Page last updated: 2024-08-17

aspartic acid and Epiphora

aspartic acid has been researched along with Epiphora in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Dingerdissen, H; Karagiannis, K; Mazumder, R; Motwani, M; Simonyan, V	1
Braun, R; Handschug, K; Huebner, A; Kaindl, AM	1

Other Studies

2 other study(ies) available for aspartic acid and Epiphora

Article	Year
Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins. The FEBS journal, 2013, Volume: 280, Issue:6 Topics: Abnormalities, Multiple; Amino Acid Substitution; Arginine; Aspartic Acid; Carbohydrate Metabolism; Catalytic Domain; Cluster Analysis; Enzyme Activation; Genetic Variation; Genome, Human; Glycogen Storage Disease; Hearing Loss; Histidine; Humans; Lacrimal Apparatus Diseases; Metabolomics; Molecular Sequence Annotation; Phenylalanine; Polymorphism, Single Nucleotide; Proteome; Proteomics; Structure-Activity Relationship; Syndactyly; Tooth Abnormalities; Tyrosine	2013
New insights into the molecular basis of the triple A syndrome. Endocrine research, 2002, Volume: 28, Issue:4 Topics: Addison Disease; Aspartic Acid; DNA Mutational Analysis; Esophageal Achalasia; Genotype; Heterozygote; Homozygote; Humans; Lacrimal Apparatus Diseases; Mutation; Nerve Tissue Proteins; Nuclear Pore Complex Proteins; Phenotype; Proteins; Repetitive Sequences, Amino Acid; Syndrome; Tryptophan	2002

Article

Year

Proteome-wide analysis of nonsynonymous single-nucleotide variations in active sites of human proteins.

The FEBS journal, 2013, Volume: 280, Issue:6

Topics: Abnormalities, Multiple; Amino Acid Substitution; Arginine; Aspartic Acid; Carbohydrate Metabolism; Catalytic Domain; Cluster Analysis; Enzyme Activation; Genetic Variation; Genome, Human; Glycogen Storage Disease; Hearing Loss; Histidine; Humans; Lacrimal Apparatus Diseases; Metabolomics; Molecular Sequence Annotation; Phenylalanine; Polymorphism, Single Nucleotide; Proteome; Proteomics; Structure-Activity Relationship; Syndactyly; Tooth Abnormalities; Tyrosine

2013

New insights into the molecular basis of the triple A syndrome.

Endocrine research, 2002, Volume: 28, Issue:4

Topics: Addison Disease; Aspartic Acid; DNA Mutational Analysis; Esophageal Achalasia; Genotype; Heterozygote; Homozygote; Humans; Lacrimal Apparatus Diseases; Mutation; Nerve Tissue Proteins; Nuclear Pore Complex Proteins; Phenotype; Proteins; Repetitive Sequences, Amino Acid; Syndrome; Tryptophan

2002