Lista de obras - Izabela Laczmanska - Dominio Público Uruguay

Assessment of chromosomal imbalances in CIMP-high and CIMP-low/CIMP-0 colorectal cancers.

artículo científico publicado en 2012

Association of select vitamin D receptor gene polymorphisms with the risk of tobacco-related cancers - a meta-analysis

artículo científico publicado en 2019

Association of the vitamin D receptor FokI gene polymorphism with sex- and non-sex-associated cancers: A meta-analysis

artículo científico publicado en 2017

Clinical Observation of a Child with Prenatally Diagnosed De Novo Partial Trisomy of Chromosome 20

scientific article published on 20 March 2019

Copy Number Variations and Schizophrenia

artículo científico publicado en 2022

Copy number alterations of chromosomal regions enclosing protein tyrosine phosphatase receptor-like genes in colorectal cancer

artículo científico publicado en 2014

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

artículo científico publicado en 2005

Customized Array Comparative Genomic Hybridization Analysis of 25 Phosphatase-encoding Genes in Colorectal Cancer Tissues.

artículo científico publicado en 2017

Exonic deletions in the NF1 gene in patients with neurofibromatosis type I from the lower Silesian region of Poland.

artículo científico publicado en 2014

Expression Analysis of Tyrosine Phosphatase Genes at Different Stages of Renal Cell Carcinoma

artículo científico publicado en 2020

Fragile X syndrome in females - a familial case report and review of the literature

artículo científico publicado en 2016

Hexasomy 13q31.3q34 due to two marker chromosomes with inverted duplication in a fetus with increased nuchal translucency

artículo científico publicado en 2015

High PTPRQ Expression and Its Relationship to Expression of PTPRZ1 and the Presence of KRAS Mutations in Colorectal Cancer Tissues

artículo científico publicado en 2016

Immunohistochemical and Western blot analysis of two protein tyrosine phosphatase receptors, R and Z1, in colorectal carcinoma, colon adenoma and normal colon tissues.

artículo científico publicado en 2013

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

artículo científico

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

artículo científico publicado en 2006

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

artículo científico publicado en 2010

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

artículo científico publicado en 2007

Meta-analysis of association between Arg326Gln (rs1503185) and Gln276Pro (rs1566734) polymorphisms of PTPRJ gene and cancer risk

article

Multilevel omic data clustering reveals variable contribution of methylator phenotype to integrative cancer subtypes

artículo científico publicado en 2018

Multiplex Ligation - dependent Probe Amplification (MLPA) as a screening test in children with developmental defects and intellectual disability of unknown etiology

artículo científico publicado el 1 de abril de 2011

Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders

scientific article published on 01 January 2020

Personalized medicine in oncology. New perspectives in management of gliomas.

artículo científico publicado en 2018

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

artículo científico publicado en 2007

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

article

Polymorphisms in nucleotide excision repair genes and basal cell carcinoma of the skin

artículo científico publicado en 2014

Protein tyrosine phosphatase receptor-like genes are frequently hypermethylated in sporadic colorectal cancer.

artículo científico publicado en 2012

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

artículo científico publicado en 2006

Response to the commentary by Gholami and Amoli

artículo científico publicado en 2020

Short stature in genetic syndromes: Selected issues

artículo científico publicado en 2018

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

artículo científico publicado en 2011

The Comparison Between Molecular Tumour Profiling in Microdissected and Surgical Tissue Samples

artículo científico publicado en 2018

The PTPN13 Y2081D (T>G) (rs989902) polymorphism is associated with an increased risk of sporadic colorectal cancer.

artículo científico publicado en 2017

The Phelan-McDermid syndrome (22q13 microdeletion) - case report

artículo científico publicado el 1 de enero de 2011

Tyrosine phosphatases as a superfamily of tumor suppressors in colorectal cancer

artículo científico publicado el 6 de diciembre de 2011

Vitamin D receptor gene polymorphisms in relation to the risk of colorectal cancer in the Polish population

artículo científico publicado en 2014

[New molecular methods in prenatal invasive diagnostics].

artículo científico publicado en 2013

[Non-invasive fetal trisomy (NIFTY) test in prenatal diagnosis]

artículo científico publicado en 2014

[Non-invasive prenatal test in the diagnosis of aneuploidy 13, 18 and 21--theoretical and practical aspects]

artículo científico publicado en 2011

[Rapid diagnosis of the most common fetal aneuploidies with the QF-PCR method--a study of 100 cases].

artículo científico publicado en 2015

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

scientific article published on 01 December 2007

[The characteristic of ribulose-1,5-biphosphate carboxylase/oxygenase(rubisco). Directions of studies]

scientific article published on 01 January 2003

Lista de obras de Izabela Laczmanska

Assessment of chromosomal imbalances in CIMP-high and CIMP-low/CIMP-0 colorectal cancers.

Association of select vitamin D receptor gene polymorphisms with the risk of tobacco-related cancers - a meta-analysis

Association of the vitamin D receptor FokI gene polymorphism with sex- and non-sex-associated cancers: A meta-analysis

Clinical Observation of a Child with Prenatally Diagnosed De Novo Partial Trisomy of Chromosome 20

Copy Number Variations and Schizophrenia

Copy number alterations of chromosomal regions enclosing protein tyrosine phosphatase receptor-like genes in colorectal cancer

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

Customized Array Comparative Genomic Hybridization Analysis of 25 Phosphatase-encoding Genes in Colorectal Cancer Tissues.

Exonic deletions in the NF1 gene in patients with neurofibromatosis type I from the lower Silesian region of Poland.

Expression Analysis of Tyrosine Phosphatase Genes at Different Stages of Renal Cell Carcinoma

Fragile X syndrome in females - a familial case report and review of the literature

Hexasomy 13q31.3q34 due to two marker chromosomes with inverted duplication in a fetus with increased nuchal translucency

High PTPRQ Expression and Its Relationship to Expression of PTPRZ1 and the Presence of KRAS Mutations in Colorectal Cancer Tissues

Immunohistochemical and Western blot analysis of two protein tyrosine phosphatase receptors, R and Z1, in colorectal carcinoma, colon adenoma and normal colon tissues.

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

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

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

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

Meta-analysis of association between Arg326Gln (rs1503185) and Gln276Pro (rs1566734) polymorphisms of PTPRJ gene and cancer risk

Multilevel omic data clustering reveals variable contribution of methylator phenotype to integrative cancer subtypes

Multiplex Ligation - dependent Probe Amplification (MLPA) as a screening test in children with developmental defects and intellectual disability of unknown etiology

Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders

Personalized medicine in oncology. New perspectives in management of gliomas.

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

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

Polymorphisms in nucleotide excision repair genes and basal cell carcinoma of the skin

Protein tyrosine phosphatase receptor-like genes are frequently hypermethylated in sporadic colorectal cancer.

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

Response to the commentary by Gholami and Amoli

Short stature in genetic syndromes: Selected issues

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

The Comparison Between Molecular Tumour Profiling in Microdissected and Surgical Tissue Samples

The PTPN13 Y2081D (T>G) (rs989902) polymorphism is associated with an increased risk of sporadic colorectal cancer.

The Phelan-McDermid syndrome (22q13 microdeletion) - case report

Tyrosine phosphatases as a superfamily of tumor suppressors in colorectal cancer

Vitamin D receptor gene polymorphisms in relation to the risk of colorectal cancer in the Polish population

[New molecular methods in prenatal invasive diagnostics].

[Non-invasive fetal trisomy (NIFTY) test in prenatal diagnosis]

[Non-invasive prenatal test in the diagnosis of aneuploidy 13, 18 and 21--theoretical and practical aspects]

[Rapid diagnosis of the most common fetal aneuploidies with the QF-PCR method--a study of 100 cases].

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

[The characteristic of ribulose-1,5-biphosphate carboxylase/oxygenase(rubisco). Directions of studies]