glycine has been researched along with Anterior Horn Cell Disease in 10 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Amyotrophic lateral sclerosis (ALS) is a devastating disease characterized by upper and lower motor neuron damage." | 1.36 | Familial amyotrophic lateral sclerosis with a novel G85S mutation of superoxide dismutase 1 gene: clinical features of lower motor neuron disease. ( Hirayama, T; Ikeda, K; Ito, H; Iwasaki, Y; Kano, O; Kawabe, K; Nakamura, Y; Sobue, G; Takazawa, T; Tanaka, F; Yoshii, Y, 2010) |
| "Amyotrophic lateral sclerosis (ALS), a multifactorial disease characterized by diffuse motor neuron degeneration, has proven to be a difficult target for stem cell therapy." | 1.32 | Intravenous administration of human umbilical cord blood cells in a mouse model of amyotrophic lateral sclerosis: distribution, migration, and differentiation. ( Chen, N; Davis, CD; Garbuzova-Davis, S; Hudson, JE; Justen, EB; Lane, JC; Sanberg, PR; Saporta, S; Willing, AE; Zigova, T, 2003) |
| "One female patient with amyotrophic lateral sclerosis (ALS) was heterozygous for G12R mutation." | 1.32 | [Peculiarities of sporadic motor neuron disease associated with D90A and G12R mutations in Russian population]. ( Alekhin, AV; Brusov, OS; Karakhan, VB; Kondrat'eva, EA; Levitskaia, NI; Levitskiĭ, GN; Limborskaia, SA; Lysko, AI; Serdiuk, AV; Shadrina, MI; Skvortsova, VI; Slominskiĭ, PA, 2003) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (40.00) | 18.2507 |
| 2000's | 4 (40.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Soares, DC | 1 |
| Barlow, PN | 1 |
| Porteous, DJ | 1 |
| Devon, RS | 1 |
| Takazawa, T | 1 |
| Ikeda, K | 1 |
| Hirayama, T | 1 |
| Kawabe, K | 1 |
| Nakamura, Y | 1 |
| Ito, H | 1 |
| Kano, O | 1 |
| Yoshii, Y | 1 |
| Tanaka, F | 1 |
| Sobue, G | 1 |
| Iwasaki, Y | 1 |
| Borghese, CM | 1 |
| Blednov, YA | 1 |
| Quan, Y | 1 |
| Iyer, SV | 1 |
| Xiong, W | 1 |
| Mihic, SJ | 1 |
| Zhang, L | 1 |
| Lovinger, DM | 1 |
| Trudell, JR | 1 |
| Homanics, GE | 1 |
| Harris, RA | 1 |
| Garbuzova-Davis, S | 1 |
| Willing, AE | 1 |
| Zigova, T | 1 |
| Saporta, S | 1 |
| Justen, EB | 1 |
| Lane, JC | 1 |
| Hudson, JE | 1 |
| Chen, N | 1 |
| Davis, CD | 1 |
| Sanberg, PR | 1 |
| Skvortsova, VI | 1 |
| Limborskaia, SA | 1 |
| Slominskiĭ, PA | 1 |
| Levitskiĭ, GN | 1 |
| Levitskaia, NI | 1 |
| Shadrina, MI | 1 |
| Kondrat'eva, EA | 1 |
| Brusov, OS | 1 |
| Lysko, AI | 1 |
| Karakhan, VB | 1 |
| Alekhin, AV | 1 |
| Serdiuk, AV | 1 |
| Cheroni, C | 1 |
| Peviani, M | 1 |
| Cascio, P | 1 |
| Debiasi, S | 1 |
| Monti, C | 1 |
| Bendotti, C | 1 |
| Virgo, L | 1 |
| de Belleroche, JS | 1 |
| Khan, JK | 1 |
| Kuo, YH | 1 |
| Haque, A | 1 |
| Lambein, F | 1 |
| Lane, RJ | 1 |
| Bandopadhyay, R | 1 |
| de Belleroche, J | 1 |
| Rodríguez-Ithurralde, D | 1 |
| Olivera, S | 1 |
| Vincent, O | 1 |
| Maruri, A | 1 |
10 other studies available for glycine and Anterior Horn Cell Disease
| Article | Year |
|---|---|
An interrupted beta-propeller and protein disorder: structural bioinformatics insights into the N-terminus of alsin.
Topics: Amino Acid Sequence; Cell Cycle Proteins; Cysteine; Glycine; Guanine Nucleotide Exchange Factors; Hu | 2009 |
Familial amyotrophic lateral sclerosis with a novel G85S mutation of superoxide dismutase 1 gene: clinical features of lower motor neuron disease.
Topics: Adult; Amyotrophic Lateral Sclerosis; Fatal Outcome; Female; Glycine; Humans; Male; Motor Neuron Dis | 2010 |
Characterization of two mutations, M287L and Q266I, in the α1 glycine receptor subunit that modify sensitivity to alcohols.
Topics: Alcohols; Amino Acid Substitution; Animals; Binding, Competitive; Brain Stem; Cells, Cultured; Drug | 2012 |
Intravenous administration of human umbilical cord blood cells in a mouse model of amyotrophic lateral sclerosis: distribution, migration, and differentiation.
Topics: Alanine; Animals; Cord Blood Stem Cell Transplantation; Disease Models, Animal; Disease Progression; | 2003 |
[Peculiarities of sporadic motor neuron disease associated with D90A and G12R mutations in Russian population].
Topics: Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Arginine; Copper; Disease Progression; Elect | 2003 |
Accumulation of human SOD1 and ubiquitinated deposits in the spinal cord of SOD1G93A mice during motor neuron disease progression correlates with a decrease of proteasome.
Topics: Alanine; Amino Acid Substitution; Animals; Female; Glycine; Humans; Mice; Mice, Inbred C57BL; Mice, | 2005 |
Differential changes in gene expression in motor neurone disease.
Topics: Amino Acid Oxidoreductases; Amino Acid Transport Systems, Neutral; Carrier Proteins; Choline O-Acety | 1994 |
Inhibitory and excitatory amino acids in cerebrospinal fluid of neurolathyrism patients, a highly prevalent motorneurone disease.
Topics: Adolescent; Adult; Aged; Alanine; Aspartic Acid; Eating; Excitatory Amino Acids; Fabaceae; Glutamic | 1995 |
Abnormal glycine metabolism in motor neurone disease: studies on plasma and cerebrospinal fluid.
Topics: Amino Acids; Female; Glycine; Humans; Male; Middle Aged; Motor Neuron Disease; Single-Blind Method | 1993 |
In vivo and in vitro studies of glycine- and glutamate-evoked acetylcholinesterase release from spinal motor neurones: implications for amyotrophic lateral sclerosis/motor neurone disease pathogenesis.
Topics: Acetylcholinesterase; Amyotrophic Lateral Sclerosis; Animals; Calcium; Glutamic Acid; Glycine; Histo | 1997 |