Publications by authors named "Phyllis Gardner"

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Analysis of the alternative splicing of an FGFR2 transcript due to a novel 5' splice site mutation (1084+1G>A): case report.
Ilana Traynis, Jonathan A Bernstein, Phyllis Gardner, Iris Schrijver

Cleft Palate Craniofac J· January 2012

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Genotyping with a 198 mutation arrayed primer extension array for hereditary hearing loss: assessment of its diagnostic value for medical practice.
Juan Rodriguez-Paris, Lynn Pique, Tahl Colen, Joseph Roberson, Phyllis Gardner

PLoS One· July 2010

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The role of the cytoskeleton in the formation of gap junctions by Connexin 30.
Chunyan Qu, Phyllis Gardner, Iris Schrijver

Exp Cell Res· June 2009

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Genetic analysis of presbycusis by arrayed primer extension.
Juan Rodriguez-Paris, Charles Ballay, Michelle Inserra, Katrina Stidham, Tahl Colen, Phyllis Gardner

Ann Clin Lab Sci· January 2009

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Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.
Rita Teek, Eneli Oitmaa, Katrin Kruustük, Riina Zordania, Kairit Joost, Phyllis Gardner

Int J Pediatr Otorhinolaryngol· January 2009

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Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis.
Maggie L Naguib, Iris Schrijver, Phyllis Gardner, Lynn M Pique, Samiha S Doss

J Cyst Fibros· April 2007

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Comprehensive arrayed primer extension array for the detection of 59 sequence variants in 15 conditions prevalent among the (Ashkenazi) Jewish population.
Iris Schrijver, Maigi Külm, Phyllis I Gardner, Eugene P Pergament, Morris B Fiddler

J Mol Diagn· April 2007

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Simultaneous multigene mutation detection in patients with sensorineural hearing loss through a novel diagnostic microarray: a new approach for newborn screening follow-up.
Phyllis Gardner, Eneli Oitmaa, Anna Messner, Lies Hoefsloot, Andres Metspalu

Pediatrics· September 2006

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Microfabricated nanochannel implantable drug delivery devices: trends, limitations and possibilities.
Phyllis Gardner

Expert Opin Drug Deliv· July 2006

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Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis.
Iris Schrijver, Phyllis Gardner

Expert Rev Mol Diagn· May 2006

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Genotyping microarray for the detection of more than 200 CFTR mutations in ethnically diverse populations.
Iris Schrijver, Eneli Oitmaa, Andres Metspalu, Phyllis Gardner

J Mol Diagn· August 2005

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Diagnostic testing by CFTR gene mutation analysis in a large group of Hispanics: novel mutations and assessment of a population-specific mutation spectrum.
Iris Schrijver, Sudha Ramalingam, Ramalingam Sankaran, Steve Swanson, Charles L M Dunlop, Phyllis Gardner

J Mol Diagn· May 2005

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Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis.
Iris Schrijver, Wikrom Karnsakul, Chanin Limwongse, Sudha Ramalingam, Ramalingam Sankaran, Phyllis Gardner

Am J Med Genet A· February 2005

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Protein kinase A negatively modulates the nuclear accumulation of NF-ATc1 by priming for subsequent phosphorylation by glycogen synthase kinase-3.
Colleen M Sheridan, E Kevin Heist, Chan R Beals, Gerald R Crabtree, Phyllis Gardner

J Biol Chem· December 2002

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A phase II, double-blind, randomized, placebo-controlled clinical trial of tgAAVCF using maxillary sinus delivery in patients with cystic fibrosis with antrostomies.
John A Wagner, Ilynn B Nepomuceno, Anna H Messner, Mary Lynn Moran, Eric P Batson, Phyllis Gardner

Hum Gene Ther· July 2002

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