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Biochimie, ISSN 0300-9084, 12/2015, Volume 119, pp. 146 - 165
GAMT | CRTR | SLC6A8 | AGAT | AMP activated protein kinase | Creatine | Secondary creatine disorders | Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Amino Acid Transport Systems, Basic - genetics | Humans | Nerve Tissue Proteins - deficiency | Movement Disorders - diagnosis | Amidinotransferases - genetics | Intellectual Disability - metabolism | Biological Transport, Active | Gyrate Atrophy - enzymology | Amino Acid Metabolism, Inborn Errors - genetics | Intellectual Disability - enzymology | Brain Diseases, Metabolic, Inborn - genetics | Hyperammonemia - diagnosis | Hyperammonemia - genetics | Creatine - genetics | Urea Cycle Disorders, Inborn - metabolism | Creatine - biosynthesis | Gyrate Atrophy - genetics | Plasma Membrane Neurotransmitter Transport Proteins - metabolism | Guanidinoacetate N-Methyltransferase - metabolism | Amidinotransferases - metabolism | Plasma Membrane Neurotransmitter Transport Proteins - genetics | Language Development Disorders - enzymology | Urea Cycle Disorders, Inborn - diagnosis | Energy Metabolism | Urea Cycle Disorders, Inborn - enzymology | Movement Disorders - genetics | Mutation | Ornithine - deficiency | Amino Acid Transport Systems, Basic - metabolism | Amino Acid Metabolism, Inborn Errors - enzymology | S-Adenosylmethionine - metabolism | AMP-Activated Protein Kinases - metabolism | Hyperammonemia - metabolism | Developmental Disabilities - metabolism | Guanidinoacetate N-Methyltransferase - genetics | Ornithine - genetics | Developmental Disabilities - genetics | Language Development Disorders - metabolism | Brain Diseases, Metabolic, Inborn - enzymology | Brain Diseases, Metabolic, Inborn - diagnosis | Intellectual Disability - genetics | Amino Acid Metabolism, Inborn Errors - diagnosis | Amino Acid Metabolism, Inborn Errors - metabolism | Mental Retardation, X-Linked - genetics | Mental Retardation, X-Linked - enzymology | Developmental Disabilities - enzymology | Language Development Disorders - diagnosis | Mental Retardation, X-Linked - diagnosis | Movement Disorders - enzymology | Creatine - metabolism | Hyperammonemia - enzymology | Creatine - deficiency | Gyrate Atrophy - diagnosis | Developmental Disabilities - diagnosis | Speech Disorders - diagnosis | Plasma Membrane Neurotransmitter Transport Proteins - deficiency | Speech Disorders - metabolism | Amidinotransferases - deficiency | Brain Diseases, Metabolic, Inborn - metabolism | Language Development Disorders - genetics | Ornithine - metabolism | Gyrate Atrophy - metabolism | Prenatal Diagnosis | Speech Disorders - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Amino Acid Transport Systems, Basic - deficiency | Movement Disorders - metabolism | Animals | Urea Cycle Disorders, Inborn - genetics | Guanidinoacetate N-Methyltransferase - deficiency | Intellectual Disability - diagnosis | Movement Disorders - congenital | Speech Disorders - enzymology | Methylation | Mental Retardation, X-Linked - metabolism | Antioxidants | Phosphates | Algorithms | Animal behavior | Physiological aspects | GABA | Glycine | Phosphotransferases | Medical research | Medicine, Experimental | Protein kinases | Index Medicus | Life Sciences
Journal Article
Rheumatology international, ISSN 0172-8172, 05/2019, Volume 39, Issue 5, pp. 911 - 919
Life Sciences & Biomedicine | Rheumatology | Science & Technology | Genetic Testing | Agammaglobulinemia - genetics | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Osteomyelitis - genetics | Anemia, Dyserythropoietic, Congenital - diagnosis | Child, Preschool | Pyrin - genetics | Agammaglobulinemia - diagnosis | Male | Mevalonate Kinase Deficiency - genetics | CARD Signaling Adaptor Proteins - genetics | Young Adult | Adult | Female | Adenosine Deaminase - deficiency | Immunologic Deficiency Syndromes - diagnosis | Child | Cryopyrin-Associated Periodic Syndromes - genetics | Adenosine Deaminase - genetics | Severe Combined Immunodeficiency - diagnosis | Anemia, Dyserythropoietic, Congenital - genetics | Familial Mediterranean Fever - genetics | Intercellular Signaling Peptides and Proteins - genetics | Nucleoside Transport Proteins - genetics | Phosphotransferases (Alcohol Group Acceptor) - genetics | Hereditary Autoinflammatory Diseases - diagnosis | Sequence Analysis, DNA | Mevalonate Kinase Deficiency - diagnosis | Severe Combined Immunodeficiency - genetics | Cryopyrin-Associated Periodic Syndromes - diagnosis | Osteomyelitis - diagnosis | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Immunologic Deficiency Syndromes - genetics | Familial Mediterranean Fever - diagnosis | High-Throughput Nucleotide Sequencing | Calcium-Binding Proteins - genetics | Hereditary Autoinflammatory Diseases - genetics | Medicine, Experimental | Genetic research | Medical research | Genes | Index Medicus
Journal Article
Journal Article
Oncogene, ISSN 0950-9232, 01/2009, Volume 28, Issue 4, pp. 509 - 517
Mutations | Mouse model | Thyroid cancer | Pten | Carcinogenesis | Biochemistry & Molecular Biology | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Fundamental and applied biological sciences. Psychology | Non tumoral diseases. Target tissue resistance. Benign neoplasms | Malignant tumors | Thyroid. Thyroid axis (diseases) | Biological and medical sciences | Endocrinopathies | Cell physiology | Molecular and cellular biology | Medical sciences | Cell transformation and carcinogenesis. Action of oncogenes and antioncogenes | Cyclin D1 - metabolism | Cell Proliferation | Chromosomes, Mammalian - genetics | Lung Neoplasms - metabolism | Caspase 3 - metabolism | Cell Survival - genetics | Apoptosis - genetics | Lung Neoplasms - pathology | NF-kappa B - metabolism | Phosphatidylinositol 3-Kinases - metabolism | Proto-Oncogene Proteins c-akt - genetics | Thyroid Hormone Receptors beta - genetics | Neoplasm Metastasis | Lung Neoplasms - secondary | Forkhead Transcription Factors - metabolism | Mice, Mutant Strains | Caspase 3 - genetics | Proto-Oncogene Proteins c-akt - metabolism | Disease Models, Animal | Lung Neoplasms - genetics | PTEN Phosphohydrolase - genetics | Thyroid Hormone Receptors beta - metabolism | Ribosomal Protein S6 Kinases, 70-kDa - metabolism | Neoplasm Invasiveness | PTEN Phosphohydrolase - metabolism | Ribosomal Protein S6 Kinases, 70-kDa - genetics | Mice, Transgenic | Phosphotransferases (Alcohol Group Acceptor) - genetics | Signal Transduction - genetics | Forkhead Transcription Factors - genetics | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Phosphatidylinositol 3-Kinases - genetics | Carrier Proteins - genetics | Thyroid Neoplasms - genetics | Animals | Carrier Proteins - metabolism | Cyclin D1 - genetics | NF-kappa B - genetics | Mice | TOR Serine-Threonine Kinases | Chromosomes, Mammalian - metabolism | Enzyme Activation - genetics | Forkhead Box Protein O3 | Thyroid Neoplasms - metabolism | Thyroid Neoplasms - pathology | Development and progression | Tumor suppressor genes | Cellular signal transduction | Genetic aspects | Research | Health aspects | Risk factors | Genetics | Rodents | Thyroid diseases | Tumors | Index Medicus | thyroid cancer | mutations | carcinogenesis | mouse model
Journal Article
The Journal of clinical investigation, ISSN 0021-9738, 11/2013, Volume 123, Issue 11, pp. 4935 - 4944
Journal Article
Oncogene, ISSN 0950-9232, 08/2018, Volume 37, Issue 33, pp. 4518 - 4533
Journal Article