ADA 2024

June 25, 2024

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Join us at the American Diabetes Association’s 84th Scientific Sessions conference in Orlando this June!


GemPharmatech has the world’s largest collection of genetically engineered mouse models. As part of this collection of over 23,000 strains, we provide scientists researching metabolic diseases a whole suite of targeted research tools to facilitate project success. To discuss these models and more at the American Diabetes Association meeting, please send an email to: sales@gempharmatech.us. 


Metabolic Disease Mouse Models


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Poster Presentations:

At this meeting, we will be presenting 2 posters on diabetes-related topics. If you are unable to attend these sessions, please stop by our booth (643), or contact at sales@gempharmatech.us to schedule a meeting.


Monday Jun 24, 2024 12:30 PM - 1:30 PM

B6-Chr1KM: A Novel Mouse Model for Spontaneous NASH Research

Category: 23-A Obesity—Animal

Board No. 1632-P

 

Monday Jun 24, 2024 12:30 PM - 1:30 PM

Tirzepatide and Efruxifermin Demonstrate Therapeutic Benefits for NASH in a Preclinical Metabolic Syndrome Animal Model, B6-Alms1-del Mice

Category: 23-A Obesity—Animal

Board No. 1639-P



A Rapid NASH Model and its Application in Candidate Drug Screening for Metabolic Syndrome and Hepatic Steatosis

A Rapid NASH Model and its Application in Candidate Drug Screening for Metabolic Syndrome and Hepatic Steatosis

Non-alcoholic steatohepatitis (NASH) is an aggressive form of non-alcoholic fatty liver disease (NAFLD) that may progress to cirrhosis and hepatocelluar carcinoma (HCC), and so far, there is limited FDA approved therapies for NASH. Animal models of NAFLD/NASH are crucial for preclinical evaluation of efficacy and safety. Given the rapidly growing recognition that NAFLD/NASH is the hepatic manifestation of metabolic syndrome, scientists are paying a lot more attention to the metabolic characteristics of NASH animal models they choose to work with. Among most classical NASH animal models, the long duration of diet treatment or the lack of metabolic phenotypes limits their application in candidate drug screening. To fill the gap, GemPharmatech developed a rapid NASH model based on Alms1 mutant mice (B6-Alms1-del mice). B6-Alms1-del mice develop a plethora of early onset metabolic phenotypes on chow diet, such as obesity, hyperglycemia, hyperlipidemia and fatty liver. To verify the applicability of this Alms1 NASH model in preclinical research, the promising preclinical drug Semaglutide was used to treat Alms1-del NASH mice.
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