J. Xia

发表

The Transfection Efficiency Improvement of hrDNA Targeting Vectors With NLS Peptide*: The Transfection Efficiency Improvement of hrDNA Targeting Vectors With NLS Peptide*

Q. Pan, D. Liang, Yan Shi, 2009 .

In vitro Efficacy of mda-7 Gene for Hepatocellular Carcinoma Gene Therapy Mediated by Human Ribosomal DNA Targeting Vector

K. Xia, Q. Pan, D. Liang, 2009 .

Non‐viral ex vivo transduction of human hepatocyte cells to express factor VIII using a human ribosomal DNA‐targeting vector

K. Xia, Q. Pan, L. Wu, 2007, Journal of thrombosis and haemostasis : JTH.

The combination of suicide gene therapy and radiation enhances the killing of nasopharyngeal carcinoma xenographs.

A. Tang, K. Xia, Q. Pan, 2004, Journal of radiation research.

A novel fusion suicide gene yeast CDglyTK plays a role in radio-gene therapy of nasopharyngeal carcinoma

A. Tang, K. Xia, Q. Pan, 2004, Cancer Gene Therapy.

Intracellular distribution, assembly and effect of disease-associated connexin 31 mutants in HeLa cells.

K. Xia, Q. Pan, D. Liang, 2005, Acta biochimica et biophysica Sinica.

Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum

N. Niikawa, K. Xia, Q. Pan, 2007, Journal of Human Genetics.

A non-viral vector for potential DMD gene therapy study by targeting a minidystrophin-GFP fusion gene into the hrDNA locus.

D. Liang, Yan Shi, Xiong-hao Liu, 2009, Acta biochimica et biophysica Sinica.

Prenatal Determination of a Variable Number of Tandem Repeats in Intron 40 of the von Willebrand Factor Gene from Maternal Peripheral Blood Using the Polymerase Chain Reaction

J. Xia, X. Ni, Jingyuan Guo, 2000, Human Heredity.

Transcriptional regulation of APH‐1A and increased γ‐secretase cleavage of APP and Notch by HIF‐1 and hypoxia

Huaxi Xu, K. Xia, J. Xia, 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.

D. Tagle, J. Xia, P. Yu, 1999, American journal of medical genetics.

Efficient Derivation of Mesenchymal Stem Cells and Neural Precursor Cells from Human Embryonic Stem Cells through Teratoma Formation

Qiao Zeng, G. Fan, K. Xia, 2008 .

[Biotoxicology and biodynamics of silica nanoparticle].

K. Xia, Q. Pan, D. Liang, 2006, Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences.

In vitro chondrogenesis of human bone marrow-derived mesenchymal progenitor cells in monolayer culture: activation by transfection with TGF-beta2.

K. Xia, J. Xia, Xiao-dong Ju, 2003, Tissue & cell.

Cx31 is assembled and trafficked to cell surface by ER-Golgi pathway and degraded by proteasomal or lysosomal pathways

K. Xia, Q. Pan, D. Liang, 2005, Cell Research.

Transcriptional Regulation of PEN-2, a Key Component of the (cid:2) -Secretase Complex, by CREB

J. Xia, Yun-wu Zhang, Xue Zhang, 2006 .

Transcriptional Regulation of The Alzheimer's Disease-related Gene, Nicastrin *: Transcriptional Regulation of The Alzheimer's Disease-related Gene, Nicastrin *

K. Xia, Q. Pan, Zhigao Long, 2009 .

Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.

Q. Pan, D. Liang, Ling-Qian Wu, 2006, Yi chuan xue bao = Acta genetica Sinica.

[Molecular cloning of the human CX 58 gene].

K. Xia, Q. Pan, J. Xia, 2002, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility.

D. Tagle, J. Xia, P. Yu, 2001, Human reproduction.

Expression of reconstructive hFVIII in the hrDNA by using hrDNA targeting vector

K. Xia, Q. Pan, D. Liang, 2005 .

Targeting of the Human Coagulation Factor IX Gene at rDNA Locus of Human Embryonic Stem Cells

D. Liang, Mai Feng, Junlin Yang, 2012, PloS one.

Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson's disease.

K. Xia, Q. Pan, Zhengmao Hu, 2006, Human molecular genetics.

Embryonic stem cells generated by nuclear transfer of human somatic nuclei into rabbit oocytes

Z. Xue, J. Xia, Ying Chen, 2003, Cell Research.

A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree

K. Xia, Q. Pan, H. Dai, 2002, Journal of Human Genetics.

A Susceptibility Locus at Chromosome 3p21 Linked to Familial Nasopharyngeal Carcinoma

Z. Zeng, W. Xiong, Gui-yuan Li, 2004, Cancer Research.

A novel PRPF31 splice-site mutation in a Chinese family with autosomal dominant retinitis pigmentosa.

K. Xia, Q. Pan, Zhengmao Hu, 2004, Molecular vision.

Efficient protein expression from the endogenous RNA polymerase I promoter using a human ribosomal DNA targeting vector.

K. Xia, Q. Pan, D. Liang, 2008, Biochemical and biophysical research communications.

Site-specific transfer of an intact beta-globin gene cluster through a new targeting vector.

K. Xia, De-Pei Liu, C. Liang, 2007, Biochemical and biophysical research communications.

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

K. Xia, Q. Pan, H. Dai, 2004, Human Genetics.

Two novel mutations of the LDL receptor gene associated with familial hypercholesterolemia in a Chinese family.

K. Xia, Zhengmao Hu, J. Xia, 2007, Chinese medical journal.

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

K. Xia, Q. Pan, H. Dai, 1998, Nature Genetics.

A boy with 9p+ resulting from maternal t(4;9) translocation: a case report

H. Dai, J. Xia, Xiumin Wang, 2007 .

A reliable method for obtaining high-resolution banded chromosome preparations from chorionic villus samples

N. Niikawa, J. Xia, H. Deng, 1990, Japanese Journal of Human Genetics.

A novel case of unilateral blepharophimosis syndrome and mental retardation associated with de novo trisomy for chromosome 3q.

D. Tagle, J. Xia, P. Yu, 1997, Journal of medical genetics.

Screening of LRRK2 interactants by yeast 2-hybrid analysis.

K. Xia, Q. Pan, H. Dai, 2008, Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences.

[Investigation on VNTR in intron 40 of vWF gene in Chinese Han population].

J. Xia, J. Guo, X. Ni, 1996, Yi chuan xue bao = Acta genetica Sinica.

[Hotspot of the mutations of keratin 9 gene in a diffuse palmoplantar keratoderma family].

K. Xia, Q. Pan, H. Dai, 2005, Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences.

[Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma].

K. Xia, Zhengmao Hu, J. Xia, 2004, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[Mutation screening of 20 candidate genes located in chromo-some 5q31-5q32 for DFNA52 locus].

K. Xia, Q. Pan, D. Liang, 2009, Yi chuan = Hereditas.

Silica nanoparticle is a possible safe carrier for gene therapy

K. Xia, Q. Pan, D. Liang, 2005 .

Investigation of hrDNA targeting vector-mediated tumor-specific suicide gene therapy for hepatocellular carcinoma

K. Xia, Q. Pan, D. Liang, 2006 .

[Identification and clone of human Alzheimer's disease related gene nicastrin promoter].

K. Xia, Q. Pan, J. Xia, 2006, Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences.

A minidystrophin-EGFP fusion gene expressed in Cos-7 cells mediated by human source vector.

K. Xia, Q. Pan, D. Liang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

A ZRS duplication causes syndactyly type IV with tibial hypoplasia

Daisuke Sato, N. Niikawa, K. Yoshiura, 2009, American journal of medical genetics. Part A.

Sodium chloride modified silica nanoparticles as a non-viral vector with a high efficiency of DNA transfer into cells.

K. Xia, Z. Xue, Z. Long, 2003, Current gene therapy.

[Growing of human embryonic stem cells on feeders derived from themselves].

Qiao Zeng, K. Xia, Q. Pan, 2009, Yi chuan = Hereditas.

Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.

Q. Pan, H. Dai, B. Tang, 2000, Archives of neurology.

[Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].

D. Liang, H. Dai, Zhigao Long, 2008, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Parental origin and mechanism of formation of X chromosome structural abnormalities: Four cases determined with RFLPs

N. Niikawa, J. Xia, M. Ishikawa, 1990, Japanese Journal of Human Genetics.

A syndactyly type IV locus maps to 7q36

Daisuke Sato, N. Niikawa, K. Yoshiura, 2007, Journal of Human Genetics.

Identification of the alternative promoters of the KChIP4 subfamily.

K. Xia, Q. Pan, D. Liang, 2005, Acta biochimica et biophysica Sinica.

Isolation and identification of a novel STR (D17S2204) in the vicinity of NF1 locus

Yurong Xin, Long Yu, Shouyuan Zhao, 1999 .

Association of PINK 1 and DJ-1 confers digenic inheritance of early-onset Parkinson ’ s disease

K. Xia, Q. Pan, Zhengmao Hu, 2006 .

[Mapping of pathogenic genes in two families with autosomal dominant ichthyosis vulgaris].

K. Xia, Q. Pan, D. Liang, 2008, Yi chuan = Hereditas.

Fragile site 1q44 involved in nasopharyngeal carcinoma. A study of a marker chromosome der(1)t(1;3)(q44;p11).

J. Xia, J. Xiao, L. Li, 1988, Cancer genetics and cytogenetics.

[The high resolution G band of human chromosomes at 1200 band stage].

H. Zhang, H. Dai, J. Xia, 1990, Yi chuan xue bao = Acta genetica Sinica.