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Xia Juan Xia

Research Profile

Disorders

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Chemicals & Drugs

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Mongolia

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Publications

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Sinem E Sahingur; Xia Juan Xia; Robert E Schifferle
Oral bacterial DNA differ in their ability to induce inflammatory responses in human monocytic cell lines.
S E Sahingur; Xia Juan Xia; S Alamgir; K Honma; A Sharma; H A Schenkein
DNA from Porphyromonas gingivalis and Tannerella forsythia induce cytokine production in human monocytic cell lines.
Mustafa Tekin; Xia Juan Xia; Radnaabazar Erdenetungalag; Filiz Basak Cengiz; Thomas W White; Janchiv Radnaabazar; Begzsuren Dangaasuren; Hakki Tastan; Walter E Nance; Arti Pandya
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf.

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All Publications

2012: Sinem E Sahingur; Xia Juan Xia; Robert E Schifferle
Oral bacterial DNA differ in their ability to induce inflammatory responses in human monocytic cell lines.
Journal of periodontology 2012;83(8):1069-77.
2010: S E Sahingur; Xia Juan Xia; S Alamgir; K Honma; A Sharma; H A Schenkein
DNA from Porphyromonas gingivalis and Tannerella forsythia induce cytokine production in human monocytic cell lines.
Molecular oral microbiology 2010;25(2):123-35.
2010: Mustafa Tekin; Xia Juan Xia; Radnaabazar Erdenetungalag; Filiz Basak Cengiz; Thomas W White; Janchiv Radnaabazar; Begzsuren Dangaasuren; Hakki Tastan; Walter E Nance; Arti Pandya
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf.
Annals of human genetics 2010;74(2):155-64.
2007: Sami Amr; Cindy Heisey; Min Zhang; Xia Juan Xia; Kathryn H Shows; Kamel M Ajlouni; Arti Pandya; Leslie S Satin; Hatem El-Shanti; Rita Shiang
A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for Wolfram syndrome 2.
American journal of human genetics 2007;81(4):673-83.
2003: Arti Pandya; Kathleen S Arnos; Xia Juan Xia; Katherine O Welch; S Blanton; Thomas B Friedman; Guillermina Garcia Sanchez; Xiu Z Liu MD; Robert J Morell; Walter E Nance
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.
Genetics in medicine : official journal of the American College of Medical Genetics 2003;5(4):295-303.
2003: Xue Zhong Liu; Xiao Mei Ouyang; Xia Juan Xia; Jing Zheng; Arti Pandya; Fang Li; Li Lin Du; Katherine O Welch; Christine Petit; Richard J H Smith; Bradley T Webb; Denise Yan; Kathleen S Arnos; David Corey; Peter Dallos; Walter E Nance; Zheng Yi Chen
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.
Human molecular genetics 2003;12(10):1155-62.
2003: Xiao Mei Ouyang; J Fielding Hejtmancik; S G Jacobson; Xia Juan Xia; A Li; Li Lin Du; V Newton; M Kaiser; Thomas J Balkany; Walter E Nance; Xue Zhong Liu
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian allele.
Clinical genetics 2003;63(2):150-3.
2002: Xue Zhong Liu; Xia Juan Xia; Xiao Mei Ke; Xiao Mei Ouyang; Li Lin Du; Yu He Liu; Simon I Angeli; Fred F Telischi; Walter E Nance; Thomas J Balkany; Li Rong Xu
The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.
Human genetics 2002;111(4-5):394-7.
2002: Xiao Mei Ouyang; Xia Juan Xia; Elisabeth Verpy; Li Lin Du; Arti Pandya; Christine Petit; Thomas J Balkany; Walter E Nance; Xue Zhong Liu
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
Human genetics 2002;111(1):26-30.
2001: Xue Zhong Liu; Xia Juan Xia; J Adams; Zheng Yi Chen; Katherine O Welch; Mustafa Tekin; Xiao Mei Ouyang; A Kristiansen; Arti Pandya; Thomas J Balkany; Kathleen S Arnos; Walter E Nance
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.
Human molecular genetics 2001;10(25):2945-51.
2001: Mustafa Tekin; N Akar; Sükrü Cin; S Blanton; Xia Juan Xia; Xue Zhong Liu; Walter E Nance; Arti Pandya
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians.
Human genetics 2001;108(5):385-9.
2001: Mustafa Tekin; Kathleen S Arnos; Xia Juan Xia; M K Oelrich; Xue Zhong Liu; Walter E Nance; Arti Pandya
W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness.
Clinical genetics 2001;59(4):269-73.
2000: Xue Zhong Liu; Xia Juan Xia; Li Rong Xu; Arti Pandya; C Y Liang; S Blanton; Steve D M Brown; Karen P Steel; Walter E Nance
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss.
Human molecular genetics 2000;9(1):63-7.
1999: Arti Pandya; Xia Juan Xia; Raadnabazar Erdenetungalag; M Amendola; BL Landa; J Radnaabazar; B Dangaasuren; G Van Tuyle; Walter E Nance
Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.
American journal of human genetics 1999;65(6):1803-6.
1997: Arti Pandya; Xia Juan Xia; S Blanton; BL Landa; T Markello; Walter E Nance
Implications of molecular diagnostic testing in families with hereditary pancreatitis.
Genetic testing 1997;1(3):207-11.
1996: Arti Pandya; Xia Juan Xia; B L Landa; K S Arnos; J Israel; J Lloyd; A L James; S R Diehl; S Blanton; Walter E Nance
Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?
Human molecular genetics 1996;5(4):497-502.