Publications
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“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