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thymine and Familial Hypobetalipoproteinemia

thymine has been researched along with Familial Hypobetalipoproteinemia in 3 studies

Research Excerpts

ExcerptRelevanceReference
"Familial hypobetalipoproteinemia (FHBL) is an monogenic co-dominant disorder characterized by reduced plasma levels of cholesterol, low density lipoproteins (LDL) and apolipoprotein B (apoB) often associated with non-alcoholic fatty liver disease (NAFLD)."1.33Pediatric gallstone disease in familial hypobetalipoproteinemia. ( Costa, L; Di Leo, E; Lancellotti, S; Lonardo, A; Tarugi, P; Zaffanello, M, 2005)

Research

Studies (3)

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

Authors

AuthorsStudies
Yue, P1
Isley, WL1
Harris, WS1
Rosipal, S1
Akin, CD1
Schonfeld, G2
Lancellotti, S1
Zaffanello, M1
Di Leo, E1
Costa, L1
Lonardo, A1
Tarugi, P1
Pulai, JI1
Zakeri, H1
Kwok, PY1
Kim, JH1
Wu, J1

Other Studies

3 other studies available for thymine and Familial Hypobetalipoproteinemia

ArticleYear
Genetic variants of ApoE account for variability of plasma low-density lipoprotein and apolipoprotein B levels in FHBL.
    Atherosclerosis, 2005, Volume: 178, Issue:1

    Topics: Adult; Apolipoproteins B; Apolipoproteins E; Female; Frameshift Mutation; Gene Deletion; Genetic Var

2005
Pediatric gallstone disease in familial hypobetalipoproteinemia.
    Journal of hepatology, 2005, Volume: 43, Issue:1

    Topics: Adenine; Adult; Apolipoproteins B; Base Sequence; Child; Codon, Nonsense; Female; Gallstones; Hetero

2005
Donor splice mutation (665 + 1 G_T) in familial hypobetalipoproteinemia with no detectable apoB truncation.
    American journal of medical genetics, 1998, Nov-16, Volume: 80, Issue:3

    Topics: Adolescent; Adult; Aged; Apolipoproteins B; Child, Preschool; Female; Guanine; Humans; Hypobetalipop

1998