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Journal Article
Journal Article
CLINICAL EPIDEMIOLOGY, ISSN 1179-1349, 2019, Volume 11, pp. 793 - 800
Journal Article
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 4, pp. 515 - 526
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 4, pp. 380 - 384
Journal Article
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1422-0067, 09/2019, Volume 20, Issue 18, p. 4402
Omega-3 fatty acids are important to pregnancy and neonatal development and health. One mechanism by which omega-3 fatty acids exert their protective effects... 
delivery | Resolvin D2 | trophoblasts | OMEGA-3-FATTY-ACIDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | RESOLUTION | SUBCELLULAR-LOCALIZATION | omega-3 fatty acids | PREECLAMPSIA | MECHANISMS | LIPID MEDIATORS | CHEMISTRY, MULTIDISCIPLINARY | SUPPLEMENTATION | inflammation | INTRAUTERINE INFECTION | specialized pro-resolving mediators | DISEASE | placenta | GPR18 | Muscle, Smooth, Vascular - metabolism | Receptors, G-Protein-Coupled - metabolism | Humans | Trophoblasts - drug effects | Young Adult | Maternal Age | Fatty Acids, Omega-3 - pharmacology | Placenta - cytology | Adult | Female | Trophoblasts - cytology | Myocytes, Smooth Muscle - drug effects | Myocytes, Smooth Muscle - cytology | Myocytes, Smooth Muscle - metabolism | Muscle, Smooth, Vascular - drug effects | Trophoblasts - metabolism | Cells, Cultured | Muscle, Smooth, Vascular - cytology | Hep G2 Cells | Gene Expression Regulation - drug effects | Placenta - drug effects | Placenta - metabolism | Pregnancy | Docosahexaenoic Acids - pharmacology | Receptors, G-Protein-Coupled - genetics | Medical research | Health | Fetuses | Acetylcysteine | Smooth muscle | Lipids | Infants | Biosynthesis | Gene expression | Docosahexaenoic acid | Fatty acids | Substrates | Proteins | Liver cancer | Placenta | Maternal & child health | Protein expression | Supplementation | Localization | Eicosapentaenoic acid | Age
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 08/2013, Volume 50, Issue 8, pp. 521 - 528
Journal Article
Clinical Chemistry, ISSN 0009-9147, 02/2019, Volume 65, Issue 2, pp. 345 - 347
[...]we successfully quantified the target sequences in diagnostic bone marrow samples as ranging between 17% and 29% (Table 1). [...]we quantified the load of... 
MEDICAL LABORATORY TECHNOLOGY | Neonates | Pediatrics | Medical research | Leukemia | Cloning | Childrens health | Genomes | Chromosome rearrangements | Patients | Gene sequencing | Children & youth | Hospitals | Councils | Bone marrow | Diagnostic systems | Children | Thermal cycling | Deoxyribonucleic acid--DNA | Cancer
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 04/2017, Volume 62, Issue 4, pp. 503 - 506
Axial spondylometaphyseal dysplasia (axial SMD) is a unique form of SMD characterized by dysplasia of axial skeleton and retinal dystrophy. Recently, C21orf2... 
MAJEWSKI | GENE | POLYCYSTIC KIDNEY-DISEASE | GENETICS & HEREDITY | IDENTIFICATION | PRENATAL-DIAGNOSIS | FAMILY | Proteins - genetics | Osteochondrodysplasias - genetics | Genetic Association Studies | Pedigree | Humans | Male | Mutation | NIMA-Related Kinase 1 - genetics | Child
Journal Article
by Jacquemont, S and Reymond, A and Zufferey, F and Harewood, L and Walters, R.G and Kutalik, Z and Martinet, D and Shen, Y and Valsesia, A and Beckmann, N.D and Thorleifsson, G and Belfiore, M and Bouquillon, S and Campion, D and Leeuw, N. de and Vries, L.B.A. de and Esko, T and Fernandez, B.A and Fernandez-Aranda, F and Fernandez-Real, J.M and Gratacos, M and Guilmatre, A and Hoyer, J and Jarvelin, M.R and Kooy, R.F and Kurg, A and Caignec, C. Le and Mannik, K and Platt, O.S and Sanlaville, D and Haelst, M.M. van and Villatoro Gomez, S and Walha, F and Wu, B.L and Yu, Y and Aboura, A and Addor, M.C and Alembik, Y and Antonarakis, S.E and Arveiler, B and Barth, M and Bednarek, N and Bena, F and Bergmann, S and Beri, M and Bernardini, L and Blaumeiser, B and Bonneau, D and Bottani, A and Boute, O and Brunner, H.G and Cailley, D and Callier, P and Chiesa, J and Chrast, J and Coin, L and Coutton, C and Cuisset, J.M and Cuvellier, J.C and David, A and Freminville, B. de and Delobel, B and Delrue, M.A and Demeer, B and Descamps, D and Didelot, G and Dieterich, K and Disciglio, V and Doco-Fenzy, M and nat, S and Duban-Bedu, B and Dubourg, C and El-Sayed Moustafa, J.S and Elliott, P and Faas, B.H.W and Faivre, L and Faudet, A and Fellmann, F and Ferrarini, A and Fisher, R and Flori, E and Forer, L and Gaillard, D and Gerard, M and Gieger, C and Gimelli, S and Gimelli, G and Grabe, H.J and Guichet, A and Guillin, O and Hartikainen, A.L and Heron, D and Hippolyte, L and Holder, M and Homuth, G and Isidor, B and Jaillard, S and Jaros, Z and Jimenez-Murcia, S and Helas, G.J and ...
Nature, ISSN 0028-0836, 2011, Volume 478, Issue 7367, pp. 97 - 102
Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI) DEPENDENT PROBE AMPLIFICATION | FAILURE-TO-THRIVE | METABOLIC SYNDROME | RELATIVE QUANTIFICATION | SNP GENOTYPING DATA | HIDDEN-MARKOV MODEL | MULTIDISCIPLINARY SCIENCES | BODY-MASS INDEX | TIME QUANTITATIVE PCR | COPY NUMBER VARIATION | CIRCULAR BINARY SEGMENTATION | Humans | Middle Aged | Child, Preschool | RNA, Messenger - analysis | Head - anatomy & histology | Infant | Male | Developmental Disabilities - genetics | Gene Expression Profiling | North America | Obesity - genetics | Case-Control Studies | Young Adult | Mental Disorders - genetics | Aging | Gene Duplication - genetics | Adult | Female | Transcription, Genetic | Energy Metabolism - genetics | Child | Infant, Newborn | Chromosomes, Human, Pair 16 - genetics | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Europe | RNA, Messenger - genetics | Mutation - genetics | Body Height - genetics | Thinness - genetics | Phenotype | Comparative Genomic Hybridization | Adolescent | Heterozygote | Aged | Cohort Studies | Sequence Deletion - genetics | Obesity | Chromosome mapping | Usage | Genetic variation | Genetic aspects | Cognition disorders | Research | Risk factors | Schizophrenia | Gender | Behavior | Gene expression | Bias | Life Sciences | Human health and pathology | Genetics | Endocrinology and metabolism | Gene Duplication | Developmental Disabilities | Sequence Deletion | Thinness | genetics | Genetic Predisposition to Disease | Head | Gene Dosage | analysis | Energy Metabolism | Mental Disorders | Chromosomes, Human, Pair 16 | Body Height | Mutation | anatomy & histology | RNA, Messenger
Journal Article