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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: Courtney Onodera, Iwei Yeh, Boris C. Bastian, Joseph T. Rabban, Jessica Van Ziffle, Karuna Garg, David A. Solomon, Charles Zaloudek, James P. Grenert, Meredith Stevers
المصدر: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, vol 32, iss 1
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Incمصطلحات موضوعية: Mesothelioma, Male, 0301 basic medicine, adenomatoid tumor, Pathology, tumor necrosis factor alpha (TNFα), Medical and Health Sciences, 0302 clinical medicine, CDKN2A, 80 and over, 2.1 Biological and endogenous factors, cdc42 GTP-Binding Protein, Peritoneal Neoplasms, Cancer, Mesothelial Neoplasm, Aged, 80 and over, mesothelial cells, BAP1, CDC42, Middle Aged, respiratory system, Tumor Necrosis Factor Receptor-Associated Peptides and Proteins, 3. Good health, medicine.anatomical_structure, 030220 oncology & carcinogenesis, malignant mesothelioma, Immunohistochemistry, Female, TRAF7, medicine.medical_specialty, Adenomatoid tumor, and over, Biology, Article, Pathology and Forensic Medicine, 03 medical and health sciences, Rare Diseases, Peritoneum, Clinical Research, SETD2, Genetics, medicine, Humans, neoplasms, well-differentiated papillary mesothelioma (WDPM), Aged, Rho family GTPase, medicine.disease, respiratory tract diseases, 030104 developmental biology, L1CAM, Mutation, nuclear factor-kappa B (NF-kB)
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c30ed1cc610629c47e76fe16db733c2Test
https://doi.org/10.1038/s41379-018-0127-2Test -
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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: Jessica Van Ziffle, Linlin Wang, Nancy Y. Greenland, Yen-Chun Liu, Sonam Prakash, Zhongxia Qi
المصدر: Human pathology. 108
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Myeloid, DNA Copy Number Variations, Cell, Biology, Somatic evolution in cancer, Polymorphism, Single Nucleotide, DNA sequencing, Pathology and Forensic Medicine, 03 medical and health sciences, Young Adult, 0302 clinical medicine, hemic and lymphatic diseases, medicine, Myeloid sarcoma, Humans, Sarcoma, Myeloid, Aged, Aged, 80 and over, Gene Expression Profiling, Myeloid leukemia, Genomic signature, Middle Aged, medicine.disease, Leukemia, Myeloid, Acute, 030104 developmental biology, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Cancer research, Cancer gene, Female, Transcriptome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8906cef56c651fae25088fb12b6b2fbTest
https://pubmed.ncbi.nlm.nih.gov/33232718Test -
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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
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3c16724cad14b3637307e3c1d08c6d9Test
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: 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: Bette K. Kleinschmidt-DeMasters, Nadejda M. Tsankova, Jessica Van Ziffle, David A. Solomon, Marc K. Rosenblum, Arie Perry, Meredith Stevers, Boris C. Bastian, Joanna J. Phillips, Tarik Tihan, Melike Pekmezci
المصدر: Acta Neuropathologica. 135:485-488
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, MAP Kinase Signaling System, Biology, Article, Pathology and Forensic Medicine, Cohort Studies, Young Adult, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, medicine, Humans, Neoplasm, Cerebellar Neoplasms, Child, Cerebrum, Extramural, Brain, Middle Aged, medicine.disease, Neoplasms, Neuroepithelial, 030104 developmental biology, medicine.anatomical_structure, Cancer research, Female, Neurology (clinical), Map kinase signaling, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e27e1fdd4b79507cdced9f4397ee8519Test
https://doi.org/10.1007/s00401-018-1820-4Test