X. Xia

发表

Oral bacterial DNA differ in their ability to induce inflammatory responses in human monocytic cell lines.

S. E. Sahingur, X. Xia, R. Schifferle, 2012, Journal of periodontology.

The prevalence of connexin 26 (GJB2) mutations in the Chinese population

F. Telischi, X. Liu, T. Balkany, 2002, Human Genetics.

Single nucleotide polymorphisms of pattern recognition receptors and chronic periodontitis.

R. Genco, J. Gunsolley, S. E. Sahingur, 2011, Journal of periodontal research.

Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.

M. Tekin, K. Arnos, A. Pandya, 2001, Human molecular genetics.

Does Universal Newborn Hearing Screening Identify All Children with GJB2 (Connexin 26) Deafness? Penetrance of GJB2 Deafness

K. Arnos, A. Pandya, W. Nance, 2006, Ear and hearing.

Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.

K. Arnos, A. Pandya, D. Corey, 2003, Human molecular genetics.

Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common Mutations

A. Pandya, S. Blanton, T. Coşkun, 1999, Human Heredity.

A20 Orchestrates Inflammatory Response in the Oral Mucosa through Restraining NF-κB Activity

A. Ma, D. Cohen, E. Mooney, 2019, The Journal of Immunology.

A20 Restricts Inflammatory Response and Desensitizes Gingival Keratinocytes to Apoptosis

E. Mooney, S. E. Sahingur, Yajie Li, 2020, Frontiers in Immunology.

Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness

A. Pandya, C. Petit, X. Liu, 2002, Human Genetics.

Quercetin Preserves Oral Cavity Health by Mitigating Inflammation and Microbial Dysbiosis

E. Mooney, S. E. Sahingur, Bin Zhu, 2021, Frontiers in Immunology.

Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?

K. Arnos, A. Pandya, S. Blanton, 1996, Human molecular genetics.

GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf

M. Tekin, A. Pandya, W. Nance, 2010, Annals of human genetics.

Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.

K. Arnos, A. Pandya, S. Blanton, 2003 .

Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands

K. Arnos, A. Pandya, S. Blanton, 2003, Genetics in Medicine.

Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.

A. Pandya, M. Amendola, X. Xia, 1999, American journal of human genetics.

Novel Compound Heterozygous Variations in MPDZ Gene Caused Isolated Bilateral Macular Coloboma in a Chinese Family

X. Sheng, Shuang Zhang, X. Xia, 2022, Cells.

Implications of molecular diagnostic testing in families with hereditary pancreatitis.

A. Pandya, T. Markello, S. Blanton, 1997, Genetic testing.

DNA from Porphyromonas gingivalis and Tannerella forsythia induce cytokine production in human monocytic cell lines.

S. E. Sahingur, H. Schenkein, K. Honma, 2010, Molecular oral microbiology.

A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for Wolfram syndrome 2.

M. Zhang, A. Pandya, R. Shiang, 2007, American journal of human genetics.

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.

A. Pandya, W. Nance, N. Fischel‐Ghodsian, 1997, Journal of medical genetics.

Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

M. Tekin, A. Pandya, S. Blanton, 2001, Human Genetics.

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss.

K. Steel, A. Pandya, S. Blanton, 2000, Human molecular genetics.

SLITRK6 mutations cause myopia and deafness in humans and mice.

Juan I. Young, M. Tekin, A. Pandya, 2013, The Journal of clinical investigation.

SLITRK 6 mutations cause myopia and deafness in humans and mice

Juan I. Young, M. Tekin, A. Pandya, 2013 .

Interplay of Toll-Like Receptor 9, Myeloid Cells, and Deubiquitinase A20 in Periodontal Inflammation

E. Mooney, S. E. Sahingur, X. Xia, 2016, Infection and Immunity.

The Clinical and Audiologic Features of Hearing Loss Due to Mitochondrial Mutations

K. Arnos, A. Pandya, W. Nance, 2013, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Toll-Like Receptor 9-Mediated Inflammation Triggers Alveolar Bone Loss in Experimental Murine Periodontitis

G. Hajishengallis, T. Abe, S. E. Sahingur, 2015, Infection and Immunity.

Increased nucleic Acid receptor expression in chronic periodontitis.

J. Gunsolley, S. E. Sahingur, X. Xia, 2013, Journal of periodontology.

GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf

M. Tekin, A. Pandya, W. Nance, 2010, Annals of human genetics.

Toll-Like Receptor 9-Mediated Inflammation Triggers Alveolar Bone Loss in Experimental Murine Periodontitis

G. Hajishengallis, K. E. Crump, T. Abe, 2015, Infection and Immunity.