P. Gardner

发表

Molecular strategies for therapy of cystic fibrosis.

J. Wagner, A. Chao, P. Gardner, 1995, Annual review of pharmacology and toxicology.

The role of the cytoskeleton in the formation of gap junctions by Connexin 30.

I. Schrijver, P. Gardner, C. Qu, 2009, Experimental cell research.

Genetic analysis of presbycusis by arrayed primer extension.

I. Schrijver, P. Gardner, J. Rodriguez-Paris, 2008, Annals of clinical and laboratory science.

Genotyping with a 198 Mutation Arrayed Primer Extension Array for Hereditary Hearing Loss: Assessment of Its Diagnostic Value for Medical Practice

I. Schrijver, P. Gardner, J. Rodriguez-Paris, 2010, PloS one.

Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis

I. Schrijver, P. Gardner, 2006, Expert review of molecular diagnostics.

Safety and Biological Efficacy of an Adeno‐Associated Virus Vector–Cystic Fibrosis Transmembrane Regulator (AAV‐CFTR) in the Cystic Fibrosis Maxillary Sinus

T. Flotte, A. Norbash, J. Wine, 1999, The Laryngoscope.

Efficient and persistent gene transfer of AAV-CFTR in maxillary sinus

T. Flotte, J. Wine, R. Moss, 1998, The Lancet.

Maxillary sinusitis as a surrogate model for CF gene therapy clinical trials in patients with antrostomies

A. Norbash, J. Wine, A. Messner, 1999, The journal of gene medicine.

Analysis of the Alternative Splicing of an FGFR2 Transcript Due to a Novel 5′ Splice Site Mutation (1084+1G>A): Case Report

J. Bernstein, I. Schrijver, P. Gardner, 2012, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Simultaneous Multigene Mutation Detection in Patients With Sensorineural Hearing Loss Through a Novel Diagnostic Microarray: A New Approach for Newborn Screening Follow-up

Andres Metspalu, Phyllis Gardner, Iris Schrijver, 2006, Pediatrics.

Genotyping microarray for the detection of more than 200 CFTR mutations in ethnically diverse populations.

Andres Metspalu, Phyllis Gardner, Iris Schrijver, 2005, The Journal of molecular diagnostics : JMD.

Comprehensive arrayed primer extension array for the detection of 59 sequence variants in 15 conditions prevalent among the (Ashkenazi) Jewish population.

I. Schrijver, P. Gardner, E. Pergament, 2007, The Journal of molecular diagnostics : JMD.

Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis.

I. Schrijver, P. Gardner, S. Nasr, 2007, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis

I. Schrijver, R. Moss, P. Gardner, 2005, American journal of medical genetics. Part A.

A phase II, double-blind, randomized, placebo-controlled clinical trial of tgAAVCF using maxillary sinus delivery in patients with cystic fibrosis with antrostomies.

Terence R Flotte, Phyllis Gardner, T. Flotte, 2002, Human gene therapy.

A Phase I/II Study of tgAAV-CF for the Treatment of Chronic Sinusitis in Patients with Cystic Fibrosis. Stanford University, Stanford, California

T. Flotte, T. Reynolds, J. Wine, 1998 .

A phase I/II study of tgAAV-CF for the treatment of chronic sinusitis in patients with cystic fibrosis.

T. Flotte, T. Reynolds, J. Wine, 1998, Human gene therapy.

Toward cystic fibrosis gene therapy.

J. Wagner, P. Gardner, J A Wagner, 1997, Annual review of medicine.

Diagnostic testing by CFTR gene mutation analysis in a large group of Hispanics: novel mutations and assessment of a population-specific mutation spectrum.

I. Schrijver, J. Oehlert, R. Moss, 2005, The Journal of molecular diagnostics : JMD.

Maxillary sinusitis as a surrogate model for CF gene therapy clinical trials in patients with antrostomies.

A. Norbash, J. Wine, A. Messner, 1999 .

Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.

N. Tõnisson, K. Õunap, R. Teek, 2009, International journal of pediatric otorhinolaryngology.

Analysis of the Alternative Splicing of an FGFR2 Transcript Due to a Novel 5′ Splice Site Mutation (1084+1G>A): Case Report

J. Bernstein, I. Schrijver, P. Gardner, 2012, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

The role of the cytoskeleton in the formation of gap junctions by Connexin 30.

I. Schrijver, P. Gardner, C. Qu, 2009, Experimental cell research.