11 Papers
112 Citations
Feng Jiao is an academic researcher from University of Tennessee Health Science Center. The author has contributed to research in topics: Candidate gene & Quantitative trait locus. The author has an hindex of 6, co-authored 11 publications. Previous affiliations of Feng Jiao include Brigham and Women's Hospital.
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Papers
A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice
Yan Jiao,Jian Yan,Feng Jiao,Hong Bin Yang,Leah Rae Donahue,Xin-Min Li,Bruce A. Roe,John M. Stuart,Weikuan Gu +8 more
TL;DR: A single nucleotide mutation of Nppc is associated with dwarfism in lbab/lbab mice and is a useful model for hereditary human achondroplasia.
Quantitative trait loci that determine mouse tibial nanoindentation properties in an F2 population derived from C57BL/6J x C3H/HeJ.
TL;DR: It is found that tibiae from mice at 16 weeks of age were mature and suitable for measurement by a nanoindentor, and both stiffness modulus and hardness modulus in the F2 population appeared to have normal distributions, which suggested that multiple genetic factors control the bone properties.
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Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouse
Jian Yan,Yan Jiao,Feng Jiao,John M. Stuart,Leah Rae Donahue,Wesley G. Beamer,Xin-Min Li,Bruce A. Roe,Mark S. LeDoux,Weikuan Gu +9 more
TL;DR: Genes involved in signaling, cell division, zinc ion-binding, synapse integrity and plasticity were downregulated and several of the upregulated genes encode proteins that function in the Golgi apparatus which suggests that Car8 deficiency has important effects on synaptic vesicle formation and transport.
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Evaluation of gene expression profiling in a mouse model of L-gulonolactone oxidase gene deficiency
TL;DR: The initial analysis of the impact of the Gulo gene deletion on the murine gene expression profiles in the liver, femur and kidney is reported on.
A deletion mutation in Slc12a6 is associated with neuromuscular disease in gaxp mice.
Yan Jiao,Xiudong Jin,Xiudong Jin,Jian Yan,Jian Yan,Chi Zhang,Chi Zhang,Feng Jiao,Feng Jiao,Xin-Min Li,Bruce A. Roe,Bruce A. Roe,David B. Mount,David B. Mount,Weikuan Gu,Weikuan Gu +15 more
TL;DR: The causative role of the exon 4 mutation within Slc12a6 in the gaxp phenotype was further confirmed by screening multiple inbred strains and by excluding the mutation of nearby genes within the gAXp locus.
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