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doi: 10.1016/s1097-2765(00)80425-6 15 PhilpottCCJadhavS

Insulin mutation screening in 1044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

The different effects of different subtypes of IFNs on the host may be related to the activated signaling pathways

Only sections where we could locate positive GFP staining within the cortex corresponding to the image area were chosen for confocal imaging and further analysis

thaliana have reported that chloroplastic GPX1 and GPX7 consisted of 236 and 233 amino acids, respectively