(Q51909851)

17 April 2018

title

Mutational analysis of the PTH 3'-untranslated region in parathyroid disorders. (English)

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17 April 2018

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Jessica Costa-Guda

1

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17 April 2018

Kelly Lauter

2

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17 April 2018

Tally Naveh-Many

3

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17 April 2018

Justin Silver

4

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17 April 2018

Andrew Arnold

5

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17 April 2018

publication date

1 December 2006

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17 April 2018

published in

Clinical Endocrinology

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17 April 2018

volume

65

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17 April 2018

issue

6

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17 April 2018

page(s)

806-809

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17 April 2018

A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidism

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

Cis and trans acting factors in the regulation of parathyroid hormone (PTH) mRNA stability by calcium and phosphate

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

The Parathyroid Hormone mRNA 3′-Untranslated Region AU-rich Element Is an Unstructured Functional Element

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

A conserved cis-acting element in the parathyroid hormone 3'-untranslated region is sufficient for regulation of RNA stability by calcium and phosphate

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

Identification and characterization of cis-acting elements in the human and bovine PTH mRNA 3'-untranslated region

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

The protein phosphatase calcineurin determines basal parathyroid hormone gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

In vitro evidence that upstream of N-ras participates in the regulation of parathyroid hormone messenger ribonucleic acid stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

Hyperparathyroid and hypoparathyroid disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

Increased efficiency of mRNA 3′ end formation: a new genetic mechanism contributing to hereditary thrombophilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

Clonal Chromosomal Defects in the Molecular Pathogenesis of Refractory Hyperparathyroidism of Uremia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2006.02670.X

10.1111/J.1365-2265.2006.02670.X

21 January 2018

Identifiers

DOI

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17 April 2018

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17 April 2018