List of works - Michael A. Levine

Genetic evidence that the human CYP2R1 enzyme is a key vitamin D 25-hydroxylase

scientific article

Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome

scientific article published on June 1, 1992

FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate

scientific article published in June 2001

Differential susceptibility to hypertension is due to selection during the out-of-Africa expansion

scientific article

Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia

scientific article published in January 2002

The hypocalciuric or benign variant of familial hypercalcemia: clinical and biochemical features in fifteen kindreds

scientific article published on 01 November 1981

Two-year results of once-weekly administration of alendronate 70 mg for the treatment of postmenopausal osteoporosis

scientific article published in November 2002

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome

scientific article published on 24 February 2004

Resistance to multiple hormones in patients with pseudohypoparathyroidism. Association with deficient activity of guanine nucleotide regulatory protein

scientific article published on 01 April 1983

Tumors associated with oncogenic osteomalacia express genes important in bone and mineral metabolism

scientific article

Molecular cloning of beta 3 subunit, a third form of the G protein beta-subunit polypeptide

scientific article

Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity

scientific article

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

scientific article

Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism

scientific article published on 01 June 1980

A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene

scientific article published on 11 August 2005

Urinary calcium excretion in familial hypocalciuric hypercalcemia. Persistence of relative hypocalciuria after induction of hypoparathyroidism.

scientific article published on 01 August 1983

Specificity of G protein beta and gamma subunit interactions

scientific article

Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy.

scientific article published on July 1996

Localisation of mesenchymal tumours by somatostatin receptor imaging

scientific article published in March 2002

G protein betagamma complex-mediated apoptosis by familial Alzheimer's disease mutant of APP.

scientific article

Retinal rods and cones have distinct G protein beta and gamma subunits

scientific article published on November 15, 1992

An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds

scientific article published on 01 February 1982

Evaluating children with fractures for child physical abuse.

scientific article published on 27 January 2014

Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a.

scientific article

Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodyst

scientific article published in March 1986

Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.

scientific article published on January 1988

A novel spliced variant of the type 1 corticotropin-releasing hormone receptor with a deletion in the seventh transmembrane domain present in the human pregnant term myometrium and fetal membranes

scientific article

Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance

scientific article

Cherubism: best clinical practice

scientific article published on May 24, 2012

A multinational study to develop universal standardization of whole-body bone density and composition using GE Healthcare Lunar and Hologic DXA systems

scientific article published on October 1, 2012

Profile of a clinical practice: Thresholds for surgery and surgical outcomes for patients with primary hyperparathyroidism: a national survey of endocrine surgeons

scientific article published on 01 August 1998

Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization

scientific article

Cloning and widespread distribution of the rat rod-type cyclic nucleotide-gated cation channel.

scientific article published on April 1997

Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification

scientific article published in November 2000

Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis

scientific article

Association between screening for osteoporosis and the incidence of hip fracture

scientific article

Urocortin, but not corticotropin-releasing hormone (CRH), activates the mitogen-activated protein kinase signal transduction pathway in human pregnant myometrium: an effect mediated via R1alpha and R2beta CRH receptor subtypes and stimulation of Gq-

scientific article

cGMP stimulates sodium and chloride currents in rat tracheal airway epithelia.

scientific article published on March 1997

Molecular cloning and primary structure of human chromogranin A (secretory protein I) cDNA

scientific article

Mapping of the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase (GNAS1) to 20q13.2----q13.3 in human by in situ hybridization

scientific article published in October 1991

Epidemiology and Diagnosis of Hypoparathyroidism

scientific article

Familial hypocalciuric hypercalcemia: the relation to primary parathyroid hyperplasia.

scientific article published on August 1982

Mutation Screening of the TNFRSF11A Gene Encoding Receptor Activator of NFkB (RANK) in Familial and Sporadic Paget's Disease of Bone and Osteosarcoma

article

The role of SH3BP2 in the pathophysiology of cherubism

scientific article

An update on the clinical and molecular characteristics of pseudohypoparathyroidism.

scientific article published on December 2012

Protein kinase A-induced negative regulation of the corticotropin-releasing hormone R1alpha receptor-extracellularly regulated kinase signal transduction pathway: the critical role of Ser301 for signaling switch and selectivity.

scientific article

Consensus development for the supplementation of vitamin D in childhood and adolescence

scientific article

National Health and Nutrition Examination Survey whole-body dual-energy X-ray absorptiometry reference data for GE Lunar systems.

scientific article

Primary hyperparathyroidism

scientific article published on 01 April 1997

Hypercalcemia in children and adolescents.

scientific article

List of works by Michael A. Levine

Genetic evidence that the human CYP2R1 enzyme is a key vitamin D 25-hydroxylase

Identification of a mutation in the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albright syndrome

FGF-23 inhibits renal tubular phosphate transport and is a PHEX substrate

Differential susceptibility to hypertension is due to selection during the out-of-Africa expansion

Paternally inherited inactivating mutations of the GNAS1 gene in progressive osseous heteroplasia

The hypocalciuric or benign variant of familial hypercalcemia: clinical and biochemical features in fifteen kindreds

Two-year results of once-weekly administration of alendronate 70 mg for the treatment of postmenopausal osteoporosis

Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome

Resistance to multiple hormones in patients with pseudohypoparathyroidism. Association with deficient activity of guanine nucleotide regulatory protein

Tumors associated with oncogenic osteomalacia express genes important in bone and mineral metabolism

Molecular cloning of beta 3 subunit, a third form of the G protein beta-subunit polypeptide

Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity

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

Deficient activity of guanine nucleotide regulatory protein in erythrocytes from patients with pseudohypoparathyroidism

A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene

Urinary calcium excretion in familial hypocalciuric hypercalcemia. Persistence of relative hypocalciuria after induction of hypoparathyroidism.

Specificity of G protein beta and gamma subunit interactions

Clinical implications of genetic defects in G proteins. The molecular basis of McCune-Albright syndrome and Albright hereditary osteodystrophy.

Localisation of mesenchymal tumours by somatostatin receptor imaging

G protein betagamma complex-mediated apoptosis by familial Alzheimer's disease mutant of APP.

Retinal rods and cones have distinct G protein beta and gamma subunits

An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds

Evaluating children with fractures for child physical abuse.

Paternal imprinting of Galpha(s) in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a.

Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodyst

Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.

A novel spliced variant of the type 1 corticotropin-releasing hormone receptor with a deletion in the seventh transmembrane domain present in the human pregnant term myometrium and fetal membranes

Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance

Cherubism: best clinical practice

A multinational study to develop universal standardization of whole-body bone density and composition using GE Healthcare Lunar and Hologic DXA systems

Profile of a clinical practice: Thresholds for surgery and surgical outcomes for patients with primary hyperparathyroidism: a national survey of endocrine surgeons

Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterization

Cloning and widespread distribution of the rat rod-type cyclic nucleotide-gated cation channel.

Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification

Mutations in SLC34A3/NPT2c are associated with kidney stones and nephrocalcinosis

Association between screening for osteoporosis and the incidence of hip fracture

Urocortin, but not corticotropin-releasing hormone (CRH), activates the mitogen-activated protein kinase signal transduction pathway in human pregnant myometrium: an effect mediated via R1alpha and R2beta CRH receptor subtypes and stimulation of Gq-

cGMP stimulates sodium and chloride currents in rat tracheal airway epithelia.

Molecular cloning and primary structure of human chromogranin A (secretory protein I) cDNA

Mapping of the gene encoding the alpha subunit of the stimulatory G protein of adenylyl cyclase (GNAS1) to 20q13.2----q13.3 in human by in situ hybridization

Epidemiology and Diagnosis of Hypoparathyroidism

Familial hypocalciuric hypercalcemia: the relation to primary parathyroid hyperplasia.

Mutation Screening of the TNFRSF11A Gene Encoding Receptor Activator of NFkB (RANK) in Familial and Sporadic Paget's Disease of Bone and Osteosarcoma

The role of SH3BP2 in the pathophysiology of cherubism

An update on the clinical and molecular characteristics of pseudohypoparathyroidism.

Protein kinase A-induced negative regulation of the corticotropin-releasing hormone R1alpha receptor-extracellularly regulated kinase signal transduction pathway: the critical role of Ser301 for signaling switch and selectivity.

Consensus development for the supplementation of vitamin D in childhood and adolescence

National Health and Nutrition Examination Survey whole-body dual-energy X-ray absorptiometry reference data for GE Lunar systems.

Primary hyperparathyroidism

Hypercalcemia in children and adolescents.