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  • ...ollaborative project to document and describe chromosome and other genomic abnormalities in cancer. This resource is supported by the [http://www.cancergenomics.org ...es V|V]]''' | '''[[:Category:Diseases W|W]]''' | '''[[:Category:Diseases X|X]]''' | '''[[:Category:Diseases Y|Y]]''' | '''[[:Category:Diseases Z|Z]]'''
    7 KB (905 words) - 03:59, 21 November 2017
  • ...collaborative effort to document and describe chromosome and other genomic abnormalities in cancer. The Wiki style interface allows for real-time editing and conten ...es V|V]]''' | '''[[:Category:Diseases W|W]]''' | '''[[:Category:Diseases X|X]]''' | '''[[:Category:Diseases Y|Y]]''' | '''[[:Category:Diseases Z|Z]]'''
    8 KB (1,008 words) - 23:03, 6 August 2020
  • == Structural == * Structural Abnormalities
    10 KB (1,089 words) - 03:30, 21 November 2017
  • ...es U]] [[Category:Diseases V]] [[Category:Diseases W]] [[Category:Diseases X]] [[Category:Diseases Y]] [[Category:Diseases Z]]
    14 KB (1,459 words) - 03:32, 21 November 2017
  • ...inclusion in any of the other AML groups (i.e. AML with Recurrent Genetic Abnormalities, AML with Myelodysplasia-Related Changes, or Therapy-Related Myeloid Neopla ...3|issn=1528-0020|pmid=21474671}}</ref>. Rearrangement of MYB/GATA1 with t(X;6)(p11;q23) has been reported in four male infants<ref name=":4" /><ref nam
    11 KB (1,534 words) - 03:22, 2 January 2020
  • ...">Arber DA, et al., (2017). Acute myeloid leukaemia with recurrent genetic abnormalities, in World Health Organization Classification of Tumours of Haematopoietic a ...cal fusions are expressed, the ''RBM15''-''MKL1'' fusion on the derivative chromosome 22 is the candidate oncoprotein because it contains all of the putative fun
    10 KB (1,331 words) - 21:10, 29 December 2019
  • ...in >50 chromosome (usually <66), typically without translocations or other structural alterations.   ...tology|volume=99|issue=1|pages=93–100|doi=10.1046/j.1365-2141.1997.3493163.x|issn=0007-1048|pmid=9359508}}</ref> <ref>{{Cite journal|last=Reismüller|fi
    16 KB (2,201 words) - 18:20, 7 November 2020
  • ...ique L.|last2=van Slegtenhorst|first2=Marjon|last3=De Menezes|first3=Renée X.|last4=Cheok|first4=Meyling H.|last5=Buijs-Gladdines|first5=Jessica G. C. A ...p A.|last9=Bräundl|first9=Kathrin|date=2017|title=Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have IGH-CRLF2 and JAK2 mutati
    19 KB (2,674 words) - 01:33, 10 May 2020
  • '''Chromothripsis:''' chromosome 11 (70% of supratentorial tumors) |Epigenetic studies suggest range of abnormalities: balanced or unbalanced genomes
    23 KB (3,015 words) - 15:05, 17 November 2018
  • ...rst9=Kip|date=2012|title=Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas|url=http !Chromosome Number!!Gain/Loss/Amp/LOH!!Region
    16 KB (2,277 words) - 20:48, 1 September 2020
  • ...mphoblastic leukemias. The majority of cases (>80%) fall within the 44-45 chromosome range. However, beyond this, there are three main groups, that although ra ...edscape Article, Drugs & Diseases, Hematology.</ref>. Hypodiploid ALL with chromosome numbers less than 44 is associated with poor prognosis.
    21 KB (2,885 words) - 21:49, 9 May 2020
  • ...Options in Oncology|volume=20|issue=1|pages=9|doi=10.1007/s11864-019-0605-x|issn=1534-6277|pmid=30715612}}</ref>. ...et age and shorter median survival<ref name=":5" />. ''RUNX2'', located on chromosome 6p21, is strongly expressed in pDCs and BPDCN cells. The t(6,8) generates m
    17 KB (2,332 words) - 21:04, 6 March 2020
  • ...noglobulin deposition disease (Randall type). Relationship with structural abnormalities of immunoglobulin chains|url=https://linkinghub.elsevier.com/retrieve/pii/S ...age=en|volume=125|issue=6|pages=681–700|doi=10.1111/j.1365-2141.2004.04970.x|issn=0007-1048}}</ref>
    40 KB (5,557 words) - 22:42, 29 July 2020