Page last updated: 2024-10-18

glycine and Hyperlipoproteinemias

glycine has been researched along with Hyperlipoproteinemias in 3 studies

Hyperlipoproteinemias: Conditions with abnormally elevated levels of LIPOPROTEINS in the blood. They may be inherited, acquired, primary, or secondary. Hyperlipoproteinemias are classified according to the pattern of lipoproteins on electrophoresis or ultracentrifugation.

Research Excerpts

ExcerptRelevanceReference
"To investigate whether a substitution of glutamine by glutamic acid at amino acid position 27 (Q/E27) and an arginine to glycine transition at amino acid 16 (R/G16) in the beta2-adrenoceptor gene are associated with lipid and lipoprotein disturbances and/or increased body weight in men."3.70The Q/E27 polymorphism in the beta2-adrenoceptor gene is associated with increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins. ( Arner, P; Ehrenborg, E; Eriksson, P; Hamsten, A; Large, V; Ruotolo, G; Skogsberg, J, 2000)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (66.67)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arai, T1
Yamashita, S1
Sakai, N1
Hirano, K1
Okada, S1
Ishigami, M1
Maruyama, T1
Yamane, M1
Kobayashi, H1
Nozaki, S1
Funahashi, T1
Kameda-Takemura, K1
Nakajima, N1
Matsuzawa, Y1
Miettinen, HE1
Gylling, H1
Tenhunen, J1
Virtamo, J1
Jauhiainen, M1
Huttunen, JK1
Kantola, I1
Miettinen, TA1
Kontula, K1
Ehrenborg, E1
Skogsberg, J1
Ruotolo, G1
Large, V1
Eriksson, P1
Arner, P1
Hamsten, A1

Other Studies

3 other studies available for glycine and Hyperlipoproteinemias

ArticleYear
A novel nonsense mutation (G181X) in the human cholesteryl ester transfer protein gene in Japanese hyperalphalipoproteinemic subjects.
    Journal of lipid research, 1996, Volume: 37, Issue:10

    Topics: Carrier Proteins; Cholesterol Ester Transfer Proteins; Cholesterol, HDL; Codon; Deoxyribonucleases,

1996
Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5% of cases with very low serum HDL cholesterol levels.
    Arteriosclerosis, thrombosis, and vascular biology, 1998, Volume: 18, Issue:4

    Topics: Adult; Arginine; Carrier Proteins; Cholesterol Ester Transfer Proteins; Cholesterol Esters; Choleste

1998
The Q/E27 polymorphism in the beta2-adrenoceptor gene is associated with increased body weight and dyslipoproteinaemia involving triglyceride-rich lipoproteins.
    Journal of internal medicine, 2000, Volume: 247, Issue:6

    Topics: Adult; Alleles; Arginine; Body Weight; Cholesterol; Cholesterol, VLDL; Genotype; Glutamic Acid; Glut

2000