/s00401-020-02144-8Test -
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المؤلفون: Patrick Devine, Yi Li, John Y.H. Kim, Lee A. Tan, David Samuel, Susan M. Chang, Sabine Mueller, David Scharnhorst, Cassie Kline, Joseph Torkildson, Peter P. Sun, Cynthia Fata, Arie Perry, Steve Braunstein, Gregory Moes, Corey Raffel, Jennifer Clarke, Anu Banerjee, Carl Koschmann, Courtney Onodera, Emily A. Sloan, Jessica Van Ziffle, David R. Raleigh, Julieann C. Lee, Tabitha Cooney, Jennie Taylor, Andrew W. Bollen, Hua Guo, Soonmee Cha, Robin A. Buerki, Vinil Shah, Philip V. Theodosopoulos, David A. Solomon, Alyssa Reddy, Michael W. McDermott, Nicholas Butowski, Dean Chou, James P. Grenert, Praveen V. Mummaneni, Joanna J. Phillips, Nancy Ann Oberheim Bush, Tarik Tihan, Nalin Gupta, Melike Pekmezci, Mitchel S. Berger
المصدر: Acta neuropathologica, vol 138, iss 5
Acta Neuropatholمصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Clinical Sciences, Article, Pathology and Forensic Medicine, Histones, Young Adult, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Humans, Spinal Cord Neoplasms, Theology, Child, Preschool, Aged, Neurology & Neurosurgery, Brain Neoplasms, Extramural, Philosophy, Neurosciences, Glioma, Middle Aged, 030104 developmental biology, Spinal Cord, Non canonical, Child, Preschool, Mutation, Female, Neurology (clinical), 030217 neurology & neurosurgery
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f450fd991d4c733880328ada22b3c5fcTest
https://doi.org/10.1007/s00401-019-02072-2Test -
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المؤلفون: Boris C. Bastian, David A. Solomon, Jessica Van Ziffle, Arie Perry, James P. Grenert, Courtney Onodera, Anuradha Banerjee, Julieann C. Lee, Samuel H. Chesier, Angelica R. Putnam, Corey Raffel
المصدر: Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-4 (2018)
Lee, Julieann; Putnam, Angelica R; Chesier, Samuel H; Banerjee, Anuradha; Raffel, Corey; Van Ziffle, Jessica; et al.(2018). Oligodendrogliomas, IDH-mutant and 1p/19q-codeleted, arising during teenage years often lack TERT promoter mutation that is typical of their adult counterparts.. Acta neuropathologica communications, 6(1), 95. doi: 10.1186/s40478-018-0598-x. UCSF: Retrieved from: http://www.escholarship.org/uc/item/69404686Test
Acta neuropathologica communications, vol 6, iss 1مصطلحات موضوعية: Male, 0301 basic medicine, Mutant, 1p/19q Codeletion, lcsh:RC346-429, CIC, Promoter Regions, Genetic, Child, Telomerase, Pediatric, Brain Neoplasms, Teenager, Isocitrate Dehydrogenase, Idh mutation, TERT promoter, Female, IDH1, Human, Molecular neuro-oncology, Adolescent, Clinical Sciences, Oligodendroglioma, Biology, Tert promoter, Chromosomes, Pathology and Forensic Medicine, Promoter Regions, 03 medical and health sciences, Cellular and Molecular Neuroscience, Genetic, medicine, Humans, Tert promoter mutation, lcsh:Neurology. Diseases of the nervous system, Pair 19, Extramural, Neurosciences, medicine.disease, Molecular biology, IDH mutation, Good Health and Well Being, FGFR1, 030104 developmental biology, Mutation, Biochemistry and Cell Biology, Neurology (clinical), Chromosomes, Human, Pair 19, 1p/19q-codeletion
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4730d20a7885ab4e64983dd5c99ca82Test
http://link.springer.com/article/10.1186/s40478-018-0598-xTest -
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المؤلفون: Ritu Roy, Jessica Van Ziffle, David A. Solomon, Michele M. Bloomer, Nicola J. Cadenas, Armin R. Afshar, James P. Grenert, Melike Pekmezci, Meredith Stevers, Courtney Onodera, Boris C. Bastian, W. Patrick Devine, Anuradha Banerjee, Bertil Damato, Adam B. Olshen
المصدر: Ophthalmology, vol 127, iss 6
Ophthalmologyمصطلحات موضوعية: Male, Tissue Fixation, Buccal swab, DNA Mutational Analysis, medicine.disease_cause, Ophthalmology & Optometry, Germline, Cohort Studies, 0302 clinical medicine, Child, Cancer, Pediatric, 0303 health sciences, Mutation, Paraffin Embedding, Retinoblastoma, High-Throughput Nucleotide Sequencing, DNA, Neoplasm, Retinoblastoma Binding Proteins, Child, Preschool, Public Health and Health Services, Female, medicine.symptom, Pediatric Research Initiative, Pediatric Cancer, Retinal Neoplasms, Ubiquitin-Protein Ligases, Clinical Sciences, Article, Eye Enucleation, 03 medical and health sciences, Germline mutation, Rare Diseases, Clinical Research, Opthalmology and Optometry, medicine, Genetics, Humans, Gene Silencing, Preschool, Anaplasia, ATRX, Germ-Line Mutation, 030304 developmental biology, business.industry, Neurosciences, Infant, DNA, medicine.disease, eye diseases, Ophthalmology, 030221 ophthalmology & optometry, Cancer research, Neoplasm, business
وصف الملف: application/pdf
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https://escholarship.org/uc/item/69x937mnTest -
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المؤلفون: Sariah Allen, Cassie Kline, Carole Brathwaite, Mouied Alashari, Gourish Mondal, Ajay Ravindranathan, Pamela Doo, Brent A. Orr, David A. Solomon, Patrick Devine, Javier Villanueva-Meyer, Joanna J. Phillips, Carol S. Bruggers, Alberto Broniscer, David Samuel, Ossama M. Maher, Jessica Van Ziffle, Alyssa Reddy, Tarik Tihan, Rong Li, Samuel H. Cheshier, Arie Perry, Nicholas S Whipple, Laura K. Metrock, Matthew Hall, James P. Grenert, Lee-Way Jin, Anu Banerjee, Andrew W. Bollen, Corey Raffel, Courtney Onodera, Julieann C. Lee, Quynh T. Tran, Melike Pekmezci, Mitchel S. Berger, Reuben Antony, Jairo Barreto, Minesh P. Mehta, Ziad Khatib, Rohit Gupta, John T. Lucas, Nalin Gupta
المصدر: Acta Neuropathol
Acta neuropathologica, vol 139, iss 6مصطلحات موضوعية: 0301 basic medicine, Male, Lung Neoplasms, Pediatric cancer, Tyrosine kinase inhibitor, medicine.disease_cause, Epigenesis, Genetic, Exon, 0302 clinical medicine, Carcinoma, Non-Small-Cell Lung, 2.1 Biological and endogenous factors, Osimertinib, Aetiology, Non-Small-Cell Lung, Child, Cancer, Pediatric, Mutation, Brain Neoplasms, Histone H3, Bithalamic glioma, Diffuse midline glioma, Glioma, ErbB Receptors, Erlotinib, Child, Preschool, Female, Tyrosine kinase, Adolescent, EGFR, Molecular neuropathology, Clinical Sciences, Antineoplastic Agents, Biology, Afatinib, Article, Pathology and Forensic Medicine, 03 medical and health sciences, Cellular and Molecular Neuroscience, Rare Diseases, Genetic, Trametinib, Genetics, medicine, Humans, Epigenetics, Preschool, Protein Kinase Inhibitors, Neurology & Neurosurgery, Carcinoma, Human Genome, Neurosciences, medicine.disease, Brain Disorders, Brain Cancer, Orphan Drug, 030104 developmental biology, Protein kinase domain, Cancer research, Neurology (clinical), 030217 neurology & neurosurgery, Epigenesis
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e08e7c3b224d9f0dfed7d7aa0d94b0feTest
https://pubmed.ncbi.nlm.nih.gov/32303840Test -
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المؤلفون: Ziad Khatib, Peter P. Sun, Corey Raffel, Marjorie R. Grafe, Julieann C. Lee, Philip V. Theodosopoulos, Liset Pelaez, Arie Perry, Joanna J. Phillips, Joseph Torkildson, Nancy Ann Oberheim-Bush, Han Lee, David Scharnhorst, Bette K. Kleinschmidt-DeMasters, Tarik Tihan, Carole Brathwaite, Lee-Way Jin, Mirna Lechpammer, James P. Grenert, Cynthia Fata, Andrew W. Bollen, Patrick Devine, Serguei Bannykh, Tabitha Cooney, Donald E. Born, Jennifer Clarke, Susan M. Chang, David Samuel, Ossama Maher, Courtney Onodera, Emily A. Sloan, Hannes Vogel, Mike McDermott, Gabriel Chamyan, Anu Banerjee, David A. Solomon, Robin Buerki, Cassie Kline, Hua Guo, Jeffrey W. Hofmann, Mitchel S. Berger, Shawn L. Hervey-Jumper, Jessica Van Ziffle, Matthew D. Wood, Lucas Calixto-Hope, Jennie Taylor, Melike Pekmezci, Manish K. Aghi, Nicholas Butowski, Nalin Gupta
المصدر: Neuro-Oncology, vol 21, iss Supplement_6
Neuro Oncolمصطلحات موضوعية: Cancer Research, Oncology and Carcinogenesis, Biology, Fourth ventricle, Ganglioglioma, Rare Diseases, CDKN2A, medicine, Genetics, Missense mutation, 2.1 Biological and endogenous factors, Oncology & Carcinogenesis, Aetiology, Anaplasia, ATRX, Cancer, Pediatric, Pilocytic astrocytoma, Neurosciences, medicine.disease, Molecular biology, Molecular Pathology and Classification - Adult and Pediatric, PTPN11, Oncology, Neurology (clinical), medicine.symptom
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffcc3f231a74ca51cd47c5caeb3b69ddTest
https://escholarship.org/uc/item/4dr7x634Test -
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المؤلفون: Ivo Buchhalter, Arie Perry, Meredith Stevers, Anuradha Banerjee, J. Bryan Iorgulescu, Lukas Chavez, Paul A. Northcott, Damian Stichel, Jessica Van Ziffle, Andrew W. Bollen, Sabine Mueller, Boris C. Bastian, Tarik Tihan, Marcel Kool, Stefan M. Pfister, Nalin Gupta, Theodore Nicolaides, Andrey Korshunov, David Samuel, James P. Grenert, David A. Solomon
المصدر: Iorgulescu, JB; Van Ziffle, J; Stevers, M; Grenert, JP; Bastian, BC; Chavez, L; et al.(2018). Deep sequencing of WNT-activated medulloblastomas reveals secondary SHH pathway activation. Acta Neuropathologica, 135(4), 635-638. doi: 10.1007/s00401-018-1819-x. UCSF: Retrieved from: http://www.escholarship.org/uc/item/5941q3p8Test
Acta neuropathologica, vol 135, iss 4مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, media_common.quotation_subject, Clinical Sciences, Andrey, Article, Deep sequencing, Pathology and Forensic Medicine, Cohort Studies, Young Adult, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Gene Frequency, Humans, Hedgehog Proteins, Theology, Cerebellar Neoplasms, Child, media_common, Neurology & Neurosurgery, Neurosciences, Wnt signaling pathway, High-Throughput Nucleotide Sequencing, Art, Wnt Proteins, 030104 developmental biology, Mutation, Disease Progression, Female, Neurology (clinical), 030217 neurology & neurosurgery, Medulloblastoma, Signal Transduction
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::702e1ba20d39f28c0b8bb3169f6e5349Test
https://doi.org/10.1007/s00401-018-1819-xTest -
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المؤلفون: William H. Yong, David A. Solomon, Arie Perry, Iwei Yeh, Courtney Onodera, Iman H. Hewedi, Andrew W. Bollen, Yu Hsiu Lin, M. Beatriz S. Lopes, Eric Talevich, Matthew P. Jacobson, Nicholas Butowski, Gourish Mondal, Benjamin Goode, Bette K. Kleinschmidt-DeMasters, Daniel J. Brat, Jessica Van Ziffle, Boris C. Bastian, Diego Garrido Ruiz, Matija Snuderl, Joanna J. Phillips, Tarik Tihan, Nancy M. Joseph, Fausto J. Rodriguez, Michael Hyun, Marc K. Rosenblum, David N. Louis, Arun P. Wiita, James P. Grenert
المصدر: Nature Communications, Vol 9, Iss 1, Pp 1-8 (2018)
Nature communications, vol 9, iss 1
Nature Communications, vol 9, iss 1
Nature Communicationsمصطلحات موضوعية: 0301 basic medicine, Male, General Physics and Astronomy, medicine.disease_cause, 0302 clinical medicine, 2.1 Biological and endogenous factors, Missense mutation, Aetiology, Phosphorylation, lcsh:Science, Extracellular Signal-Regulated MAP Kinases, Cancer, Mutation, Multidisciplinary, Lamina terminalis, Glioma, Middle Aged, 3. Good health, medicine.anatomical_structure, Female, Adult, Protein Kinase C-alpha, Science, Mutation, Missense, Brain tumor, Biology, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, Rare Diseases, Protein Domains, Clinical Research, Genetics, medicine, Humans, Protein kinase C, Third Ventricle, Aged, Third ventricle, Oncogene, Human Genome, Neurosciences, General Chemistry, medicine.disease, Brain Disorders, Brain Cancer, 030104 developmental biology, Protein kinase domain, Cancer research, lcsh:Q, Missense, Cerebral Ventricle Neoplasms, 030217 neurology & neurosurgery
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a58554b151e1c6f2901a5a43a96e3f03Test
https://doaj.org/article/8ff58d0463294f3b9772e2541cb2ebc5Test -
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المؤلفون: Zahra Al‐Hajri, Tara A. Saunders, Matthew Schniederjan, Andrew W. Bollen, Cassie Kline, Soonmee Cha, Dianne Wilson, Sean P. Ferris, Joanna J. Phillips, Irune Ruiz‐Diaz, Mariam Aboian, Jessica Van Ziffle, Corey Raffel, José E. Velázquez Vega, Tarik Tihan, Janna H. Neltner, Melike Pekmezci, Julieann C. Lee, Anu Banerjee, David A. Solomon, David Samuel, Nalin Gupta, Shino Magaki, Arie Perry, Courtney Onodera, Yunn-Yi Chen, James P. Grenert
المصدر: Brain Pathol
Brain pathology (Zurich, Switzerland), vol 30, iss 1مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, Kaplan-Meier Estimate, Central Nervous System Neoplasms, Exon, 0302 clinical medicine, CDKN2A, Neoplasms, Child, Telomerase, Cancer, screening and diagnosis, Tumor, biology, Brain Neoplasms, General Neuroscience, molecular neurooncology, Methylation, Exons, Genomics, Glioma, Neoplasms, Neuroepithelial, Neuroepithelial cell, Detection, HGNET, Child, Preschool, Female, brain tumor, Biotechnology, 4.2 Evaluation of markers and technologies, medicine.medical_specialty, Adolescent, Clinical Sciences, Brain tumor, Neuroepithelial, molecular neuro-oncology, Article, Pathology and Forensic Medicine, OLIG2, BCOR exon 15 internal tandem duplication, 03 medical and health sciences, Rare Diseases, Proto-Oncogene Proteins, Genetics, medicine, Biomarkers, Tumor, Humans, Preschool, EP300, Cyclin-Dependent Kinase Inhibitor p16, Neurology & Neurosurgery, high-grade neuroepithelial tumor, Neurosciences, Infant, Oligodendrocyte Transcription Factor 2, medicine.disease, Brain Disorders, Brain Cancer, molecular neuropathology, Repressor Proteins, Orphan Drug, 030104 developmental biology, Synaptophysin, biology.protein, Neurology (clinical), E1A-Associated p300 Protein, Biomarkers, 030217 neurology & neurosurgery, Transcription Factors
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0cc248f5a171382f1e7dc14495ac077Test
https://pubmed.ncbi.nlm.nih.gov/31104347Test