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Molecular and Cellular Biochemistry, ISSN 0300-8177, 2/2018, Volume 439, Issue 1, pp. 53 - 63
Necrotizing enterocolitis (NEC) is one of the most severe and unpredictable complications of prematurity. There are two possible mechanisms involved in the... 
Life Sciences | Biochemistry, general | Gene | Preterm newborn | Medical Biochemistry | Oncology | Necrotizing enterocolitis | Cardiology | Polymorphism | MANAGEMENT | VARIANTS | PROMOTER POLYMORPHISM | SEPSIS | CELL BIOLOGY | BIRTH-WEIGHT INFANTS | TNF-ALPHA | OUTCOMES | RECEPTOR ALPHA-CHAIN | SINGLE NUCLEOTIDE POLYMORPHISMS | Infant, Newborn, Diseases - epidemiology | Prevalence | Enterocolitis, Necrotizing - genetics | Humans | Infant, Newborn, Diseases - surgery | Male | Polymorphism, Genetic | Enterocolitis, Necrotizing - epidemiology | Infant, Premature | Female | Infant, Newborn, Diseases - genetics | Infant, Newborn | Enterocolitis, Necrotizing - surgery | Enterocolitis, Pseudomembranous | Enterocolitis, Neonatal necrotizing | Ischemia | Interleukins | Tumor necrosis factor | Infants (Premature) | Genes | Genetic polymorphisms | Neonates | Pathogenesis | Interleukin | Pregnancy complications | Inflammatory response | Population studies | Infants | Gestation | Interleukin 1 receptors | Enterocolitis | Gene polymorphism | Blood | Arteries | Interleukin 6 | Intestine | Surgery | Interleukin 1 | Children | Genotypes | Statistical analysis | Complications | Interleukin 1 receptor antagonist | Abnormalities | Blood vessels | Inflammation | Tumor necrosis factor-α | Blood flow | Population (statistical) | Gene flow | Alleles | Steroid hormones | Steroids
Journal Article
Journal Article
Nutrition & dietetics: the journal of the Dietitians Association of Australia, ISSN 1446-6368, 05/2019
Physiological homocysteine (Hcy) concentrations depend on several factors, both dietary (including folate and choline intake) and biological (such as... 
Journal Article
Ginekologia polska, ISSN 0017-0011, 2018, Volume 89, Issue 4, p. 211
Adequate folate intake constitutes a significant problem in the periconceptional period and early pregnancy but can be achieved by folic acid (FA)... 
Pregnancy | Young Adult | Prenatal Care - statistics & numerical data | Humans | Adolescent | Pregnant Women | Poland | Adult | Female | Folic Acid - administration & dosage | Dietary Supplements - statistics & numerical data | Socioeconomic Factors
Journal Article
Maturitas, ISSN 0378-5122, 2015, Volume 84, pp. 42 - 54
Highlights • We found associations between the MAOA c.1460C > T, COMT c.472G > A, MTHFR c.677C > T and ESR1 454-351 A > G polymorphisms to mild and moderate... 
Internal Medicine | Obstetrics and Gynecology | MTHFR | COMT | MAOA | ESR1 | Gene polymorphism | Menopausal depression | MONOAMINE-OXIDASE | FUNCTIONAL POLYMORPHISM | ESTROGEN-RECEPTORS | HORMONE REPLACEMENT THERAPY | GERIATRICS & GERONTOLOGY | OBSTETRICS & GYNECOLOGY | CATECHOL-O-METHYLTRANSFERASE | BREAST-CANCER RISK | MOOD DISORDERS | POSTMENOPAUSAL WOMEN | LOW ACTIVITY ALLELE | PARKINSONS-DISEASE | Receptor, Serotonin, 5-HT2A - genetics | Minor Histocompatibility Antigens | Humans | Middle Aged | Menopause - psychology | Monoamine Oxidase - genetics | Catechol O-Methyltransferase - genetics | Depression - genetics | Psychiatric Status Rating Scales | Methylenetetrahydrofolate Reductase (NADPH2) - genetics | Norepinephrine Plasma Membrane Transport Proteins - genetics | Receptor, Serotonin, 5-HT1B - genetics | Adult | Female | Methylenetetrahydrofolate Dehydrogenase (NADP) - genetics | Depressive Disorder - genetics | Risk Factors | Genotype | Tryptophan Hydroxylase - genetics | Estrogen Receptor alpha - genetics | Receptors, GABA-A - genetics | 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase - genetics | Aged | Polymorphism, Single Nucleotide | Receptor, Serotonin, 5-HT2C - genetics | Women | Psychological aspects | Monoamine oxidase | Menopause | Genes | Genetic research | Genetic aspects | Risk factors | Genetic polymorphisms | Neurophysiology
Journal Article
Ginekologia Polska, ISSN 0017-0011, 2017, Volume 88, Issue 7, pp. 385 - 392
Introduction: The aim of the study was to evaluate the contribution of genetic variants determining inherited thrombophilia to recurrent miscarriage (RM) in... 
Recurrent miscarriage | Inherited thrombophilia | Genetic polymorphism | METAANALYSIS | PROTHROMBIN GENE | PREGNANCY LOSS | VASCULAR-DISEASE | OBSTETRICS & GYNECOLOGY | METHYLENETETRAHYDROFOLATE REDUCTASE | recurrent miscarriage | WOMEN | FACTOR-V-LEIDEN | POLYMORPHISMS | inherited thrombophilia | MUTATION | genetic polymorphism | ASSOCIATION
Journal Article
Ginekologia polska, ISSN 0017-0011, 2017, Volume 88, Issue 4, pp. 205 - 211
Objectives: Choline and folate metabolism disturbances may be involved in the occurrence of intrauterine fetal death (IUFD). The proper activity of this... 
choline | genetic polymorphism | intrauterine fetal death | POPULATION | METAANALYSIS | NEURAL-TUBE DEFECTS | PHOSPHOCHOLINE CYTIDYLYLTRANSFERASE | HUMANS | OBSTETRICS & GYNECOLOGY | METABOLISM | PHOSPHATIDYLCHOLINE | ESSENTIAL NUTRIENT | STILLBIRTH | REQUIREMENT
Journal Article