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Items: 1 to 20 of 77

1.
MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion
Laura Fontana, Silvia Tabano, Eleonora Bonaparte, Giovanni Marfia, Chiara Pesenti, Rossella Falcone, Claudia Augello, Nicole Carlessi, Rosamaria Silipigni, Silvana Guerneri, Rolando Campanella, Manuela Caroli, Silvia Maria Sirchia, Silvano Bosari, Monica Miozzo
J Neuropathol Exp Neurol. 2016 Aug; 75(8): 791–800. Published online 2016 Jun 24. doi: 10.1093/jnen/nlw052
PMCID:
PMC5409217
AbstractArticlePDF–843K
2.
Clinical and genetic characterization of patients with Pierre Robin sequence and spinal disease: review of the literature and novel terminal 10q deletion
Anudeep Yekula, Connor Grant, Mihir Gupta, David R. Santiago-Dieppa, Pate J. Duddleston, David Gonda, Michael Levy
Childs Nerv Syst. 2020; 36(7): 1367–1377. Published online 2020 May 12. doi: 10.1007/s00381-020-04642-2
PMCID:
PMC7300078
AbstractArticlePDF–523K
3.
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Hinke F van Thuijl, Ilari Scheinin, Daoud Sie, Agusti Alentorn, Hendrik F van Essen, Martijn Cordes, Ruth Fleischeuer, Anja M Gijtenbeek, Guus Beute, Wimar A van den Brink, Gerrit A Meijer, Miek Havenith, Ahmed Idbaih, Khê Hoang-Xuan, Karima Mokhtari, Roel GW Verhaak, Paul van der Valk, Mark A van de Wiel, Jan J Heimans, Eleonora Aronica, Jaap C Reijneveld, Pieter Wesseling, Bauke Ylstra
Genome Biol. 2014; 15(9): 471. Published online 2014 Sep 23. doi: 10.1186/s13059-014-0471-6
PMCID:
PMC4195855
AbstractArticlePDF–1.8M
4.
Distinct genomic alterations in prostate cancers in Chinese and Western populations suggest alternative pathways of prostate carcinogenesis
Xueying Mao, Yongwei Yu, Lara K Boyd, Guoping Ren, Dongmei Lin, Tracy Chaplin, Sakunthala C. Kudahetti, Elzbieta Stankiewicz, Liyan Xue, Luis Beltran, Manu Gupta, R. Tim D. Oliver, Nick R Lemoine, Dan M. Berney, Bryan D. Young, Yong-Jie Lu
Cancer Res. Author manuscript; available in PMC 2011 Jan 1.
Published in final edited form as: Cancer Res. 2010 Jul 1; 70(13): 5207–5212. Published online 2010 Jun 1. doi: 10.1158/0008-5472.CAN-09-4074
PMCID:
PMC2896548
AbstractArticlePDF–918K
5.
Contribution of 1p, 19q, 9p and 10q Automated Analysis by FISH to the Diagnosis and Prognosis of Oligodendroglial Tumors According to WHO 2016 Guidelines
Karine Michaud, Marie de Tayrac, Myreille D’Astous, Céline Duval, Claudie Paquet, Oumar Samassekou, Peter Vincent Gould, Stéphan Saikali
PLoS One. 2016; 11(12): e0168728. Published online 2016 Dec 28. doi: 10.1371/journal.pone.0168728
PMCID:
PMC5193469
AbstractArticlePDF–2.2M
6.
Pediatric and adult sonic hedgehog medulloblastomas are clinically and molecularly distinct
Paul A. Northcott, Thomas Hielscher, Adrian Dubuc, Stephen Mack, David Shih, Marc Remke, Hani Al-Halabi, Steffen Albrecht, Nada Jabado, Charles G. Eberhart, Wieslawa Grajkowska, William A. Weiss, Steven C. Clifford, Eric Bouffet, James T. Rutka, Andrey Korshunov, Stefan Pfister, Michael D. Taylor
Acta Neuropathol. Author manuscript; available in PMC 2015 Aug 17.
Published in final edited form as: Acta Neuropathol. 2011 Aug; 122(2): 231–240. Published online 2011 Jun 17. doi: 10.1007/s00401-011-0846-7
PMCID:
PMC4538327
AbstractArticlePDF–715K
7.
Concurrent somatic KRAS mutation and germline 10q22.3-q23.2 deletion in a patient with juvenile myelomonocytic leukemia, developmental delay, and multiple malformations: a case report
Ruen Yao, Tingting Yu, Yufei Xu, Guoqiang Li, Lei Yin, Yunfang Zhou, Jian Wang, Zhilong Yan
BMC Med Genomics. 2018; 11: 60. Published online 2018 Jul 16. doi: 10.1186/s12920-018-0377-3
PMCID:
PMC6048798
AbstractArticlePDF–722K
8.
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
Acta Neuropathol. 2013; 126(6): 917–929. Published online 2013 Oct 31. doi: 10.1007/s00401-013-1198-2
PMCID:
PMC3830749
AbstractArticlePDF–800K
9.
Association between glioma susceptibility loci and tumour pathology defines specific molecular etiologies
Anna Luisa Di Stefano, Victor Enciso-Mora, Yannick Marie, Virginie Desestret, Marianne Labussière, Blandine Boisselier, Karima Mokhtari, Ahmed Idbaih, Khe Hoang-Xuan, Jean-Yves Delattre, Richard S. Houlston, Marc Sanson
Neuro Oncol. 2013 May; 15(5): 542–547. Published online 2012 Nov 16. doi: 10.1093/neuonc/nos284
PMCID:
PMC3635509
AbstractArticlePDF–138K
10.
An unbalanced translocation involving loss of 10q26.2 and gain of 11q25 in a pedigree with autism spectrum disorder and cerebellar juvenile pilocytic astrocytoma
Hassan M. Minhas, Matthew F. Pescosolido, Matthew Schwede, Justyna Piasecka, John Gaitanis, Umadevi Tantravahi, Eric M. Morrow
Am J Med Genet A. Author manuscript; available in PMC 2014 Apr 1.
Published in final edited form as: Am J Med Genet A. 2013 Apr; 161(4): 787–791. Published online 2013 Mar 12. doi: 10.1002/ajmg.a.35841
PMCID:
PMC3606653
AbstractArticlePDF–790K
11.
A case of interstitial deletion of 10q25.2----q26.1.
D E Rooney, K Williams, D V Coleman, A Habel
J Med Genet. 1989 Jan; 26(1): 58–60. doi: 10.1136/jmg.26.1.58
PMCID:
PMC1015539
SummaryPage BrowsePDF–485K
12.
Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities
J B Ravnan, J H Tepperberg, P Papenhausen, A N Lamb, J Hedrick, D Eash, D H Ledbetter, C L Martin
J Med Genet. 2006 Jun; 43(6): 478–489. Published online 2005 Sep 30. doi: 10.1136/jmg.2005.036350
PMCID:
PMC2564531
AbstractArticlePDF–984K
13.
Somatic mutation of PTEN in bladder carcinoma
J S Aveyard, A Skilleter, T Habuchi, M A Knowles
Br J Cancer. 1999 May; 80(5-6): 904–908. doi: 10.1038/sj.bjc.6690439
PMCID:
PMC2362287
SummaryPDF–120K
14.
Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p.
I. Petersen, H. Langreck, G. Wolf, A. Schwendel, R. Psille, P. Vogt, M. B. Reichel, T. Ried, M. Dietel
Br J Cancer. 1997; 75(1): 79–86. doi: 10.1038/bjc.1997.13
PMCID:
PMC2222682
SummaryPage BrowsePDF–1.8M
15.
Loss of heterozygosity analysis of keratoacanthoma reveals multiple differences from cutaneous squamous cell carcinoma.
A. J. Waring, M. Takata, I. Rehman, J. L. Rees
Br J Cancer. 1996 Mar; 73(5): 649–653. doi: 10.1038/bjc.1996.113
PMCID:
PMC2074334
SummaryPage BrowsePDF–1.6M
16.
Chromosomal alterations in the clonal evolution to the metastatic stage ofquamous cell carcinomas of the lung
S Petersen, M Aninat-Meyer, K Schlüns, K Gellert, M Dietel, I Petersen
Br J Cancer. 2000 Jan; 82(1): 65–73. Published online 1999 Dec 8. doi: 10.1054/bjoc.1999.0878
PMCID:
PMC2363206
SummaryPDF–348K
17.
High-resolution genome-wide allelotype analysis identifies loss of chromosome 14q as a recurrent genetic alteration in astrocytic tumours
J Hu, JC-s Pang, CY-k Tong, B Lau, X-l Yin, W-S Poon, C-C Jiang, L-F Zhou, H-K Ng
Br J Cancer. 2002 Jul 15; 87(2): 218–224. Published online 2002 Jul 2. doi: 10.1038/sj.bjc.6600430
PMCID:
PMC2376105
AbstractArticlePDF–133K
18.
Deletion mapping of gliomas suggest the presence of two small regions for candidate tumor-suppressor genes in a 17-cM interval on chromosome 10q.
R. Albarosa, B. M. Colombo, L. Roz, I. Magnani, B. Pollo, N. Cirenei, C. Giani, A. M. Conti, S. DiDonato, G. Finocchiaro
Am J Hum Genet. 1996 Jun; 58(6): 1260–1267.
PMCID:
PMC1915052
SummaryPage BrowsePDF–2.1M
19.
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.
J. A. Kaukonen, P. Amati, A. Suomalainen, A. Rötig, M. G. Piscaglia, F. Salvi, J. Weissenbach, G. Fratta, G. Comi, L. Peltonen, M. Zeviani
Am J Hum Genet. 1996 Apr; 58(4): 763–769.
PMCID:
PMC1914672
SummaryPage BrowsePDF–1.1M
20.
Molecular analysis of anaplastic oligodendroglial tumors in a prospective randomized study: A report from EORTC study 26951
Mathilde C.M. Kouwenhoven, Thierry Gorlia, Johan M. Kros, Ahmed Ibdaih, Alba A. Brandes, Jacolien E.C. Bromberg, Karima Mokhtari, Sjoerd G. van Duinen, Johannes L. Teepen, Pieter Wesseling, Fanny Vandenbos, Wolfgang Grisold, László Sipos, Rene Mirimanoff, Charles J. Vecht, Anouk Allgeier, Denis Lacombe, Martin J. van den Bent
Neuro Oncol. 2009 Dec; 11(6): 737–746. doi: 10.1215/15228517-2009-011
PMCID:
PMC2802394
AbstractArticlePDF–353K

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