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Involvement of the osteoinductive factors, Tmem119 and BMP-2, and the ER stress response PERK-eIF2α-ATF4 pathway in the commitment of myoblastic into osteoblastic cells.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Interdependence between Chromogranin-A, Alternatively Activated Macrophages, Tight Junction Proteins and the Epithelial Functions. A Human and In-Vivo/In-Vitro Descriptive Study.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 21, p. 7976, doi. 10.3390/ijms21217976
- By:
- Publication type:
- Article
Catestatin Regulates Epithelial Cell Dynamics to Improve Intestinal Inflammation.
- Published in:
- Vaccines, 2018, v. 6, n. 4, p. 67, doi. 10.3390/vaccines6040067
- By:
- Publication type:
- Article
Parathyroid hormone signaling via Gαs is selectively inhibited by an NH<sub>2</sub>-terminally truncated Gαs: Implications for pseudohypoparathyroidism.
- Published in:
- Journal of Bone & Mineral Research, 2011, v. 26, n. 10, p. 2473, doi. 10.1002/jbmr.461
- By:
- Publication type:
- Article
The Calcium-Sensing Receptor and 25-Hydroxyvitamin D-1 α-Hydroxylase Interact to Modulate Skeletal Growth and Bone Turnover.
- Published in:
- Journal of Bone & Mineral Research, 2010, v. 25, n. 7, p. 1627, doi. 10.1002/jbmr.58
- By:
- Publication type:
- Article
Exogenous PTH and Endogenous 1,25-Dihydroxyvitamin D Are Complementary in Inducing an Anabolic Effect on Bone.
- Published in:
- Journal of Bone & Mineral Research, 2008, v. 23, n. 8, p. 1257, doi. 10.1359/jbmr.080318
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- Publication type:
- Article
Exogenous PTH-Related Protein and PTH Improve Mineral and Skeletal Status in 25-Hydroxyvitamin D-1α-Hydroxylase and PTH Double Knockout Mice.
- Published in:
- Journal of Bone & Mineral Research, 2005, v. 20, n. 10, p. 1766, doi. 10.1359/JBMR.050608
- By:
- Publication type:
- Article
25-Hydroxyvitamin D 1α-Hydroxylase: Structure of the Mouse Gene, Chromosomal Assignment, and Developmental Expression.
- Published in:
- Journal of Bone & Mineral Research, 2001, v. 16, n. 1, p. 46, doi. 10.1359/jbmr.2001.16.1.46
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- Publication type:
- Article
Bone mineral metabolism in T lymphocyte-deficient and -replete strains of rat.
- Published in:
- Journal of Bone & Mineral Research, 1995, v. 10, n. 10, p. 1556, doi. 10.1002/jbmr.5650101018
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- Publication type:
- Article
Expression of the 1,25-dihydroxyvitamin D<sub>3</sub>-24-hydroxylase gene in rat intestine: Response to calcium, vitamin D<sub>3</sub> and calcitriol administration in vivo.
- Published in:
- Journal of Bone & Mineral Research, 1995, v. 10, n. 8, p. 1148, doi. 10.1002/jbmr.5650100803
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- Publication type:
- Article
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2017, p. 3961, doi. 10.1210/jc.2017-00250
- By:
- Publication type:
- Article
Autosomal Dominant PTH Gene Signal Sequence Mutation in a Family With Familial Isolated Hypoparathyroidism.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Codon Arg15 Mutations of the AP2S1 Gene: Common Occurrence in Familial Hypocalciuric Hypercalcemia Cases Negative for Calcium-Sensing Receptor (CASR) Mutations.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Ruling in a suspect: the role of AP2S1 mutations in familial hypocalciuric hypercalcemia type 3.
- Published in:
- 2013
- By:
- Publication type:
- Editorial
Decreased transcriptional activity of calcium-sensing receptor gene promoter 1 is associated with calcium nephrolithiasis.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Menin missense mutants encoded by the MEN1 gene that are targeted to the proteasome: restoration of expression and activity by CHIP siRNA.
- Published in:
- 2012
- By:
- Publication type:
- journal article
Neonatal Hyperparathyroidism with a Heterozygous Calcium-Sensing Receptor (CASR) R185Q Mutation: Clinical Benefit from Cinacalcet.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 4, p. E707, doi. 10.1210/jc.2010-1306
- By:
- Publication type:
- Article
Large intragenic deletion of CDC73 (exons 4–10) in a three-generation hyperparathyroidism-jaw tumor (HPT-JT) syndrome family.
- Published in:
- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0445-0
- By:
- Publication type:
- Article
Effect of Menin Deletion in Early Osteoblast Lineage on the Mineralization of an In Vitro 3D Osteoid-like Dense Collagen Gel Matrix.
- Published in:
- Biomimetics (2313-7673), 2022, v. 7, n. 3, p. 101, doi. 10.3390/biomimetics7030101
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- Publication type:
- Article
Identification and Functional Characterization of Three NoLS (Nucleolar Localisation Signals) Mutations of the CDC73 Gene.
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0082292
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- Publication type:
- Article
Circulating concentrations of parathyroid hormone-like peptide in malignancy and in hyperparathyroidism.
- Published in:
- Journal of Bone & Mineral Research, 1990, v. 5, n. 2, p. 105, doi. 10.1002/jbmr.5650050203
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- Publication type:
- Article
Regulation by calcium of parathyroid hormone mRNA in cultured parathyroid tissue.
- Published in:
- Journal of Bone & Mineral Research, 1986, v. 1, n. 6, p. 529, doi. 10.1002/jbmr.5650010607
- By:
- Publication type:
- Article
Calcium-Sensing Receptor (CASR) Mutations in Hypercalcemic States: Studies from a Single Endocrine Clinic Over Three Years.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 4, p. 1819, doi. 10.1210/jc.2008-2430
- By:
- Publication type:
- Article
Identification and Functional Characterization of a Novel Mutation in the Calcium-Sensing Receptor Gene in Familial Hypocalciuric Hypercalcemia: Modulation of Clinical Severity by Vitamin D Status.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 7, p. 2616, doi. 10.1210/jc.2007-0123
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- Publication type:
- Article
Primary Hyperparathyroidism and the Presence of Kidney Stones Are Associated with Different Haplotypes of the Calcium-Sensing Receptor.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 1, p. 277, doi. 10.1210/jc.2006-0857
- By:
- Publication type:
- Article
A Hypocalcemic Child with a Novel Activating Mutation of the Calcium-Sensing Receptor Gene: Successful Treatment with Recombinant Human Parathyroid Hormone.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 7, p. 2474, doi. 10.1210/jc.2005-2605
- By:
- Publication type:
- Article
Functional Characterization of Calcium-Sensing Receptor Codon 227 Mutations Presenting as Either Familial (Benign) Hypocalciuric Hypercalcemia or Neonatal Hyperparathyroidism.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 2, p. 864, doi. 10.1210/jc.2004-1791
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- Publication type:
- Article
Blood Ionized Calcium Is Associated with Clustered Polymorphisms in the Carboxyl-Terminal Tail of the Calcium-Sensing Receptor.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 11, p. 5634, doi. 10.1210/jc.2004-0129
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- Publication type:
- Article
Familial Isolated Hyperparathyroidism Is Rarely Caused by Germline Mutation in HRPT2, the Gene for the Hyperparathyroidism-Jaw Tumor Syndrome.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 1, p. 96, doi. 10.1210/jc.2003-030675
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- Publication type:
- Article
Recurrent Familial Hypocalcemia Due to Germline Mosaicism for an Activating Mutation of the CalciumSensing Receptor Gene.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 8, p. 3674, doi. 10.1210/jc.2003-030409
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- Publication type:
- Article
A Syndrome of Hypocalciuric Hypercalcemia Caused by Autoantibodies Directed at the Calcium-Sensing Receptor.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 1, p. 60, doi. 10.1210/jc.2002-020249
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- Publication type:
- Article
Association between AAAG Repeat Polymorphism in the P3 Promoter of the Human Parathyroid Hormone (PTH)/ PTH-Related Peptide Receptor Gene and Adult Height, Urinary Pyridinoline Excretion, and Promoter Activity.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 4, p. 1791, doi. 10.1210/jcem.87.4.8419
- By:
- Publication type:
- Article
Gαs Transcripts Are Biallelically Expressed in the Human Kidney Cortex: Implications for Pseudohypoparathyroidism Type 1b.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 10, p. 4627, doi. 10.1210/jcem.86.10.7940
- By:
- Publication type:
- Article
Analysis of the P3 Promoter of the Human Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Gene in Pseudohypoparathyroidism Type 1b.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 3, p. 1394, doi. 10.1210/jcem.86.3.7364
- By:
- Publication type:
- Article
Cloning and Characterization of the Promoter Regions of the Human Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Gene: Analysis of Deoxyribonucleic Acid from Normal Subjects and Patients with Pseudohypoparathyroidism Type 1b.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1997, v. 82, n. 4, p. 1031, doi. 10.1210/jc.82.4.1031
- By:
- Publication type:
- Article
Role of Smad3, acting independently of transforming growth factor-β, in the early induction of Wnt-β-catenin signaling by parathyroid hormone in mouse osteoblastic cells.
- Published in:
- Journal of Cellular Biochemistry, 2009, v. 108, n. 1, p. 285, doi. 10.1002/jcb.22252
- By:
- Publication type:
- Article
A functional polymorphism in the PTHR1 promoter region is associated with adult height and BMD measured at the femoral neck in a large cohort of young caucasian women.
- Published in:
- Human Genetics, 2006, v. 119, n. 4, p. 416, doi. 10.1007/s00439-006-0155-8
- By:
- Publication type:
- Article
Novel calcium-sensing receptor cytoplasmic tail deletion mutation causing autosomal dominant hypocalcemia: molecular and clinical study.
- Published in:
- European Journal of Endocrinology, 2016, v. 174, n. 4, p. K1, doi. 10.1530/EJE-15-1216
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- Publication type:
- Article
Factors associated with vertebral fracture risk in patients with primary hyperparathyroidism.
- Published in:
- European Journal of Endocrinology, 2014, v. 171, n. 3, p. 399, doi. 10.1530/EJE-14-0343
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- Publication type:
- Article
Calcium-Sensing Receptor Gene: Regulation of Expression.
- Published in:
- Frontiers in Physiology, 2016, p. 1, doi. 10.3389/fphys.2016.00394
- By:
- Publication type:
- Article
Maternal Activating Mutation of the Calcium-Sensing Receptor: Implications for Calcium Metabolism in the Neonate.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2004, v. 17, n. 4, p. 673, doi. 10.1515/jpem.2004.17.4.673
- By:
- Publication type:
- Article
Regulation of Parathyroid Hormonelike Protein Production in Cultured Normal and Malignant Keratinocytes.
- Published in:
- Journal of Investigative Dermatology, 1992, v. 98, n. 2, p. 198, doi. 10.1111/1523-1747.ep12555864
- By:
- Publication type:
- Article
Transferrin‐mediated uptake of aluminium by human parathyroid cells results in reduced parathyroid hormone secretion.
- Published in:
- Nephrology Dialysis Transplantation, 2000, v. 15, n. 9, p. 1328, doi. 10.1093/ndt/15.9.1328
- By:
- Publication type:
- Article
Pancreastatin Reduces Alternatively Activated Macrophages, Disrupts the Epithelial Homeostasis and Aggravates Colonic Inflammation. A Descriptive Analysis.
- Published in:
- Biomedicines, 2021, v. 9, n. 2, p. 134, doi. 10.3390/biomedicines9020134
- By:
- Publication type:
- Article
Smad7 inhibits differentiation and mineralization of mouse osteoblastic cells.
- Published in:
- Endocrine Journal, 2012, v. 59, n. 8, p. 653, doi. 10.1507/endocrj.ej12-0022
- By:
- Publication type:
- Article
Homozygous Calcium-Sensing Receptor Polymorphism R544Q Presents as Hypocalcemic Hypoparathyroidism.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Glial Cells Missing-2 (GCM2) transactivates the calcium-sensing receptor gene: effect of a dominant-negative GCM2 mutant associated with autosomal dominant hypoparathyroidism.
- Published in:
- Human Mutation, 2009, v. 30, n. 1, p. 85, doi. 10.1002/humu.20827
- By:
- Publication type:
- Article
CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.
- Published in:
- Human Mutation, 2004, v. 24, n. 2, p. 107, doi. 10.1002/humu.20067
- By:
- Publication type:
- Article
Chromogranin-A Regulates Macrophage Function and the Apoptotic Pathway in Murine DSS colitis.
- Published in:
- Journal of Molecular Medicine, 2018, v. 96, n. 2, p. 183, doi. 10.1007/s00109-017-1613-6
- By:
- Publication type:
- Article
Novel association of MEN1 gene mutations with parathyroid carcinoma.
- Published in:
- 2017
- By:
- Publication type:
- Case Study