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Human calcium-sensing receptor gene. Vitamin D response elements in promoters P1 and P2 confer transcriptional responsiveness to 1,25-dihydroxyvitamin D

The Journal of biological chemistry, 2002-08, Vol.277 (33), p.30337-30350

2002

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Inactivation of the 25-Hydroxyvitamin D 1α-Hydroxylase and Vitamin D Receptor Demonstrates Independent and Interdependent Effects of Calcium and Vitamin D on Skeletal and Mineral Homeostasis

The Journal of biological chemistry, 2004-04, Vol.279 (16), p.16754-16766

2004

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Targeted Ablation of the 25-Hydroxyvitamin D 1α-Hydroxylase Enzyme: Evidence for Skeletal, Reproductive, and Immune Dysfunction

Proceedings of the National Academy of Sciences - PNAS, 2001-06, Vol.98 (13), p.7498-7503

2001

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Parathyroid Hormone Increases β-Catenin Levels through Smad3 in Mouse Osteoblastic Cells

Endocrinology (Philadelphia), 2006-05, Vol.147 (5), p.2583-2590

2006

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Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused by AP2S1 Mutation

The journal of clinical endocrinology and metabolism, 2015-07, Vol.100 (7), p.2515-2518

2015

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Menin Is Required for Bone Morphogenetic Protein 2- and Transforming Growth Factor β-regulated Osteoblastic Differentiation through Interaction with Smads and Runx2

The Journal of biological chemistry, 2004-09, Vol.279 (39), p.40267-40275

2004

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CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia

Human mutation, 2004-08, Vol.24 (2), p.107-111

2004

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Inactivation of Menin, A Smad3-Interacting Protein, Blocks Transforming Growth Factor Type β Signaling

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (7), p.3837-3842

2001

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Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS

The Journal of clinical investigation, 2003-10, Vol.112 (8), p.1255-1263

2003

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New insights into mineral and skeletal regulation by active forms of vitamin D

Kidney international, 2006-01, Vol.69 (2), p.218-223

2006

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Familial Isolated Hyperparathyroidism Is Rarely Caused by Germline Mutation in HRPT2, the Gene for the Hyperparathyroidism-Jaw Tumor Syndrome

The journal of clinical endocrinology and metabolism, 2004-01, Vol.89 (1), p.96-102

2004

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Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia

Human mutation, 2000-10, Vol.16 (4), p.281-296

2000

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Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds

Medicine (Baltimore), 2002-01, Vol.81 (1), p.1-26

2002

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A Syndrome of Hypocalciuric Hypercalcemia Caused by Autoantibodies Directed at the Calcium-Sensing Receptor

The journal of clinical endocrinology and metabolism, 2003-01, Vol.88 (1), p.60-72

2003

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Blood Ionized Calcium Is Associated with Clustered Polymorphisms in the Carboxyl-Terminal Tail of the Calcium-Sensing Receptor

The journal of clinical endocrinology and metabolism, 2004-11, Vol.89 (11), p.5634-5638

2004

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Inactivation of Menin, the Product of the Multiple Endocrine Neoplasia Type 1 Gene, Inhibits the Commitment of Multipotential Mesenchymal Stem Cells into the Osteoblast Lineage

The Journal of biological chemistry, 2003-06, Vol.278 (23), p.21058-21069

2003

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Skeletal Abnormalities in Pth-Null Mice Are Influenced by Dietary Calcium

Endocrinology (Philadelphia), 2004-04, Vol.145 (4), p.2046-2053

2004

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Menin Suppresses Osteoblast Differentiation by Antagonizing the AP-1 Factor, JunD

The Journal of biological chemistry, 2005-02, Vol.280 (6), p.4785-4791

2005

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Menin and TGF-β Superfamily Member Signaling via the Smad Pathway in Pituitary, Parathyroid and Osteoblast

Hormone and metabolic research, 2005-06, Vol.37 (6), p.375-379

2005

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Coding GNAS Mutations Leading to Hormone Resistance Impair in Vitro Agonist- and Cholera Toxin-Induced Adenosine Cyclic 3′,5′-Monophosphate Formation Mediated by Human XLαs

Endocrinology (Philadelphia), 2006-05, Vol.147 (5), p.2253-2262

2006

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Impaired cotranslational processing of the calcium-sensing receptor due to signal peptide missense mutations in familial hypocalciuric hypercalcemia

Human molecular genetics, 2005-06, Vol.14 (12), p.1679-1690

2005

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Effects of calcium and of the Vitamin D system on skeletal and calcium homeostasis: lessons from genetic models

Journal of steroid biochemistry and molecular biology, 2004-05, Vol.89 (1-5), p.485-489

2004

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Menin inactivation leads to loss of transforming growth factor β inhibition of parathyroid cell proliferation and parathyroid hormone secretion

Cancer research (Chicago, Ill.), 2004-03, Vol.64 (6), p.2222-2228

2004

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Exogenous PTH‐Related Protein and PTH Improve Mineral and Skeletal Status in 25‐Hydroxyvitamin D‐1α‐Hydroxylase and PTH Double Knockout Mice

Journal of bone and mineral research, 2005-10, Vol.20 (10), p.1766-1777

2005

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Identification and Functional Characterization of Novel Calcium-Sensing Receptor Mutations in Familial Hypocalciuric Hypercalcemia and Autosomal Dominant Hypocalcemia

The journal of clinical endocrinology and metabolism, 2002-03, Vol.87 (3), p.1309-1318

2002

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Human calcium-sensing receptor gene. Vitamin D response elements in promoters P1 and P2 confer transcriptional responsiveness to 1,25-dihydroxyvitamin D

Inactivation of the 25-Hydroxyvitamin D 1α-Hydroxylase and Vitamin D Receptor Demonstrates Independent and Interdependent Effects of Calcium and Vitamin D on Skeletal and Mineral Homeostasis

Targeted Ablation of the 25-Hydroxyvitamin D 1α-Hydroxylase Enzyme: Evidence for Skeletal, Reproductive, and Immune Dysfunction

Parathyroid Hormone Increases β-Catenin Levels through Smad3 in Mouse Osteoblastic Cells

Cinacalcet Treatment in an Adolescent With Concurrent 22q11.2 Deletion Syndrome and Familial Hypocalciuric Hypercalcemia Type 3 Caused by AP2S1 Mutation

Menin Is Required for Bone Morphogenetic Protein 2- and Transforming Growth Factor β-regulated Osteoblastic Differentiation through Interaction with Smads and Runx2

CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia

Inactivation of Menin, A Smad3-Interacting Protein, Blocks Transforming Growth Factor Type β Signaling

Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS

New insights into mineral and skeletal regulation by active forms of vitamin D

Familial Isolated Hyperparathyroidism Is Rarely Caused by Germline Mutation in HRPT2, the Gene for the Hyperparathyroidism-Jaw Tumor Syndrome

Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia

Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds

A Syndrome of Hypocalciuric Hypercalcemia Caused by Autoantibodies Directed at the Calcium-Sensing Receptor

Blood Ionized Calcium Is Associated with Clustered Polymorphisms in the Carboxyl-Terminal Tail of the Calcium-Sensing Receptor

Inactivation of Menin, the Product of the Multiple Endocrine Neoplasia Type 1 Gene, Inhibits the Commitment of Multipotential Mesenchymal Stem Cells into the Osteoblast Lineage

Skeletal Abnormalities in Pth-Null Mice Are Influenced by Dietary Calcium

Menin Suppresses Osteoblast Differentiation by Antagonizing the AP-1 Factor, JunD

Menin and TGF-β Superfamily Member Signaling via the Smad Pathway in Pituitary, Parathyroid and Osteoblast

Coding GNAS Mutations Leading to Hormone Resistance Impair in Vitro Agonist- and Cholera Toxin-Induced Adenosine Cyclic 3′,5′-Monophosphate Formation Mediated by Human XLαs

Impaired cotranslational processing of the calcium-sensing receptor due to signal peptide missense mutations in familial hypocalciuric hypercalcemia

Effects of calcium and of the Vitamin D system on skeletal and calcium homeostasis: lessons from genetic models

Menin inactivation leads to loss of transforming growth factor β inhibition of parathyroid cell proliferation and parathyroid hormone secretion

Exogenous PTH‐Related Protein and PTH Improve Mineral and Skeletal Status in 25‐Hydroxyvitamin D‐1α‐Hydroxylase and PTH Double Knockout Mice

Identification and Functional Characterization of Novel Calcium-Sensing Receptor Mutations in Familial Hypocalciuric Hypercalcemia and Autosomal Dominant Hypocalcemia

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