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1.
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.
Internet cím:
Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
Borító:
Saját polcon:
2.
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.
Internet cím:
Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
Borító:
Saját polcon:
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.
Internet cím:
Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
Borító:
Saját polcon:
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.
Internet cím:
Szerző által megadott URL
DOI
Intézményi repozitóriumban (DEA) tárolt változat
Borító:
Saját polcon:
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.
Internet cím:
Szerző által megadott URL
DOI
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Saját polcon:
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
Internet cím:
DOI
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