Publications by authors named "Phyllis Gardner"

15Publications

Analysis of the alternative splicing of an FGFR2 transcript due to a novel 5' splice site mutation (1084+1G>A): case report.

Cleft Palate Craniofac J 2012 Jan 27;49(1):104-8. Epub 2011 Apr 27.

Department of Pathology, L235 Stanford University Medical Center, 300 Pasteur Drive, Stanford, CA 94305, USA.

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January 2012

Genotyping with a 198 mutation arrayed primer extension array for hereditary hearing loss: assessment of its diagnostic value for medical practice.

PLoS One 2010 Jul 26;5(7):e11804. Epub 2010 Jul 26.

Department of Pathology, Stanford University School of Medicine, Stanford, California, United States of America.

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July 2010

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

Exp Cell Res 2009 Jun 13;315(10):1683-92. Epub 2009 Mar 13.

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.

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June 2009

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

Int J Pediatr Otorhinolaryngol 2009 Jan 22;73(1):103-7. Epub 2008 Nov 22.

Department of Oto-Rhino-Laryngology, University of Tartu, Tartu, Estonia.

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January 2009

Genetic analysis of presbycusis by arrayed primer extension.

Ann Clin Lab Sci 2008 ;38(4):352-60

Department of Pathology, L235, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USA.

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January 2009

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

J Cyst Fibros 2007 Apr 11;6(2):111-6. Epub 2006 Jul 11.

Department of Pediatrics, Division of Pulmonology, Cairo University Children's Hospital, Faculty of Medicine Cairo, Egypt.

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April 2007

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

Authors:
Phyllis Gardner

Expert Opin Drug Deliv 2006 Jul;3(4):479-87

Department of Medicine, Lane 308A, 300 Pasteur Drive, Stanford, CA 94305-5127, USA.

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July 2006

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

Expert Rev Mol Diagn 2006 May;6(3):375-86

Stanford University School of Medicine, Department of Pathology & Pediatrics, L235, 300 Pasteur Drive, Stanford, CA 94305, USA.

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May 2006

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

J Mol Diagn 2005 Aug;7(3):375-87

Department of Pathology, L235, Stanford University Medical Center, 300 Pasteur Drive, Stanford, CA 94305, USA.

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August 2005

Protein kinase A negatively modulates the nuclear accumulation of NF-ATc1 by priming for subsequent phosphorylation by glycogen synthase kinase-3.

J Biol Chem 2002 Dec 25;277(50):48664-76. Epub 2002 Sep 25.

Program in Immunology, Department of Molecular Pharmacology, Howard Hughes Medical Institute, California 94305, USA.

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December 2002