Technologies
Sub Categories
Therapeutic hardware/ software/medical devices
Transgenic mice which express only PRLR-L, ubiquitously (Tg-RL)
Transgenic mice which express only PRLR-L, in a CL-specific manner (CL-RL)
Periodontal disease is one of the major reasons for tooth loss in the United States and may be associated with systemic effects, including heart disease and rheumatoid arthritis. Although tooth retention has greatly improved over the past few decades, a significant percentage of older Americans do not have functional dentitions and only 42.4% of the U.S.
Loss of dental and craniofacial tissues due to disease, injury or genetic disorders negatively affects the quality of life of millions of Americans. Presently, the gold standard in clinical treatment for craniofacial bone defects is autografts and demineralized bone matrix (DBM). Autografts perform exceptionally well, but are known to induce donor site morbidity and DBMs poorly induce regeneration of lost tissue.
UIC Scientists have designed an automated chemical structure dereplication software capable of identifying the chemical structure of an unknown molecule from raw NMR data using dereplication and data mining principles. The dereplication tool provides information about chemical shifts of methyl groups within the triterpenoid family of molecules. This software provides a standardized model for naming the compounds based on the structure and variation to the methyl group location including members of the cycloartane triterpenes family.
UIC Scientists have designed an automated chemical structure dereplication software capable of identifying the chemical structure of an unknown molecule from raw NMR data using dereplication and data mining principles. The dereplication tool provides information about chemical shifts of methyl groups within the triterpenoid family of molecules. This software provides a standardized model for naming the compounds based on the structure and variation to the methyl group location including members of the cycloartane triterpenes family.
UIC Scientists have designed an automated chemical structure dereplication software capable of identifying the chemical structure of an unknown molecule from raw NMR data using dereplication and data mining principles. The dereplication tool provides information about chemical shifts of methyl groups within the triterpenoid family of molecules. This software provides a standardized model for naming the compounds based on the structure and variation to the methyl group location including members of the cycloartane triterpenes family.
UIC Scientists have designed an automated chemical structure dereplication software capable of identifying the chemical structure of an unknown molecule from raw NMR data using dereplication and data mining principles. The dereplication tool provides information about chemical shifts of methyl groups within the triterpenoid family of molecules. This software provides a standardized model for naming the compounds based on the structure and variation to the methyl group location including members of the cycloartane triterpenes family.
UIC Scientists have designed an automated chemical structure dereplication software capable of identifying the chemical structure of an unknown molecule from raw NMR data using dereplication and data mining principles. The dereplication tool provides information about chemical shifts of methyl groups within the triterpenoid family of molecules. This software provides a standardized model for naming the compounds based on the structure and variation to the methyl group location including members of the cycloartane triterpenes family.
UIC Scientists have designed an automated chemical structure dereplication software capable of identifying the chemical structure of an unknown molecule from raw NMR data using dereplication and data mining principles. The dereplication tool provides information about chemical shifts of methyl groups within the triterpenoid family of molecules. This software provides a standardized model for naming the compounds based on the structure and variation to the methyl group location including members of the cycloartane triterpenes family.
Below the knee muscle weakness, defined by weak
dorsiflexor (shin) or plantarflexor (calf) muscle groups, can result from a
variety of physical impairments or congenital abnormalities. Stroke, spinal
cord injuries, polio and multiple sclerosis are among some of the physical injuries
and congenital defects responsible for the condition. The largest complication
from below the knee muscle weakness is abnormal gait, which when compensated
for can lead to further complications in other muscles and joints.