Compounds > arginine

arginine and Dunnigan Syndrome

arginine has been researched along with Dunnigan Syndrome in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cyganek, K; Klupa, T; Kowalska, I; Malecki, MT; Skupien, J; Szopa, M; Wojtyczek, K1
Brouwer, CB; Cao, H; Hegele, RA; Jeninga, EH; Kalkhoven, E; Leff, T; Li, G; Maas, M; Monajemi, H; Stroes, E; Zhang, L1
Berger, R; Bonvin, AM; Hamers, N; Hendriks-Stegeman, BI; Jeninga, EH; Kalkhoven, E; van Beekum, O; van Dijk, AD1

Other Studies

3 other study(ies) available for arginine and Dunnigan Syndrome

ArticleYear
LMNA gene mutation search in Polish patients: new features of the heterozygous Arg482Gln mutation phenotype.
    Endocrine, 2009, Volume: 36, Issue:3

    Topics: Amino Acid Substitution; Arginine; Body Mass Index; Diabetes Mellitus, Type 2; DNA Mutational Analysis; Female; Genetic Association Studies; Glutamine; Heterozygote; Humans; Insulin Resistance; Lamin Type A; Lipodystrophy, Familial Partial; Male; Middle Aged; Point Mutation; Poland; Pulmonary Fibrosis; Skinfold Thickness

2009
Familial partial lipodystrophy phenotype resulting from a single-base mutation in deoxyribonucleic acid-binding domain of peroxisome proliferator-activated receptor-gamma.
    The Journal of clinical endocrinology and metabolism, 2007, Volume: 92, Issue:5

    Topics: Adult; Animals; Arginine; Cells, Cultured; Cloning, Molecular; DNA; Electrophoretic Mobility Shift Assay; Exons; Female; Genes, Dominant; Humans; Lipodystrophy, Familial Partial; Magnetic Resonance Imaging; Mice; Phenotype; Point Mutation; PPAR gamma; Transcription, Genetic; Tryptophan; Zinc Fingers

2007
Impaired peroxisome proliferator-activated receptor gamma function through mutation of a conserved salt bridge (R425C) in familial partial lipodystrophy.
    Molecular endocrinology (Baltimore, Md.), 2007, Volume: 21, Issue:5

    Topics: Amino Acid Substitution; Arginine; Base Sequence; Bone Neoplasms; Cell Line, Tumor; Cysteine; DNA; DNA Mutational Analysis; DNA Probes; Genetic Carrier Screening; Humans; Lipodystrophy, Familial Partial; Models, Molecular; Osteosarcoma; PPAR gamma; Protein Conformation; Transcription, Genetic; Transfection

2007