Fengtao Luo
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Explore the profile of Fengtao Luo including associated specialties, affiliations and a list of published articles.
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36
Citations
785
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Recent Articles
11.
Tan Q, Wang Q, Kuang L, Zhang J, Peng X, Liang S, et al.
J Cell Physiol
. 2021 Jan;
236(7):5278-5292.
PMID: 33452687
Osteoarthritis (OA) is the most common joint disease. The surface of joint cartilage is a defensive and first affected structure of articular cartilage (AC) during the pathogenesis of OA. Alk5...
12.
Xie Y, Su N, Yang J, Tan Q, Huang S, Jin M, et al.
Signal Transduct Target Ther
. 2020 Sep;
5(1):181.
PMID: 32879300
Growing evidences suggest that the fibroblast growth factor/FGF receptor (FGF/FGFR) signaling has crucial roles in a multitude of processes during embryonic development and adult homeostasis by regulating cellular lineage commitment,...
13.
Sun X, Zhang R, Chen H, Du X, Chen S, Huang J, et al.
Theranostics
. 2020 Jul;
10(16):7111-7130.
PMID: 32641982
CATSHL syndrome, characterized by camptodactyly, tall stature and hearing loss, is caused by loss-of-function mutations of fibroblast growth factor receptors 3 (FGFR3) gene. Most manifestations of patients with CATSHL syndrome...
14.
Sun X, Zhou Y, Zhang R, Wang Z, Xu M, Zhang D, et al.
Nat Commun
. 2020 Jan;
11(1):479.
PMID: 31980602
Congenital scoliosis (CS) is a complex genetic disorder characterized by vertebral malformations. The precise etiology of CS is not fully defined. Here, we identify that mutation in dual serine/threonine and...
15.
Kuang L, Wu J, Su N, Qi H, Chen H, Zhou S, et al.
Ann Rheum Dis
. 2019 Oct;
79(1):112-122.
PMID: 31662319
Objectives: This study aims to investigate the role and mechanism of FGFR3 in macrophages and their biological effects on the pathology of arthritis. Methods: Mice with conditional knockout of FGFR3...
16.
Sun X, Zhang R, Liu M, Chen H, Chen L, Luo F, et al.
J Bone Miner Res
. 2019 Jun;
34(11):2101-2116.
PMID: 31237961
Cartilage-hair hypoplasia (CHH) is an autosomal recessive metaphyseal chondrodysplasia characterized by bone dysplasia and many other highly variable features. The gene responsible for CHH is the RNA component of the...
17.
Chen B, Tan Q, Chen H, Luo F, Xu M, Zhao J, et al.
J Orthop Translat
. 2019 Jun;
17:103-111.
PMID: 31194037
Objective: Scoliosis is a common disease characterized by spinal curvature with variable severities. There is no generally accepted theory about the physical origin of the spinal deformation of scoliosis. The...
18.
Luo F, Xie Y, Wang Z, Huang J, Tan Q, Sun X, et al.
Mol Ther Nucleic Acids
. 2018 Oct;
13:291-302.
PMID: 30321816
Apert syndrome (AS), the most severe form of craniosynostosis, is caused by missense mutations including Pro253Arg(P253R) of fibroblast growth factor receptor 2 (FGFR2), which leads to enhanced FGF/FGFR2-signaling activity. Surgical...
19.
Wang Z, Huang J, Zhou S, Luo F, Tan Q, Sun X, et al.
J Biol Chem
. 2018 Apr;
293(23):8761-8774.
PMID: 29691281
Temporomandibular joint osteoarthritis (TMJ OA) is a common degenerative disease with few effective disease-modifying treatments in the clinic. Fibroblast growth factor (FGF) signaling is implicated in articular cartilage homeostasis, but...
20.
Xie Y, Luo F, Xu W, Wang Z, Sun X, Xu M, et al.
Int J Biol Sci
. 2017 Sep;
13(8):1029-1037.
PMID: 28924384
Bone fracture healing is processed through multiple biological stages that partly recapitulates the skeletal development process. FGFR3 is a negative regulator of chondrogenesis during embryonic stage and plays an important...