A non-deterministic decoding algorithm for binary coded genetic algorithms is presented. The proposed algorithm enhances the precision of the GA solutions by introducing a Gaussian perturbation to the ...

Researchers from the University of Maryland's Department of Nutrition and Food Science are shedding new light on how a ...

Abstract: We introduce a genetic model based on stochastic crossover to solve the Hamiltonian cycle problem (DHCP) for random digraphs containing a random Hamiltonian cycle. The genetic model ...

Hyderabad: Doctors recommend checking hemoglobin levels in school children to test blood disorders Hyderabad: Medical experts have called for raising awareness about inherited blood disorders among ...

In preclinical studies using clinically-translatable human cell models, CLY-124 increased fetal hemoglobin above 20%, with no evidence of cytotoxicity.

This gene-editing technology used for thalassemia is also used to treat sickle cell disease. Both are genetic diseases that affect hemoglobin within red blood cells.

Severe anemia and a 1-day history of nausea and 'coffee ground' vomiting are presented in a 56-year-old male with a history of excess alcohol consumption and type 2 diabetes. What's the diagnosis?

In addition, the dissociation of maternal CO-Hb creates a pressure gradient between maternal and fetal blood, causing placental CO diffusion. Once the CO reaches the fetal blood, it easily combines ...

The BEAM-101 edit is designed to inhibit the transcriptional repressor BCL11A from binding to the promoter without disrupting BCL11A expression, leading to increased production of non-sickling and ...

Updated data from 17 patients treated with BEAM-101 demonstrated robust and durable increases in fetal hemoglobin (HbF) and reductions in sickle hemoglobin (HbS), rapid neutrophil and platelet ...