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001-es BibID:BIBFORM052708
035-os BibID:WOS:000327100500011
Első szerző:Remke, Marc
Cím:TERT promoter mutations are highly recurrent in SHH subgroup medulloblastoma / Marc Remke, Vijay Ramaswamy, John Peacock, David J. H. Shih, Christian Koelsche, Paul A. Northcott, Nadia Hill, Florence M. G. Cavalli, Marcel Kool, Xin Wang, Stephen C. Mack, Mark Barszczyk, A. Sorana Morrissy, Xiaochong Wu, Sameer Agnihotri, Betty Luu, David T. W. Jones, Livia Garzia, Adrian M. Dubuc, Nataliya Zhukova, Robert Vanner, Johan M. Kros, Pim J. French, Erwin G. Van Meir, Rajeev Vibhakar, Karel Zitterbart, Jennifer A. Chan, László Bognár, Almos Klekner, Boleslaw Lach, Shin Jung, Ali G. Saad, Linda M. Liau, Steffen Albrecht, Massimo Zollo, Michael K. Cooper, Reid C. Thompson, Oliver O. Delattre, Franck Bourdeaut, François F. Doz, Miklós Garami, Peter Hauser, Carlos G. Carlotti, Timothy E. Van Meter, Luca Massimi, Daniel Fults, Scott L. Pomeroy, Toshiro Kumabe, Young Shin Ra, Jeffrey R. Leonard, Samer K. Elbabaa, Jaume Mora, Joshua B. Rubin, Yoon-Jae Cho, Roger E. McLendon, Darell D. Bigner, Charles G. Eberhart, Maryam Fouladi, Robert J. Wechsler-Reya, Claudia C. Faria, Sidney E. Croul, Annie Huang, Eric Bouffet, Cynthia E. Hawkins, Peter B. Dirks, William A. Weiss, Ulrich Schüller, Ian F. Pollack, Stefan Rutkowski, David Meyronet, Anne Jouvet, Michelle Fèvre-Montange, Nada Jabado, Marta Perek-Polnik, Wieslawa A. Grajkowska, Seung-Ki Kim, James T. Rutka, David Malkin, Uri Tabori, Stefan M. Pfister, Andrey Korshunov, Andreas von Deimling, Michael D. Taylor
Dátum:2013
ISSN:0001-6322
Megjegyzések:Telomerase reverse transcriptase (TERT) promoter mutations were recently shown to drive telomerase activity in various cancer types, including medulloblastoma. However, the clinical and biological implications of TERT mutations in medulloblastoma have not been described. Hence, we sought to describe these mutations and their impact in a subgroup-specific manner. We analyzed the TERT promoter by direct sequencing and genotyping in 466 medulloblastomas. The mutational distributions were determined according to subgroup affiliation, demographics, and clinical, prognostic, and molecular features. Integrated genomics approaches were used to identify specific somatic copy number alterations in TERT promoter-mutated and wild-type tumors. Overall, TERT promoter mutations were identified in 21 % of medulloblastomas. Strikingly, the highest frequencies of TERT mutations were observed in SHH (83 %; 55/66) and WNT (31 %; 4/13) medulloblastomas derived from adult patients. Group 3 and Group 4 harbored this alteration in <5 % of cases and showed no association with increased patient age. The prognostic implications of these mutations were highly subgroup-specific. TERT mutations identified a subset with good and poor prognosis in SHH and Group 4 tumors, respectively. Monosomy 6 was mostly restricted to WNT tumors without TERT mutations. Hallmark SHH focal copy number aberrations and chromosome 10q deletion were mutually exclusive with TERT mutations within SHH tumors. TERT promoter mutations are the most common recurrent somatic point mutation in medulloblastoma, and are very highly enriched in adult SHH and WNT tumors. TERT mutations define a subset of SHH medulloblastoma with distinct demographics, cytogenetics, and outcomes.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Acta Neuropathologica 126 : 6 (2013), p. 917-929. -
További szerzők:Ramaswamy, Vijay Peacock, John Shih, David J. H. Koelsche, Christian Northcott, Paul A. Hill, Nadia Cavalli, Florence M. G. Kool, Marcel Wang, Xin Mack, Stephen Barszczyk, Mark Morrissy, Sorana Wu, Xiaochong Agnihotri, Sameer Luu, Betty Jones, David T. W. Garzia, Livia Dubuc, Adrian Zhukova, Nataliya Vanner, Robert Kros, Johan M. French, Pim J. van Meir, Erwin G. Vibhakar, Rajeev Zitterbart, Karel Chan, Jennifer A. Bognár László (1958-) (idegsebész, gyermekidegsebész) Klekner Álmos (1970-) (idegsebész) Lach, Boleslaw Jung, Shin Saad, Ali G. Liau, Linda M. Albrecht, Stephen Zollo, Massimo Cooper, Michael K. Thompson, Reid C. Delattre, Olivier Bourdeaut, Franck Doz, François F. Garami Miklós Hauser Péter Carlotti, Carlos G. van Meter, Timothy E. Massimi, Luca Fults, Daniel Pomeroy, Scott L. Kumabe, Toshihiro Shin Ra, Young Leonard, Jeffrey R. Elbabaa, Samer K. Mora, Jaume Rubin, Joshua B. Cho, Yoon-Jae McLendon, Roger E. Bigner, Darell Eberhart, Charles G. Fouladi, Maryam Wechsler-Reya, Robert J. Faria, Claudia C. Croul, Sidney E. Huang, Annie Bouffet, Eric Hawkins, Cynthia E. Dirks, Peter Weiss, William A. Schüller, Ulrich Pollack, Ian F. Rutkowski, Stefan Meyronet, David Jouvet, Anne Fèvre-Montange, Michelle Jabado, Nada Perek-Polnik, Marta Grajkowska, Wieslawa A. Kim, Seung-Ki Rutka, James T. Malkin, David Tabori, Uri Pfister, Stefan M. Korshunov, Andrey von Deimling, Andreas Taylor, Michael D.
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001-es BibID:BIBFORM052715
Első szerző:Shih, David J. H.
Cím:Cytogenetic prognostication within medulloblastoma subgroups / David J. H. Shih, Paul A. Northcott, Marc Remke, Andrey Korshunov, Vijay Ramaswamy, Marcel Kool, Betty Luu, Yuan Yao, Xin Wang, Adrian M. Dubuc, Livia Garzia, John Peacock, Stephen C. Mack, Xiaochong Wu, Adi Rolider, A. Sorana Morrissy, Florence M. G. Cavalli, David T. W. Jones, Karel Zitterbart, Claudia C. Faria, Ulrich Schüller, Leos Kren, Toshihiro Kumabe, Teiji Tominaga, Young Shin Ra, Miklós Garami, Peter Hauser, Jennifer A. Chan, Shenandoah Robinson, László Bognár, Almos Klekner, Ali G. Saad, Linda M. Liau, Steffen Albrecht, Adam Fontebasso, Giuseppe Cinalli, Pasqualino De Antonellis, Massimo Zollo, Michael K. Cooper, Reid C. Thompson, Simon Bailey, Janet C. Lindsey, Concezio Di Rocco, Luca Massimi, Erna M. C. Michiels, Stephen W. Scherer, Joanna J. Phillips, Nalin Gupta, Xing Fan, Karin M. Muraszko, Rajeev Vibhakar, Charles G. Eberhart, Maryam Fouladi, Boleslaw Lach, Shin Jung, Robert J. Wechsler-Reya, Michelle Fèvre-Montange, Anne Jouvet, Nada Jabado, Ian F. Pollack, William A. Weiss, Ji-Yeoun Lee, Byung-Kyu Cho, Seung-Ki Kim, Kyu-Chang Wang, Jeffrey R. Leonard, Joshua B. Rubin, Carmen de Torres, Cinzia Lavarino, Jaume Mora, Yoon-Jae Cho, Uri Tabori, James M. Olson, Amar Gajjar, Roger J. Packer, Stefan Rutkowski, Scott L. Pomeroy, Pim J. French, Nanne K. Kloosterhof, Johan M. Kros, Erwin G. Van Meir, Steven C. Clifford, Franck Bourdeaut, Olivier Delattre, François F. Doz, Cynthia E. Hawkins, David Malkin, Wieslawa A. Grajkowska, Marta Perek-Polnik, Eric Bouffet, James T. Rutka, Stefan M. Pfister, Michael D. Taylor
Dátum:2014
ISSN:0732-183X 1527-7755
Megjegyzések:Purpose Medulloblastoma comprises four distinct molecular subgroups: WNT, SHH, Group 3, and Group 4. Current medulloblastoma protocols stratify patients based on clinical features: patient age, metastatic stage, extent of resection, and histologic variant. Stark prognostic and genetic differences among the four subgroups suggest that subgroup-specific molecular biomarkers could improve patient prognostication.Patients and Methods Molecular biomarkers were identified from a discovery set of 673 medulloblastomas from 43 cities around the world. Combined risk stratification models were designed based on clinical and cytogenetic biomarkers identified by multivariable Cox proportional hazards analyses. Identified biomarkers were tested using fluorescent in situ hybridization (FISH) on a nonoverlapping medulloblastoma tissue microarray (n = 453), with subsequent validation of the risk stratification models.Results Subgroup information improves the predictive accuracy of a multivariable survival model compared with clinical biomarkers alone. Most previously published cytogenetic biomarkers are only prognostic within a single medulloblastoma subgroup. Profiling six FISH biomarkers (GLI2, MYC, chromosome 11 [chr11], chr14, 17p, and 17q) on formalin-fixed paraffin-embedded tissues, we can reliably and reproducibly identify very low-risk and very high-risk patients within SHH, Group 3, and Group 4 medulloblastomas.Conclusion Combining subgroup and cytogenetic biomarkers with established clinical biomarkers substantially improves patient prognostication, even in the context of heterogeneous clinical therapies. The prognostic significance of most molecular biomarkers is restricted to a specific subgroup. We have identified a small panel of cytogenetic biomarkers that reliably identifies very high-risk and very low-risk groups of patients, making it an excellent tool for selecting patients for therapy intensification and therapy de-escalation in future clinical trials.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Journal of Clinical Oncology. - 32 : 9 (2014), p. 886-896. -
További szerzők:Northcott, Paul A. Remke, Marc Korshunov, Andrey Ramaswamy, Vijay Kool, Marcel Luu, Betty Yao, Yuan Wang, Xin Dubuc, Adrian Garzia, Livia Peacock, John Mack, Stephen Wu, Xiaochong Rolider, Adi Morrissy, Sorana Cavalli, Florence M. G. Jones, David T. W. Zitterbart, Karel Faria, Claudia C. Schüller, Ulrich Kren, Leos Kumabe, Toshihiro Tominaga, Teiji Shin Ra, Young Garami Miklós Hauser, Peter Chan, Jennifer A. Robinson, Shenandoah Bognár László (1958-) (idegsebész, gyermekidegsebész) Klekner Álmos (1970-) (idegsebész) Saad, Ali G. Liau, Linda M. Albrecht, Stephen Fontebasso, Adam M. Cinalli, Giuseppe De Antonellis, Pasqualino Zollo, Massimo Cooper, Michael K. Thompson, Reid C. Bailey, Simon Lindsey, Janet C. Di Rocco, Concezio Massimi, Luca Michiels, Erna M. C. Scherer, Stephen W. Phillips, Joanna J. Gupta, Nalin Fan, Xing Muraszko, Karin M. Vibhakar, Rajeev Eberhart, Charles G. Fouladi, Maryam Lach, Boleslaw Jung, Shin Wechsler-Reya, Robert J. Fèvre-Montange, Michelle Jouvet, Anne Jabado, Nada Pollack, Ian F. Weiss, William A. Lee, Ji-Yeoun Cho, Byung-Kyu Kim, Seung-Ki Wang, Kyu-Chang Leonard, Jeffrey R. Rubin, Joshua B. Torres, Carmen, de Lavarino, Cinzia Mora, Jaume Cho, Yoon-Jae Tabori, Uri Olson, James M. Gajjar, Amar Packer, Roger J. Rutkowski, Stefan Pomeroy, Scott L. French, Pim J. Kloosterhof, Nanne K. Kros, Johan M. van Meir, Erwin G. Clifford, Steven C. Bourdeaut, Franck Delattre, Olivier Doz, François F. Hawkins, Cynthia E. Malkin, David Grajkowska, Wieslawa A. Perek-Polnik, Marta Bouffet, Eric Rutka, James T. Pfister, Stefan M. Taylor, Michael D.
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3.

001-es BibID:BIBFORM096045
035-os BibID:(cikkazonosító)1749 (WoS)000631928500006 (Scopus)85102687135
Első szerző:Skowron, Patryk
Cím:The transcriptional landscape of Shh medulloblastoma / Patryk Skowron, Hamza Farooq, Florence M. G. Cavalli1, A. Sorana Morrissy, Michelle Ly, Liam D. Hendrikse, Evan Y. Wang, Haig Djambazian, Helen Zhu, Karen L. Mungall, Quang M. Trinh, Tina Zheng, Shizhong Dai, Ana S. Guerreiro Stucklin, Maria C. Vladoiu, Vernon Fong, Borja L. Holgado, Carolina Nor, Xiaochong Wu, Diala Abd-Rabbo, Pierre Bérubé, Yu Chang Wang, Betty Luu, Raul A. Suarez, Avesta Rastan, Aaron H. Gillmor, John J. Y. Lee, Xiao Yun Zhang, Craig Daniels, Peter Dirks, David Malkin, Eric Bouffet, Uri Tabori, James Loukides, François P. Doz, Franck Bourdeaut, Olivier O. Delattre, Julien Masliah-Planchon, Olivier Ayrault, Seung-Ki Kim, David Meyronet, Wieslawa A. Grajkowska, Carlos G. Carlotti, Carmen de Torres, Jaume Mora, Charles G. Eberhart, Erwin G. Van Meir, Toshihiro Kumabe, Pim J. French, Johan M. Kros, Nada Jabado, Boleslaw Lach, Ian F. Pollack, Ronald L. Hamilton, Amulya A. Nageswara Rao, Caterina Giannini, James M. Olson, László Bognár, Almos Klekner, Karel Zitterbart, Joanna J. Phillips, Reid C. Thompson, Michael K. Cooper, Joshua B. Rubin, Linda M. Liau, Miklós Garami, Peter Hauser, Kay Ka Wai Li, Ho-Keung Ng, Wai Sang Poon, G. Yancey Gillespie, Jennifer A. Chan, Shin Jung, Roger E. McLendon, Eric M. Thompson, David Zagzag, Rajeev Vibhakar, Young Shin Ra, Maria Luisa Garre, Ulrich Schüller, Tomoko Shofuda, Claudia C. Faria, Enrique López-Aguilar, Gelareh Zadeh, Chi-Chung Hui, Vijay Ramaswamy, Swneke D. Bailey, Steven J. Jones, Andrew J. Mungall, Richard A. Moore, John A. Calarco, Lincoln D. Stein, Gary D. Bader, Jüri Reimand, Jiannis Ragoussis, William A. Weiss, Marco A. Marra, Hiromichi Suzuki, Michael D. Taylor
Dátum:2021
ISSN:2041-1723
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Nature Communications. - 12 : 1 (2021), p. 1-17. -
További szerzők:Farooq, Hamza Cavalli, Florence M. G. Morrissy, Sorana Ly, Michelle Hendrikse, Liam D. Wang, Evan Y. Djambazian, Haig Zhu, Helen Mungall, Karen L. Trinh, Quang M. Zheng, Tina Dai, Shizhong Stucklin, Ana S. Guerreiro Vladoiu, Maria C. Fong, Vernon Holgado, Borja L. Nor, Carolina Wu, Xiaochong Abd-Rabbo, Diala Berube, Pierre Wang, Yu Chang Luu, Betty Suarez, Raul A. Rastan, Avesta Gillmor, Aaron H. Lee, John J. Y. Zhang, Xiao Yun Daniels, Craig Dirks, Peter Malkin, David Bouffet, Eric Tabori, Uri Loukides, James Doz, François P. Bourdeaut, Franck Delattre, Olivier Masliah-Planchon, Julien Ayrault, Olivier Kim, Seung-Ki Meyronet, David Grajkowska, Wieslawa A. Carlotti, Carlos G. Torres, Carmen, de Mora, Jaume Eberhart, Charles G. van Meir, Erwin G. Kumabe, Toshihiro French, Pim J. Kros, Johan M. Jabado, Nada Lach, Boleslaw Pollack, Ian F. Hamilton, Ronald L. Rao, Amulya A. Nageswara Giannini, Caterina Olson, James M. Bognár László (1958-) (idegsebész, gyermekidegsebész) Klekner Álmos (1970-) (idegsebész) Zitterbart, Karel Phillips, Joanna J. Thompson, Reid C. Cooper, Michael K. Rubin, Joshua B. Liau, Linda M. Garami Miklós Hauser, Peter Li, Kay Ka Wai Ng, Ho-Keung Poon, Wai Sang Yancey Gillespie, G. Chan, Jennifer A. Jung, Shin McLendon, Roger E. Thompson, Eric M. Zagzag, David Vibhakar, Rajeev Shin Ra, Young Garre, Maria Luisa Schüller, Ulrich Shofuda, Tomoko Faria, Claudia C. Lopez-Aguilar, Enrique Zadeh, Gelareh Hui, Chi-chung Ramaswamy, Vijay Bailey, Swneke D. Jones, Steven J. M. Mungall, Andrew J. Moore, Richard A. Calarco, John A. Stein, Lincoln Bader, Gary D. Reimand, Jüri Ragoussis, Jiannis Weiss, William A. Marra, Marco A. Suzuki, Hiromichi Taylor, Michael D.
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4.

001-es BibID:BIBFORM040477
Első szerző:Sturm, Dominik
Cím:Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma / Dominik Sturm, Hendrik Witt, Volker Hovestadt, Dong-Anh Khuong-Quang, David T. W. Jones, Carolin Konermann, Elke Pfaff, Martje Tönjes, Martin Sill, Sebastian Bender, Marcel Kool, Marc Zapatka, Natalia Becker, Manuela Zucknick, Thomas Hielscher, Xiao-Yang Liu, Adam M. Fontebasso, Marina Ryzhova, Steffen Albrecht, Karine Jacob, Marietta Wolter, Martin Ebinger, Martin U. Schuhmann, Timothy van Meter, Michael C. Frühwald, Holger Hauch, Arnulf Pekrun, Bernhard Radlwimmer, Tim Niehues, Gregor von Komorowski, Matthias Dürken, Andreas E. Kulozik, Jenny Madden, Andrew Donson, Nicholas K. Foreman, Rachid Drissi, Maryam Fouladi, Wolfram Scheurlen, Andreas von Deimling, Camelia Monoranu, Wolfgang Roggendorf, Christel Herold-Mende, Andreas Unterberg, Christof M. Kramm, Jörg Felsberg, Christian Hartmann, Benedikt Wiestler, Wolfgang Wick, Till Milde, Olaf Witt, Anders M. Lindroth, Jeremy Schwartzentruber, Damien Faury, Adam Fleming, Magdalena Zakrzewska, Pawel P. Liberski, Krzysztof Zakrzewski, Peter Hauser, Miklos Garami, Almos Klekner, Laszlo Bognar, Sorana Morrissy, Florence Cavalli, Michael D. Taylor, Peter van Sluis, Jan Koster, Rogier Versteeg, Richard Volckmann, Tom Mikkelsen, Kenneth Aldape, Guido Reifenberger, V. Peter Collins, Jacek Majewski, Andrey Korshunov, Peter Lichter, Christoph Plass, Nada Jabado, Stefan M. Pfister
Dátum:2012
ISSN:1535-6108
Megjegyzések:Glioblastoma (GBM) is a brain tumor that carries a dismal prognosis and displays considerable heterogeneity. We have recently identified recurrent H3F3A mutations affecting two critical amino acids (K27 and G34) of histone H3.3 in one-third of pediatric GBM. Here, we show that each H3F3A mutation defines an epigenetic subgroup of GBM with a distinct global methylation pattern, and that they are mutually exclusive with IDH1 mutations, which characterize a third mutation-defined subgroup. Three further epigenetic subgroups were enriched for hallmark genetic events of adult GBM and/or established transcriptomic signatures. We also demonstrate that the two H3F3A mutations give rise to GBMs in separate anatomic compartments, with differential regulation of transcription factors OLIG1, OLIG2, and FOXG1, possibly reflecting different cellular origins.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
külföldön készült közlemény
Megjelenés:Cancer Cell. - 22 : 4 (2012), p. 425-437. -
További szerzők:Witt, Hendrik Hovestadt, Volker Khuong-Quang, Dong-Anh Jones, David T. W. Konermann, Carolin Pfaff, Elke Tönjes, Martje Sill, Martin Bender, Sebastian Kool, Marcel Zapatka, Marc Becker, Natalia Zucknick, Manuela Hielscher, Thomas Liu, Xiao-Yang Fontebasso, Adam M. Ryzhova, Marina Albrecht, Stephen Jacob, Karine Wolter, Marietta Ebinger, Martin Schuhmann, Martin U. van Meter, Timothy E. Frühwald, Michael C. Hauch, Holger Pekrun, Arnulf Radlwimmer, Bernhard Niehues, Tim von Komorowski, Gregor Dürken, Matthias Kulozik, Andreas E. Madden, Jenny Donson, Andrew Foreman, Nicholas K. Drissi, Rachid Fouladi, Maryam Scheurlen, Wolfram von Deimling, Andreas Monoranu, Camelia Roggendorf, Wolfgang Herold-Mende, Christel Unterberg, Andreas Kramm, Christoph Felsberg, Jörg Hartmann, Christian Wiestler, Benedikt Wick, Wolfgang Milde, Till Witt, Olaf Lindroth, Anders Schwartzentruber, Jeremy Faury, Damien Fleming, Adam Zakrzewska, Magdalena Liberski, Pawel P. Zakrzewski, Krzystof Hauser Péter Garami Miklós Klekner Álmos (1970-) (idegsebész) Bognár László (1958-) (idegsebész, gyermekidegsebész) Morrissy, Sorana Cavalli, Florence Taylor, Michael D. van Sluis, Peter Koster, Jan Versteeg, Rogier Volckmann, Richard Mikkelsen, Tom Aldape, Kenneth Reifenberger, Guido Collins, V. Peter Majewski, Jacek Korshunov, Andrey Lichter, Peter Plass, Christoph Jabado, Nada Pfister, Stefan M.
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5.

001-es BibID:BIBFORM082160
035-os BibID:(WoS)000493807800049 (Scopus)85074231650 (PMID)31664194
Első szerző:Suzuki, Hiromichi
Cím:Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma / Suzuki, Hiromichi; Kumar, Sachin A.; Shuai, Shimin; Diaz-Navarro, Ander; Gutierrez-Fernandez, Ana; De Antonellis, Pasqualino; Cavalli, Florence M. G.; Juraschka, Kyle; Farooq, Hamza; Shibahara, Ichiyo; Vladoiu, Maria C.; Zhang, Jiao; Abeysundara, Namal; Przelicki, David; Skowron, Patryk; Gauer, Nicole; Luu, Betty; Daniels, Craig; Wu, Xiaochong; Forget, Antoine; Momin, Ali; Wang, Jun; Dong, Weifan; Kim, Seung-Ki; Grajkowska, Wieslawa A.; Jouvet, Anne; Fèvre-Montange, Michelle; Garre, Maria Luisa; Nageswara Rao, Amulya A.; Giannini, Caterina; Kros, Johan M.; French, Pim J.; Jabado, Nada; Ng, Ho-Keung; Poon, Wai Sang; Eberhart, Charles G.; Pollack, Ian F.; Olson, James M.; Weiss, William A.; Kumabe, Toshihiro; López-Aguilar, Enrique; Lach, Boleslaw; Massimino, Maura; Van Meir, Erwin G.; Rubin, Joshua B.; Vibhakar, Rajeev; Chambless, Lola B.; Kijima, Noriyuki; Klekner, Almos; Bognár, László; Chan, Jennifer A.; Faria, Claudia C.; Ragoussis, Jiannis; Pfister, Stefan M.; Goldenberg, Anna; Wechsler-Reya, Robert J.; Bailey, Swneke D.; Garzia, Livia; Morrissy, A. Sorana; Marra, Marco A.; Huang, Xi; Malkin, David; Ayrault, Olivier; Ramaswamy, Vijay; Puente, Xose S.; Calarco, John A.; Stein, Lincoln; Taylor, Michael D.
Dátum:2019
ISSN:0028-0836
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Megjelenés:Nature. - 574 : 7780 (2019), p. 707-711. -
További szerzők:Kumar, Sachin A. Shuai, Shimin Diaz-Navarro, Ander Gutierrez-Fernandez, Ana De Antonellis, Pasqualino Cavalli, Florence M. G. Juraschka, Kyle Farooq, Hamza Shibahara, Ichiyo Vladoiu, Maria C. Zhang, Jiao Abeysundara, Namal Przelicki, David Skowron, Patryk Gauer, Nicole Luu, Betty Daniels, Craig Wu, Xiaochong Forget, Antoine Momin, Ali Wang, Jun Dong, Weifan Kim, Seung-Ki Grajkowska, Wieslawa A. Jouvet, Anne Fèvre-Montange, Michelle Garre, Maria Luisa Nageswara Rao, Amulya A. Giannini, Caterina Kros, Johan M. French, Pim J. Jabado, Nada Ng, Ho-Keung Poon, Wai Sang Eberhart, Charles G. Pollack, Ian F. Olson, James M. Weiss, William A. Kumabe, Toshihiro Lopez-Aguilar, Enrique Lach, Boleslaw Massimino, Maura van Meir, Erwin G. Rubin, Joshua B. Vibhakar, Rajeev Chambless, Lola B. Kijima, Noriyuki Klekner Álmos (1970-) (idegsebész) Bognár László (1958-) (idegsebész, gyermekidegsebész) Chan, Jennifer A. Faria, Claudia C. Ragoussis, Jiannis Pfister, Stefan M. Goldenberg, Anna Wechsler-Reya, Robert J. Bailey, Swneke D. Garzia, Livia Morrissy, Sorana Marra, Marco A. Huang, Xi Malkin, David Ayrault, Olivier Ramaswamy, Vijay Puente, Xose S. Calarco, John A. Stein, Lincoln Taylor, Michael D.
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6.

001-es BibID:BIBFORM066682
Első szerző:Torchia, Jonathon
Cím:Integrated (epi)-Genomic Analyses Identify Subgroup-Specific Therapeutic Targets in CNS Rhabdoid Tumors / Torchia Jonathon, Golbourn Brian, Feng Shengrui, Ho King Ching, Sin-Chan Patrick, Vasiljevic Alexandre, Norman Joseph D., Guilhamon Paul, Garzia Livia, Agamez Natalia R., Lu Mei, Chan Tiffany S. Y., Picard Daniel, de Antonellis Pasqualino, Khuong-Quang Dong-Anh, Planello Aline C., Zeller Constanze, Barsyte-Lovejoy Dalia, Lafay-Cousin Lucie, Letourneau Louis, Bourgey Mathieu, Yu Man, Gendoo Deena M. A., Dzamba Misko, Barszczyk Mark, Medina Tiago, Riemenschneider Alexandra N., Morrissy A. Sorana, Ra Young-Shin, Ramaswamy Vijay, Remke Marc, Dunham Christopher P., Yip Stephen, Ng Ho-keung, Lu Jian-Qiang, Mehta Vivek, Albrecht Steffen, Pimentel Jose, Chan Jennifer A., Somers Gino R., Faria Claudia C., Roque Lucia, Fouladi Maryam, Hoffman Lindsey M., Moore Andrew S., Wang Yin, Choi Seung Ah, Hansford Jordan R., Catchpoole Daniel, Birks Diane K., Foreman Nicholas K., Strother Doug, Klekner Almos, Bognár Laszló, Garami Miklós, Hauser Péter, Hortobágyi Tibor, Wilson Beverly, Hukin Juliette, Carret Anne-Sophie, Van Meter Timothy E., Hwang Eugene I., Gajjar Amar, Chiou Shih-Hwa, Nakamura Hideo, Toledano Helen, Fried Iris, Fults Daniel, Wataya Takafumi, Fryer Chris, Eisenstat David D., Scheineman Katrin, Fleming Adam J., Johnston Donna L., Michaud Jean, Zelcer Shayna, Hammond Robert, Afzal Samina, Ramsay David A., Sirachainan Nongnuch, Hongeng Suradej, Larbcharoensub Noppadol, Grundy Richard G., Lulla Rishi R., Fangusaro Jason R., Druker Harriet, Bartels Ute, Grant Ronald, Malkin David, McGlade C. Jane, Nicolaides Theodore, Tihan Tarik, Phillips Joanna, Majewski Jacek, Montpetit Alexandre, Bourque Guillaume, Bader Gary D., Reddy Alyssa T., Gillespie G. Yancey, Warmuth-Metz Monika, Rutkowski Stefan, Tabori Uri, Lupien Mathieu, Brudno Michael, Schüller Ulrich, Pietsch Torsten, Judkins Alexander R., Hawkins Cynthia E., Bouffet Eric, Kim Seung-Ki, Dirks Peter B., Taylor Michael D., Erdreich-Epstein Anat, Arrowsmith Cheryl H., De Carvalho Daniel D., Rutka James T., Jabado Nada, Huang Annie
Dátum:2016
ISSN:1535-6108
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:Cancer Cell 30 : 6 (2016), p. 891-908. -
További szerzők:Golbourn, Brian Feng, Shengrui Ho, King Ching Sin-Chan, Patrick Vasiljevic, Alexandre Norman, Joseph D. Guilhamon, Paul Garzia, Livia Agamez, Natalia R. Lu, Mei Chan, Tiffany Sin Yu Picard, Daniel De Antonellis, Pasqualino Khuong-Quang, Dong-Anh Planello, Aline C. Zeller, Constanze Barsyte-Lovejoy, Dalia Lafay-Cousin, Lucie Letourneau, Louis Bourgey, Mathieu Yu, Man Gendoo, Deena M. A. Dzamba, Misko Barszczyk, Mark Medina, Tiago Riemenschneider, Alexandra N. Morrissy, Sorana Ra, Young-Shin Ramaswamy, Vijay Remke, Marc Dunham, Christopher P. Yip, Stephen Ng, Ho-Keung Lu, Jian-Qiang Mehta, Vivek Albrecht, Stephen Pimentel, José Chan, Jennifer A. Somers, Gino R. Faria, Claudia C. Roque, Lucia Fouladi, Maryam Hoffman, Lindsey M. Moore, Andrew S. Wang, Yin Choi, Seung Ah Hansford, Jordan R. Catchpoole, Daniel Birks, Diane Foreman, Nicholas K. Strother, Douglas Klekner Álmos (1970-) (idegsebész) Bognár László (1958-) (idegsebész, gyermekidegsebész) Garami Miklós Hauser Péter Hortobágyi Tibor (1965-) (patológus) Wilson, Beverly Hukin, Juliette Carret, Anne-Sophie van Meter, Timothy E. Hwang, Eugene Gajjar, Amar Chiou, Shih-Hwa Nakamura, Hideo Toledano, Helen Fried, Iris Fults, Daniel Wataya, Takafumi Fryer, Chris Eisenstat, David D. Scheineman, Katrin Fleming, Adam Johnston, Donna Michaud, Jean Zelcer, Shayna Hammond, Robert Afzal, Samina Ramsay, David A. Sirachainan, Nongnuch Hongeng, Suradej Larbcharoensub, Noppadol Grundy, Richard G. Lulla, Rishi R. Fangusaro, Jason R. Druker, Harriet Bartels, Ute Grant, Ronald Malkin, David McGlade, C. Jane Nicolaides, Theodore Tihan, Tarik Phillips, Joanna J. Majewski, Jacek Montpetit, Alexandre Bourque, Guillaume Bader, Gary D. Reddy, Alyssa T. Gillespie, G. Yancey Warmuth-Metz, Monika Rutkowski, Stefan Tabori, Uri Lupien, Mathieu Brudno, Michael Schüller, Ulrich Pietsch, Torsten Judkins, Alexander R. Hawkins, Cynthia E. Bouffet, Eric Kim, Seung-Ki Dirks, Peter Taylor, Michael D. Erdreich-Epstein, Anat Arrowsmith, Cheryl H. De Carvalho, Daniel D. Rutka, James T. Jabado, Nada Huang, Annie
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