tryptophan has been researched along with Gaucher Disease in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (25.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (75.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Alam, A; Amato, D; Assouline, S; Dupre, N; Fon, EA; Franche, LA; Gan-Or, Z; Kalia, LV; Postuma, RB; Rivard, GE; Roncière, L; Ruskey, JA; Santiago, R; Spiegelman, D; Trempe, JF; Zhou, S | 1 |
Blackie, J; Chu, S; Ellis, M; Hayes, M; Kennerson, M; Lubomski, M; Nicholson, G; O'Sullivan, JD | 1 |
Barros, M; Curtis, JE; Gruschus, JM; Heinrich, F; Jiang, Z; Lee, JC; Pfefferkorn, CM; Sidransky, E; Yap, TL | 1 |
Eriksson, O; Hultberg, B; Ockerman, PA | 1 |
4 other study(ies) available for tryptophan and Gaucher Disease
Article | Year |
---|---|
The GBA p.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies.
Topics: Adolescent; Adult; Aged; Child, Preschool; Female; Founder Effect; Gaucher Disease; Glucosylceramidase; Glycine; Haplotypes; Heterozygote; Humans; Infant; Male; Middle Aged; Mutation; Polymorphism, Single Nucleotide; Principal Component Analysis; Quebec; Synucleins; Tryptophan; Young Adult | 2018 |
A novel Parkinson's disease risk variant, p. W378R, in the Gaucher's disease GBA gene.
Topics: Adult; Aged; Arginine; Family Health; Female; Gaucher Disease; Glucosylceramidase; Humans; Male; Middle Aged; Mutation; Parkinson Disease; Tryptophan | 2018 |
Structural features of membrane-bound glucocerebrosidase and α-synuclein probed by neutron reflectometry and fluorescence spectroscopy.
Topics: alpha-Synuclein; Gaucher Disease; Glucosylceramidase; Humans; Lipid Bilayers; Mutation; Neutron Diffraction; Parkinson Disease; Protein Binding; Spectrometry, Fluorescence; Surface Plasmon Resonance; Tryptophan | 2015 |
Urinary amino acids in storage disorders: mucopolysaccharidosis, Gaucher's disease and metachromatic leucodystrophy.
Topics: Adolescent; Adult; Amino Acids; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diffuse Cerebral Sclerosis of Schilder; Female; Gaucher Disease; Glycolipids; Glycoproteins; Glycosaminoglycans; Humans; Intellectual Disability; Lysosomes; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Serine; Threonine; Tryptophan | 1969 |