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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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Vitamin D and its receptor during late development

Biochimica et biophysica acta, 2015-02, Vol.1849 (2), p.171-180

2015

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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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Nuclear Localization of the Type 1 PTH/PTHrP Receptor in Rat Tissues

Journal of bone and mineral research, 2000-06, Vol.15 (6), p.1033-1044

2000

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The Gene Responsible for Pseudohypoparathyroidism Type Ib Is Paternally Imprinted and Maps in Four Unrelated Kindreds to Chromosome 20q13.3

Proceedings of the National Academy of Sciences - PNAS, 1998-09, Vol.95 (20), p.11798-11803

1998

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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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A986S polymorphism of the calcium-sensing receptor and circulating calcium concentrations

The Lancet (British edition), 1999-01, Vol.353 (9147), p.112-115

1999

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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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Cell cycle regulation of menin expression

Cancer research (Chicago, Ill.), 1999-10, Vol.59 (20), p.5097-5101

1999

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Nuclear localization of the type 1 parathyroid hormone/parathyroid hormone-related peptide receptor in MC3T3-E1 cells: association with serum-induced cell proliferation

Bone (New York, N.Y.), 2000-03, Vol.26 (3), p.221-225

2000

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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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Characterization of the human parathyroid hormone-like peptide gene. Functional and evolutionary aspects

The Journal of biological chemistry, 1989-05, Vol.264 (13), p.7720-7725

1989

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Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism : effects of mutant gene dosage on phenotype

The Journal of clinical investigation, 1994-03, Vol.93 (3), p.1108-1112

1994

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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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Comparison of the biochemical responses to human parathyroid Hormone-(1-31)NH2 and hPTH-(1-34) in healthy humans

The journal of clinical endocrinology and metabolism, 1999-08, Vol.84 (8), p.2739-2743

1999

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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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Organization and evolution of the human growth hormone receptor gene 5'-flanking region

Endocrinology (Philadelphia), 2001-05, Vol.142 (5), p.1923-1934

2001

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Regulation of parathyroid hormone-like peptide in cultured normal human keratinocytes : effect of growth factors and 1,25 dihydroxyvitamin D3 on gene expression and secretion

The Journal of clinical investigation, 1991-03, Vol.87 (3), p.884-893

1991

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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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Alu elements in human growth hormone receptor gene 5' untranslated region exons

Journal of molecular endocrinology, 2001-12, Vol.27 (3), p.357-366

2001

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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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Abundant expression of parathyroid hormone-related protein in primary rat aortic smooth muscle cells accompanies serum-induced proliferation

The Journal of clinical investigation, 1991-12, Vol.88 (6), p.1841-1847

1991

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Menin interacts with β-catenin in osteoblast differentiation

Hormone and metabolic research, 2011-03, Vol.43 (3), p.183-187

2011

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

Vitamin D and its receptor during late development

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

Nuclear Localization of the Type 1 PTH/PTHrP Receptor in Rat Tissues

The Gene Responsible for Pseudohypoparathyroidism Type Ib Is Paternally Imprinted and Maps in Four Unrelated Kindreds to Chromosome 20q13.3

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

A986S polymorphism of the calcium-sensing receptor and circulating calcium concentrations

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

Cell cycle regulation of menin expression

Nuclear localization of the type 1 parathyroid hormone/parathyroid hormone-related peptide receptor in MC3T3-E1 cells: association with serum-induced cell proliferation

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

Characterization of the human parathyroid hormone-like peptide gene. Functional and evolutionary aspects

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism : effects of mutant gene dosage on phenotype

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

Comparison of the biochemical responses to human parathyroid Hormone-(1-31)NH2 and hPTH-(1-34) in healthy humans

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

Organization and evolution of the human growth hormone receptor gene 5'-flanking region

Regulation of parathyroid hormone-like peptide in cultured normal human keratinocytes : effect of growth factors and 1,25 dihydroxyvitamin D3 on gene expression and secretion

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

Alu elements in human growth hormone receptor gene 5' untranslated region exons

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

Abundant expression of parathyroid hormone-related protein in primary rat aortic smooth muscle cells accompanies serum-induced proliferation

Menin interacts with β-catenin in osteoblast differentiation

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