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Journal Article
Traffic (Copenhagen, Denmark), ISSN 1398-9219, 10/2013, Volume 14, Issue 10, pp. 1091 - 1104
Journal Article
American journal of human genetics, ISSN 0002-9297, 06/2015, Volume 96, Issue 6, pp. 971 - 978
Heparan and chondroitin/dermatan sulfated proteoglycans have a wide range of roles in cellular and tissue homeostasis including growth factor function,... 
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Immunohistochemistry | Osteochondrodysplasias - pathology | Retinal Detachment - pathology | Humans | Cataract - pathology | Molecular Sequence Data | Male | Retinal Detachment - drug therapy | Hearing Disorders - genetics | Osteochondrodysplasias - drug therapy | Osteochondrodysplasias - genetics | Base Sequence | Osteoporosis - diagnostic imaging | Diphosphonates - therapeutic use | Craniofacial Abnormalities - pathology | Osteoporosis - genetics | Pentosyltransferases - blood | Real-Time Polymerase Chain Reaction | Craniofacial Abnormalities - genetics | Frameshift Mutation - genetics | Pentosyltransferases - genetics | Eye Diseases, Hereditary - pathology | Craniofacial Abnormalities - drug therapy | Retinal Detachment - genetics | Sequence Analysis, DNA | Eye Diseases, Hereditary - drug therapy | Eye Diseases, Hereditary - genetics | Radiography | Homozygote | Exome - genetics | Pedigree | Hearing Disorders - pathology | Cataract - genetics | Cataract - drug therapy | Genetic disorders | Proteoglycans | Gene mutations | Physiological aspects | Nucleotide sequencing | Identification and classification | Health aspects | Methods | DNA sequencing | Homeostasis | Genotype & phenotype | Genetics | Mutation | RNA-protein interactions | Index Medicus | Report
Journal Article
American journal of medical genetics. Part A, ISSN 1552-4825, 02/2018, Volume 176, Issue 2, pp. 465 - 469
Journal Article
American journal of human genetics, ISSN 0002-9297, 10/2015, Volume 97, Issue 4, pp. 521 - 534
Journal Article
The Journal of clinical investigation, ISSN 0021-9738, 04/2015, Volume 125, Issue 5, pp. 2161 - 2170
.... How TREM2 deficiency mediates demyelination and disease is unknown. Here, we addressed the basis for this genetic association using Trem2(-/-) mice... 
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Receptors, Immunologic - physiology | Cell Count | Humans | Nerve Tissue Proteins - deficiency | Gene Expression Profiling | Phagocytosis - genetics | Myelin Sheath - metabolism | Membrane Glycoproteins - physiology | Microglia - immunology | Osteochondrodysplasias - genetics | Nerve Tissue Proteins - biosynthesis | Microglia - pathology | Transcription, Genetic | Demyelinating Diseases - chemically induced | Demyelinating Diseases - pathology | Genes, Reporter | Disease Models, Animal | Cuprizone - toxicity | Myelin Sheath - physiology | Nerve Tissue Proteins - physiology | Receptors, Immunologic - deficiency | Nerve Tissue Proteins - genetics | Membrane Glycoproteins - genetics | Mice, Knockout | Lipodystrophy - genetics | Regeneration | Animals | Axons - pathology | Subacute Sclerosing Panencephalitis - genetics | Brain - pathology | Mice | Receptors, Immunologic - genetics | Membrane Glycoproteins - deficiency | Aging - metabolism | Physiological aspects | Development and progression | Cell receptors | Research | Demyelinating diseases | Phosphorylation | Statistical analysis | Lipids | Data processing | Genomes | Kinases | Gene expression | Brain research | Blood-brain barrier | Rodents | Morphology | Aging | Alzheimers disease | Expansion | Apoptosis | Index Medicus | Abridged Index Medicus
Journal Article
Nature communications, ISSN 2041-1723, 10/2019, Volume 10, Issue 1, pp. 1 - 19
Journal Article