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Identification of Brain-Specific Treatment Effects in NPC1 Disease by Focusing on Cellular and Molecular Changes of Sphingosine-1-Phosphate Metabolism.
Author: BrandtNicola, BräuerAnja Ursula, ColdeweySina M, FrechMoritz J, GläserAnne, GrälerMarkus H, HammerlFranziska, HeimesDiana, KorenkeGeorg Christoph, LuoJiankai, NeidhardtJohn, NeßlauerAnna-Maria, Owczarek-LipskaMarta, RolfsArndt, TönniesEric, VölknerChristin, WittMartin, WreeAndreas, YangFan, von Bohlen Und HalbachOliver
Original Abstract of the Article :
Niemann-Pick type C1 (NPC1) is a lysosomal storage disorder, inherited as an autosomal-recessive trait. Mutations in the <i>Npc1</i> gene result in malfunction of the NPC1 protein, leading to an accumulation of unesterified cholesterol and glycosphingolipids. Beside visceral symptoms like hepatosple...See full text at original site
Dr.Camel's Paper Summary Blogラクダ博士について
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352403/
データ提供:米国国立医学図書館(NLM)
NPC1 Disease: A Desert of Cellular Chaos
The world of Niemann-Pick type C1 (NPC1) disease is a complex desert landscape, characterized by cellular dysfunction and neurological challenges. This study, a meticulous exploration of the sphingosine-1-phosphate (S1P)/S1P receptor (S1PR) axis in the brains of NPC1 mice, aims to navigate the cellular pathways affected by this rare and debilitating disease. The researchers, like meticulous desert archaeologists, delve into the intricacies of S1P metabolism, uncovering the potential role of this signaling pathway in NPC1 disease. Their findings shed light on the complex interplay of cellular processes, providing valuable insights into the disease's progression and highlighting the challenges of finding effective treatments.
A New Perspective on the Desert of NPC1 Disease
This study offers a fresh perspective on the desert of NPC1 disease, suggesting a potential link between the S1P/S1PR axis and the disease's progression. The findings highlight the importance of understanding the intricate details of cellular processes to develop effective treatment strategies. The researchers' exploration of the S1P/S1PR axis provides a valuable roadmap for future research endeavors.
Navigating the Desert of NPC1 Disease with Hope
While the desert of NPC1 disease is a challenging one, this study offers a beacon of hope. The researchers' dedication to understanding the disease's complexities and their meticulous exploration of the S1P/S1PR axis pave the way for the development of new and effective treatment strategies.
Dr.Camel's Conclusion
Like a camel seeking a path through the desert, this study navigates the complexities of NPC1 disease. The researchers' exploration of the S1P/S1PR axis provides valuable insights into the disease's cellular mechanisms, offering a new perspective and paving the way for potential therapeutic breakthroughs.
Date :
- Date Completed 2021-03-22
- Date Revised 2021-12-04
Further Info :
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