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Effects of BRCA Germline Mutations on Triple-Negative Breast Cancer Prognosis

Journal of oncology, 2020, Vol.2020 (2020), p.1-10

2020

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NTHL1 Gene Mutations in Polish Polyposis Patients—Weighty Player or Vague Background?

International journal of molecular sciences, 2023-10, Vol.24 (19), p.14548

2023

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Association of TLR3 L412F Polymorphism with Cytomegalovirus Infection in Children

PloS one, 2017-01, Vol.12 (1), p.e0169420-e0169420

2017

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Toll-like receptors genes polymorphisms and the occurrence of HCMV infection among pregnant women

Virology journal, 2017-03, Vol.14 (1), Article 64

2017

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TLR9 -1486T/C and 2848C/T SNPs Are Associated with Human Cytomegalovirus Infection in Infants

PloS one, 2016-04, Vol.11 (4), p.e0154100-e0154100

2016

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TLR9 2848 GA heterozygotic status possibly predisposes fetuses and newborns to congenital infection with human cytomegalovirus

PloS one, 2015-04, Vol.10 (4), p.e0122831-e0122831

2015

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A novel germline PALB2 deletion in Polish breast and ovarian cancer patients

BMC medical genetics, 2010-02, Vol.11 (1), p.20-20, Article 20

2010

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Genotyping of Toxoplasma gondii by Multiplex PCR and Peptide-Based Serological Testing of Samples from Infants in Poland Diagnosed with Congenital Toxoplasmosis

Journal of Clinical Microbiology, 2006-04, Vol.44 (4), p.1382-1389

2006

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Influence of ionizing radiation on human body

Family medicine & primary care review, 2016, Vol.2 (2), p.174-179

2016

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Mannan-binding lectin-2 (MBL2) gene polymorphisms in prenatal and perinatal cytomegalovirus infections

Molecular immunology, 2011-09, Vol.48 (15-16), p.2203-2206

2011

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Fetal bilateral primary chylothorax – report of the two cases

Ginekologia polska, 2014, Vol.85 (10)

2014

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Clinical challenges in the management of a prenatally diagnosed cloacal malformation

Congenital anomalies, 2011-06, Vol.51 (2), p.92-95

2011

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INTHL1/I Gene Mutations in Polish Polyposis Patients—Weighty Player or Vague Background?

International journal of molecular sciences, 2023-09, Vol.24 (19)

2023

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Detection of cytomegalovirus in human placental cells by polymerase chain reaction

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2006-11, Vol.114 (11), p.764-771

2006

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Genetic modifications of cytokine genes and Toxoplasma gondii infections in pregnant women

Microbial pathogenesis, 2018-08, Vol.121, p.283-292

2018

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Genetic alterations within TLR genes in development of Toxoplasma gondii infection among Polish pregnant women

Advances in medical sciences, 2017-09, Vol.62 (2), p.216-222

2017

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New recurrent BRCA1/2 mutations in Polish patients with familial breast/ovarian cancer detected by next generation sequencing

BMC medical genomics, 2015-05, Vol.8 (1), p.19-19, Article 19

2015

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Alterations in TLRs as new molecular markers of congenital infections with Human cytomegalovirus?

Pathogens and disease, 2014-02, Vol.70 (1), p.3-16

2014

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Toll-like receptors genes polymorphisms and the occurrence of HCMV infection among pregnant women

Virology journal, 2017-03, Vol.14 (1), p.64-64

2017

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PALB2 mutations in BRCA1/2-mutation negative breast and ovarian cancer patients from Poland

BMC medical genomics, 2017-03, Vol.10 (1), p.14-14, Article 14

2017

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DNA repair mechanisms and Toxoplasma gondii infection

Archives of microbiology, 2014-01, Vol.196 (1), p.1-8

2014

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Prenatal sonographic diagnosis of premature constriction of the fetal ductus arteriosus after maternal self-medication with benzydamine hydrochloride: report of 3 cases and review of the literature

Journal of ultrasound in medicine, 2015-03, Vol.34 (3), p.531-535

2015

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The role of single nucleotide polymorphisms, contained in proinflammatory cytokine genes, in the development of congenital infection with human cytomegalovirus in fetuses and neonates

Microbial pathogenesis, 2017-04, Vol.105, p.106-116

2017

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TLR2 2258 GA single nucleotide polymorphism and the risk of congenital infection with human cytomegalovirus

Virology journal, 2017-01, Vol.14 (1)

2017

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Effects of BRCA Germline Mutations on Triple-Negative Breast Cancer Prognosis

NTHL1 Gene Mutations in Polish Polyposis Patients—Weighty Player or Vague Background?

Association of TLR3 L412F Polymorphism with Cytomegalovirus Infection in Children

Toll-like receptors genes polymorphisms and the occurrence of HCMV infection among pregnant women

TLR9 -1486T/C and 2848C/T SNPs Are Associated with Human Cytomegalovirus Infection in Infants

TLR9 2848 GA heterozygotic status possibly predisposes fetuses and newborns to congenital infection with human cytomegalovirus

Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis

A novel germline PALB2 deletion in Polish breast and ovarian cancer patients

Genotyping of Toxoplasma gondii by Multiplex PCR and Peptide-Based Serological Testing of Samples from Infants in Poland Diagnosed with Congenital Toxoplasmosis

Influence of ionizing radiation on human body

Mannan-binding lectin-2 (MBL2) gene polymorphisms in prenatal and perinatal cytomegalovirus infections

Fetal bilateral primary chylothorax – report of the two cases

Clinical challenges in the management of a prenatally diagnosed cloacal malformation

INTHL1/I Gene Mutations in Polish Polyposis Patients—Weighty Player or Vague Background?

Detection of cytomegalovirus in human placental cells by polymerase chain reaction

Genetic modifications of cytokine genes and Toxoplasma gondii infections in pregnant women

Genetic alterations within TLR genes in development of Toxoplasma gondii infection among Polish pregnant women

New recurrent BRCA1/2 mutations in Polish patients with familial breast/ovarian cancer detected by next generation sequencing

Alterations in TLRs as new molecular markers of congenital infections with Human cytomegalovirus?

Toll-like receptors genes polymorphisms and the occurrence of HCMV infection among pregnant women

PALB2 mutations in BRCA1/2-mutation negative breast and ovarian cancer patients from Poland

DNA repair mechanisms and Toxoplasma gondii infection

Prenatal sonographic diagnosis of premature constriction of the fetal ductus arteriosus after maternal self-medication with benzydamine hydrochloride: report of 3 cases and review of the literature

The role of single nucleotide polymorphisms, contained in proinflammatory cytokine genes, in the development of congenital infection with human cytomegalovirus in fetuses and neonates

TLR2 2258 GA single nucleotide polymorphism and the risk of congenital infection with human cytomegalovirus

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