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The Journal of Architecture, ISSN 1360-2365, 07/2019, Volume 24, Issue 5, pp. 676 - 698
This article looks at discussions of communist urban planning in relation to both the Marxist theory of ideology and communication theory in the 1960s in the... 
Architecture | Urban planning | Communication theory
Journal Article
Architectural Histories, 2018, Volume 6, Issue 1
Journal Article
BIOMOLECULES, ISSN 2218-273X, 09/2019, Volume 9, Issue 9, p. 422
Methylation is a widespread modification occurring in DNA, RNA and proteins. The N6AMT1 (HEMK2) protein has DNA N6-methyladenine as well as the protein... 
N6AMT1 | METHYLATION | methyltransferase | alternative splicing | BIOCHEMISTRY & MOLECULAR BIOLOGY | WBSCR22/MERM1 | TRANSLATION | protein stability | TRMT112 | SUBSTRATE-SPECIFICITY | BIOGENESIS | HEMK2 PROTEIN | DNA | ADENINE | TRM112
Journal Article
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
The Journal of Architecture, ISSN 1360-2365, 07/2019, Volume 24, Issue 5, pp. 593 - 603
Journal Article
Oncology Letters, ISSN 1792-1074, 07/2018, Volume 16, Issue 1, pp. 211 - 218
Melanoma-associated antigen A (MAGEA) represent a class of tumor antigens that are expressed in a variety of malignant tumors, however, their expression in... 
Antibodies | Cancer-testis antigens | Melanoma antigens | Melanoma | Cancer | cancer-testis antigens | COMPLEXES | melanoma | P53 FUNCTION | UBIQUITIN LIGASES | T-CELL RESPONSES | ONCOLOGY | IMMUNOTHERAPY | CUTANEOUS MELANOMA | melanoma antigens | antibodies | cancer | A FAMILY | PROTEINS | EXPRESSION | CARCINOMA
Journal Article
Journal Article
AA files, ISSN 0261-6823, 01/2015, Issue 71, pp. 68 - 74
On dissident artists and architects in Estonia in the 1970s and 1980s who questioned the relationship between design, art and the environment; features the... 
Journal Article
Home Cultures, ISSN 1740-6315, 11/2012, Volume 9, Issue 3, pp. 225 - 231
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 5616 - 9
Non-invasive prenatal testing (NIPT) is a recent and rapidly evolving method for detecting genetic lesions, such as aneuploidies, of a fetus. However, there is... 
FRACTION | MATERNAL PLASMA | DNA | MULTIDISCIPLINARY SCIENCES | Genetic variance | Software packages | Fetuses | Genomes | Software | Gene mapping | Computer programs
Journal Article
2000, Dissertationes biologicae Universitatis Tartuensis, ISBN 9789985564691, Volume 58.
Dissertation
American Journal of Medical Genetics, Part A, ISSN 1552-4825, 04/2013, Volume 161, Issue 4, pp. 865 - 870
The 2p15-p16.1 microdeletion syndrome is a novel, rare disorder characterized by developmental delay, intellectual disability, microcephaly, growth... 
Autism | Copy number variation | Intellectual disability | SNP array | 2p15-p16.1 microdeletion syndrome | Developmental delay | RESOURCES | VARIANTS | PHENOTYPE |