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Search Results - ins-mck-mut
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Novel mouse model of methylmalonic acidemia (MMA) Mut-/- Tg
INS-Mck-Mut
Methylmalonic acidemia (MMA) is an autosomal recessive disorder, caused by the deficiency of the mitochondrial enzyme methylmalonyl-CoA mutase (MUT). It is characterized by metabolic instability, multiorgan pathology, and poor prognosis for long-term survival. Deletion of Mut in mice results in neonathal lethality, thus, to overcome this limitation,...
Published: 10/28/2024
|
Inventor(s):
Eirini (Irini) Manoli
,
Randy Chandler
,
Charles Venditti
Keywords(s):
Acidemia
,
INS-Mck-Mut
,
Methylmalonic
,
MMA
,
Model
,
Mouse
,
Mut-/-
,
Novel
,
Tg
,
VPXXXX
,
WIXXXX
,
XEXXXX
Category(s):
TherapeuticArea > Cardiology
,
TherapeuticArea > Oncology
,
TherapeuticArea > Dental
,
TherapeuticArea > Endocrinology
,
Application > Therapeutics
,
TherapeuticArea > Ophthalmology
,
TherapeuticArea > Infectious Disease
,
Application > Research Materials