Laczmanska I - Search Results

1

Irrelevance of CHEK2 variants to diagnosis of breast/ovarian cancer predisposition in Polish cohort.

Myszka A, Karpinski P, Slezak R, Czemarmazowicz H, Stembalska A, Gil J, Laczmanska I, Bednarczyk D, Szmida E, Sasiadek MM. Myszka A, et al. Among authors: laczmanska i. J Appl Genet. 2011 May;52(2):185-91. doi: 10.1007/s13353-010-0013-1. Epub 2010 Dec 1. J Appl Genet. 2011. PMID: 21120647

2

Influence of GSTT1, mEH, CYP2E1 and RAD51 polymorphisms on diepoxybutane-induced SCE frequency in cultured human lymphocytes.

Schlade-Bartusiak K, Rozik K, Laczmanska I, Ramsey D, Sasiadek M. Schlade-Bartusiak K, et al. Among authors: laczmanska i. Mutat Res. 2004 Mar 14;558(1-2):121-30. doi: 10.1016/j.mrgentox.2003.11.007. Mutat Res. 2004. PMID: 15036125

3

Cri du chat syndrome determined by the 5p15.3-->pter deletion--diagnostic problems.

Laczmanska I, Stembalska A, Gil J, Czemarmazowicz H, Sasiadek M. Laczmanska I, et al. Eur J Med Genet. 2006 Jan-Feb;49(1):87-92. doi: 10.1016/j.ejmg.2005.04.023. Epub 2005 Jul 6. Eur J Med Genet. 2006. PMID: 16473315

4

Recombinant chromosome 4 resulting from a maternal pericentric inversion in two sisters presenting consistent dysmorphic features.

Stembalska A, Laczmanska I, Schlade-Bartusiak K, Czemarmazowicz H, Murawski M, Sasiadek M. Stembalska A, et al. Among authors: laczmanska i. Eur J Pediatr. 2007 Jan;166(1):67-71. doi: 10.1007/s00431-006-0214-0. Epub 2006 Sep 30. Eur J Pediatr. 2007. PMID: 17013597

5

Influence of polymorphisms in xenobiotic-metabolizing genes and DNA-repair genes on diepoxybutane-induced SCE frequency.

Laczmanska I, Gil J, Karpinski P, Stembalska A, Kozlowska J, Busza H, Trusewicz A, Pesz K, Ramsey D, Schlade-Bartusiak K, Blin N, Sasiadek MM. Laczmanska I, et al. Environ Mol Mutagen. 2006 Dec;47(9):666-73. doi: 10.1002/em.20253. Environ Mol Mutagen. 2006. PMID: 17078101

6

Maternal complex chromosome rearrangements involving five chromosomes 1, 4, 10, 12 and 20 ascertained through a del(4)(p14p15) detected in a mother's first affected daughter.

Smigiel R, Laczmanska I, Sasiadek M. Smigiel R, et al. Among authors: laczmanska i. Clin Dysmorphol. 2007 Jan;16(1):63-64. doi: 10.1097/01.mcd.0000220615.55402.d8. Clin Dysmorphol. 2007. PMID: 17159519

7

Polymorphism in nucleotide excision repair gene XPC correlates with bleomycin-induced chromosomal aberrations.

Laczmanska I, Gil J, Karpinski P, Stembalska A, Trusewicz A, Pesz K, Ramsey D, Schlade-Bartusiak K, Blin N, Sasiadek MM. Laczmanska I, et al. Environ Mol Mutagen. 2007 Oct;48(8):666-71. doi: 10.1002/em.20333. Environ Mol Mutagen. 2007. PMID: 17685459

8

[Rapid-FISH--fast and reliable method of detecting common numerical chromosomal aberrations in prenatal diagnosis].

Laczmańska I, Stembalska A, Slezak R, Kozłowska J, Makowska I, Czemarmazowicz H, Pesz KA, Smigiel R, Jakiel A, Sasiadek MM. Laczmańska I, et al. Ginekol Pol. 2007 Dec;78(12):952-5. Ginekol Pol. 2007. PMID: 18411918 Polish.

9

Polymorphisms in methyl-group metabolism genes and risk of sporadic colorectal cancer with relation to the CpG island methylator phenotype.

Karpinski P, Myszka A, Ramsey D, Misiak B, Gil J, Laczmanska I, Grzebieniak Z, Sebzda T, Smigiel R, Stembalska A, Sasiadek MM. Karpinski P, et al. Among authors: laczmanska i. Cancer Epidemiol. 2010 Jun;34(3):338-44. doi: 10.1016/j.canep.2010.03.002. Epub 2010 Apr 8. Cancer Epidemiol. 2010. PMID: 20381446

10

The C/A polymorphism in intron 11 of the XPC gene plays a crucial role in the modulation of an individual's susceptibility to sporadic colorectal cancer.

Gil J, Ramsey D, Stembalska A, Karpinski P, Pesz KA, Laczmanska I, Leszczynski P, Grzebieniak Z, Sasiadek MM. Gil J, et al. Among authors: laczmanska i. Mol Biol Rep. 2012 Jan;39(1):527-34. doi: 10.1007/s11033-011-0767-5. Epub 2011 May 11. Mol Biol Rep. 2012. PMID: 21559836

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