Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lucie V. Ngaba"'
Autor:
Joshua C. Chang, Molly R. Ryan, Marie C. Stark, Su Liu, Pravinkumar Purushothaman, Fria Bolan, Caitlin A. Johnson, Mark Champe, Hui Meng, Michael W. Lawlor, Sarah Halawani, Lucie V. Ngaba, David R. Lynch, Crystal Davis, Elena Gonzalo-Gil, Cathleen Lutz, Fabrizia Urbinati, Bala Medicherla, Carlos Fonck
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 32, Iss 1, Pp 101193- (2024)
Friedreich’s ataxia (FRDA) is an autosomal-recessive disorder primarily attributed to biallelic GAA repeat expansions that reduce expression of the mitochondrial protein frataxin (FXN). FRDA is characterized by progressive neurodegeneration, with m
Externí odkaz:
https://doaj.org/article/622f3ceaccb84a80bfa5ed76dfdd8605
Autor:
Yesica Mercado-Ayon, Sarah M. Halawani, Elizabeth Mercado-Ayon, Lucie V. Ngaba, David A. Lynch, Yi Na Dong, Joseph Johnson
Publikováno v:
Archives of Biochemistry and Biophysics. 702:108698
In addition to ATP synthesis, mitochondria are highly dynamic organelles that modulate apoptosis, ferroptosis, and inflammasome activation. Through executing these varied functions, the mitochondria play critical roles in the development and progress
Autor:
Natalie A. Terry, Benjamin J. Wilkins, Danielle Pi, Lucie V. Ngaba, Klaus H. Kaestner, Nishi Gheewala
Publikováno v:
American journal of physiology. Gastrointestinal and liver physiology. 315(4)
Infants with congenital diarrheal disorders caused by enteroendocrine cell dysgenesis, or the loss of intestinal endocrine cells, causes severe malabsorptive diarrhea, though the mechanism is not fully understood. The transcription factor “aristale