Z. Chen

发表

Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.

S. Jacobson, C. Cremers, D. Corey, 1996, American journal of human genetics.

A bidirectional YAC walk from the Norrie disease (NDP) locus.

K. Davies, I. Craig, M. Coleman, 1995, Genomics.

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene.

I. Craig, R. Hendriks, R. Schuurman, 1992, Human molecular genetics.

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

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

Genetic effect of an A/G polymorphism in the HSP70 gene on thermotolerance in chicken.

W. Zhang, L. Kong, X. Zhang, 2016, Genetics and molecular research : GMR.

The properdin structural locus (Pfc) lies close to the locus for tissue inhibitor of metallothionine proteases (Timp) on the mouse X chromosome.

S. Laval, Y. Boyd, Z. Chen, 1991, Genomics.

Organization of the human monoamine oxidase genes and long-range physical mapping around them.

X. Breakefield, I. Craig, J. Powell, 1992, Genomics.

Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

S. Schwartz, A. Zinn, V. Tonk, 1998, American journal of human genetics.

Investigation of AZF microdeletions in patients with Klinefelter syndrome.

X. Ding, H. Dai, Z. Chen, 2015, Genetics and molecular research : GMR.

The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome.

I. Craig, R. Hendriks, H. Hinds, 1992, Genomics.

Norrie disease and MAO genes: nearest neighbors.

X. Breakefield, R. Denney, Z. Chen, 1995, Human molecular genetics.

Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif.

I. Craig, R. Hendriks, H. Hinds, 1992, Genomics.

Structure of the human gene for monoamine oxidase type A.

X. Breakefield, I. Craig, G. Hotamisligil, 1991, Nucleic acids research.

Dinucleotide repeat polymorphism at the MAOA locus.

I. Craig, J. Powell, G. Black, 1991, Nucleic acids research.

An isoform of GTPase regulator DOCK4 localizes to the stereocilia in the inner ear and binds to harmonin (USH1C).

D. Yan, C. Giallourakis, V. Yajnik, 2006, Journal of molecular biology.

Investigation of polymorphisms in exon7 of the NSUN7 gene among Chinese Han men with asthenospermia.

X. Ding, Z. Chen, Y. Jing, 2015, Genetics and molecular research : GMR.

Myosin-VIIb, a novel unconventional myosin, is a constituent of microvilli in transporting epithelia.

D. Corey, T. Hasson, M. Mooseker, 2001, Genomics.

Promoter methylation negatively correlated with mRNA expression but not tissue differential expression after heat stress.

X. Zhang, Q. Luo, D. He, 2013, Genetics and molecular research : GMR.

Characterization of a mutation within the NDP gene in a family with a manifesting female carrier.

X. Breakefield, I. Craig, E. Battinelli, 1993, Human molecular genetics.

Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.

D. Corey, W. Kimberling, M. Ramakrishnan, 1996, Genomics.

Mapping of unconventional myosins in mouse and human.

L. Greene, D. Corey, N. Copeland, 1996, Genomics.

A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter

A. Pandya, X. Liu, S. Blanton, 2002, Journal of medical genetics.

Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp)

X. Breakefield, I. Craig, E. Battinelli, 1996, Mammalian Genome.

The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).

D. Corey, W. Kimberling, T. Hasson, 1997, Genomics.

The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3.

X. Breakefield, G. Bruns, I. Craig, 1992, Human molecular genetics.

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A gene.

I. Craig, R. Hendriks, R. Schuurman, 1992, Human molecular genetics.