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2011
A. Movafagh, Mortazavi-Tabatabaei, S. A., and Kolahi, A. A., The role of α-satellite DNA and heterochromatin polymorphism in leukemia patients and illicit drug addicts, vol. 10, pp. 3999-4005, 2011.
Atkin NB and Brito-Babapulle V (1981). Heterochromatin polymorphism and human cancer. Cancer Genet. Cytogenet. 3: 261-272. http://dx.doi.org/10.1016/0165-4608(81)90093-5 Bennett LM, Wang Y, Ramsey MJ, Harger GF, et al. (2010). Cigarette smoking during pregnancy: chromosome translocations and phenotypic susceptibility in mothers and newborns. Mutat. Res. 696: 81-88. http://dx.doi.org/10.1016/j.mrgentox.2009.12.015 PMid:20060061 Berger R, Bernheim A, Kristoffersson U, Mitelman F, et al. (1985). C-band heteromorphism in breast cancer patients. Cancer Genet. Cytogenet. 18: 37-42. http://dx.doi.org/10.1016/0165-4608(85)90037-8 Brothman AR, Persons DL and Shaffer LG (2009). Nomenclature evolution: Changes in the ISCN from the 2005 to the 2009 edition. Cytogenet. Genome Res. 127: 1-4. http://dx.doi.org/10.1159/000279442 PMid:20110655 Cortés A, Huertas D, Marsellach FX, Ferrer-Miralles N, et al. (2003). Analysing the contribution of nucleic acids to the structure and properties of centric heterochromatin. Genetica 117: 117-125. http://dx.doi.org/10.1023/A:1022947921402 PMid:12723691 de Assis KR, Ladeira MS, Bueno RC, Dos Santos BF, et al. (2009). Genotoxicity of cigarette smoking in maternal and newborn lymphocytes. Mutat. Res. 679: 72-78. http://dx.doi.org/10.1016/j.mrgentox.2009.02.006 PMid:19773089 Enukashvily NI, Donev R, Waisertreiger IS and Podgornaya OI (2007). Human chromosome 1 satellite 3 DNA is decondensed, demethylated and transcribed in senescent cells and in A431 epithelial carcinoma cells. Cytogenet. Genome Res. 118: 42-54. http://dx.doi.org/10.1159/000106440 PMid:17901699 Grewal SI and Moazed D (2003). Heterochromatin and epigenetic control of gene expression. Science 301: 798-802. http://dx.doi.org/10.1126/science.1086887 PMid:12907790 Le Coniant M, Vecchione D, Bernheim A and Berger R (1982). C-banding studies in acute nonlymphocytic leukemia. Cancer Genet. Cytogenet. 5: 327-331. http://dx.doi.org/10.1016/0165-4608(82)90098-X Madon PF, Athalye AS and Parikh FR (2005). Polymorphic variants on chromosomes probably play a significant role in infertility. Reprod. Biomed. Online 11: 726-732. http://dx.doi.org/10.1016/S1472-6483(10)61691-4 National Toxicology Program (2010). Final report on carcinogens background document for formaldehyde. Rep. Carcinog. Backgr. Doc. (10-5981): i-512. Neglia M, Bertoni L, Zoli W and Giulotto E (2003). Amplification of the pericentromeric region of chromosome 1 in a newly established colon carcinoma cell line. Cancer Genet. Cytogenet. 142: 99-106. http://dx.doi.org/10.1016/S0165-4608(02)00802-6 Plohl M, Luchetti A, Mestrovic N and Mantovani B (2008). Satellite DNAs between selfishness and functionality: structure, genomics and evolution of tandem repeats in centromeric (hetero)chromatin. Gene 409: 72-82. http://dx.doi.org/10.1016/j.gene.2007.11.013 PMid:18182173 Pluth JM, Ramsey MJ and Tucker JD (2000). Role of maternal exposures and newborn genotypes on newborn chromosome aberration frequencies. Mutat. Res. 465: 101-111. http://dx.doi.org/10.1016/S1383-5718(99)00217-X Pujol A, Benet J, Staessen C, Van AE, et al. (2006). The importance of aneuploidy screening in reciprocal translocation carriers. Reproduction 131: 1025-1035. http://dx.doi.org/10.1530/rep.1.01063 PMid:16735542 Ranni NS, Labal VM, Mudry de PM, Slavutsky I, et al. (1987). Heterochromatic variants and their association with neoplasias: III. Multiple myeloma. Cancer Genet. Cytogenet. 28: 101-105. http://dx.doi.org/10.1016/0165-4608(87)90358-X Rey JA, Bello MJ, de Campos JM, Kusak ME, et al. (1987). C-band pattern in patients with nervous system tumors. Cancer Genet. Cytogenet. 27: 185-190. http://dx.doi.org/10.1016/0165-4608(87)90275-5 Rivera H, Gutierrez-Angulo M and Gonzalez-Garcia JR (1999). Chromosome 9qh inversions may not be true inversions. Hum. Genet. 105: 181-184. PMid:10480378 Rossnerova A, Balascak I, Rossner P, Jr. and Sram RJ (2010). Frequency of chromosomal aberrations in Prague mothers and their newborns. Mutat. Res. 699: 29-34. http://dx.doi.org/10.1016/j.mrgentox.2010.04.015 PMid:20417307 Sivakumaran TA, Ghose S, Kumar H, Singha U, et al. (1997). Absence of pericentromeric heterochromatin (9qh-) in a patient with bilateral retinoblastoma. Acta Genet. Med. Gemellol. 46: 193-198. Sumner AT (1982). The nature and mechanisms of chromosome banding. Cancer Genet. Cytogenet. 6: 59-87. http://dx.doi.org/10.1016/0165-4608(82)90022-X Tsuda H, Takarabe T, Kanai Y, Fukutomi T et al. (2002). Correlation of DNA hypomethylation at pericentric heterochromatin regions of chromomes 1 and 16 with histological features and chromosomal abnormalities of human breast carcinomas. Am. J. Pathol. 161: 859-866. http://dx.doi.org/10.1016/S0002-9440(10)64246-0