phenylalanine has been researched along with Amyotrophic Lateral Sclerosis in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 4 (57.14) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Čerček, U; Hermann, A; Ho, MT; Malnar Črnigoj, M; Mayr, M; Neumann, M; Repic Lampret, B; Rogelj, B; Rouleau, G; Suter, B; Yin, X | 1 |
| Connor, JR; Lee, SY; Mitchell, RM; Simmons, Z; Stephens, HE; Su, XW | 1 |
| Gourie-Devi, M; Kukreti, R; Ramachandran, S; Taneja, B; Taneja, V; Vats, A; Verma, M | 1 |
| Battistini, S; Benigni, M; Bondavalli, M; Cereda, C; Ceroni, M; Gagliardi, S; Lotti, EM; Marcello, N; Ricci, C; Zucco, R | 1 |
| Baek, W; Ki, CS; Kim, HY; Kim, SH; Kim, YS; Koh, SH; Kwon, MJ; Park, JS | 1 |
| Amoroso, A; Bordo, D; Caponnetto, C; Ferrera, L; Garrè, C; Marini, V; Origone, P; Penco, S; Rizzi, D | 1 |
| Kuncl, RW; Martin, LJ; Rothstein, JD | 1 |
7 other study(ies) available for phenylalanine and Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
Phenylalanine-tRNA aminoacylation is compromised by ALS/FTD-associated C9orf72 C4G2 repeat RNA.
Topics: Aminoacylation; Amyotrophic Lateral Sclerosis; C9orf72 Protein; Frontotemporal Dementia; Humans; Phenylalanine; RNA, Antisense; RNA, Transfer, Phe; Transfer RNA Aminoacylation | 2023 |
H63D HFE polymorphisms are associated with increased disease duration and decreased muscle superoxide dismutase-1 expression in amyotrophic lateral sclerosis patients.
Topics: Adult; Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Female; Gene Expression Regulation; Genetic Association Studies; Genotype; Hemochromatosis Protein; Histidine; Histocompatibility Antigens Class I; Humans; Male; Membrane Proteins; Middle Aged; Muscle, Skeletal; Phenylalanine; Polymorphism, Single Nucleotide; Superoxide Dismutase; Superoxide Dismutase-1 | 2013 |
Identification of L84F mutation with a novel nucleotide change c.255G > T in the superoxide dismutase gene in a North Indian family with amyotrophic lateral sclerosis.
Topics: Aged; Amyotrophic Lateral Sclerosis; DNA-Binding Proteins; Family Health; Female; Genetic Testing; Genotype; Humans; India; Lysine; Male; Middle Aged; Models, Molecular; Phenylalanine; Polymorphism, Single Nucleotide; Superoxide Dismutase-1 | 2016 |
Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene.
Topics: Adult; Alanine; Amyotrophic Lateral Sclerosis; DNA Mutational Analysis; Exons; Family Health; Female; Humans; Male; Middle Aged; Models, Molecular; Mutation; Phenylalanine; Superoxide Dismutase; Superoxide Dismutase-1 | 2010 |
A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosis.
Topics: Alanine; Amyotrophic Lateral Sclerosis; DNA Mutational Analysis; Family Health; Female; Humans; Male; Middle Aged; Mutation; Phenylalanine; Superoxide Dismutase; Superoxide Dismutase-1 | 2011 |
An Italian dominant FALS Leu144Phe SOD1 mutation: genotype-phenotype correlation.
Topics: Adolescent; Adult; Aged; Amyotrophic Lateral Sclerosis; DNA Mutational Analysis; Family Health; Female; Genotype; Humans; Italy; Leucine; Male; Mutation; Phenotype; Phenylalanine; Polymerase Chain Reaction; Superoxide Dismutase; Superoxide Dismutase-1 | 2003 |
Decreased glutamate transport by the brain and spinal cord in amyotrophic lateral sclerosis.
Topics: Aged; Alzheimer Disease; Amyotrophic Lateral Sclerosis; Biological Transport; Brain; Female; gamma-Aminobutyric Acid; Glutamates; Glutamic Acid; Humans; Huntington Disease; In Vitro Techniques; Male; Middle Aged; Motor Cortex; Phenylalanine; Somatosensory Cortex; Spinal Cord; Synaptosomes; Visual Cortex | 1992 |