carotenoids 发表于 2025-3-25 07:01:10
Molecular Genetics of Phosphorylase Kinase: cDNA Cloning, Chromosomal Mapping and Isoform Structure gene. The . subunit gene was mapped to chromosome Xq12-q13 and the . subunit gene to chromosome 16q12-q13. Isoform cDNAs reveal differential mRNA splicing. Thus, the stage is set for the molecular characterization of the genes and their deficiency mutations.Anthropoid 发表于 2025-3-25 11:23:53
http://reply.papertrans.cn/23/2216/221536/221536_22.pngagonist 发表于 2025-3-25 11:48:10
http://reply.papertrans.cn/23/2216/221536/221536_23.png提名 发表于 2025-3-25 16:45:32
Mechanisms of Blood Glucose Homeostasis,thesis. When glycogen synthesis is intense, the concentrations of UDPG and of glucose 6-phosphate in the liver decrease, allowing a net glucose uptake by the liver. Glucose uptake is indeed the difference between the activities of glucokinase and glucose 6-phosphatase. Since the K. of the latter enzresistant 发表于 2025-3-25 21:43:34
http://reply.papertrans.cn/23/2216/221536/221536_25.pngharmony 发表于 2025-3-26 00:43:26
http://reply.papertrans.cn/23/2216/221536/221536_26.pngparsimony 发表于 2025-3-26 04:57:16
http://reply.papertrans.cn/23/2216/221536/221536_27.png纹章 发表于 2025-3-26 11:19:53
http://reply.papertrans.cn/23/2216/221536/221536_28.pngConducive 发表于 2025-3-26 14:29:56
http://reply.papertrans.cn/23/2216/221536/221536_29.png夹克怕包裹 发表于 2025-3-26 20:21:32
Advances in the Molecular Genetics of Metachromatic Leukodystrophy,bstantial arylsulphatase A deficiency can also occur in healthy individuals, a phenotype termed pseudodeficiency. Two concurrent mutations have been identified in this low arylsulphatase A activity allele. This permitted the development of a rapid assay which allows the detection of the pseudodefici