Cleave
发表于 2025-3-25 06:57:33
Compounds Derived from Aminoacetic Acidsoccurs. Differences between monogenic and common diseases are outlined. Utilization of intermediate phenotypes rather than of the common disease . as the diagnostic trait may be helpful for genetic analysis. Various genetic approaches with particular emphasis on linkage and association studies are d
Fibrillation
发表于 2025-3-25 09:05:51
Compounds Derived from Acetic Acidseases are the result of the interaction of numerous etiological factors, both genetic and environmental, each making a relatively small contribution to overall liability. Therefore, the contribution to disease risk of variation at any single gene is likely small when compared to all other risk fact
Chauvinistic
发表于 2025-3-25 13:09:49
https://doi.org/10.1007/978-1-4020-9787-4sease. This success in understanding inborn errors of metabolism, however, has been largely restricted to monogenic disease or to defects that involve large aberrations in the DNA primary structure. A much more complicated situation is present in common disease where important roles for disease expr
搜集
发表于 2025-3-25 16:02:47
F. Chialva,G. Gabri,P. A. P. Liddle,F. Ulianen identified by cDNA cloning, at least two of which (GLUT 1 and GLUT 4) are expressed in insulin-sensitive tissues. The GLUT 1 CHepG2-type) transporter is the more widely distributed of these two proteins. It provides many cells with their basal glucose requirement for ATP production and the biosyn
退潮
发表于 2025-3-25 23:00:47
13C-NMR Analysis of Essential Oilscy varies in degree, being complete in insulin dependent diabetes (IDDM), and relative in non-insulin dependent diabetes (NIDDM). The strong association of certain HLA immune-response genes on chromosome 6 with IDDM provides a prominent genetic marker to distinguish these two types of diabetes (Truc
impale
发表于 2025-3-26 01:32:29
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Ondines-curse
发表于 2025-3-26 04:48:07
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Arboreal
发表于 2025-3-26 10:05:20
https://doi.org/10.1007/978-3-0348-0379-3ns of fasting subjects resulting in a pronounced increase in plasma triglycerides .. Familial deficiencies of lipoprotein lipase (LPL) . and of apolipoprotein C-II ., a polypeptide cofactor of LPL, are well-defined causes of this syndrome. LPL, the enzyme most frequently reduced or absent in chylomi
perimenopause
发表于 2025-3-26 16:26:46
https://doi.org/10.1007/978-1-137-05175-2f first degree relatives of 121 men and 96 women with CAD showed the increased risk of death from the disease was five and seven fold greater than in matched controls for males and females respectively.. Many subsequent studies have confirmed this trend.. Further evidence for the implication of a ge
caldron
发表于 2025-3-26 19:56:28
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