Compounds > arginine

arginine and Fibrous Dysplasia, Polyostotic

arginine has been researched along with Fibrous Dysplasia, Polyostotic in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (37.50)18.2507
2000's5 (62.50)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
de Sanctis, C; de Sanctis, L; Genitori, L; Greggio, N; Lala, R; Romagnolo, D1
Brinkman, AD; Davis, MM; Eugster, EA; Hannon, TS; King, DW; Pescovitz, OH; Steinmetz, R1
Avsar, M; Bircan, R; Bozbuga, M; Cirakoglu, B; Ekinci, G; Gozu, H; Gulec, I; Sargin, H; Sargin, M; Tanakol, R; Yayla, A1
Boney, CM; Charest, NJ; Feuillan, PP; Merino, MJ; Moran, A; Pescovitz, OH; Shenker, A; Spiegel, AM; Van Wyk, JJ; Weinstein, LS1
Matalon, R; Warner, DR; Weinstein, LS; Weng, G; Yu, S1
Warner, DR; Weinstein, LS1
Gillerot, Y; Lumbroso, S; Medina, M; Silva, ES; Sokal, EM; Sultan, C1
Iwamoto, Y; Oda, Y; Sakamoto, A; Tsuneyoshi, M1

Trials

1 trial(s) available for arginine and Fibrous Dysplasia, Polyostotic

ArticleYear
Premature thelarche and granulosa cell tumors: a search for FSH receptor and G5alpha activating mutations.
    Journal of pediatric endocrinology & metabolism : JPEM, 2002, Volume: 15 Suppl 3

    Topics: Age Determination by Skeleton; Arginine; Child; DNA; Female; Fibrous Dysplasia, Polyostotic; Genetic Testing; Granulosa Cell Tumor; GTP-Binding Protein alpha Subunits, Gs; Humans; Male; Mutation; Polymorphism, Genetic; Puberty, Precocious; Receptors, FSH; Reverse Transcriptase Polymerase Chain Reaction

2002

Other Studies

7 other study(ies) available for arginine and Fibrous Dysplasia, Polyostotic

ArticleYear
Searching for Arg201 mutations in the GNAS1 gene in Italian patients with McCune-Albright syndrome.
    Journal of pediatric endocrinology & metabolism : JPEM, 2002, Volume: 15 Suppl 3

    Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Arginine; Child; Child, Preschool; Exons; Female; Fibrous Dysplasia, Polyostotic; GTP-Binding Protein alpha Subunits, Gs; Humans; Italy; Male; Mutation; Reverse Transcriptase Polymerase Chain Reaction

2002
A case of McCune-Albright syndrome associated with Gs alpha mutation in the bone tissue.
    Endocrine journal, 2006, Volume: 53, Issue:1

    Topics: Acromegaly; Arginine; Bone and Bones; Cysteine; DNA; DNA Mutational Analysis; Facial Bones; Fibrous Dysplasia, Polyostotic; GTP-Binding Protein alpha Subunits, Gs; Humans; Hyperthyroidism; Leukocytes; Male; Middle Aged; Mutation; Polymerase Chain Reaction; Radiography; Sequence Analysis, DNA; Skull

2006
Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein GS.
    The Journal of pediatrics, 1993, Volume: 123, Issue:4

    Topics: Adolescent; Antisense Elements (Genetics); Arginine; Cyclic AMP; Death, Sudden; Endocrine System Diseases; Female; Fibrous Dysplasia, Polyostotic; GTP-Binding Proteins; Humans; Infant, Newborn; Male; Mosaicism; Mutation; Polymerase Chain Reaction; Risk Factors

1993
A novel mutation in the switch 3 region of Gsalpha in a patient with Albright hereditary osteodystrophy impairs GDP binding and receptor activation.
    The Journal of biological chemistry, 1998, Sep-11, Volume: 273, Issue:37

    Topics: Adenylyl Cyclases; Adult; Alanine; Aluminum Compounds; Amino Acid Sequence; Arginine; Base Sequence; Binding Sites; Cloning, Molecular; Erythrocyte Membrane; Escherichia coli; Exons; Female; Fibrous Dysplasia, Polyostotic; Fluorides; GTP-Binding Protein alpha Subunits, Gs; Guanosine 5'-O-(3-Thiotriphosphate); Guanosine Diphosphate; Humans; Male; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Point Mutation; Polymerase Chain Reaction; Protein Biosynthesis; Protein Structure, Secondary; Receptors, Cell Surface; Recombinant Proteins; RNA, Messenger; Transcription, Genetic; Tryptophan

1998
A mutation in the heterotrimeric stimulatory guanine nucleotide binding protein alpha-subunit with impaired receptor-mediated activation because of elevated GTPase activity.
    Proceedings of the National Academy of Sciences of the United States of America, 1999, Apr-13, Volume: 96, Issue:8

    Topics: Adenylyl Cyclases; Aluminum Compounds; Amino Acid Substitution; Animals; Arginine; Cattle; Cloning, Molecular; Escherichia coli; Fibrous Dysplasia, Polyostotic; Fluorides; Glutamine; GTP Phosphohydrolases; GTP-Binding Protein alpha Subunits, Gs; Guanosine 5'-O-(3-Thiotriphosphate); Guanosine Diphosphate; Humans; Isoproterenol; Kinetics; Macromolecular Substances; Mutagenesis, Site-Directed; Polymerase Chain Reaction; Protein Structure, Secondary; Recombinant Proteins

1999
Demonstration of McCune-Albright mutations in the liver of children with high gammaGT progressive cholestasis.
    Journal of hepatology, 2000, Volume: 32, Issue:1

    Topics: Arginine; Cholestasis, Intrahepatic; DNA; DNA Mutational Analysis; DNA Primers; Female; Fibrous Dysplasia, Polyostotic; gamma-Glutamyltransferase; GTP-Binding Protein alpha Subunits, Gs; Humans; Infant, Newborn; Liver; Male; Mutation; Polymerase Chain Reaction

2000
A comparative study of fibrous dysplasia and osteofibrous dysplasia with regard to Gsalpha mutation at the Arg201 codon: polymerase chain reaction-restriction fragment length polymorphism analysis of paraffin-embedded tissues.
    The Journal of molecular diagnostics : JMD, 2000, Volume: 2, Issue:2

    Topics: Adolescent; Adult; Aged; Arginine; Base Sequence; Case-Control Studies; Child; Child, Preschool; Codon; DNA Primers; Female; Fibrous Dysplasia of Bone; Fibrous Dysplasia, Monostotic; Fibrous Dysplasia, Polyostotic; GTP-Binding Protein alpha Subunits, Gs; Humans; Male; Point Mutation

2000