thymine has been researched along with Hypobetalipoproteinemias in 3 studies
Hypobetalipoproteinemias: Conditions with abnormally low levels of BETA-LIPOPROTEINS (low density lipoproteins or LDL) in the blood. It is defined as LDL values equal to or less than the 5th percentile for the population. They include the autosomal dominant form involving mutation of the APOLIPOPROTEINS B gene, and the autosomal recessive form involving mutation of the microsomal triglyceride transfer protein. All are characterized by low LDL and dietary fat malabsorption.
| 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 Hypobetalipoproteinemias
| 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 |