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"authors": "Wang F, Li H, Xu M, Li H, Zhao L, Yang L, Zaneveld JE, Wang K, Li Y, Sui R, Chen R", "reference": { "type": "PubMed", "id": "25477324", "url": "https://pubmed.ncbi.nlm.nih.gov/25477324" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q13562-1", "protein_name": "Neurogenic differentiation factor 1", "gene_name": "NEUROD1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q13562", "url": "https://www.uniprot.org/uniprotkb/Q13562" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.25477324", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { 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Haeringen A, Vanakker O, Van Hecke A, Amrom D, Kury S, Ratner C, Jethva R, Gamble C, Jacq B, Fasano L, Santpere G, Lorente-Galdos B, Sestan N, Gelot A, Giacuzz S, Goebbels S, Represa A, Cardoso C, Cremer H, de Chevigny A", "reference": { "type": "PubMed", "id": "34188164", "url": "https://pubmed.ncbi.nlm.nih.gov/34188164" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q15784-1", "protein_name": "Neurogenic differentiation factor 2", "gene_name": "NEUROD2", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q15784", "url": "https://www.uniprot.org/uniprotkb/Q15784" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.34188164", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { 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[] } ] }, { "title": "Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome.", "journal": "Journal of medical genetics", "date": "2010", "authors": "Gerards M, Sluiter W, van den Bosch BJ, de Wit LE, Calis CM, Frentzen M, Akbari H, Schoonderwoerd K, Scholte HR, Jongbloed RJ, Hendrickx AT, de Coo IF, Smeets HJ", "reference": { "type": "PubMed", "id": "19542079", "url": "https://pubmed.ncbi.nlm.nih.gov/19542079" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q5TEU4-1", "protein_name": "Arginine-hydroxylase NDUFAF5, mitochondrial", "gene_name": "NDUFAF5", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q5TEU4", "url": "https://www.uniprot.org/uniprotkb/Q5TEU4" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.19542079", "abstract": "", "glycosylation": [], "mutagenesis": [], 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"glycosylation_automatic_literature_mining", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { "field": "o_linked_glycan_sites", "count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "Structural features in the glycine-binding sites of the GluN1 and GluN3A subunits regulate the surface delivery of NMDA receptors.", "journal": "Scientific reports", "date": "2019", "authors": "Skrenkova K, Hemelikova K, Kolcheva M, Kortus S, Kaniakova M, Krausova B, Horak M", "reference": { "type": "PubMed", "id": "31444392", "url": "https://pubmed.ncbi.nlm.nih.gov/31444392" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q8TCU5-1", "protein_name": "Glutamate receptor ionotropic, NMDA 3A", "gene_name": "GRIN3A", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q8TCU5", "url": "https://www.uniprot.org/uniprotkb/Q8TCU5" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.31444392", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": "referenced_glycans", "table_stats": [ { "field": "total", "count": 0 } ], "sort_fields": [] }, { "table_id": "glycosylation", "table_stats": [ { "field": "total", "count": 0 }, { "field": "total_sites", "count": 0 }, { "field": "n_linked_sites", "count": 0 }, { "field": "o_linked_sites", "count": 0 }, { "field": "n_linked_glycan_sites", "count": 0 }, { 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