F J Tsai
Overview
Explore the profile of F J Tsai including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
126
Citations
458
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Liu H, Lin W, Wang W, Tsai C, Wu W, Chiou M, et al.
J Biol Regul Homeost Agents
. 2013 Jul;
27(2):319-27.
PMID: 23830383
Previous experiments demonstrated that transgenic mice carrying both amyloid precursor protein and mutant ATP7B transgenes reduce amyloid plaques and diminish plasma Abeta levels. These experiments showed that a structural change...
2.
Lin W, Wu B, Lee C, Sheu J, Liu S, Wang W, et al.
J Biol Regul Homeost Agents
. 2012 Oct;
26(3):401-10.
PMID: 23034259
Defects in dopaminergic transmission play important roles in the disturbance of synaptic plasticity and even in advanced cognitive behavior. However, the relationship between genes involved in the regulation of dopamine...
3.
Chen C, Lin S, Su Y, Chern S, Tsai F, Chen W, et al.
Genet Couns
. 2011 Oct;
22(3):327-31.
PMID: 22029177
No abstract available.
4.
Chen C, Lin S, Chen M, Su Y, Chern S, Wang T, et al.
Genet Couns
. 2011 Oct;
22(3):273-80.
PMID: 22029168
We report molecular cytogenetic characterization of mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses. The supernumerary r(1) is associated with...
5.
Chen C, Lin S, Su Y, Chern S, Tsai F, Wu P, et al.
Genet Couns
. 2011 Oct;
22(3):255-61.
PMID: 22029166
We report molecular and cytogenetic characterization of proximal deletion of chromosome 4q, del(4)(q12 --> q21.21) in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects,...
6.
Chen C, Lin S, Chern S, Tsai F, Lee C, Pan C, et al.
Genet Couns
. 2011 Feb;
21(4):457-60.
PMID: 21290975
No abstract available.
7.
Chen C, Chern S, Tsai F, Lin H, Wui P, Lee C, et al.
Genet Couns
. 2011 Feb;
21(4):451-5.
PMID: 21290974
No abstract available.
8.
Chen S, Wan L, Huang C, Huang Y, Sheu J, Lin Y, et al.
J Appl Genet
. 2010 Nov;
51(4):519-21.
PMID: 21063071
Rheumatoid arthritis (RA) is a chronic autoimmune disease and can lead to deformities and severe disabilities, due to irreversible damage of tendons, joints, and bones. A previous study indicated that...
9.
Chen C, Tsai F, Lee C, Chen W, Pan C, Wu P, et al.
Genet Couns
. 2010 Oct;
21(3):353-7.
PMID: 20964129
No abstract available.
10.
Wang C, Lin W, Bau D, Chou I, Tsai C, Tsai F
J Pediatr Endocrinol Metab
. 2010 Sep;
23(7):653-60.
PMID: 20857837
Acanthosis nigricans (AN) is most commonly related to obesity as a manifestation of cutaneous insulin resistance in children and adolescents, while the interaction and time course between AN and obesity...