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Evaluation of the therapeutic potential of a CNP analog in a Fgfr3 mouse model recapitulating achondroplasia.
Author: BellSean M, Benoist-LasselinCatherine, BullensSherry, BuntingStuart, Di RoccoFederico, KaciNabil, Legeai-MalletLaurence, LorgetFlorence, MugnieryEmilie, MunnichArnold, O'NeillCharles A, OppeneerTodd, PengJeff, TsurudaLaurie S, WendtDan J
Original Abstract of the Article :
Achondroplasia (ACH), the most common form of dwarfism, is an inherited autosomal-dominant chondrodysplasia caused by a gain-of-function mutation in fibroblast-growth-factor-receptor 3 (FGFR3). C-type natriuretic peptide (CNP) antagonizes FGFR3 downstream signaling by inhibiting the pathway of mitog...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516592/
データ提供:米国国立医学図書館(NLM)
Achondroplasia: Seeking a Solution in the Desert of Bone Growth
Imagine a vast desert landscape where a lone oasis, representing the growth plate, is stunted and underdeveloped. This is the reality for individuals with achondroplasia (ACH), a genetic disorder characterized by dwarfism. This study investigates the potential of a CNP analog, a naturally occurring substance involved in bone growth, as a treatment option for ACH. The study examines the effects of this analog in a mouse model of ACH, offering hope for a new therapeutic approach to this challenging condition.
A Potential Oasis for Growth: CNP Analog Shows Promise for ACH
This study showcases the promising potential of a CNP analog as a treatment option for ACH. The positive results in a mouse model of ACH offer a glimmer of hope for developing a new therapy for this challenging condition.
Navigating the Desert of Bone Growth Disorders: Seeking Expert Care
Bone growth disorders require specialized care and management. It is essential to consult an endocrinologist, orthopedic surgeon, or other qualified healthcare professionals for accurate diagnosis, individualized treatment plans, and ongoing support.
Dr.Camel's Conclusion
This study sheds light on a potential oasis in the desert of bone growth disorders, showcasing the promising potential of a CNP analog as a treatment option for achondroplasia. This research holds the potential to transform the lives of individuals with this condition, offering a glimmer of hope for achieving normal growth and development.
Date :
- Date Completed 2013-02-14
- Date Revised 2021-12-24
Further Info :
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