4.6 Article

PTH1R Mutants Found in Patients with Primary Failure of Tooth Eruption Disrupt G-Protein Signaling

Related references

Note: Only part of the references are listed.
Article Dentistry, Oral Surgery & Medicine

Expanding the spectrum of PTH1R mutations in patients with primary failure of tooth eruption

Helmut Roth et al.

CLINICAL ORAL INVESTIGATIONS (2014)

Article Dentistry, Oral Surgery & Medicine

Novel Mutations in PTH1R Associated with Primary Failure of Eruption and Osteoarthritis

S. A. Frazier-Bowers et al.

JOURNAL OF DENTAL RESEARCH (2014)

Article Dentistry, Oral Surgery & Medicine

Differential diagnosis of primary failure of eruption (PFE) with and without evidence of pathogenic mutations in the PTHR1 gene

Peter Pilz et al.

JOURNAL OF OROFACIAL ORTHOPEDICS-FORTSCHRITTE DER KIEFERORTHOPADIE (2014)

Editorial Material Cell Biology

Regulation of VASP by phosphorylation Consequences for cell migration

Heike Doeppler et al.

CELL ADHESION & MIGRATION (2013)

Article Biochemistry & Molecular Biology

From parathyroid hormone to cytosolic Ca2+ signals

Colin W. Taylor et al.

BIOCHEMICAL SOCIETY TRANSACTIONS (2012)

Article Endocrinology & Metabolism

Exome Resequencing Combined With Linkage Analysis Identifies Novel PTH1R Variants in Primary Failure of Tooth Eruption in Japanese

Tetsutaro Yamaguchi et al.

JOURNAL OF BONE AND MINERAL RESEARCH (2011)

Review Endocrinology & Metabolism

G protein-coupled receptors: mutations and endocrine diseases

Gilbert Vassart et al.

NATURE REVIEWS ENDOCRINOLOGY (2011)

Article Cell Biology

Cellular Strategies of Protein Quality Control

Bryan Chen et al.

COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2011)

Review Cell Biology

PTH and PTHrP signaling in osteoblasts

Nabanita S. Datta et al.

CELLULAR SIGNALLING (2009)

Article Dentistry, Oral Surgery & Medicine

Genetic analysis of familial non-syndromic primary failure of eruption

S. A. Frazier-Bowers et al.

ORTHODONTICS & CRANIOFACIAL RESEARCH (2009)

Article Genetics & Heredity

PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption

Eva Decker et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2008)

Article Biochemistry & Molecular Biology

PTHR1 mutations associated with Ollier disease result in receptor loss of function

Alain Couvineau et al.

HUMAN MOLECULAR GENETICS (2008)

Article Endocrinology & Metabolism

Novel mutations in the parathyroid hormone (PTH)/PTH-related peptide receptor type 1 causing blomstrand osteochondrodysplasia types I and II

J. Hoogendam et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2007)

Review Biochemistry & Molecular Biology

Parathyroid hormone and parathyroid hormone-related peptide, and their receptors

RC Gensure et al.

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2005)

Article Biochemistry & Molecular Biology

Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes

S Duchatelet et al.

HUMAN MOLECULAR GENETICS (2005)

Review Multidisciplinary Sciences

Osteoclast differentiation and activation

WJ Boyle et al.

NATURE (2003)