A. Madetko‐Talowska

发表

Transcriptome profiling of the newborn mouse lung after hypoxia and reoxygenation: hyperoxic reoxygenation affects mTOR signaling pathway, DNA repair, and JNK-pathway regulation

M. Wright, S. Nygård, P. Kwinta, 2013, Pediatric Research.

Transcriptome profiling of the newborn mouse brain after hypoxia–reoxygenation: hyperoxic reoxygenation induces inflammatory and energy failure responsive genes

M. Wright, S. Nygård, P. Kwinta, 2014, Pediatric Research.

Cardiovascular Anomalies among 1005 Fetuses Referred to Invasive Prenatal Testing—A Comprehensive Cohort Study of Associated Chromosomal Aberrations

A. Wójtowicz, H. Huras, K. Szewczyk, 2022, International journal of environmental research and public health.

[The use of microarrays for gene expression analysis in premature children--new strategy of searching for genetic basis of late complications of prematurity--preliminary research].

P. Kwinta, J. Pietrzyk, M. Bik-Multanowski, 2011, Przeglad lekarski.

Comparison of whole genome expression profile between preterm and full-term newborns.

L. Baumbusch, P. Kwinta, Cecilie Revhaug, 2017, Ginekologia polska.

The rs113883650 variant of SLC7A5 (LAT1) gene may alter brain phenylalanine content in PKU

M. Bik-Multanowski, A. Madetko‐Talowska, Kinga Bik-Multanowska, 2021, Molecular genetics and metabolism reports.

Carriership of the rs113883650/rs2287120 haplotype of the SLC7A5 (LAT1) gene increases the risk of obesity in infants with phenylketonuria

M. Bik-Multanowski, E. Starostecka, R. Mozrzymas, 2020, Molecular genetics and metabolism reports.

Immune System Regulation Affected by a Murine Experimental Model of Bronchopulmonary Dysplasia: Genomic and Epigenetic Findings

L. Baumbusch, M. Zasada, P. Kwinta, 2019, Neonatology.

Human Induced Pluripotent Stem Cell‐Derived Microvesicles Transmit RNAs and Proteins to Recipient Mature Heart Cells Modulating Cell Fate and Behavior

Z. Madeja, S. Kędracka-Krok, B. Dawn, 2015, Stem cells.

Genetic analysis of the paired box transcription factor (PAX8) gene in a cohort of Polish patients with primary congenital hypothyroidism and dysgenetic thyroid glands

A. Madetko-Talowska, M. Kumorowicz-Czoch, A. Dudek, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

Identification of deletions in children with congenital hypothyroidism and thyroid dysgenesis with the use of multiplex ligation-dependent probe amplification

A. Madetko-Talowska, J. Pietrzyk, J. Starzyk, 2015, Journal of pediatric endocrinology & metabolism : JPEM.

New insight into the pathogenesis of retinopathy of prematurity: assessment of whole-genome expression

S. Nygård, T. Tomasik, P. Kwinta, 2013, Pediatric Research.

[Fetal CD34+ cells isolated from maternal blood and cytogenetics array as potential tools in screening, non-invasive prenatal diagnosis--preliminary research].

A. Grabowska, J. Pietrzyk, M. Majka, 2011, Przeglad lekarski.

Gene Expression Profiling in Preterm Infants: New Aspects of Bronchopulmonary Dysplasia Development

Clara-Cecilie Günther, Jacek J. Pietrzyk, T. Tomasik, 2013, PloS one.

Comparative two time-point proteome analysis of the plasma from preterm infants with and without bronchopulmonary dysplasia

L. Baumbusch, M. Zasada, P. Kwinta, 2019, Italian Journal of Pediatrics.

An iTRAQ-Based Quantitative Proteomic Analysis of Plasma Proteins in Preterm Newborns With Retinopathy of Prematurity.

L. Baumbusch, M. Zasada, P. Kwinta, 2018, Investigative ophthalmology & visual science.

Short- and long-term impact of hyperoxia on the blood and retinal cells’ transcriptome in a mouse model of oxygen-induced retinopathy

L. Baumbusch, M. Zasada, P. Kwinta, 2019, Pediatric Research.

Transcriptome analysis reveals dysregulation of genes involved in oxidative phosphorylation in a murine model of retinopathy of prematurity

L. Baumbusch, M. Zasada, P. Kwinta, 2020, Pediatric Research.

Hyperoxia induces epigenetic changes in newborn mice lungs

M. Zasada, Cecilie Revhaug, A. Grabowska, 2018, Free radical biology & medicine.

Paternal uniparental disomy of chromosome 2 resulting in a concurrent presentation of Crigler–Najjar syndrome type I and long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency

P. Kwinta, A. Madetko‐Talowska, Katarzyna Końska, 2022, American journal of medical genetics. Part A.

Development and Maturation of the Immune System in Preterm Neonates: Results from a Whole Genome Expression Study

M. Zasada, P. Kwinta, J. Pietrzyk, 2014, BioMed research international.

Hypoxia-reoxygenation affects whole-genome expression in the newborn eye.

M. Wright, S. Nygård, P. Kwinta, 2014, Investigative ophthalmology & visual science.

Polymorphisms of SLC19A1 80 G>A, MTHFR 677 C>T, and Tandem TS Repeats Influence Pharmacokinetics, Acute Liver Toxicity, and Vomiting in Children With Acute Lymphoblastic Leukemia Treated With High Doses of Methotrexate

M. Bik-Multanowski, W. Balwierz, A. Wieczorek, 2020, Frontiers in Pediatrics.

Additional risk factor for the development of ALL

J. Pietrzyk, M. Bik-Multanowski, M. Ołtarzewski, 2009, Pediatric blood & cancer.

Pulmonary vascular disease is evident in gene regulation of experimental bronchopulmonary dysplasia

L. Baumbusch, M. Zasada, P. Kwinta, 2020, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Hypoxia-reoxygenation affects whole-genome expression in the newborn eye.

M. Wright, S. Nygård, P. Kwinta, 2014, Investigative ophthalmology & visual science.

Analysis of miRNAs in Osteogenesis imperfecta Caused by Mutations in COL1A1 and COL1A2: Insights into Molecular Mechanisms and Potential Therapeutic Targets

Joanna Witecka, A. Sieron, M. Bik-Multanowski, 2023, Pharmaceuticals.