thymine has been researched along with Familial Hypobetalipoproteinemia in 3 studies
Excerpt | Relevance | Reference |
---|---|---|
"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)." | 1.33 | Pediatric gallstone disease in familial hypobetalipoproteinemia. ( Costa, L; Di Leo, E; Lancellotti, S; Lonardo, A; Tarugi, P; Zaffanello, M, 2005) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (33.33) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Yue, P | 1 |
Isley, WL | 1 |
Harris, WS | 1 |
Rosipal, S | 1 |
Akin, CD | 1 |
Schonfeld, G | 2 |
Lancellotti, S | 1 |
Zaffanello, M | 1 |
Di Leo, E | 1 |
Costa, L | 1 |
Lonardo, A | 1 |
Tarugi, P | 1 |
Pulai, JI | 1 |
Zakeri, H | 1 |
Kwok, PY | 1 |
Kim, JH | 1 |
Wu, J | 1 |
3 other studies available for thymine and Familial Hypobetalipoproteinemia
Article | Year |
---|---|
Genetic variants of ApoE account for variability of plasma low-density lipoprotein and apolipoprotein B levels in FHBL.
Topics: Adult; Apolipoproteins B; Apolipoproteins E; Female; Frameshift Mutation; Gene Deletion; Genetic Var | 2005 |
Pediatric gallstone disease in familial hypobetalipoproteinemia.
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.
Topics: Adolescent; Adult; Aged; Apolipoproteins B; Child, Preschool; Female; Guanine; Humans; Hypobetalipop | 1998 |