Page last updated: 2024-11-08

serine and Diseases in Twins

serine has been researched along with Diseases in Twins in 3 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.

Diseases in Twins: Disorders affecting TWINS, one or both, at any age.

Research Excerpts

ExcerptRelevanceReference
"Investigation of a 15-year old boy with progressive optic atrophy and spinocerebellar degeneration revealed elevated plasma, cerebrospinal fluid, and urine glycine concentrations."3.66Late-onset nonketotic hyperglycinemia and spinocerebellar degeneration. ( Berman, PH; Blazer-Yost, B; Segal, S; Steiman, GS; Yudkoff, M, 1979)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Suda, N1
Hattori, M1
Kosaki, K1
Banshodani, A1
Kozai, K1
Tanimoto, K1
Moriyama, K1
Munhoz, RP1
Wakutani, Y1
Marras, C1
Teive, HA1
Raskin, S1
Werneck, LC1
Moreno, D1
Sato, C1
Lang, AE1
Rogaeva, E1
Steiman, GS1
Yudkoff, M1
Berman, PH1
Blazer-Yost, B1
Segal, S1

Other Studies

3 other studies available for serine and Diseases in Twins

ArticleYear
Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.
    Orthodontics & craniofacial research, 2010, Volume: 13, Issue:4

    Topics: Adenine; Adolescent; Adult; Arginine; Child; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Su

2010
The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.
    Movement disorders : official journal of the Movement Disorder Society, 2008, Jan-30, Volume: 23, Issue:2

    Topics: Adult; Age of Onset; Aged; Aged, 80 and over; Brazil; Diseases in Twins; Female; Glycine; Humans; Le

2008
Late-onset nonketotic hyperglycinemia and spinocerebellar degeneration.
    The Journal of pediatrics, 1979, Volume: 94, Issue:6

    Topics: Adolescent; Diseases in Twins; Glycine; Humans; Male; Nervous System Diseases; Optic Atrophy; Serine

1979