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PLoS ONE, ISSN 1932-6203, 09/2014, Volume 9, Issue 9, pp. e107428 - e107428
MID1 is a microtubule-associated protein that belongs to the TRIM family. MID1 functions as an ubiquitin E3 ligase, and recently was shown to catalyze the... 
BINDING DOMAINS | SERINE/THREONINE PHOSPHATASES | ZINC FINGERS | SYNDROME GENE-PRODUCT | MICROTUBULES | PHOSPHORYLATION | REGULATORY SUBUNIT ALPHA-4 | MULTIDISCIPLINARY SCIENCES | GBBB SYNDROME | LIGASE MID1 | OPITZ-G/BBB SYNDROME | Transcription Factors - chemistry | Protein Phosphatase 2 - chemistry | Humans | Molecular Sequence Data | Cleft Palate - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Recombinant Fusion Proteins - metabolism | Ubiquitination | Microtubule Proteins - chemistry | Genetic Diseases, X-Linked - genetics | Microtubule Proteins - genetics | Nuclear Proteins - genetics | Intracellular Signaling Peptides and Proteins - genetics | Fibroblasts - metabolism | Protein Structure, Tertiary | Amino Acid Sequence | Hypertelorism - metabolism | Hypospadias - metabolism | Signal Transduction | Gene Expression Regulation | Hypertelorism - genetics | Protein Phosphatase 2 - genetics | Ubiquitin-Protein Ligases - metabolism | Esophagus - metabolism | Microtubule Proteins - metabolism | Models, Molecular | Hypospadias - genetics | Nuclear Proteins - metabolism | Genetic Diseases, X-Linked - metabolism | Hypertelorism - pathology | Recombinant Fusion Proteins - chemistry | Transcription Factors - genetics | Esophagus - abnormalities | Fibroblasts - pathology | Nuclear Proteins - chemistry | Ubiquitin-Protein Ligases - chemistry | Sequence Homology, Amino Acid | Transcription Factors - metabolism | Esophagus - pathology | Sequence Alignment | Intracellular Signaling Peptides and Proteins - chemistry | Cleft Palate - pathology | Protein Phosphatase 2 - metabolism | Genetic Diseases, X-Linked - pathology | Recombinant Fusion Proteins - genetics | Cleft Palate - metabolism | Ubiquitin-Protein Ligases - genetics | Hypospadias - pathology | Ubiquitin | Genetic aspects | Phosphatases | Ligases | Phosphoprotein phosphatase | Birth defects | Phosphatase | Kinases | Zinc | Proteins | Fibroblasts | Protein phosphatase | Mutation | Catalysis | Ubiquitin-protein ligase | Apoptosis | Index Medicus
Journal Article
Oncotarget, ISSN 1949-2553, 2016, Volume 7, Issue 42, pp. 67934 - 67947
Journal Article
PLoS Genetics, ISSN 1553-7390, 06/2012, Volume 8, Issue 6, pp. e1002749 - e1002749
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2013, Volume 110, Issue 48, pp. 19525 - 19530
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2016, Volume 25, Issue 3, pp. 546 - 557
Journal Article
PLoS Genetics, ISSN 1553-7390, 10/2013, Volume 9, Issue 10, pp. e1003857 - e1003857
Roberts syndrome (RBS) is a human disease characterized by defects in limb and craniofacial development and growth and mental retardation. RBS is caused by... 
SISTER-CHROMATID COHESION | MAMMALIAN TARGET | SKELETAL-MUSCLE | ACTIVATED PROTEIN-KINASE | TRANSFER-RNA SYNTHETASE | GENETICS & HEREDITY | DIAMOND-BLACKFAN ANEMIA | C-MYC | INITIATION-FACTOR 4E | TRANSLATION INITIATION | CELL-GROWTH | TOR Serine-Threonine Kinases - metabolism | Humans | Multiprotein Complexes - genetics | Zebrafish - embryology | Acetyltransferases - genetics | RNA, Ribosomal - genetics | Tumor Suppressor Protein p53 - genetics | Mechanistic Target of Rapamycin Complex 1 | Multiprotein Complexes - metabolism | TOR Serine-Threonine Kinases - genetics | Ectromelia - genetics | Cell Cycle Proteins - genetics | Craniofacial Abnormalities - metabolism | Leucine - genetics | Craniofacial Abnormalities - genetics | Chromosome Segregation | Hypertelorism - metabolism | Chromosomal Proteins, Non-Histone - metabolism | Signal Transduction | Cell Cycle Proteins - metabolism | Hypertelorism - genetics | Tumor Suppressor Protein p53 - metabolism | Embryonic Development | Ectromelia - metabolism | Chromosomal Proteins, Non-Histone - genetics | Animals | Physiological aspects | Rapamycin | Genetic aspects | Genetic disorders | Leucine | Health aspects | Index Medicus | Proteins | Yeast | Cyclin-dependent kinases | Cell division | Biosynthesis | Mutation | Kinases | Gene expression | Chromosomes | Evacuations & rescues | Defects
Journal Article
The FEBS Journal, ISSN 1742-464X, 07/2017, Volume 284, Issue 14, pp. 2183 - 2193
Mutations of human MID 1 are associated with X‐linked Opitz G Syndrome ( XLOS ), which is characterized by midline birth defects. XLOS ‐observed mutations... 
Ubiquitination | PP2A | E3 ligase | B‐box | TRIM | B-box | REGULATORY SUBUNIT | CATALYTIC SUBUNIT | B-BOXES | UBIQUITIN LIGASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEIN PHOSPHATASE 2A | BINDING PROTEIN | G/BBB SYNDROME | SENSITIVE SIGNAL-TRANSDUCTION | RING | Transcription Factors - chemistry | Humans | Nuclear Proteins - ultrastructure | Substrate Specificity | Cleft Palate - genetics | Microtubule Proteins - chemistry | Protein Domains | Genetic Diseases, X-Linked - genetics | Microtubule Proteins - genetics | Nuclear Proteins - genetics | Protein Structure, Tertiary | Amino Acid Sequence | Hypertelorism - metabolism | Hypospadias - metabolism | Hypertelorism - genetics | Esophagus - metabolism | Microtubule Proteins - metabolism | Models, Molecular | Hypospadias - genetics | Microtubule Proteins - ultrastructure | Nuclear Proteins - metabolism | Genetic Diseases, X-Linked - metabolism | Hypertelorism - pathology | Transcription Factors - genetics | Transcription Factors - ultrastructure | Esophagus - abnormalities | Nuclear Proteins - chemistry | Sequence Homology, Amino Acid | Transcription Factors - metabolism | Esophagus - pathology | Cleft Palate - pathology | Protein Phosphatase 2 - metabolism | Genetic Diseases, X-Linked - pathology | Cleft Palate - metabolism | Protein Processing, Post-Translational | Mutation | Hypospadias - pathology | Embryonic development | Genetic aspects | Congenital defects | Tertiary structure | Birth defects | Cleft lip/palate | Embryonic growth stage | Embryogenesis | Opitz syndrome | Catalysis | Protein structure | Ubiquitin-protein ligase | Structure-function relationships | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 11/2011, Volume 286, Issue 46, pp. 39945 - 39957
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 5, pp. e20051 - e20051
The human developmental diseases Cornelia de Lange Syndrome (CdLS) and Roberts Syndrome (RBS) are both caused by mutations in proteins responsible for sister... 
SISTER-CHROMATID COHESION | DROSOPHILA NIPPED-B | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | C-MYC | S-PHASE | DE-LANGE-SYNDROME | MUTATIONS | ESTABLISHMENT | HUMAN HOMOLOG | DNA-REPLICATION | Transcription, Genetic - drug effects | Acetyltransferases - metabolism | Animal Fins - growth & development | Apoptosis - drug effects | Humans | Craniofacial Abnormalities - embryology | Embryo, Nonmammalian - metabolism | Animal Fins - drug effects | Zebrafish - embryology | Acetyltransferases - genetics | Ectromelia - pathology | Embryo, Nonmammalian - drug effects | G2 Phase - drug effects | Caspases - metabolism | Acetyltransferases - deficiency | Larva - drug effects | Craniofacial Abnormalities - pathology | Larva - genetics | Disease Models, Animal | Oligonucleotides, Antisense - pharmacology | Chromosomal Proteins, Non-Histone - metabolism | Zebrafish Proteins - metabolism | Cell Cycle Proteins - metabolism | Embryonic Development - genetics | Gene Expression Regulation, Developmental - drug effects | Tumor Suppressor Protein p53 - metabolism | Hypertelorism - pathology | Enzyme Activation - drug effects | Zebrafish Proteins - deficiency | Animals | Mitosis - drug effects | Zebrafish - metabolism | Zebrafish Proteins - genetics | Cell Cycle - drug effects | Embryonic Development - drug effects | Proteins | Embryonic development | DNA microarrays | RNA | Cell death | Analysis | Cell cycle | Genetic aspects | Genetic transcription | Mediation | Chromosomes | Cell proliferation | Cohesion | Regulators | Transcription | Laboratories | Genes | Cytology | Genomes | Defects | Pathways | Fibroblasts | Acetylation | Deoxyribonucleic acid--DNA | Abnormalities | Cell division | Zebrafish | Runx1 protein | Gene expression | Ribonucleic acid--RNA | Embryos | Mutants | Medicine | Pathology | Depletion | Insects | S phase | Stem cells | Cohesin | Mutation | Apoptosis | Index Medicus | Deoxyribonucleic acid | Ribonucleic acid | DNA
Journal Article
DMM Disease Models and Mechanisms, ISSN 1754-8403, 08/2015, Volume 8, Issue 8, pp. 941 - 955
Journal Article
BMC Genomics, ISSN 1471-2164, 01/2016, Volume 17, Issue 1, pp. 25 - 25
Journal Article