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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
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:
- Calcified Tissue International, 2014, v. 94, n. 4, p. 454, doi. 10.1007/s00223-013-9828-1
- By:
- Publication type:
- Article
Author Correction: Transforming Growth Factor-beta Regulation of Ephrin Type-A Receptor 4 Signaling in Breast Cancer Cellular Migration.
- Published in:
- 2022
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- Publication type:
- Correction Notice
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
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- Publication type:
- 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
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
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
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
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- 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
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
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
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
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- Publication type:
- Article
Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders.
- Published in:
- European Journal of Endocrinology, 2022, v. 186, n. 3, p. 351, doi. 10.1530/EJE-21-0433
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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
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- Publication type:
- Article
Calcium Sensing Receptor as a Novel Mediator of Adipose Tissue Dysfunction: Mechanisms and Potential Clinical Implications.
- Published in:
- Frontiers in Physiology, 2016, p. 1, doi. 10.3389/fphys.2016.00395
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- Publication type:
- Article
Breast Cancer Anti-Estrogen Resistance-3 inhibits transforming growth factor-β/Smad signaling and associates with favorable breast cancer disease outcomes.
- Published in:
- Breast Cancer Research, 2014, v. 16, n. 6, p. 19, doi. 10.1186/s13058-014-0476-9
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- Publication type:
- Article
Breast cancer anti-estrogen resistance 3 inhibits transforming growth factor β/Smad signaling and associates with favorable breast cancer disease outcomes.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Multiple Endocrine Neoplasia Type 1 Regulates TGFβ-Mediated Suppression of Tumor Formation and Metastasis in Melanoma.
- Published in:
- Cells (2073-4409), 2024, v. 13, n. 11, p. 973, doi. 10.3390/cells13110973
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- Publication type:
- Article
CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohort.
- Published in:
- Cellular Oncology (2211-3428), 2012, v. 35, n. 6, p. 411, doi. 10.1007/s13402-012-0100-x
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- 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
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- 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
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- Publication type:
- Article
Calcium-sensing receptor dimerizes in the endoplasmic reticulum: biochemical and biophysical characterization of CASR mutants retained intracellularly.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 14, p. 2200, doi. 10.1093/hmg/ddl145
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- Publication type:
- Article
Impaired cotranslational processing of the calcium-sensing receptor due to signal peptide missense mutations in familial hypocalciuric hypercalcemia.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 12, p. 1679, doi. 10.1093/hmg/ddi176
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- Publication type:
- Article
The leukemia inhibitory factor (LIF) and p21 mediate the TGFβ tumor suppressive effects in human cutaneous melanoma.
- Published in:
- BMC Cancer, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12885-015-1177-1
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- Publication type:
- Article
The leukemia inhibitory factor (LIF) and p21 mediate the TGFβ tumor suppressive effects in human cutaneous melanoma
- Published in:
- BMC Cancer, 2015, v. 15, n. 1, p. 200, doi. 10.1186/s12885-015-1177-1
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- Publication type:
- Article
The leukemia inhibitory factor (LIF) and p21 mediate the TGFβ tumor suppressive effects in human cutaneous melanoma.
- Published in:
- 2015
- By:
- Publication type:
- journal article
A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohort.
- Published in:
- 2012
- By:
- Publication type:
- Letter
An acceptor splice site mutation in the calcium-sensing receptor (CASR) gene in familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.
- Published in:
- Human Mutation, 2001, v. 18, n. 5, p. 411, doi. 10.1002/humu.1212
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- Publication type:
- Article
Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.
- Published in:
- Human Mutation, 2000, v. 16, n. 4, p. 281, doi. 10.1002/1098-1004(200010)16:4<281::AID-HUMU1>3.0.CO;2-A
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- Publication type:
- Article
Genetic Deletion of Menin in Mouse Mesenchymal Stem Cells: An Experimental and Computational Analysis.
- Published in:
- JBMR Plus, 2022, v. 6, n. 5, p. 1, doi. 10.1002/jbm4.10622
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- Publication type:
- Article
Extracellular Mg[sup2+]- and ca[sup2+]-sensing in mouse distal convoluted tubule cells.
- Published in:
- Kidney International, 1998, v. 53, n. 3, p. 583, doi. 10.1046/j.1523-1755.1998.00790.x
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- Publication type:
- Article