Lista de obras - Marzena Gajęcka - Dominio Público Uruguay

16-Membered Macrolide Lactone Derivatives Bearing a Triazole-Functionalized Arm at the Aglycone C13 Position as Antibacterial and Anticancer Agents.

artículo científico publicado en 2016

A Combined Metabolomic and Proteomic Analysis of Gestational Diabetes Mellitus

artículo científico publicado en 2015

Accumulation of sequence variants in genes of Wnt signaling and focal adhesion pathways in human corneas further explains their involvement in keratoconus

scientific article published on 14 April 2020

Are dietary supplements containing plant-derived ingredients safe microbiologically?

scientific article published on 10 November 2018

CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region.

artículo científico publicado en 2017

CYP1A1, CYP2D6, CYP2E1, NAT2, GSTM1 and GSTT1 polymorphisms or their combinations are associated with the increased risk of the laryngeal squamous cell carcinoma.

artículo científico publicado en 2005

Changes in Nuclear Gene Expression Related to Mitochondrial Function Affect Extracellular Matrix, Collagens, and Focal Adhesion in Keratoconus

artículo científico publicado en 2021

Characterization of a complex rearrangement with interstitial deletions and inversion on human chromosome 1

artículo científico publicado en 2006

Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13).

artículo científico publicado en 2008

Collagen synthesis disruption and downregulation of core elements of TGF-β, Hippo, and Wnt pathways in keratoconus corneas

artículo científico publicado en 2017

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.

artículo científico publicado en 2008

Contribution of polymorphism in codon 72 of TP53 gene to laryngeal cancer in Polish patients.

artículo científico publicado en 2008

Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function

artículo científico publicado en 2011

Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes

artículo científico publicado en 2011

Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure

artículo científico publicado en 2005

Epigenetically dysregulated genes and pathways implicated in the pathogenesis of non-syndromic high myopia

article

Evidence against ZNF469 being causative for keratoconus in Polish patients

artículo científico publicado en 2016

Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.

artículo científico publicado en 2009

Further evaluation of differential expression of keratoconus candidate genes in human corneas

artículo científico publicado en 2020

Genetic factors influencing the reduction of central corneal thickness in disorders affecting the eye.

artículo científico publicado en 2017

Genomic strategies to understand causes of keratoconus.

scientific article published on 28 December 2016

Halloysite nanotubes as carriers of vancomycin in alginate-based wound dressing.

artículo científico publicado en 2017

IGF-1 gene polymorphisms in Polish families with high-grade myopia

artículo científico publicado en 2011

Identification of a novel polymorphism--the duplication of the NPHP1 (nephronophthisis 1) gene.

artículo científico publicado en 2006

Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.

artículo científico publicado en 2006

Identification of novel suggestive loci for high-grade myopia in Polish families

artículo científico publicado en 2011

Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations

artículo científico publicado en 2006

Increasing Resistance and Changes in Distribution of Serotypes of Streptococcus agalactiae in Poland

artículo científico publicado en 2020

Is the role of human female reproductive tract microbiota underestimated?

artículo científico publicado en 2017

KTCNlncDB-a first platform to investigate lncRNAs expressed in human keratoconus and non-keratoconus corneas.

artículo científico publicado en 2017

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.

artículo científico publicado en 2008

Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.

artículo científico publicado en 2014

Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing some terminal deletions

artículo científico publicado en 2004

Monosomy 1p36 deletion syndrome.

artículo científico publicado en 2007

Multiple Differentially Methylated Regions Specific to Keratoconus Explain Known Keratoconus Linkage Loci

artículo científico publicado en 2019

Myopia in systemic disorders

artículo científico publicado en 2009

Myopia: Risk Factors, Disease Mechanisms, Diagnostic Modalities, and Therapeutic Options

artículo científico publicado en 2018

Myopia: Risk Factors, Disease Mechanisms, Diagnostic Modalities, and Therapeutic Options 2019

scientific article published on 07 March 2020

Non-allergic eye rubbing is a major behavioral risk factor for keratoconus

artículo científico publicado en 2023

Non-random distribution of chromatid breaks in lymphocytes of laryngeal squamous cell carcinoma patients

artículo científico publicado en 2004

Nonrandom Distribution of miRNAs Genes and Single Nucleotide Variants in Keratoconus Loci.

artículo científico publicado en 2015

Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus.

artículo científico publicado en 2011

Polymorphic variants of folate metabolism genes and the risk of laryngeal cancer

artículo científico publicado en 2009

Polymorphism of the DNA repair genes RAD51 and XRCC2 in smoking- and drinking-related laryngeal cancer in a Polish population

artículo científico publicado en 2012

Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2).

artículo científico publicado en 2014

Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints

scientific article published on 01 December 2010

Reduced DNA Repair Capacity in Laryngeal Cancer Subjects

scholarly article published 2004

Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus

artículo científico publicado en 2011

Significance of genetic factor in pathogenesis of laryngeal squamous cell carcinoma

artículo científico publicado el 1 de enero de 2003

Structure-activity relationship studies of new rifamycins containing l-amino acid esters as inhibitors of bacterial RNA polymerases.

artículo científico publicado en 2016

Substitution at IL1RN and deletion at SLC4A11 segregating with phenotype in familial keratoconus

artículo científico publicado en 2013

Synthesis and antibacterial activity of new N-alkylammonium and carbonate-triazole derivatives within desosamine of 14- and 15-membered lactone macrolides

artículo científico publicado en 2020

Synthesis, Antibacterial, and Anticancer Evaluation of Novel Spiramycin-Like Conjugates Containing C(5) Triazole Arm.

artículo científico publicado en 2016

Synthesis, docking and antibacterial studies of more potent amine and hydrazone rifamycin congeners than rifampicin

scientific article published on 04 February 2019

Synthesis, structure and antimicrobial evaluation of a new gossypol triazole conjugates functionalized with aliphatic chains and benzyloxy groups

article

The effect of complexation of 3-formylrifamycin SV macrocyclic ether derivatives with metal cations and small nitrogen-containing organic molecules on antibacterial activity against S. aureus and S. epidermidis

scientific article published on 22 July 2015

The genetics of keratoconus

article

The impact of genetic factors on the incidence of multiple primary tumors (MPT) of the head and neck

artículo científico publicado en 2005

The role of genetic factor in etiopathogenesis of squamous cell carcinoma of the head and neck in young adults

artículo científico publicado en 2007

Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.

artículo científico publicado en 2003

Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)

artículo científico publicado en 2008

Unrevealed mosaicism in the next-generation sequencing era

artículo científico publicado en 2016

Vancomycin-modified silica: Synthesis, controlled release and biological activity of the drug

artículo científico publicado en 2015

Variant c.2262A>C in DOCK9 Leads to Exon Skipping in Keratoconus Family.

artículo científico publicado en 2015

Variants in SKP1, PROB1, and IL17B genes at keratoconus 5q31.1-q35.3 susceptibility locus identified by whole-exome sequencing

artículo científico publicado en 2016

Will the use of double barrier result in sustained release of vancomycin? Optimization of parameters for preparation of a new antibacterial alginate-based modern dressing

artículo científico publicado en 2015

[An analysis of the fundus changes in families with high myopia]

artículo científico publicado en 2007

[Mutagen sensitivity in patients with multiple primary tumors (MPT) of the head and neck region--quantitative and qualitative assessment based on bleomycin assay]

scientific article published on 01 January 2004

[Mutations in mitochondrial DNA in ocular diseases--Leher's hereditary optic neuropathy and Kearns' syndrome]

scientific article published on 01 January 2008

Lista de obras de Marzena Gajęcka

16-Membered Macrolide Lactone Derivatives Bearing a Triazole-Functionalized Arm at the Aglycone C13 Position as Antibacterial and Anticancer Agents.

A Combined Metabolomic and Proteomic Analysis of Gestational Diabetes Mellitus

Accumulation of sequence variants in genes of Wnt signaling and focal adhesion pathways in human corneas further explains their involvement in keratoconus

Are dietary supplements containing plant-derived ingredients safe microbiologically?

CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region.

CYP1A1, CYP2D6, CYP2E1, NAT2, GSTM1 and GSTT1 polymorphisms or their combinations are associated with the increased risk of the laryngeal squamous cell carcinoma.

Changes in Nuclear Gene Expression Related to Mitochondrial Function Affect Extracellular Matrix, Collagens, and Focal Adhesion in Keratoconus

Characterization of a complex rearrangement with interstitial deletions and inversion on human chromosome 1

Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13).

Collagen synthesis disruption and downregulation of core elements of TGF-β, Hippo, and Wnt pathways in keratoconus corneas

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.

Contribution of polymorphism in codon 72 of TP53 gene to laryngeal cancer in Polish patients.

Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function

Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes

Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure

Epigenetically dysregulated genes and pathways implicated in the pathogenesis of non-syndromic high myopia

Evidence against ZNF469 being causative for keratoconus in Polish patients

Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.

Further evaluation of differential expression of keratoconus candidate genes in human corneas

Genetic factors influencing the reduction of central corneal thickness in disorders affecting the eye.

Genomic strategies to understand causes of keratoconus.

Halloysite nanotubes as carriers of vancomycin in alginate-based wound dressing.

IGF-1 gene polymorphisms in Polish families with high-grade myopia

Identification of a novel polymorphism--the duplication of the NPHP1 (nephronophthisis 1) gene.

Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.

Identification of novel suggestive loci for high-grade myopia in Polish families

Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations

Increasing Resistance and Changes in Distribution of Serotypes of Streptococcus agalactiae in Poland

Is the role of human female reproductive tract microbiota underestimated?

KTCNlncDB-a first platform to investigate lncRNAs expressed in human keratoconus and non-keratoconus corneas.

Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.

Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.

Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing some terminal deletions

Monosomy 1p36 deletion syndrome.

Multiple Differentially Methylated Regions Specific to Keratoconus Explain Known Keratoconus Linkage Loci

Myopia in systemic disorders

Myopia: Risk Factors, Disease Mechanisms, Diagnostic Modalities, and Therapeutic Options

Myopia: Risk Factors, Disease Mechanisms, Diagnostic Modalities, and Therapeutic Options 2019

Non-allergic eye rubbing is a major behavioral risk factor for keratoconus

Non-random distribution of chromatid breaks in lymphocytes of laryngeal squamous cell carcinoma patients

Nonrandom Distribution of miRNAs Genes and Single Nucleotide Variants in Keratoconus Loci.

Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus.

Polymorphic variants of folate metabolism genes and the risk of laryngeal cancer

Polymorphism of the DNA repair genes RAD51 and XRCC2 in smoking- and drinking-related laryngeal cancer in a Polish population

Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2).

Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints

Reduced DNA Repair Capacity in Laryngeal Cancer Subjects

Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus

Significance of genetic factor in pathogenesis of laryngeal squamous cell carcinoma

Structure-activity relationship studies of new rifamycins containing l-amino acid esters as inhibitors of bacterial RNA polymerases.

Substitution at IL1RN and deletion at SLC4A11 segregating with phenotype in familial keratoconus

Synthesis and antibacterial activity of new N-alkylammonium and carbonate-triazole derivatives within desosamine of 14- and 15-membered lactone macrolides

Synthesis, Antibacterial, and Anticancer Evaluation of Novel Spiramycin-Like Conjugates Containing C(5) Triazole Arm.

Synthesis, docking and antibacterial studies of more potent amine and hydrazone rifamycin congeners than rifampicin

Synthesis, structure and antimicrobial evaluation of a new gossypol triazole conjugates functionalized with aliphatic chains and benzyloxy groups

The effect of complexation of 3-formylrifamycin SV macrocyclic ether derivatives with metal cations and small nitrogen-containing organic molecules on antibacterial activity against S. aureus and S. epidermidis

The genetics of keratoconus

The impact of genetic factors on the incidence of multiple primary tumors (MPT) of the head and neck

The role of genetic factor in etiopathogenesis of squamous cell carcinoma of the head and neck in young adults

Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.

Unexpected complexity at breakpoint junctions in phenotypically normal individuals and mechanisms involved in generating balanced translocations t(1;22)(p36;q13)

Unrevealed mosaicism in the next-generation sequencing era

Vancomycin-modified silica: Synthesis, controlled release and biological activity of the drug

Variant c.2262A>C in DOCK9 Leads to Exon Skipping in Keratoconus Family.

Variants in SKP1, PROB1, and IL17B genes at keratoconus 5q31.1-q35.3 susceptibility locus identified by whole-exome sequencing

Will the use of double barrier result in sustained release of vancomycin? Optimization of parameters for preparation of a new antibacterial alginate-based modern dressing

[An analysis of the fundus changes in families with high myopia]

[Mutagen sensitivity in patients with multiple primary tumors (MPT) of the head and neck region--quantitative and qualitative assessment based on bleomycin assay]

[Mutations in mitochondrial DNA in ocular diseases--Leher's hereditary optic neuropathy and Kearns' syndrome]