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The Lancet Oncology, ISSN 1470-2045, 01/2019, Volume 20, Issue 1, pp. e54 - e64
Immune checkpoint inhibitors are reshaping the prognosis of many cancer and are progressively becoming the standard of care in the treatment of many tumour... 
RHEUMATOID-ARTHRITIS | MELANOMA | ONCOLOGY | RITUXIMAB | PATIENT | INDUCTION | MYASTHENIA-GRAVIS | MAINTENANCE THERAPY | T-CELLS | IPILIMUMAB | TOCILIZUMAB
Journal Article
Cytopathology, ISSN 0956-5507, 01/2019, Volume 30, Issue 1, pp. 51 - 60
Fine needle aspiration cytology (FNAC) is the current gold standard diagnostic method utilised for the initial investigation of thyroid nodules, although it is... 
thyroid nodule | Raman spectroscopy | cell lines | thyroid neoplasms | SYSTEM | AMERICAN ASSOCIATION | CYTOLOGY | PATHOLOGY | CELL BIOLOGY | CLINICAL ENDOCRINOLOGISTS | MALIGNANCY | FINE-NEEDLE-ASPIRATION | EXPERIENCE | Carbohydrates | Cytology | Benign | Lipids | Principal components analysis | Malignancy | Nodules | Thyroid cancer | Cellular biology | Spectrum analysis | Cell lines | Diagnosis | Thyroid
Journal Article
Oxidative Medicine and Cellular Longevity, ISSN 1942-0900, 2016, Volume 2016, pp. 7476241 - 2
  [...]the paper from E. Al Jaaly et al. entitled "Pulmonary Protection Strategies in Cardiac Surgery: Are We Making Any Progress?" discusses the... 
CELL BIOLOGY | Proteostasis Deficiencies - metabolism | Animals | Oxidation-Reduction | Humans | Proteostasis Deficiencies - pathology | Aging - metabolism | Aging - pathology | Proteins | Oxidative stress | Phosphorylation | Colleges & universities | Quality control | Aging | Biomarkers | Homeostasis | Biology | Alzheimers disease | Index Medicus
Journal Article
Modern Pathology, ISSN 0893-3952, 02/2017, Volume 30, Issue 2, p. 236
  Various histological variants of papillary thyroid carcinoma have been reported, some with clinical implications, some with peculiar, sometimes misleading... 
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2010, Volume 107, Issue 34, pp. 15140 - 15144
Between the genetic extremes of rare monogenic and common polygenic diseases lie diverse oligogenic disorders involving mutations in more than one locus in... 
Deficiency diseases | Sex hormones | Nervous system diseases | Disease models | Medical genetics | Genetic diseases | Genetic mutation | Kallmann syndrome | Human genetics | Hypogonadism | Rare variant | Digenic | Idiopathic hypogonadotropic hypogonadism | FGFR1 | idiopathic hypogonadotropic hypogonadism | GPR54 | MULTIDISCIPLINARY SCIENCES | CLINICAL HETEROGENEITY | MISSENSE MUTATIONS | PUBERTY | digenic | GENE | BARDET-BIEDL-SYNDROME | LINKED KALLMANN-SYNDROME | FIBROBLAST-GROWTH-FACTOR-RECEPTOR-1 | GNRH RECEPTOR | rare variant | Receptors, LHRH - genetics | Humans | Male | Gene Regulatory Networks | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Case-Control Studies | Receptors, Peptide - genetics | Genetic Variation | DNA Mutational Analysis | Female | Neuropeptides - genetics | Fibroblast Growth Factor 8 - genetics | Kallmann Syndrome - genetics | Extracellular Matrix Proteins - genetics | Transcription Factors - genetics | Nerve Tissue Proteins - genetics | Hypogonadism - genetics | Homozygote | Phenotype | Pedigree | Gastrointestinal Hormones - genetics | Heterozygote | Models, Genetic | Receptors, G-Protein-Coupled - genetics | Mutation | Receptors, Kisspeptin-1 | Gonadotropin-Releasing Hormone - deficiency | Cohort Studies | Multifactorial diseases | Genetic aspects | Hormones | Gonadotropin | Health aspects | Pathogens | Genetics | Genetic disorders | Pathogenesis | Index Medicus | Biological Sciences
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2013, Volume 92, Issue 5, pp. 725 - 743
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2011, Volume 108, Issue 28, pp. 11524 - 11529
Neuronal development is the result of a multitude of neural migrations, which require extensive cell-cell communication. These processes are modulated by... 
Enzymes | Phenotypes | Neurons | Medical genetics | Ligands | Sulfates | Genetic mutation | Kallmann syndrome | Human genetics | Hypogonadism | Heparan sulfotransferase | SPECIFICITY | GONADOTROPIN-RELEASING-HORMONE | MULTIDISCIPLINARY SCIENCES | DEFICIENCY | FGF RECEPTOR | FAMILY | heparan sulfotransferase | CAENORHABDITIS-ELEGANS | KALLMANN-SYNDROME | MUTATIONS | EXPRESSION | HEPARAN-SULFATE 6-O-SULFOTRANSFERASE | Species Specificity | Humans | Middle Aged | Genes, Helminth | Receptor, Fibroblast Growth Factor, Type 1 - metabolism | Caenorhabditis elegans Proteins - metabolism | Molecular Sequence Data | Kallmann Syndrome - enzymology | Male | Mutation, Missense | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Sulfotransferases - deficiency | Intercellular Signaling Peptides and Proteins - metabolism | Receptors, Fibroblast Growth Factor - genetics | Adult | Female | Sulfotransferases - metabolism | Child | Extracellular Matrix Proteins - metabolism | Sulfotransferases - genetics | Amino Acid Sequence | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - genetics | Kallmann Syndrome - genetics | Extracellular Matrix Proteins - genetics | Intercellular Signaling Peptides and Proteins - genetics | Models, Molecular | Nerve Tissue Proteins - genetics | Hypogonadism - enzymology | Hypogonadism - genetics | Nerve Tissue Proteins - metabolism | Sequence Homology, Amino Acid | Animals | Pedigree | Receptors, Fibroblast Growth Factor - metabolism | Mutation | In Vitro Techniques | Caenorhabditis elegans Proteins - genetics | Sulfotransferases - chemistry | Amino Acid Substitution | Index Medicus | Heparan sulfate | Fibroblast growth factor | Puberty | Intercellular signalling | Polysaccharides | Hedgehog protein | Infertility | Extracellular matrix | Gonadotropin-releasing hormone | Cell migration | Sugar | Biological Sciences
Journal Article
Journal Article
Clinical Genetics, ISSN 0009-9163, 08/2017, Volume 92, Issue 2, pp. 213 - 216
Journal Article