Page last updated: 2024-11-08

serine and Ataxia

serine has been researched along with Ataxia in 9 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Ataxia: Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions.

Research Excerpts

ExcerptRelevanceReference
"D-Serine, a selective agonist at the strychnine-insensitive glycine binding site, antagonized PCP-induction of stereotyped behavior and ataxia in a dose-dependent manner."7.68D-serine antagonized phencyclidine- and MK-801-induced stereotyped behavior and ataxia. ( Contreras, PC, 1990)
"Effects of systemic injection of the glycine(B) agonist, d-serine, the GlyT-1 glycine transporter inhibitor, ALX-5407, and the glycine(B) antagonist, L-701,324, were tested for the effects on EtOH-induced ataxia, hypothermia, and loss of righting reflex (LORR) duration in C57BL/6J (B6) and 129S1/SvImJ (S1) inbred mice."3.79Probing the modulation of acute ethanol intoxication by pharmacological manipulation of the NMDAR glycine co-agonist site. ( Camp, M; Debrouse, L; Grant, SG; Gunduz-Cinar, O; Holmes, A; Hurd, B; Kiselycznyk, C; Mishina, M; Plitt, A; Todaro, A, 2013)
"D-Serine, a selective agonist at the strychnine-insensitive glycine binding site, antagonized PCP-induction of stereotyped behavior and ataxia in a dose-dependent manner."3.68D-serine antagonized phencyclidine- and MK-801-induced stereotyped behavior and ataxia. ( Contreras, PC, 1990)
"Familial hemiplegic migraine is an episodic neurological disorder characterized by transient sensory and motor symptoms and signs."1.56Astrocyte deletion of α2-Na/K ATPase triggers episodic motor paralysis in mice via a metabolic pathway. ( Bice, AR; Bonni, A; Brier, LM; Bumstead, JR; Chen, X; Crowley, JR; Culver, JP; Dikranian, K; Haigis, MC; Ippolito, JE; Oldenborg, A; Papouin, T; Rensing, NR; Ringel, AE; Shin, H; Smith, SE; Wong, M; Zhao, G, 2020)
"Spinocerebellar ataxia type 1 (SCA1) is a polyglutamine (polyQ) repeat neurodegenerative disease in which a primary site of pathogenesis are cerebellar Purkinje cells."1.48Reduction of protein kinase A-mediated phosphorylation of ATXN1-S776 in Purkinje cells delays onset of Ataxia in a SCA1 mouse model. ( Adamski, CJ; Duvick, L; Friedrich, J; Hawkinson, JE; Henzler, C; Lagalwar, S; Mollema, N; O'Callaghan, B; Orr, HT; Pérez Ortiz, JM; Strasser, J; Toker, N; Walters, MA; Zoghbi, HY, 2018)

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19901 (11.11)18.7374
1990's3 (33.33)18.2507
2000's1 (11.11)29.6817
2010's3 (33.33)24.3611
2020's1 (11.11)2.80

Authors

AuthorsStudies
Smith, SE1
Chen, X1
Brier, LM1
Bumstead, JR1
Rensing, NR1
Ringel, AE1
Shin, H1
Oldenborg, A1
Crowley, JR1
Bice, AR1
Dikranian, K1
Ippolito, JE1
Haigis, MC1
Papouin, T1
Zhao, G1
Wong, M1
Culver, JP1
Bonni, A1
Pérez Ortiz, JM1
Mollema, N1
Toker, N1
Adamski, CJ1
O'Callaghan, B1
Duvick, L1
Friedrich, J1
Walters, MA1
Strasser, J1
Hawkinson, JE1
Zoghbi, HY1
Henzler, C1
Orr, HT1
Lagalwar, S1
Pelayo-Negro, AL1
Sánchez-Quintana, C1
Rodríguez-Oroz, MC1
Volpini, V1
Zeviani, M1
Tola-Arribas, MA1
Berciano, J1
Infante, J1
Debrouse, L1
Hurd, B1
Kiselycznyk, C1
Plitt, A1
Todaro, A1
Mishina, M1
Grant, SG1
Camp, M1
Gunduz-Cinar, O1
Holmes, A1
Sawada, K1
Ando, M1
Sakata-Haga, H1
Sun, XZ1
Jeong, YG1
Hisano, S1
Takeda, N1
Fukui, Y1
Tanii, Y1
Nishikawa, T1
Hashimoto, A1
Takahashi, K1
Bank, WJ1
Pizer, L1
Pfendner, W1
Sorrels, TL1
Bostock, E1
Contreras, PC1

Other Studies

9 other studies available for serine and Ataxia

ArticleYear
Astrocyte deletion of α2-Na/K ATPase triggers episodic motor paralysis in mice via a metabolic pathway.
    Nature communications, 2020, 12-02, Volume: 11, Issue:1

    Topics: Animals; Astrocytes; Ataxia; Brain; Disease Models, Animal; Electroencephalography; Female; Function

2020
Reduction of protein kinase A-mediated phosphorylation of ATXN1-S776 in Purkinje cells delays onset of Ataxia in a SCA1 mouse model.
    Neurobiology of disease, 2018, Volume: 116

    Topics: Animals; Ataxia; Ataxin-1; Cyclic AMP-Dependent Protein Kinases; Female; Humans; Male; Mice; Mice, T

2018
Screening for POLG W748S and A467T mutations in ataxia patients from Spain.
    Movement disorders : official journal of the Movement Disorder Society, 2012, Sep-01, Volume: 27, Issue:10

    Topics: Adult; Age of Onset; Aged; Alanine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Femal

2012
Probing the modulation of acute ethanol intoxication by pharmacological manipulation of the NMDAR glycine co-agonist site.
    Alcoholism, clinical and experimental research, 2013, Volume: 37, Issue:2

    Topics: Alcoholic Intoxication; Animals; Ataxia; Cycloserine; Disease Models, Animal; Disks Large Homolog 4

2013
Abnormal expression of tyrosine hydroxylase not accompanied by phosphorylation at serine 40 in cerebellar Purkinje cells of ataxic mutant mice, rolling mouse Nagoya and dilute-lethal.
    Congenital anomalies, 2004, Volume: 44, Issue:1

    Topics: Animals; Ataxia; Cerebellum; Female; Immunohistochemistry; Male; Mice; Phosphorylation; Purkinje Cel

2004
Stereoselective antagonism by enantiomers of alanine and serine of phencyclidine-induced hyperactivity, stereotypy and ataxia in the rat.
    The Journal of pharmacology and experimental therapeutics, 1994, Volume: 269, Issue:3

    Topics: Alanine; Animals; Ataxia; Injections, Intraventricular; Male; Motor Activity; Phencyclidine; Rats; R

1994
Glycine metabolism and spinal cord disorders.
    Advances in neurology, 1978, Volume: 21

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Animals; Ataxia; Cats; Cells, Cultured; Chi

1978
Induction of feeding by 7-chlorokynurenic acid, a strychnine-insensitive glycine binding site antagonist.
    Brain research, 1992, Feb-14, Volume: 572, Issue:1-2

    Topics: Analysis of Variance; Animals; Ataxia; Dose-Response Relationship, Drug; Feeding Behavior; Glycine;

1992
D-serine antagonized phencyclidine- and MK-801-induced stereotyped behavior and ataxia.
    Neuropharmacology, 1990, Volume: 29, Issue:3

    Topics: Animals; Ataxia; Dibenzocycloheptenes; Dizocilpine Maleate; Dose-Response Relationship, Drug; Inject

1990
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