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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1979 1
1985 1
1986 3
1987 1
1989 1
1990 2
1991 1
1992 3
1994 3
1995 3
1996 1
1997 1
1998 4
1999 2
2000 2
2001 2
2002 7
2003 3
2004 3
2005 3
2007 2
2008 1
2009 1
2010 3
2011 2
2013 1
2014 1
2015 1
2016 1
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2020 3
2023 2
2024 0

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64 results

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Quoted phrase not found in phrase index: "Rearrangement of 3q"
Page 1
Role of chromosomal imbalances in the pathogenesis of DSD: A retrospective analysis of 115 prenatal samples.
Mary L, Fradin M, Pasquier L, Quelin C, Loget P, Le Lous M, Le Bouar G, Nivot-Adamiak S, Lokchine A, Dubourg C, Jauffret V, Nouyou B, Henry C, Launay E, Odent S, Jaillard S, Belaud-Rotureau MA. Mary L, et al. Eur J Med Genet. 2023 Jun;66(6):104748. doi: 10.1016/j.ejmg.2023.104748. Epub 2023 Mar 21. Eur J Med Genet. 2023. PMID: 36948288 Free article. Review.
Almost half of the cases resulted from an unbalanced chromosomal rearrangement. Chromosome 9p/q, 4p/q, 3q and 11q anomalies were more frequently observed. ...
Almost half of the cases resulted from an unbalanced chromosomal rearrangement. Chromosome 9p/q, 4p/q, 3q and 11q anomalies we …
Impact of chromosome alterations, genetic mutations and clonal hematopoiesis of indeterminate potential (CHIP) on the classification and risk stratification of MDS.
Ganguly BB, Banerjee D, Agarwal MB. Ganguly BB, et al. Blood Cells Mol Dis. 2018 Mar;69:90-100. doi: 10.1016/j.bcmd.2017.10.001. Epub 2017 Oct 16. Blood Cells Mol Dis. 2018. PMID: 29079134 Review.
The advent of technological development has undoubtedly advanced biological and molecular inputs for better understanding the heterogeneous hematopoietic pre-malignant disorder of the stem cells known as myelodysplastic syndromes (MDS). Chromosomal rearrangements, includin …
The advent of technological development has undoubtedly advanced biological and molecular inputs for better understanding the heterogeneous …
The complex landscape of genetic alterations in mantle cell lymphoma.
Royo C, Salaverria I, Hartmann EM, Rosenwald A, Campo E, Beà S. Royo C, et al. Semin Cancer Biol. 2011 Nov;21(5):322-34. doi: 10.1016/j.semcancer.2011.09.007. Epub 2011 Sep 18. Semin Cancer Biol. 2011. PMID: 21945515 Review.
Several aberrations have been found to be associated with worse prognosis, 3q gains and losses of 8p, 9p, and 17p. An increased number of secondary alterations and blastoid morphology have also been shown to be associated with cases with short survival. On the contrary, in …
Several aberrations have been found to be associated with worse prognosis, 3q gains and losses of 8p, 9p, and 17p. An increased numbe …
High frequency of BCL2 gene rearrangement-negative follicular lymphoma in northwestern Italy.
Magnoli F, Marchiori D, Facchi S, Martin V, Campiotti L, Merli M, Sessa F, Tibiletti MG, Uccella S. Magnoli F, et al. Cancer Genet. 2023 Jun;274-275:1-9. doi: 10.1016/j.cancergen.2023.03.001. Epub 2023 Mar 6. Cancer Genet. 2023. PMID: 36917896
Karyotype analysis was available in a subset of cases. BCL2 rearrangements were detected in 39 cases (51,3%). Of the remaining 37, 6 showed IGH rearrangement, and were further tested: 1 showed variant BCL2 translocation, 1 had BCL6 rearrangement, and the othe …
Karyotype analysis was available in a subset of cases. BCL2 rearrangements were detected in 39 cases (51,3%). Of the remaining 37, 6 …
Retrospective evaluation of the clinical and laboratory data from 300 patients of various hematological malignancies with chromosome 3 abnormalities.
Liu D, Zhang Y, Chen S, Pan J, He X, Liang J, Chen Z. Liu D, et al. Cancer Genet. 2015 Jun;208(6):333-40. doi: 10.1016/j.cancergen.2015.03.013. Epub 2015 Apr 9. Cancer Genet. 2015. PMID: 26032184
This retrospective study was designed to evaluate the clinical and laboratory behaviors of chromosome 3 abnormalities by analyzing the morphological, cytogenetic, and follow-up data from 300 patients of various hematological malignancies with chromosome 3 abnormalities. From the …
This retrospective study was designed to evaluate the clinical and laboratory behaviors of chromosome 3 abnormalities by analyzing the morph …
Atypical 3q26/MECOM rearrangements genocopy inv(3)/t(3;3) in acute myeloid leukemia.
Ottema S, Mulet-Lazaro R, Beverloo HB, Erpelinck C, van Herk S, van der Helm R, Havermans M, Grob T, Valk PJM, Bindels E, Haferlach T, Haferlach C, Smeenk L, Delwel R. Ottema S, et al. Blood. 2020 Jul 9;136(2):224-234. doi: 10.1182/blood.2019003701. Blood. 2020. PMID: 32219447 Free article.
The full-length MECOM transcript, MDS1-EVI1, is not expressed as the result of the 3q26 rearrangement. Besides the classical inv(3)/t(3;3), a number of other 3q26/MECOM rearrangements with poor treatment response have been reported in AML. ...Therefore, we conclude …
The full-length MECOM transcript, MDS1-EVI1, is not expressed as the result of the 3q26 rearrangement. Besides the classical inv(3)/t …
Molecular cytogenetic characterization of pancreas cancer cell lines reveals high complexity chromosomal alterations.
Griffin CA, Morsberger L, Hawkins AL, Haddadin M, Patel A, Ried T, Schrock E, Perlman EJ, Jaffee E. Griffin CA, et al. Cytogenet Genome Res. 2007;118(2-4):148-56. doi: 10.1159/000108295. Cytogenet Genome Res. 2007. PMID: 18000365 Review.
Comparative genomic hybridization (CGH) analysis of all 15 lines identified genomic gains of 3q, 8q, 11q, 17q, and chromosome 20 in nine or more cell lines. ...Multicolor FISH (Spectral Karyotyping, or SKY) of 11 lines identified many complex structural chromosomal aberrat …
Comparative genomic hybridization (CGH) analysis of all 15 lines identified genomic gains of 3q, 8q, 11q, 17q, and chromosome 20 in n …
The value of molecular genetic analysis in the diagnosis and prognosis of renal cell tumours.
Kovacs G. Kovacs G. World J Urol. 1994;12(2):64-8. doi: 10.1007/BF00184238. World J Urol. 1994. PMID: 8087142 Review.
Chromophobe renal cell carcinomas are marked by a highly specific combination of loss of chromosomes 1, 2, 6, 10, 13, 17 and 21 and gross rearrangement of mitochondrial DNA. Subsets of renal oncocytomas show minimal karyotype alterations or translocation 11q13;? ...There a …
Chromophobe renal cell carcinomas are marked by a highly specific combination of loss of chromosomes 1, 2, 6, 10, 13, 17 and 21 and gross …
Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patients.
Ribeiro IP, Carreira IM, Esteves L, Caramelo F, Liehr T, Melo JB. Ribeiro IP, et al. Genomics. 2020 Jan;112(1):297-303. doi: 10.1016/j.ygeno.2019.02.009. Epub 2019 Feb 23. Genomics. 2020. PMID: 30802597 Free article.
Array-CGH was performed in HNSCC patients and the chromosomal breakpoints involved in gene amplification/loss were analyzed. Frequent breakpoints were clustered in chromosomes 12p, 8p, 3q, 14q, 6p, 4q, Xq and 8q. ...We conclude that in our cohort specific peri-centr …
Array-CGH was performed in HNSCC patients and the chromosomal breakpoints involved in gene amplification/loss were analyzed. Frequent …
Identification of two subgroups of mantle cell leukemia with distinct clinical and biological features.
Vizcarra E, Martínez-Climent JA, Benet I, Marugan I, Terol MJ, Prosper F, Marco J, Sanchez D, Ferrandez A, Tormo M, Sarsotti E, Ferrer R, García M, Ortuño F, Montagud M, García-Conde J. Vizcarra E, et al. Hematol J. 2001;2(4):234-41. doi: 10.1038/sj.thj.6200111. Hematol J. 2001. PMID: 11920255
METHODS: Seven cases of MCLeu with t(11;14)(q13;q32) and BCL1-IGH gene rearrangement were ascertained among 140 newly diagnosed chronic B-cell lymphoproliferative disorders with leukemic expression. ...Comparative genomic hybridization analysis identified genomic im …
METHODS: Seven cases of MCLeu with t(11;14)(q13;q32) and BCL1-IGH gene rearrangement were ascertained among 140 newly diagnose …
64 results