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Quoted phrase not found in phrase index: "Tetrasomy 17"
Page 1
A novel coexistence of tetrasomy 8 and FLT3-ITD along with variant 3 way translocation t(4;17;15) in acute promyelocytic leukemia: Case study and literature review.
Pais A, Fernandes C, Dalvi R, Bafna V, Pawar R, Chavan D, Ahmad F. Pais A, et al. Cancer Genet. 2022 Apr;262-263:111-117. doi: 10.1016/j.cancergen.2022.02.004. Epub 2022 Feb 16. Cancer Genet. 2022. PMID: 35219054 Review.
Although chromosome 4 is most commonly associated chromosome in three way translocation, present case is the first report with four novel co-existent findings of new break point region on chromosome 4, new cyclic mechanism with simultaneous breaks, presence of a co-existent te …
Although chromosome 4 is most commonly associated chromosome in three way translocation, present case is the first report with four novel co …
Coexistence of tetrasomy 8 and trisomy 8 in acute promyelocytic leukemia (AML-M3) with t(15;17)(q22;q12).
Wang HP, Li GX, Qiao ZH, Ren WY, Wang HW. Wang HP, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2004 Aug;12(4):406-10. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2004. PMID: 15363120
The patient survival time was just 10 days. It is concluded that tetrasomy 8 is secondary cytogenetic event after t(15;17) in this case. It may be a consequence of clonal evolution of trisomy 8. t(15;17) AML-M(3) with tetrasomy 8 heralds a poor prognosis....
The patient survival time was just 10 days. It is concluded that tetrasomy 8 is secondary cytogenetic event after t(15;17) in this ca …
FISH cytogenetics and prognosis in breast and non-small cell lung cancers.
Massoner A, Augustin F, Duba HC, Zojer N, Fiegl M. Massoner A, et al. Cytometry B Clin Cytom. 2004 Nov;62(1):52-6. doi: 10.1002/cyto.b.20023. Cytometry B Clin Cytom. 2004. PMID: 15468329 Free article.
Likewise, in effusions with aneuploidy, there was no difference in overall survival rate among patients with different modal chromosome copy numbers (e.g., trisomy vs. tetrasomy 11) or among patients with a low or high grade of intratumor complexity (defined by the intratu …
Likewise, in effusions with aneuploidy, there was no difference in overall survival rate among patients with different modal chromosome copy …
Schmid-Fraccaro syndrome: severe neurologic features.
Romagna ES, Appel da Silva MC, Ballardin PA. Romagna ES, et al. Pediatr Neurol. 2010 Feb;42(2):151-3. doi: 10.1016/j.pediatrneurol.2009.07.020. Pediatr Neurol. 2010. PMID: 20117756
Schmid-Fraccaro syndrome is a rare genetic disease, characterized by modifications of chromosome 22 (partial trisomy or tetrasomy), accompanied by eye abnormality (coloboma) and anal atresia. ...Life expectancy in Schmid-Fraccaro syndrome depends on the number and variety …
Schmid-Fraccaro syndrome is a rare genetic disease, characterized by modifications of chromosome 22 (partial trisomy or tetrasomy), a …
Tetrasomy 6 and 6q14 deletion are associated with better survival in hepatocellular carcinomas. a fluorescence in situ hybridization study of 77 cases.
Huang SF, Hsu HC, Chen JC, Chie WC, Lai P. Huang SF, et al. Cancer Genet Cytogenet. 2003 Jul 1;144(1):23-30. doi: 10.1016/s0165-4608(02)00860-9. Cancer Genet Cytogenet. 2003. PMID: 12810252
For patients with 6q14 deletion, both disomy and tetrasomy groups had significantly better survival rates than trisomy and hypersomy groups. In contrast, no differences in survival rates could be observed among these four groups for patients without the 6q14 deletion. The …
For patients with 6q14 deletion, both disomy and tetrasomy groups had significantly better survival rates than trisomy and hypersomy …
Isochromosome 7q in adult Wilms' tumors: diagnostic and pathogenetic implications.
Rubin BP, Pins MR, Nielsen GP, Rosen S, Hsi BL, Fletcher JA, Renshaw AA. Rubin BP, et al. Am J Surg Pathol. 2000 Dec;24(12):1663-9. doi: 10.1097/00000478-200012000-00011. Am J Surg Pathol. 2000. PMID: 11117788
Wilms' tumors affecting adults are rare and are thought to have a worse prognosis than similar stage tumors in the pediatric population. To understand these tumors better, the authors reviewed their multi-institutional experience in a series of nine lesions diagnosed as Wi …
Wilms' tumors affecting adults are rare and are thought to have a worse prognosis than similar stage tumors in the pediatric populati …
Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia.
Heerema NA, Raimondi SC, Anderson JR, Biegel J, Camitta BM, Cooley LD, Gaynon PS, Hirsch B, Magenis RE, McGavran L, Patil S, Pettenati MJ, Pullen J, Rao K, Roulston D, Schneider NR, Shuster JJ, Sanger W, Sutcliffe MJ, van Tuinen P, Watson MS, Carroll AJ. Heerema NA, et al. Genes Chromosomes Cancer. 2007 Jul;46(7):684-93. doi: 10.1002/gcc.20451. Genes Chromosomes Cancer. 2007. PMID: 17431878 Free article.
Children with acute lymphoblastic leukemia (ALL) and high hyperdiploidy (>50 chromosomes) are considered to have a relatively good prognosis. The specific extra chromosomes are not random; extra copies of some chromosomes occur more frequently than those of others. ...T …
Children with acute lymphoblastic leukemia (ALL) and high hyperdiploidy (>50 chromosomes) are considered to have a relatively good pro …
Tetrasomy 8 in a patient with acute monoblastic leukemia.
Kim J, Park TS, Song J, Lee KA, Lee SG, Cheong JW, Choi JR. Kim J, et al. Korean J Lab Med. 2008 Aug;28(4):262-6. doi: 10.3343/kjlm.2008.28.4.262. Korean J Lab Med. 2008. PMID: 18728374 Free article.
In contrast to trisomy 8, tetrasomy 8 is a rare chromosomal aberration, in that only 17 reported AML cases with isolated tetrasomy 8 have been documented. ...Here, we report a patient with acute monoblastic leukemia having tetrasomy 8 and a very aggressive di …
In contrast to trisomy 8, tetrasomy 8 is a rare chromosomal aberration, in that only 17 reported AML cases with isolated tetrasomy …
Chromosome-wide aneuploidy study of cultured circulating myeloid progenitor cells from workers occupationally exposed to formaldehyde.
Lan Q, Smith MT, Tang X, Guo W, Vermeulen R, Ji Z, Hu W, Hubbard AE, Shen M, McHale CM, Qiu C, Liu S, Reiss B, Beane-Freeman L, Blair A, Ge Y, Xiong J, Li L, Rappaport SM, Huang H, Rothman N, Zhang L. Lan Q, et al. Carcinogenesis. 2015 Jan;36(1):160-7. doi: 10.1093/carcin/bgu229. Epub 2014 Nov 12. Carcinogenesis. 2015. PMID: 25391402 Free PMC article.
We found statistically significant increases in the frequencies of monosomy, trisomy, tetrasomy and SCAs of multiple chromosomes in exposed workers compared with controls, with particularly notable effects for monosomy 1 [P = 6.02E-06, incidence rate ratio (IRR) = 2.31], m …
We found statistically significant increases in the frequencies of monosomy, trisomy, tetrasomy and SCAs of multiple chromosomes in e …
Chromosomal alterations in exfoliated urothelial cells from bladder cancer cases and healthy men: a prospective screening study.
Bonberg N, Pesch B, Behrens T, Johnen G, Taeger D, Gawrych K, Schwentner C, Wellhäußer H, Kluckert M, Leng G, Nasterlack M, Oberlinner C, Stenzl A, Brüning T. Bonberg N, et al. BMC Cancer. 2014 Nov 20;14:854. doi: 10.1186/1471-2407-14-854. BMC Cancer. 2014. PMID: 25412927 Free PMC article.
A generalized estimating equation model was applied to evaluate the influence of age, smoking, and urine status on CNVs in cells from tumor-free men. RESULTS: Tetrasomy of chromosomes 3, 7 and 17, and DNA loss at 9p21 were the most frequently observed forms of CNV. ...
A generalized estimating equation model was applied to evaluate the influence of age, smoking, and urine status on CNVs in cells from tumor- …
23 results