cysteine and g(m2) ganglioside

cysteine has been researched along with g(m2) ganglioside in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Itoh, K; Kuroki, Y; Nadaoka, Y; Sakuraba, H; Tanaka, T	1
Deng, H; Mahuran, D; Rigat, B; Smiljanic-Georgijev, N; Xie, B	1

Other Studies

2 other study(ies) available for cysteine and g(m2) ganglioside

Article	Year
A novel missense mutation (C522Y) is present in the beta-hexosaminidase beta-subunit gene of a Japanese patient with infantile Sandhoff disease. Biochemical and biophysical research communications, 1995, Jul-17, Volume: 212, Issue:2 Topics: Base Sequence; beta-N-Acetylhexosaminidases; Codon; Consanguinity; Conserved Sequence; Cysteine; DNA Mutational Analysis; Female; Fibroblasts; Fluorescent Antibody Technique; G(M2) Ganglioside; Humans; Infant; Japan; Molecular Sequence Data; Mutation; Protein Structure, Secondary; Sandhoff Disease; Tyrosine	1995
Biochemical characterization of the Cys138Arg substitution associated with the AB variant form of GM2 gangliosidosis: evidence that Cys138 is required for the recognition of the GM2 activator/GM2 ganglioside complex by beta-hexosaminidase A. Biochemistry, 1998, Jan-20, Volume: 37, Issue:3 Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; beta-N-Acetylhexosaminidases; CHO Cells; Cricetinae; Cysteine; Disulfides; Escherichia coli; G(M2) Activator Protein; G(M2) Ganglioside; Gangliosidoses; Genetic Variation; Molecular Sequence Data; Oligopeptides; Peptides; Protein Folding; Proteins; Recombinant Fusion Proteins	1998

Article

Year

A novel missense mutation (C522Y) is present in the beta-hexosaminidase beta-subunit gene of a Japanese patient with infantile Sandhoff disease.

Biochemical and biophysical research communications, 1995, Jul-17, Volume: 212, Issue:2

Topics: Base Sequence; beta-N-Acetylhexosaminidases; Codon; Consanguinity; Conserved Sequence; Cysteine; DNA Mutational Analysis; Female; Fibroblasts; Fluorescent Antibody Technique; G(M2) Ganglioside; Humans; Infant; Japan; Molecular Sequence Data; Mutation; Protein Structure, Secondary; Sandhoff Disease; Tyrosine

1995

Biochemical characterization of the Cys138Arg substitution associated with the AB variant form of GM2 gangliosidosis: evidence that Cys138 is required for the recognition of the GM2 activator/GM2 ganglioside complex by beta-hexosaminidase A.

Biochemistry, 1998, Jan-20, Volume: 37, Issue:3

Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Arginine; beta-N-Acetylhexosaminidases; CHO Cells; Cricetinae; Cysteine; Disulfides; Escherichia coli; G(M2) Activator Protein; G(M2) Ganglioside; Gangliosidoses; Genetic Variation; Molecular Sequence Data; Oligopeptides; Peptides; Protein Folding; Proteins; Recombinant Fusion Proteins

1998