Compounds > tryptophan

tryptophan and Gaucher Disease

tryptophan has been researched along with Gaucher Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's3 (75.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
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, S1
Blackie, J; Chu, S; Ellis, M; Hayes, M; Kennerson, M; Lubomski, M; Nicholson, G; O'Sullivan, JD1
Barros, M; Curtis, JE; Gruschus, JM; Heinrich, F; Jiang, Z; Lee, JC; Pfefferkorn, CM; Sidransky, E; Yap, TL1
Eriksson, O; Hultberg, B; Ockerman, PA1

Other Studies

4 other study(ies) available for tryptophan and Gaucher Disease

ArticleYear
The GBA p.Trp378Gly mutation is a probable French-Canadian founder mutation causing Gaucher disease and synucleinopathies.
    Clinical genetics, 2018, Volume: 94, Issue:3-4

    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.
    Movement disorders : official journal of the Movement Disorder Society, 2018, Volume: 33, Issue:10

    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.
    The Journal of biological chemistry, 2015, Jan-09, Volume: 290, Issue:2

    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.
    Metabolism: clinical and experimental, 1969, Volume: 18, Issue:8

    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