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

Year Number of Results
1970 1
1976 1
1979 1
1980 4
1981 2
1983 3
1984 2
1985 2
1986 1
1987 2
1988 3
1989 2
1990 2
1991 3
1992 2
1993 1
1994 2
1995 5
1996 6
1997 6
1998 5
1999 5
2000 7
2001 10
2002 9
2003 5
2004 6
2005 10
2006 9
2007 12
2008 9
2009 17
2010 22
2011 25
2012 22
2013 15
2014 15
2015 18
2016 16
2017 15
2018 12
2019 10
2020 13
2021 20
2022 10
2023 13
2024 3

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345 results

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Page 1
Genomic and transcriptomic profiling reveals distinct molecular subsets associated with outcomes in mantle cell lymphoma.
Yi S, Yan Y, Jin M, Bhattacharya S, Wang Y, Wu Y, Yang L, Gine E, Clot G, Chen L, Yu Y, Zou D, Wang J, Phan AT, Cui R, Li F, Sun Q, Zhai Q, Wang T, Yu Z, Liu L, Liu W, Lyv R, Sui W, Huang W, Xiong W, Wang H, Li C, Xiao Z, Hao M, Wang J, Cheng T, Bea S, Herrera AF, Danilov A, Campo E, Ngo VN, Qiu L, Wang L. Yi S, et al. J Clin Invest. 2022 Feb 1;132(3):e153283. doi: 10.1172/JCI153283. J Clin Invest. 2022. PMID: 34882582 Free PMC article. Clinical Trial.
C1 featured mutated immunoglobulin heavy variable (IGHV), CCND1 mutation, amp(11q13), and active B cell receptor (BCR) signaling. C2 was enriched with del(11q)/ATM mutations and upregulation of NF-kappaB and DNA repair pathways. C3 was characterized by mutations in SP140, …
C1 featured mutated immunoglobulin heavy variable (IGHV), CCND1 mutation, amp(11q13), and active B cell receptor (BCR) signaling. C2 was enr …
An Anomaly with Potential as a New Prognostic Marker in CLL with del(13q): Gain of 16p13.3.
Isik S, Gunden G, Gunduz E, Akay OM, Aslan A, Ozen H, Cilingir O, Erzurumluoglu Gokalp E, Kocagil S, Artan S, Gulbas Z, Durak Aras B. Isik S, et al. Cytogenet Genome Res. 2021;161(10-11):479-487. doi: 10.1159/000520242. Epub 2021 Dec 15. Cytogenet Genome Res. 2021. PMID: 34915466
Deletion 13q [del(13q)] is a favorable prognostic marker if it is detected as a sole abnormality in chronic lymphocytic leukemia (CLL). However the clinical courses of cases with isolated del(13q) are quite heterogeneous. In our study, we invest …
Deletion 13q [del(13q)] is a favorable prognostic marker if it is detected as a sole abnormality in chronic lymphocytic …
Myeloproliferative disorders.
Bench AJ, Cross NC, Huntly BJ, Nacheva EP, Green AR. Bench AJ, et al. Best Pract Res Clin Haematol. 2001 Sep;14(3):531-51. doi: 10.1053/beha.2001.0153. Best Pract Res Clin Haematol. 2001. PMID: 11640868 Review.
Consistent acquired changes seen at diagnosis include deletion of the long arm of chromosome 20, del(13q), trisomy 8 and 9 and duplication of parts of 1q. Furthermore del(20q), trisomy 8 and dupl(lq) all arise in multipotent progenitor cells. Molecular mappin …
Consistent acquired changes seen at diagnosis include deletion of the long arm of chromosome 20, del(13q), trisomy 8 and 9 and …
Precision diagnostics in chronic lymphocytic leukemia: Past, present and future.
Mollstedt J, Mansouri L, Rosenquist R. Mollstedt J, et al. Front Oncol. 2023 Mar 21;13:1146486. doi: 10.3389/fonc.2023.1146486. eCollection 2023. Front Oncol. 2023. PMID: 37035166 Free PMC article. Review.
In diagnostics of patients with chronic lymphocytic leukemia (CLL), we currently apply fluorescence in situ hybridization (FISH)-based analysis to detect recurrent chromosomal aberrations (del(11q), del(13q), del(17p) and trisomy 12) as well as targete …
In diagnostics of patients with chronic lymphocytic leukemia (CLL), we currently apply fluorescence in situ hybridization (FISH)-based analy …
Impact of trisomy 12, del(13q), del(17p), and del(11q) on the immunophenotype, DNA ploidy status, and proliferative rate of leukemic B-cells in chronic lymphocytic leukemia.
Quijano S, López A, Rasillo A, Sayagués JM, Barrena S, Sánchez ML, Teodosio C, Giraldo P, Giralt M, Pérez MC, Romero M, Perdiguer L, Orfao A. Quijano S, et al. Cytometry B Clin Cytom. 2008 May;74(3):139-49. doi: 10.1002/cyto.b.20390. Cytometry B Clin Cytom. 2008. PMID: 18061951 Free article.
B-cell chronic lymphocytic leukemia (B-CLL) is a well-defined clinical entity with heterogeneous molecular and cytogenetic features. Here, we analyze the impact of trisomy 12, del(13q), del(17p), and del(11q) as determined by interphase fluorescence in …
B-cell chronic lymphocytic leukemia (B-CLL) is a well-defined clinical entity with heterogeneous molecular and cytogenetic features. Here, w …
13q-/r(13) mosaicism.
Niikawa N, Tamura T, Tomiyasu F, Kajii T. Niikawa N, et al. J Med Genet. 1980 Aug;17(4):316-9. doi: 10.1136/jmg.17.4.316. J Med Genet. 1980. PMID: 7205909 Free PMC article.
A 2-month-old female infant with typical features of the 13q-syndrome was found to be a hitherto unreported mosaic consisting of 46,XX,del(13)(q22)-46,XX,r(13)(p13q22). Both of the 13q- and r(13) chromosomes were Ag N banding positive. Therefore, it was assum …
A 2-month-old female infant with typical features of the 13q-syndrome was found to be a hitherto unreported mosaic consisting of 46,X …
Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature.
Kotani T, Tsuda H, Ito Y, Nakamura N, Ushida T, Imai K, Iitani Y, Fuma K, Muramatsu Y, Hayakawa M, Kajiyama H. Kotani T, et al. J Med Case Rep. 2022 Dec 27;16(1):481. doi: 10.1186/s13256-022-03713-z. J Med Case Rep. 2022. PMID: 36572904 Free PMC article. Review.
BACKGROUND: Chromosome 13q deletion syndrome shows variable clinical features related to the different potential breakpoints in chromosome 13q. ...The infant presented with isolated esophageal atresia (Gross type A), Dandy-Walker malformation, right microphthalmia, …
BACKGROUND: Chromosome 13q deletion syndrome shows variable clinical features related to the different potential breakpoints in chrom …
Cytogenetic Abnormalities in Myelodysplastic Syndromes: An Overview.
Zahid MF, Malik UA, Sohail M, Hassan IN, Ali S, Shaukat MHS. Zahid MF, et al. Int J Hematol Oncol Stem Cell Res. 2017 Jul 1;11(3):231-239. Int J Hematol Oncol Stem Cell Res. 2017. PMID: 28989590 Free PMC article. Review.
Karyotype is one of the main constituents of the International Prognostic Scoring System (IPSS) and revised-IPSS that are the cornerstones for the prognostication of patients with myelodysplastic syndromes (MDS). Del(5q), -7/del(7q), +8 and -Y are among the most ext …
Karyotype is one of the main constituents of the International Prognostic Scoring System (IPSS) and revised-IPSS that are the cornerstones f …
Fold-back mechanism originating inv-dup-del rearrangements in chromosomes 13 and 15.
Burssed B, Zamariolli M, Favilla BP, Meloni VA, Goloni-Bertollo EM, Bellucco FT, Melaragno MI. Burssed B, et al. Chromosome Res. 2023 Feb 24;31(1):10. doi: 10.1007/s10577-023-09720-0. Chromosome Res. 2023. PMID: 36826604
Inverted duplications associated with terminal deletions, known as inv-dup-del rearrangements, were found in 13q and 15q in these patients. ...
Inverted duplications associated with terminal deletions, known as inv-dup-del rearrangements, were found in 13q and 15q in th …
Rare cytogenetic abnormalities in myelodysplastic syndromes.
Bacher U, Schanz J, Braulke F, Haase D. Bacher U, et al. Mediterr J Hematol Infect Dis. 2015 May 1;7(1):e2015034. doi: 10.4084/MJHID.2015.034. eCollection 2015. Mediterr J Hematol Infect Dis. 2015. PMID: 25960862 Free PMC article. Review.
The karyotype represents one of the main cornerstones for the International Prognostic Scoring System (IPSS) and the revised IPSS-R (IPSS-R) that are most widely used for prognostication in patients with myelodysplastic syndromes (MDS). The most frequent cytogenetic abnormalities …
The karyotype represents one of the main cornerstones for the International Prognostic Scoring System (IPSS) and the revised IPSS-R (IPSS-R) …
345 results