H. Dai

发表

Common genetic variants on 1p13.2 associate with risk of autism

Z. Hu, D. St. Clair, Y. Hu, 2014, Molecular Psychiatry.

Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia

K. Xia, Q. Pan, H. Dai, 2006, Journal of the Neurological Sciences.

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.

Mutation in PITX2 is associated with ring dermoid of the cornea

K. Xia, Q. Pan, L. Wu, 2004, Journal of Medical Genetics.

An improved mechanical technique for assisted hatching.

Y. P. Li, L. Wu, D. Liang, 2005, Human reproduction.

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.

Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.

K. Xia, Q. Pan, H. Dai, 2004, Archives of neurology.

Identification and characterization of human neuronal voltage-gated calcium channel gamma 3 subunit gene

Q. Pan, H. Dai, J. Xia, 2000 .

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.

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

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

A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1–26.1

H. Dai, J. Xia, Q. Pan, 2002, The British journal of dermatology.

Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1.

K. Xia, H. Dai, B. Tang, 2000, The Journal of investigative dermatology.

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.

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L

K. Xia, Q. Pan, H. Dai, 2005, Human Genetics.

Confirmation and refinement of a genetic locus for disseminated superficial actinic porokeratosis (DSAP1) at 12q23.2‐24.1

K. Xia, H. Dai, Y. Feng, 2004, The British journal of dermatology.

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.

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.

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.

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 .

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.

[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.

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 .

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.

[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.

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.

[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.

Mutation in PITX2 is associated with ring dermoid of the cornea

K. Xia, Q. Pan, D. Liang, 2004, Journal of Medical Genetics.