Marzena Gajęcka
Gajęcka, Marzena
VIAF ID: 9260147270718035700001 (Personal)
Permalink: http://viaf.org/viaf/9260147270718035700001
Preferred Forms
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- 100 0 _ ‡a Marzena Gajęcka
4xx's: Alternate Name Forms (3)
Works
Title | Sources |
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16-Membered Macrolide Lactone Derivatives Bearing a Triazole-Functionalized Arm at the Aglycone C13 Position as Antibacterial and Anticancer Agents. | |
Accumulation of sequence variants in genes of Wnt signaling and focal adhesion pathways in human corneas further explains their involvement in keratoconus | |
[An analysis of the fundus changes in families with high myopia] | |
Are dietary supplements containing plant-derived ingredients safe microbiologically? | |
Association of arylamine N-acetyltransferase (NAT1 and NAT2) genotypes with urinary bladder cancer risk | |
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 | |
A Combined Metabolomic and Proteomic Analysis of Gestational Diabetes Mellitus | |
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2. | |
Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function | |
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. | |
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 | |
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 | |
Epigenetically dysregulated genes and pathways implicated in the pathogenesis of non-syndromic high myopia | |
Etiologia stożka rogówki i molekularne aspekty choroby : aktualny stan wiedzy | |
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. | |
Genetic factors influencing the reduction of central corneal thickness in disorders affecting the eye. | |
The genetics of keratoconus | |
Halloysite nanotubes as carriers of vancomycin in alginate-based wound dressing. | |
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 | |
The impact of genetic factors on the incidence of multiple primary tumors | |
Increasing Resistance and Changes in Distribution of Serotypes of Streptococcus agalactiae in Poland | |
Is the role of human female reproductive tract microbiota underestimated? | |
Krótkowzroczność w schorzeniach ogólnoustrojowych | |
KTCNlncDB-a first platform to investigate lncRNAs expressed in human keratoconus and non-keratoconus corneas. | |
Metody bioinformatyczne stosowane w procesie identyfikacji nowych genów warunkujących choroby narządu wzroku | |
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 deletion syndrome. | |
Multiple Differentially Methylated Regions Specific to Keratoconus Explain Known Keratoconus Linkage Loci | |
Mutacje mitochondrialnego DNA w chorobach narządu wzroku - dziedziczna neuropatia nerwu wzrokowego Lebera oraz zespół Kearnsa | |
[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] | |
Myopia in systemic disorders | |
Myopia: Risk Factors, Disease Mechanisms, Diagnostic Modalities, and Therapeutic Options | |
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. | |
Polymorphism of the DNA repair genes "RAD 51" 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 | |
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. | |
Typy dziedziczenia w genetycznie uwarunkowanych chorobach narządu wzroku | |
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. | |
W poszukiwaniu genu warunkującego stożek rogówki | |
Wartość poznawcza i diagnostyczna oceny niestabilności chromosomowej w płaskonabłonkowym raku krtani | |
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. |