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Quoted phrase not found in phrase index: "Rearrangement of 3q"
Page 1
Copy-number variations in adult patients with chronic immune thrombocytopenia.
Yucesan E, Hatirnaz Ng O, Yalniz FF, Yilmaz H, Salihoglu A, Sudutan T, Eskazan AE, Ongoren S, Baslar Z, Soysal T, Ozbek U, Sayitoglu M, Ar MC. Yucesan E, et al. Expert Rev Hematol. 2020 Nov;13(11):1277-1287. doi: 10.1080/17474086.2020.1819786. Epub 2020 Sep 23. Expert Rev Hematol. 2020. PMID: 32885695
RESULTS: Several CNV losses and gains were defined (losses:2q,7q,17q,19p, and gains: 1q,2p,3q,4q,7q,10q,12p,13q,14q,15q,17p,20q,21p,22q,Xp). Mosaic changes of different sizes (0.2-17.77Mb) were identified in five patients and three of them showed clonality. ...
RESULTS: Several CNV losses and gains were defined (losses:2q,7q,17q,19p, and gains: 1q,2p,3q,4q,7q,10q,12p,13q,14q,15q,17p,20q,21p,2 …
Biology of HPV in HIV infection.
Palefsky J. Palefsky J. Adv Dent Res. 2006 Apr 1;19(1):99-105. doi: 10.1177/154407370601900120. Adv Dent Res. 2006. PMID: 16672559 Review.
With increasing grades of IN and cancer, the proportion of tissues with copy-number abnormalities (CNA) increases, with one of the most common genetic changes being amplification of chromosome 3q. The presence of CNA is associated with the integration of HPV DNA into the h …
With increasing grades of IN and cancer, the proportion of tissues with copy-number abnormalities (CNA) increases, with one of the most comm …
Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients.
Haltrich I, Kost-Alimova M, Kovács G, Klein G, Fekete G, Imreh S. Haltrich I, et al. Eur J Haematol. 2006 Feb;76(2):124-33. doi: 10.1111/j.1600-0609.2005.00576.x. Eur J Haematol. 2006. PMID: 16405433
We detected non-random 3p losses and 3q gains on well-determined regions in both murine and human tumors using a microcell hybrid-based model system called 'elimination test'. ...The poor outcome in pediatric patients with 3q rearrangements appears to …
We detected non-random 3p losses and 3q gains on well-determined regions in both murine and human tumors using a microcell hyb …
Chromosome abnormalities in adult T-cell leukemia/lymphoma: a karyotype review committee report.
Kamada N, Sakurai M, Miyamoto K, Sanada I, Sadamori N, Fukuhara S, Abe S, Shiraishi Y, Abe T, Kaneko Y, et al. Kamada N, et al. Cancer Res. 1992 Mar 15;52(6):1481-93. Cancer Res. 1992. PMID: 1540956 Clinical Trial.
Of 373 structural abnormalities in all the 103 aneuploid cases, translocations involving 14q32 (28%) or 14q11 (14%) and deletion of 6q (23%) were most frequent, followed by deletion of 10p (9%), 3q (8%), 5q, 9q, and 13q (7% each), and 1p and 7p (6% each). The proportion of …
Of 373 structural abnormalities in all the 103 aneuploid cases, translocations involving 14q32 (28%) or 14q11 (14%) and deletion of 6q (23%) …
Regional cancer cytogenetics: a report on 1,143 diagnostic cases.
Perkins D, Brennan S, Carstairs K, Bailey D, Pantalony D, Poon A, Fernandes B, Dubé I. Perkins D, et al. Cancer Genet Cytogenet. 1997 Jul 1;96(1):64-80. doi: 10.1016/s0165-4608(96)00363-9. Cancer Genet Cytogenet. 1997. PMID: 9209473
Common structural changes observed were changes resulting in loss of material from the long arm of chromosomes 5 and 7, trisomy 8, rearrangements of 11q23, t(15;17), t(8;21), rearrangements of 12q13 and 3q, inversion 16, trisomy 11, Ph, trisomy 21, t(6;9) and …
Common structural changes observed were changes resulting in loss of material from the long arm of chromosomes 5 and 7, trisomy 8, rearra …
Intra-tumour genetic heterogeneity and poor chemoradiotherapy response in cervical cancer.
Cooke SL, Temple J, Macarthur S, Zahra MA, Tan LT, Crawford RA, Ng CK, Jimenez-Linan M, Sala E, Brenton JD. Cooke SL, et al. Br J Cancer. 2011 Jan 18;104(2):361-8. doi: 10.1038/sj.bjc.6605971. Epub 2010 Nov 9. Br J Cancer. 2011. PMID: 21063398 Free PMC article.
METHODS: To investigate intra-tumour genetic heterogeneity and chemoradiation response in advanced cervical cancer, we analysed 10 cases treated on the CTCR-CE01 clinical study. Core biopsies for molecular profiling were taken from four quadrants of the cervix pre-treatmen …
METHODS: To investigate intra-tumour genetic heterogeneity and chemoradiation response in advanced cervical cancer, we analysed 10 cases tre …
Azacitidine treatment for patients with myelodysplastic syndrome and acute myeloid leukemia with chromosome 3q abnormalities.
Wanquet A, Prebet T, Berthon C, Sebert M, Roux C, Kulasekararaj A, Micol JB, Esterni B, Itzykson R, Thepot S, Recher C, Delaunay J, Dreyfus F, Mufti G, Fenaux P, Vey N. Wanquet A, et al. Am J Hematol. 2015 Oct;90(10):859-63. doi: 10.1002/ajh.24099. Epub 2015 Jul 14. Am J Hematol. 2015. PMID: 26113240 Free article.
Acute Myeloid Leukemia (AML) and myelodysplasia (MDS) with chromosome 3q abnormalities have a dismal outcome either untreated or with conventional treatments. ...Median age was 65 years, 40 patients (25%) had inv(3)(q21q26.2) or t(3;3)(q21;q26.2), 36 patients (23%) had oth …
Acute Myeloid Leukemia (AML) and myelodysplasia (MDS) with chromosome 3q abnormalities have a dismal outcome either untreated or with …
Detection of novel copy number variants in uterine leiomyomas using high-resolution SNP arrays.
Bowden W, Skorupski J, Kovanci E, Rajkovic A. Bowden W, et al. Mol Hum Reprod. 2009 Sep;15(9):563-8. doi: 10.1093/molehr/gap050. Epub 2009 Jun 30. Mol Hum Reprod. 2009. PMID: 19567454 Free PMC article.
In the current study, we employed a high resolution SNP microarray on 16 randomly selected ULs and normal myometrium samples to detect submicroscopic (<5 Mb) chromosomal aberrations. ...Novel submicroscopic aberrations on chromosomal segments 1q42.13, 11q13.1 and 13q12. …
In the current study, we employed a high resolution SNP microarray on 16 randomly selected ULs and normal myometrium samples to detec …
Report from the Maryland Epidemiology Schizophrenia Linkage Study: no evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model.
Karayiorgou M, Kasch L, Lasseter VK, Hwang J, Elango R, Bernardini DJ, Kimberland M, Babb R, Francomano CA, Wolyniec PS, et al. Karayiorgou M, et al. Am J Med Genet. 1994 Dec 15;54(4):345-53. doi: 10.1002/ajmg.1320540413. Am J Med Genet. 1994. PMID: 7726207
An initial sample of 39 families, each having two or more affecteds, was available for genotyping candidate genes, candidate regions, and highly polymorphic markers randomly distributed throughout the genome. We used a single complex dominant model (with a disease gene …
An initial sample of 39 families, each having two or more affecteds, was available for genotyping candidate genes, candidate regions, and hi …
Cytogenetics of childhood acute myeloid leukemia: United Kingdom Medical Research Council Treatment trials AML 10 and 12.
Harrison CJ, Hills RK, Moorman AV, Grimwade DJ, Hann I, Webb DK, Wheatley K, de Graaf SS, van den Berg E, Burnett AK, Gibson BE. Harrison CJ, et al. J Clin Oncol. 2010 Jun 1;28(16):2674-81. doi: 10.1200/JCO.2009.24.8997. Epub 2010 May 3. J Clin Oncol. 2010. PMID: 20439644
PATIENTS AND METHODS: This cytogenetic study of 729 childhood patients classified them into 22 subgroups and evaluated their incidence and risk. RESULTS: Rearrangements of 11q23 were the most frequent abnormality found in approximately 16% of patients, with 50% of these in …
PATIENTS AND METHODS: This cytogenetic study of 729 childhood patients classified them into 22 subgroups and evaluated their incidence and r …
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