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Quoted phrase not found in phrase index: "Gain of Chromosome 13"
Page 1
Parent-reported histories of adults with trisomy 13 syndrome.
Lebedoff AN, Carey JC. Lebedoff AN, et al. Am J Med Genet A. 2021 Jun;185(6):1743-1756. doi: 10.1002/ajmg.a.62165. Epub 2021 Mar 22. Am J Med Genet A. 2021. PMID: 33750000
The goal of this study was to collect the medical histories of adult individuals (18 years old) with apparent non-mosaic trisomy 13/Patau syndrome to help gain further insight in to the clinical course for individuals with this condition and to characterize the manifestati …
The goal of this study was to collect the medical histories of adult individuals (18 years old) with apparent non-mosaic trisomy 13/Patau sy …
Germline CHEK2 and ATM Variants in Myeloid and Other Hematopoietic Malignancies.
Stubbins RJ, Korotev S, Godley LA. Stubbins RJ, et al. Curr Hematol Malig Rep. 2022 Aug;17(4):94-104. doi: 10.1007/s11899-022-00663-7. Epub 2022 Jun 8. Curr Hematol Malig Rep. 2022. PMID: 35674998 Review.
Peripheral blood shows a small population of lymphocytes with a chronic lymphocytic leukemia immunophenotype, and FISH demonstrates a complex karyotype: gain of one to two copies of IGH and FGFR3; gain of two copies of CDKN2C at 1p32.3; gain of two copies of …
Peripheral blood shows a small population of lymphocytes with a chronic lymphocytic leukemia immunophenotype, and FISH demonstrates a comple …
Clinical characteristics and treatment outcomes of newly diagnosed multiple myeloma with chromosome 1q abnormalities.
Abdallah N, Greipp P, Kapoor P, Gertz MA, Dispenzieri A, Baughn LB, Lacy MQ, Hayman SR, Buadi FK, Dingli D, Go RS, Hwa YL, Fonder A, Hobbs M, Lin Y, Leung N, Kourelis T, Warsame R, Siddiqui M, Lust J, Kyle RA, Bergsagel L, Ketterling R, Rajkumar SV, Kumar SK. Abdallah N, et al. Blood Adv. 2020 Aug 11;4(15):3509-3519. doi: 10.1182/bloodadvances.2020002218. Blood Adv. 2020. PMID: 32750129 Free PMC article.
A gain in chromosome 1q (+1q) is among the most common cytogenetic abnormalities in multiple myeloma (MM). ...We included 1376 Mayo Clinic patients diagnosed with MM from 2005 to 2018 who underwent fluorescence in situ hybridization testing at diagnosis with a panel includ …
A gain in chromosome 1q (+1q) is among the most common cytogenetic abnormalities in multiple myeloma (MM). ...We included 1376 Mayo C …
Cytogenetic analysis in the examination of solid tumors in children.
Mertens F, Mandahl N, Mitelman F, Heim S. Mertens F, et al. Pediatr Hematol Oncol. 1994 Jul-Aug;11(4):361-77. doi: 10.3109/08880019409140536. Pediatr Hematol Oncol. 1994. PMID: 7947009 Review.
At the cytogenetic level, however, aberrations of 13q are seen in less than 25% of retinoblastomas; instead, the presumably progression-related i(6p) and aberrations leading to gain of 1q predominate, each being present in one-third of the tumors. ...Most osteosarcomas are …
At the cytogenetic level, however, aberrations of 13q are seen in less than 25% of retinoblastomas; instead, the presumably progression-rela …
Pathogenesis of testicular germ cell tumours.
Looijenga LH, Oosterhuis JW. Looijenga LH, et al. Rev Reprod. 1999 May;4(2):90-100. doi: 10.1530/ror.0.0040090. Rev Reprod. 1999. PMID: 10357096 Review.
The pathogenetically relevant genes on 12p11.2-p12.1 are probably on a fragment of about 1.7 mb. Gain of 12p sequences may be related to invasive growth. Gain of chromosome 9 is the only consistent chromosomal anomaly of spermatocytic seminomas. ...
The pathogenetically relevant genes on 12p11.2-p12.1 are probably on a fragment of about 1.7 mb. Gain of 12p sequences may be related …
Biology and therapy of pediatric rhabdomyosarcoma.
Pappo AS, Shapiro DN, Crist WM, Maurer HM. Pappo AS, et al. J Clin Oncol. 1995 Aug;13(8):2123-39. doi: 10.1200/JCO.1995.13.8.2123. J Clin Oncol. 1995. PMID: 7636557 Review.
Recognition of prognostically important patient groups primarily identified by tumor extent, site, and histology, and development of effective risk-based multimodal therapy in randomized trials, have increased long-term survival in RMS from 25% in 1970 to more than 70% in current …
Recognition of prognostically important patient groups primarily identified by tumor extent, site, and histology, and development of effecti …
Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India.
Govindasamy P, Pandurangan P, Tarigopula A, Mani R, R Samuel C. Govindasamy P, et al. Asian Pac J Cancer Prev. 2019 Jan 25;20(1):235-241. doi: 10.31557/APJCP.2019.20.1.235. Asian Pac J Cancer Prev. 2019. PMID: 30678438 Free PMC article.
The most frequent aberration was trisomy(ies) involving only gain of chromosomes in 48 (22.3%) cases. A translocation involving the IGH gene alone or accompanied by trisomy(ies) or by monosomy 13/13q deletion or by both was registered in 80 (37.2%) patients. ...Conclusions …
The most frequent aberration was trisomy(ies) involving only gain of chromosomes in 48 (22.3%) cases. A translocation involving the I …
Association of a microRNA/TP53 feedback circuitry with pathogenesis and outcome of B-cell chronic lymphocytic leukemia.
Fabbri M, Bottoni A, Shimizu M, Spizzo R, Nicoloso MS, Rossi S, Barbarotto E, Cimmino A, Adair B, Wojcik SE, Valeri N, Calore F, Sampath D, Fanini F, Vannini I, Musuraca G, Dell'Aquila M, Alder H, Davuluri RV, Rassenti LZ, Negrini M, Nakamura T, Amadori D, Kay NE, Rai KR, Keating MJ, Kipps TJ, Calin GA, Croce CM. Fabbri M, et al. JAMA. 2011 Jan 5;305(1):59-67. doi: 10.1001/jama.2010.1919. JAMA. 2011. PMID: 21205967 Free PMC article.
The functional relationship between these genes was studied using in vitro gain- and loss-of-function experiments in cell lines and primary samples and was validated in a separate cohort of primary CLL samples. ...
The functional relationship between these genes was studied using in vitro gain- and loss-of-function experiments in cell lines and p …
Gain of chromosome 3 and loss of 13q are frequent alterations in pituitary adenomas.
Fan X, Paetau A, Aalto Y, Välimäki M, Sane T, Poranen A, Castresana JS, Knuutila S. Fan X, et al. Cancer Genet Cytogenet. 2001 Jul 15;128(2):97-103. doi: 10.1016/s0165-4608(01)00398-3. Cancer Genet Cytogenet. 2001. PMID: 11463446
These data indicate that the 13q region may harbor tumor suppressor genes determining the tumorigenesis of PA and gain in chromosome 3 may be related to hormone secretion. These findings provide a basis to search for candidate diagnostic markers of HSPA....
These data indicate that the 13q region may harbor tumor suppressor genes determining the tumorigenesis of PA and gain in chromosome …
High resolution SNP array profiling identifies variability in retinoblastoma genome stability.
Mol BM, Massink MP, van der Hout AH, Dommering CJ, Zaman JM, Bosscha MI, Kors WA, Meijers-Heijboer HE, Kaspers GJ, Riele Ht, Moll AC, Cloos J, Dorsman JC. Mol BM, et al. Genes Chromosomes Cancer. 2014 Jan;53(1):1-14. doi: 10.1002/gcc.22111. Epub 2013 Nov 5. Genes Chromosomes Cancer. 2014. PMID: 24249257
In contrast, copy number neutral loss of heterozygosity was detected mainly on chromosome 13, where RB1 resides, irrespective of hereditary status or age. Focal amplifications and deletions and copy number neutral loss of heterozygosity besides chromosome …
In contrast, copy number neutral loss of heterozygosity was detected mainly on chromosome 13, where RB1 resides, irrespective …
35 results