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European Journal of Human Genetics, ISSN 1018-4813, 01/2018, Volume 26, Issue 1, pp. 117 - 123
Journal Article
JOURNAL OF PATHOLOGY, ISSN 0022-3417, 08/2006, Volume 209, Issue 4, pp. 474 - 483
Langerhans cell histiocytosis (LCH) is a neoplastic disorder that results in clonal proliferation of cells with a Langerhans cell (LQ phenotype. The... 
MMP12 | GSN | Langerhans cell histiocytosis | FSCN1 | Langerhans cells | SAGE | CD1a | HODGKINS LYMPHOMA | REED-STERNBERG CELLS | CYTOKINES | DENDRITIC CELLS | MACROPHAGES | BONE-MARROW | TUMOR-CELLS | PATHOLOGY | METALLOELASTASE MMP-12 | FASCIN | ACTIN-BUNDLING PROTEIN | CD34 antigen | Cell proliferation | Immunohistochemistry | Prognosis | Serial analysis of gene expression | Data processing | Histiocytosis | Hemopoiesis | Polymerase chain reaction | CCL22 protein | Stem cells | Umbilical cord | CCL17 protein | Metalloendopeptidases - genetics | Oligonucleotide Array Sequence Analysis | Humans | Chemokine CCL22 | Gene Expression Profiling | Antigens, CD1 - analysis | Lectins, C-Type - genetics | Antigens, CD - genetics | Chemokines, CC - analysis | Antigens, CD - analysis | Histiocytosis, Langerhans-Cell - metabolism | Lectins, C-Type - analysis | Mannose-Binding Lectins - analysis | Muramidase - analysis | Carrier Proteins - analysis | Microfilament Proteins - genetics | Metalloendopeptidases - analysis | Gene Expression | Chemokine CCL17 | Gene Library | Langerhans Cells - chemistry | Muramidase - genetics | Biomarkers - analysis | Microfilament Proteins - analysis | Immunophenotyping | Gelsolin - analysis | Reverse Transcriptase Polymerase Chain Reaction | Matrix Metalloproteinase 12 | Immunohistochemistry - methods | Carrier Proteins - genetics | Mannose-Binding Lectins - genetics | Chemokines, CC - genetics | Gelsolin - genetics | Antigens, CD1 - genetics | Index Medicus
Journal Article
Journal Article
Molecular and Cellular Biochemistry, ISSN 0300-8177, 5/2014, Volume 390, Issue 1, pp. 263 - 270
Journal Article
Molecular Genetics and Genomics, ISSN 1617-4615, 12/2004, Volume 272, Issue 5, pp. 550 - 561
Glycogen synthase, an enzyme involved in glycogen biosynthesis, is regulated by phosphorylation and by the allosteric ligand glucose-6-phosphate (G6P). In... 
Neurospora crassa | HSE and STRE elements | Promoter region | gsn gene | Heat shock | RESERVE CARBOHYDRATE-METABOLISM | CELLS | ACTIVATION | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | YEAST GLYCOGEN-SYNTHASE | heat shock | INDUCTION | DNA-BINDING PROTEIN | SACCHAROMYCES-CEREVISIAE | HSP70 GENE | GENETICS & HEREDITY | promoter region | EXPRESSION | Enzymes | Phosphorylation | Introns | Glycogen synthase | Glycogen | Gene regulation | Regulatory sequences | Gene expression | 5' Untranslated regions | Neuromodulation | Glucose-6-phosphate | Promoters | Stress | Allosteric properties | Electrophoretic mobility | genomics | cDNA | Open reading frames | Transcription initiation | Gene Expression Regulation, Fungal | Genomic Library | Molecular Sequence Data | DNA Primers | Sequence Analysis, DNA | Proteins | Gene Expression Regulation, Enzymologic | Heat-Shock Response | Base Sequence | Cloning, Molecular | Electrophoretic Mobility Shift Assay | Gene Components | Glycogen Synthase | Binding sites | DNA, Complementary | DNA-Binding Proteins | 5' Untranslated Regions | DNA | Glycogen Synthase - genetics | DNA, Complementary - genetics | DNA-Binding Proteins - genetics | Heat-Shock Response - genetics | DNA-Binding Proteins - metabolism | Neurospora crassa - enzymology | Neurospora crassa - genetics | Binding Sites | Index Medicus
Journal Article
Muscle & Nerve, ISSN 0148-639X, 05/2016, Volume 53, Issue 5, pp. 762 - 769
IntroductionHereditary gelsolin amyloidosis (GA) is a rare condition caused by the gelsolin gene mutation. The diagnostic triad includes corneal lattice... 
cranial neuropathy | amyloidosis | gelsolin | bilateral facial paresis | facial paresis grading | Facial paresis grading | Amyloidosis | Gelsolin | Cranial neuropathy | Bilateral facial paresis | GSN GENE | NEUROSCIENCES | FINNISH TYPE FAF | POLYNEUROPATHY TYPE-IV | CLINICAL NEUROLOGY | LATTICE CORNEAL-DYSTROPHY | HEARING-LOSS | NEUROPATHY | FAMILIAL AMYLOIDOSIS | MERETOJAS SYNDROME | HEREDITARY AMYLOIDOSIS | MUTATION | Wood products | Workshops | Cornea | Motor units | Muscles | Facial nerve | Acoustics | Surgery | Cranial nerves | Point mutation | Skin | Dystrophy | Age | Injuries | EMG | Bell's palsy | Vestibulocochlear Nerve Diseases - physiopathology | Cutis Laxa - etiology | Humans | Middle Aged | Vestibulocochlear Nerve Diseases - etiology | Oculomotor Nerve Diseases - etiology | Male | Amyloid Neuropathies, Familial - physiopathology | Facial Nerve Diseases - etiology | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | Facial Paralysis - physiopathology | Aged, 80 and over | Adult | Female | Electromyography | Amyloidosis - complications | Cranial Nerve Diseases - physiopathology | Hypoglossal Nerve Diseases - etiology | Trigeminal Nerve Diseases - physiopathology | Trigeminal Nerve Diseases - etiology | Amyloid Neuropathies, Familial - complications | Amyloidosis - physiopathology | Neural Conduction | Facial Nerve Diseases - physiopathology | Oculomotor Nerve Diseases - physiopathology | Facial Muscles - physiopathology | Cranial Nerve Diseases - etiology | Corneal Dystrophies, Hereditary - complications | Aged | Facial Paralysis - etiology | Development and progression | Paralysis, Facial | Gene mutations | Index Medicus
Journal Article
Soil Science & Plant Nutrition, ISSN 0038-0768, 04/2008, Volume 54, Issue 2, pp. 197 - 203
Bradyrhizobium japonicum Is‐1 is incompatible with soybean ( Glycine max L. Merr.) cv. CNS ( Rj 2 Rj 3 ) and compatible with cv. Hill ( Rj 4 ) and is,... 
strain Is‐1 | mutant | gene | compatibility | Rj‐gsn | Bradyrhizobium japonicum | Rj | Bradyrhizobium japonicum strain Is-1 | Compatibility | Tn5 mutant | Rj-gsn gene
Journal Article
Journal Article