tryptophan and Hypophosphatemia, Familial

tryptophan has been researched along with Hypophosphatemia, Familial 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
Adiceam, P; Brouillard, F; Garabedian, M; Garnier, JM; Guillozo, H; Kottler, ML; Lagier, P; Nguyen, TM; Palix, C; Rizk-Rabin, M	1

Other Studies

1 other study(ies) available for tryptophan and Hypophosphatemia, Familial

Article	Year
Tryptophan missense mutation in the ligand-binding domain of the vitamin D receptor causes severe resistance to 1,25-dihydroxyvitamin D. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2002, Volume: 17, Issue:9 Topics: Amino Acid Sequence; Animals; Base Sequence; Binding Sites; Calcitriol; Cells, Cultured; Child, Preschool; COS Cells; Cytochrome P-450 Enzyme System; DNA, Complementary; Female; Hair Follicle; Humans; Hypophosphatemia, Familial; Infant; Ligands; Male; Mutation, Missense; Receptors, Calcitriol; Recombinant Proteins; RNA, Messenger; Steroid Hydroxylases; Transfection; Tryptophan; Vitamin D3 24-Hydroxylase	2002

Article

Year

Tryptophan missense mutation in the ligand-binding domain of the vitamin D receptor causes severe resistance to 1,25-dihydroxyvitamin D.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2002, Volume: 17, Issue:9

Topics: Amino Acid Sequence; Animals; Base Sequence; Binding Sites; Calcitriol; Cells, Cultured; Child, Preschool; COS Cells; Cytochrome P-450 Enzyme System; DNA, Complementary; Female; Hair Follicle; Humans; Hypophosphatemia, Familial; Infant; Ligands; Male; Mutation, Missense; Receptors, Calcitriol; Recombinant Proteins; RNA, Messenger; Steroid Hydroxylases; Transfection; Tryptophan; Vitamin D3 24-Hydroxylase

2002