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المصدر: PLoS Genetics, Vol 17, Iss 2, p e1009144 (2021)
Verhoef, E, Shapland, C Y, Fisher, S E, Dale, P S & St Pourcain, B 2021, ' The developmental genetic architecture of vocabulary skills during the first three years of life : Capturing emerging associations with later-life reading and cognition ', PLoS Genetics, vol. 17, no. 2, e1009144 . https://doi.org/10.1371/JOURNAL.PGEN.1009144Test
Plos Genetics, 17, 2, pp. 1-19
PLoS Genetics
Plos Genetics, 17, 1-19

مصطلحات موضوعية: Male, Cancer Research, Vocabulary, Heredity, Genetic Linkage, Intelligence, Social Sciences, QH426-470, Developmental psychology, Cohort Studies, Cognition, 0302 clinical medicine, Psychology, Longitudinal Studies, Child, Correlation of Data, Genetics (clinical), Language, media_common, Grammar, 0303 health sciences, education.field_of_study, Verbal reasoning, Semantics, Phenotypes, Phenotype, Child, Preschool, Female, Research Article, Neuroinformatics, Genotype, media_common.quotation_subject, Population, Biology, Phonology, Language Development, Polymorphism, Single Nucleotide, Structural equation modeling, 03 medical and health sciences, Genetic variation, Genetics, Humans, Cognitive skill, education, Molecular Biology, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Evolutionary Biology, Population Biology, Human intelligence, Cognitive Psychology, Infant, Biology and Life Sciences, Linguistics, Human Genetics, Genetic architecture, Reading, Multivariate Analysis, Genetic Polymorphism, Cognitive Science, Software, Population Genetics, 030217 neurology & neurosurgery, Genome-Wide Association Study, Neuroscience

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df5a95c449dda32300645ddca0b01c6aTest
https://doaj.org/article/14883abe84fd408eb716d1bbdcf521f1Test

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Dysfunctional stem and progenitor cells impair fracture healing with age

المؤلفون: Philip S. Low, Jiliang Li, Diane R. Wagner, Matthias Clauss, Melissa A. Kacena, Jeffery J Nielsen, Sonali Karnik, Alanna Fennimore, Zachary J. Gunderson, Hunter J Promer, Jonathan W. Lowery, M. Terry Loghmani, Todd O. McKinley

المصدر: World Journal of Stem Cells

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c8db35d222dc0061d0ebc2e5784f88eTest
http://europepmc.org/articles/PMC6600851Test

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Neoplasm Risk Among Individuals With a Pathogenic Germline Variant in DICER1

المؤلفون: Douglas R. Stewart, Ana F. Best, Ann G. Carr, Christian P. Kratz, Laura A. Harney, D. Ashley Hill, Anne K. Harris, Yoav H. Messinger, Louis P. Dehner, Kris Ann P. Schultz, Philip S. Rosenberg, Gretchen M. Williams

المصدر: Journal of Clinical Oncology. 37:668-676

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db47a1182ab11aa445df107e8276f6ecTest
https://doi.org/10.1200/jco.2018.78.4678Test

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Reprogramming of profibrotic macrophages for treatment of bleomycin-induced pulmonary fibrosis

المؤلفون: Cheryl Nickerson-Nutter, Ehab A. Ayaub, Yen-Hsing Li, Estela Puchulu-Campanella, Madduri Srinivasarao, Philip S. Low, Spencer D. Lindeman, Fenghua Zhang, Konstantin Tsoyi, Bingbing Wang, Suraj U. Hettiarachchi, Sasmita Rout, Abigail Cox, Ivan O. Rosas, Qian Luo

المصدر: EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 12, Iss 8, Pp n/a-n/a (2020)

مصطلحات موضوعية: 0301 basic medicine, Medicine (General), medicine.medical_treatment, Pulmonary Fibrosis, Respiratory System, QH426-470, Bleomycin, Article, Extracellular matrix, 03 medical and health sciences, chemistry.chemical_compound, Idiopathic pulmonary fibrosis, Mice, 0302 clinical medicine, R5-920, Fibrosis, Pulmonary fibrosis, Macrophages, Alveolar, Chemical Biology, medicine, Genetics, Animals, toll‐like receptor 7, folate receptor β, bleomycin, business.industry, Macrophages, virus diseases, TLR7, Articles, Fibroblasts, medicine.disease, idiopathic pulmonary fibrosis, Mice, Inbred C57BL, 030104 developmental biology, Cytokine, chemistry, Toxicity, Cancer research, Molecular Medicine, business, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d8ec9037972638af948a59b037c0d8cTest
https://pubmed.ncbi.nlm.nih.gov/32597014Test

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A missense variant in mitochondrial amidoxime reducing component 1 gene and protection against liver disease

المساهمون: Institute for Molecular Medicine Finland, University of Helsinki, Complex Disease Genetics, Genomics of Neurological and Neuropsychiatric Disorders, HUS Helsinki and Uusimaa Hospital District, Emdin, Connor A. [0000-0003-2337-1229], Haas, Mary E. [0000-0002-2816-9268], Khera, Amit V. [0000-0001-6535-5839], Chaffin, Mark [0000-0002-1234-5562], Klarin, Derek [0000-0002-4636-5780], Jiang, Lan [0000-0002-2583-3661], Wei, Wei-Qi [0000-0003-4985-056X], Feng, Qiping [0000-0002-6213-793X], Havulinna, Aki [0000-0002-4787-8959], Kiiskinen, Tuomo [0000-0002-6306-8227], Bick, Alexander [0000-0001-5824-9595], Ardissino, Diego [0000-0003-0410-3528], Schunkert, Heribert [0000-0001-6428-3001], McPherson, Ruth [0000-0002-9087-6107], Erdmann, Jeanette [0000-0002-4486-6231], Chang, Kyong-Mi [0000-0001-6811-9364], Vujkovic, Marijana [0000-0003-4924-5714], Voight, Ben [0000-0002-6205-9994], Damrauer, Scott [0000-0001-8009-1632], Lynch, Julie [0000-0003-0108-2127], Kaplan, David [0000-0002-3839-336X], Serper, Marina [0000-0003-4899-2160], Tsao, Philip [0000-0001-7274-9318], Mercader, Josep [0000-0001-8494-3660], Hanis, Craig [0000-0002-4880-5348], Denny, Joshua [0000-0002-3049-7332], Apollo - University of Cambridge Repository, Emdin, Connor A [0000-0003-2337-1229], Haas, Mary E [0000-0002-2816-9268], Khera, Amit V [0000-0001-6535-5839]

المصدر: PLoS Genetics, Vol 16, Iss 4, p e1008629 (2020)
PLoS Genetics, Vol 17, Iss 4, p e1009503 (2021)
PLoS Genetics

مصطلحات موضوعية: Liver Cirrhosis, Male, Cancer Research, Cirrhosis, Datasets as Topic, PROTEIN, Coronary Artery Disease, QH426-470, Fetge -- Malalties, Biochemistry, Vascular Medicine, Liver disease, chemistry.chemical_compound, 0302 clinical medicine, Sociology, ANGPTL3, Consortia, Liver Cirrhosis, Alcoholic, Loss of Function Mutation, Psychology, Coronary Heart Disease, CONFERS SUSCEPTIBILITY, Genetics (clinical), 0303 health sciences, Liver Diseases, Homozygote, Fatty liver, 1184 Genetics, developmental biology, physiology, Middle Aged, Lipids, Addicts, 3. Good health, Cholesterol, Liver, Alkaline phosphatase, Female, Oxidoreductases, ENZYMES, Colesterol, Research Article, medicine.medical_specialty, Cirrosi hepàtica, Cardiology, Mutation, Missense, Addiction, Gastroenterology and Hepatology, Biology, Social sciences, TM6SF2, Mitochondrial Proteins, 03 medical and health sciences, Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Alcoholics, GENOME-WIDE ASSOCIATION, Molecular Biology, Alleles, Ecology, Evolution, Behavior and Systematics, PNPLA3, 030304 developmental biology, Medicine and health sciences, Biology and life sciences, MORTALITY, Correction, Cholesterol, LDL, medicine.disease, RISK LOCI, Mitochondrial amidoxime reducing component 1, Fatty Liver, Endocrinology, YIELD, chemistry, Alanine transaminase, Genetic Loci, biology.protein, 3111 Biomedicine, Proteïnes, 030217 neurology & neurosurgery

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الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b2aeafb245632b250e5e05c8a2d99cdTest
http://hdl.handle.net/10230/47380Test

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دورية أكاديمية

The C-terminal region of S100A4 is important for its metastasis-inducing properties

المؤلفون: Zhang, Shu, Wang, Guozheng, Liu, Dong, Bao, Zhengzheng, Fernig, David G, Rudland, Philip S, Barraclough, Roger

المصدر: Oncogene ; volume 24, issue 27, page 4401-4411 ; ISSN 0950-9232 1476-5594

مصطلحات موضوعية: Cancer Research, Genetics, Molecular Biology

الإتاحة: https://doi.org/10.1038/sj.onc.1208663Test
https://www.nature.com/articles/1208663.pdfTest
https://www.nature.com/articles/1208663Test

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