tryptophan and Dunnigan Syndrome

tryptophan has been researched along with Dunnigan Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Brouwer, CB; Cao, H; Hegele, RA; Jeninga, EH; Kalkhoven, E; Leff, T; Li, G; Maas, M; Monajemi, H; Stroes, E; Zhang, L	1

Other Studies

1 other study(ies) available for tryptophan and Dunnigan Syndrome

Article	Year
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

Article

Year

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