खोज परिणाम - Ana Novokmet
- प्रदर्शित 1 - 12 परिणाम 12
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Recurrent Focal Copy-Number Changes and Loss of Heterozygosity Implicate Two Noncoding RNAs and One Tumor Suppressor Gene at Chromosome 3q13.31 in Osteosarcoma द्वारा Ivan Pašić, Adam Shlien, Adam D. Durbin, Dimitrios J. Stavropoulos, Berivan Baskin, Peter N. Ray, Ana Novokmet, David Malkin
प्रकाशित 2010Artigo -
2
Prevalence and Functional Consequence of <i>TP53</i> Mutations in Pediatric Adrenocortical Carcinoma: A Children's Oncology Group Study द्वारा Jonathan D. Wasserman, Ana Novokmet, Claudia Eichler-Jonsson, Raul C. Ribeiro, Carlos Rodríguez‐Galindo, Gerard P. Zambetti, David Malkin
प्रकाशित 2015Artigo -
3
Excessive genomic DNA copy number variation in the Li–Fraumeni cancer predisposition syndrome द्वारा Adam Shlien, Uri Tabori, Christian R. Marshall, Małgorzata Pieńkowska, Lars Feuk, Ana Novokmet, Sonia Nanda, Harriet Druker, Stephen W. Scherer, David Malkin
प्रकाशित 2008Artigo -
4
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5
A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes द्वारा Adam Shlien, Berivan Baskin, Maria Isabel Achatz, Dimitrios J. Stavropoulos, Kim E. Nichols, Louanne Hudgins, Chantal F. Morel, Margaret P Adam, Nataliya Zhukova, Lianne E. Rotin, Ana Novokmet, Harriet Druker, Mary Shago, Peter N. Ray, Pierre Hainaut, David Malkin
प्रकाशित 2010Artigo -
6
Monoallelic Expression Determines Oncogenic Progression and Outcome in Benign and Malignant Brain Tumors द्वारा Erin J. Walker, Cindy Zhang, Pedro Castelo‐Branco, Cynthia Hawkins, Wesley V. Wilson, Nataliya Zhukova, Noa Alon, Ana Novokmet, Berivan Baskin, Peter N. Ray, Christiane B. Knobbe‐Thomsen, Peter B. Dirks, Michael D. Taylor, Sidney Croul, David Malkin, Uri Tabori
प्रकाशित 2011Artigo -
7
Parent decision‐making around the genetic testing of children for germline <i>TP53</i> mutations द्वारा Melissa A. Alderfer, Kristin Zelley, Robert B. Lindell, Ana Novokmet, L. Phuong, Judy E. Garber, Deepika Nathan, Sarah Scollon, Nicolette M. Chun, Andrea Farkas Patenaude, James M. Ford, Sharon E. Plon, Joshua D. Schiffman, Lisa Diller, Sharon A. Savage, David Malkin, Carol A. Ford, Kim E. Nichols
प्रकाशित 2014Artigo -
8
Molecular Characterization of Choroid Plexus Tumors Reveals Novel Clinically Relevant Subgroups द्वारा Diana M. Merino, Adam Shlien, Anita Villani, Małgorzata Pieńkowska, Stephen C. Mack, Vijay Ramaswamy, David Shih, Ruth Tatevossian, Ana Novokmet, Sanaa Choufani, Rina Dvir, Myran Ben-Arush, Brent T. Harris, Eugene Hwang, Rishi Lulla, Stefan M. Pfister, Maria Isabel Achatz, Nada Jabado, Jonathan L. Finlay, Rosanna Weksberg, Éric Bouffet, Cynthia Hawkins, Michael D. Taylor, Uri Tabori, David W. Ellison, Richard J. Gilbertson, David Malkin
प्रकाशित 2014Artigo -
9
Genome-Wide DNA Methylation Analysis Reveals Epigenetic Dysregulation of MicroRNA-34A in <i>TP53</i>-Associated Cancer Susceptibility द्वारा Nardin Samuel, Gavin W. Wilson, Mathieu Lemire, Badr Id Said, Youliang Lou, Weili Li, Diana M. Merino, Ana Novokmet, James Tran, Kim E. Nichols, Jonathan L. Finlay, Sanaa Choufani, Marc Remke, Vijay Ramaswamy, Florence M.G. Cavalli, Christine Elser, Lynn Meister, Michael D. Taylor, Uri Tabori, Meredith S. Irwin, Rosanna Weksberg, Jonathan D. Wasserman, Andrew D. Paterson, Jordan R. Hansford, Maria Isabel Achatz, Thomas J. Hudson, David Malkin
प्रकाशित 2016Artigo -
10
Li-Fraumeni Exploration Consortium Data Coordinating Center: Building an Interactive Web-Based Resource for Collaborative International Cancer Epidemiology Research for a Rare Cond... द्वारा L. Phuong, Sharon Sand, Neiladri Saha, Mauricio Oberti, Tom Dolafi, L. Digianni, Elizabeth J. Root, Xianhua Kong, Renée C. Bremer, Karina Miranda Santiago, Jasmina Bojadzieva, Derek Barley, Ana Novokmet, Karen A. Ketchum, Ngoc Thanh Nguyên, Shine Jacob, Kim E. Nichols, Christian P. Kratz, Joshua D. Schiffman, D. Gareth Evans, Maria Isabel Achatz, Louise C. Strong, Judy E. Garber, Sweta A. Ladwa, David Malkin, Jeffrey N. Weitzel
प्रकाशित 2020Artigo -
11
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis द्वारा Nicholas Light, Mehdi Layeghifard, Ayush Attery, Vallijah Subasri, Matthew Zatzman, Nathaniel D. Anderson, Rupal Hatkar, Sasha Blay, David Chen, Ana Novokmet, Fabio Fuligni, James Tran, Richard de Borja, Himanshi Agarwal, Larissa Waldman, Lisa M. Abegglen, Daniel J. Albertson, Jonathan L. Finlay, Jordan R. Hansford, Sam Behjati, Anita Villani, Moritz Gerstung, Ludmil B. Alexandrov, Gino R. Somers, Joshua D. Schiffman, Varda Rotter, David Malkin, Adam Shlien
प्रकाशित 2023Artigo -
12
Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors द्वारा Nathaniel D. Anderson, Richard de Borja, Matthew D. Young, Fabio Fuligni, Andrej Rosic, Nicola D. Roberts, Simon Hajjar, Mehdi Layeghifard, Ana Novokmet, Paul E. Kowalski, Matthew Anaka, Scott Davidson, Mehdi Zarrei, Badr Id Said, Laura Schreiner, Remi Marchand, Joseph Sitter, Nalan Gökgöz, Ledia Brunga, Garrett T. Graham, Anthony Fullam, Nischalan Pillay, Jeffrey A. Toretsky, Akihiko Yoshida, Tatsuhiro Shibata, Markus Metzler, Gino R. Somers, Stephen W. Scherer, Adrienne M. Flanagan, Peter J. Campbell, Joshua D. Schiffman, Mary Shago, Ludmil B. Alexandrov, Jay S. Wunder, Irene L. Andrulis, David Malkin, Sam Behjati, Adam Shlien
प्रकाशित 2018Artigo
खोज साधन:
संबंधित विषय
Biology
Gene
Genetics
Medicine
Mutation
Cancer
Cancer research
Germline
Germline mutation
Pathology
Copy-number variation
Genome
Allele
Carcinogenesis
Gene expression
Internal medicine
Chromosome
Comparative genomic hybridization
DNA methylation
Epigenetics
Gene duplication
Li–Fraumeni syndrome
Loss of heterozygosity
Methylation
Oncology
Somatic cell
Acoustics
Adrenocortical carcinoma
Alternative medicine
Brain tumor