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Nature Reviews Endocrinology, ISSN 1759-5029, 12/2018, Volume 15, Issue 1, pp. 33 - 51
The Ca2+-sensing receptor (CaSR) is a dimeric family C G protein-coupled receptor that is expressed in calcitropic tissues such as the parathyroid glands and... 
HYPERPLASTIC PARATHYROID-GLANDS | EXTRACELLULAR CA2+-SENSING RECEPTOR | OF-FUNCTION MUTATION | VITAMIN-D | HORMONE-RELATED PROTEIN | NEONATAL SEVERE HYPERPARATHYROIDISM | CELL-SURFACE EXPRESSION | ENDOCRINOLOGY & METABOLISM | AUTOSOMAL-DOMINANT HYPOCALCEMIA | FAMILIAL HYPOCALCIURIC HYPERCALCEMIA | HUMAN BREAST-CANCER | Hypocalcemia - physiopathology | Prognosis | Humans | Hypoparathyroidism - physiopathology | Male | Hypoparathyroidism - genetics | Nephrolithiasis - drug therapy | Incidence | Hypocalcemia - drug therapy | Female | Hypercalcemia - drug therapy | Hypercalciuria - genetics | Genetic Predisposition to Disease - epidemiology | Nephrolithiasis - genetics | Nephrolithiasis - physiopathology | Hypercalcemia - genetics | Hypoparathyroidism - drug therapy | Risk Assessment | Hypoparathyroidism - congenital | Hypercalciuria - physiopathology | Gene Expression Regulation | Treatment Outcome | Mutation - genetics | Calcimimetic Agents - therapeutic use | Hypercalciuria - drug therapy | Hypercalcemia - physiopathology | Hypocalcemia - genetics | Receptors, Calcium-Sensing - drug effects | Receptors, Calcium-Sensing - genetics | Hypercalcemia - congenital | Breastfeeding & lactation | Lactation | Colorectal carcinoma | Homeostasis | Arrestin | Hormones | Neuroblastoma | Drug development | Cell surface | Parathyroid | Calcium homeostasis | Calcium (urinary) | Excretion | Wound healing | Secretion | Therapeutic applications | Metabolism | Insulin | Asthma | Neurological diseases | Parathyroid hormone | Mutation | Cardiovascular diseases | Prostate | Brain injury | Hyperparathyroidism | Calcium-sensing receptors
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2015, Volume 10, Issue 4, pp. e0122650 - e0122650
Ectopic calcification (EC), which is the pathological deposition of calcium and phosphate in extra-skeletal tissues, may be associated with hypercalcaemic and... 
FAMILIAL TUMORAL CALCINOSIS | MUTANT MICE | MUTAGENESIS | HOMEOSTASIS | PROTEIN | GALNT3 | MULTIDISCIPLINARY SCIENCES | MISSENSE MUTATION | DRIVEN | DIFFERENTIATION | FGF23 | Longevity - drug effects | Humans | Glucuronidase - metabolism | Cercopithecus aethiops | Endoplasmic Reticulum - metabolism | Ethylnitrosourea - toxicity | Fibroblast Growth Factors - genetics | Molecular Sequence Data | Male | Genetic Loci | Mutation, Missense | Kidney - metabolism | N-Acetylgalactosaminyltransferases - genetics | Phosphates - blood | Calcinosis - metabolism | Disease Models, Animal | Amino Acid Sequence | Mice, Inbred C57BL | Genotype | Glucuronidase - chemistry | Codon, Nonsense | Vitamin D - blood | Phenotype | Sequence Alignment | Animals | Glucuronidase - genetics | Fibroblast Growth Factors - blood | Alleles | Vitamin D - analogs & derivatives | Mice | Polymorphism, Single Nucleotide | Calcinosis - pathology | COS Cells | Gene mutations | Genetic variation | Calcification | Causes of | Physiological aspects | Genetic aspects | Research | Calcification (ectopic) | Phosphates | Fibroblast growth factor | Animal models | Calcium | Fibroblast growth factor 23 | Disorders | Mapping | Metastasis | Proteins | Rodents | Tomography | Aging | Genetics | Growth factors | Deoxyribonucleic acid--DNA | Chronic illnesses | Medical research | Enzymes | Phenotypes | Nucleotide sequence | Abnormalities | Dihydroxyvitamin D | Chromosome 5 | Metabolism | Mutants | Mineral metabolism | Calcium phosphates | Medicine | Organic chemistry | Progeny | Ethyl nitrosourea | Councils | Life span | Calcinosis | Klotho protein | Metabolic pathways | Diabetes | Mutation | Gene mapping | Endoplasmic reticulum | Endocrinology | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2016, Volume 11, Issue 12, pp. e0167916 - e0167916
Non-syndromic kyphosis is a common disorder that is associated with significant morbidity and has a strong genetic involvement; however, the causative genes... 
ETIOLOGY | MUTAGENESIS | SKELETAL GROWTH | GENE | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | VERTEBRAL SEGMENTATION | DYSPLASIA | DWARFISM | SCHEUERMANN-DISEASE | Bone Density | Kyphosis - metabolism | Spine - metabolism | Tibia - diagnostic imaging | Cercopithecus aethiops | Ethylnitrosourea - toxicity | Male | Glycosylation | Mutation, Missense | Kyphosis - genetics | MAP Kinase Signaling System | Spine - diagnostic imaging | Animals | Receptors, Atrial Natriuretic Factor - genetics | Female | Mice | Mice, Inbred BALB C | Protein Processing, Post-Translational | Tibia - metabolism | COS Cells | Kyphosis - pathology | Disease Models, Animal | Immunohistochemistry | Kyphosis | Care and treatment | Usage | Gene mutations | Analysis | Risk factors | Drinking water | Peptides | Spine | Signal transduction | Conserved sequence | Genetics | Physiology | Bone (endochondral) | C-Type natriuretic peptide | Deoxyribonucleic acid--DNA | Medical research | Vertebrae | Neuromuscular diseases | MAP kinase | Heredity | Metabolism | Radiography | Bone mineral content | Studies | Chondrocytes | Mutation | Endoplasmic reticulum | Endocrinology | Alkaline phosphatase | Recombination | Phosphorylation | Genes | Body length | Genomes | Activation | Kinases | Dwarfism | Missense mutation | Rodents | Elongation | Dual energy X-ray absorptiometry | Nucleotide sequence | Morbidity | Medicine | Progeny | Signaling | Ethyl nitrosourea | Protein kinase | Potash | Diabetes | Gene mapping | Females | Potassium | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 11/2019, Volume 10, Issue 1, pp. 5175 - 10
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 1931-857X, 02/2010, Volume 298, Issue 2, pp. 365 - 380
Renal tubular reabsorption is important for extracellular fluid homeostasis and much of this occurs via the receptor-mediated endocytic pathway. This pathway... 
Hypercalciuric nephrolithiasis | Chloride/proton antiporter | Receptor-mediated endocytosis | Kinesin family | Proximal tubular reabsorption | proximal tubular reabsorption | PHYSIOLOGY | chloride/proton antiporter | hypercalciuric nephrolithiasis | kinesin family | receptor-mediated endocytosis | ALBUMIN ENDOCYTOSIS | PROXIMAL TUBULE CELLS | KIDNEY-CELLS | RENAL CHLORIDE CHANNEL | IMPAIRS ENDOCYTOSIS | UROLOGY & NEPHROLOGY | CYSTIC-FIBROSIS | PROTEINS | APICAL MEMBRANE | MOLECULAR-BASIS | Kidney Diseases - physiopathology | Up-Regulation | Humans | Cercopithecus aethiops | Electric Conductivity | Kidney - metabolism | Microtubules - metabolism | Drug Interactions | Adult | Protein Interaction Domains and Motifs | Genetic Diseases, X-Linked - physiopathology | Cell Line | Kidney Tubules, Proximal - cytology | Gene Library | Albumins - metabolism | Down-Regulation | Kidney - cytology | Endocytosis - physiology | Kinesin - metabolism | Mice, Knockout | Protein Transport | Chloride Channels - metabolism | Two-Hybrid System Techniques | Animals | Kidney Tubules, Proximal - metabolism | Mice | COS Cells | Chloride Channels - physiology | DNA, Complementary | Endocytosis | Gene mutations | Physiological aspects | Chloride channels | Genetic aspects | Research | Kidney diseases | Health aspects | Risk factors | chloride | proton antiporter
Journal Article
Nephron Physiology, ISSN 1660-2137, 05/2009, Volume 112, Issue 2, pp. p27 - p36
Journal Article