S. Wayne

发表

AP-2 participates in the transcriptional control of the amyloid precursor protein (APP) gene in oral squamous cell carcinoma.

F. Domann, R. Robinson, M. Fitzgerald, 2007, Experimental and molecular pathology.

Expression of human papillomavirus type 16 E6-E7 open reading frame varies quantitatively in biopsy tissue from different grades of cervical intraepithelial neoplasia

F. Guijon, R. Hidajat, S. Wayne, 1995, Journal of clinical microbiology.

Group of Neurogenic Genes

Eric Johnson, R. Nagoshi, S. Wayne, 2002 .

fs (1) Yb is required for ovary follicle cell differentiation in Drosophila melanogaster and has genetic interactions with the Notch group of neurogenic genes.

R. Nagoshi, E. Johnson, S. Wayne, 1995, Genetics.

A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6.

V. Sheffield, D. Nishimura, G. Van Camp, 1996, Human molecular genetics.

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F.

S. Schwartz, C. Lee, C. Morton, 2001, Human molecular genetics.

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.

M. Bitner-Glindzicz, S. Riazuddin, Z. Ahmed, 2001, American journal of human genetics.

Localization of the Usher syndrome type ID gene (Ush1D) to chromosome 10.

V. Sheffield, V. D. Der Kaloustian, J. Hejtmancik, 1996, Human molecular genetics.

New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.

V. Sheffield, M. Lovett, C. Srisailapathy, 1997, American journal of medical genetics.

Upper aerodigestive tract squamous dysplasia: correlation with p16, p53, pRb, and Ki-67 expression.

R. Robinson, S. Wayne, 2006, Archives of pathology & laboratory medicine.

Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.

C. Morton, K. Verhoeven, F. Declau, 2001, Human molecular genetics.

Passage to India: The Search for Genes Causing Autosomal Recessive Nonsyndromic Hearing Loss

C. Srisailapathy, A. Ramesh, K. Fukushima, 1998, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Two Sites of Head and Neck Squamous Cell Carcinoma: Utility of Loss of Heterozygosity

M. Nikiforova, R. Walvekar, Jonas T. Johnson, 2008, The Annals of otology, rhinology, and laryngology.

The DFNA10 Phenotype

Richard J. H. Smith, P. Huygen, S. Wayne, 2001, The Annals of otology, rhinology, and laryngology.

DFNA10/EYA4--the clinical picture.

C. Cremers, F. Declau, Richard J. H. Smith, 2002, Advances in oto-rhino-laryngology.

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.

Shelley D. Smith, P. Coucke, C. Srisailapathy, 1995, Genome research.

Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.

M. Lovett, P. Coucke, C. Srisailapathy, 1998, American journal of medical genetics.

Genetic characterization of small ovaries, a gene required in the soma for the development of the Drosophila ovary and the female germline.

R. Nagoshi, J. Pettus, S. Wayne, 1995, Genetics.

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment

T. Fagerheim, K. Verhoeven, Richard J. H. Smith, 2000, Human Genetics.