P. M. Kelley

发表

Antibodies to two major chicken heat shock proteins cross-react with similar proteins in widely divergent species

M. Schlesinger, P. M. Kelley, Philip M. KELLEYt, 1982, Molecular and cellular biology.

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

S. Jacobson, C. Cremers, D. Corey, 2007 .

Characterization of a maize cDNA that complements an enolase-deficient mutant of Escherichia coli

Scott K. Johnson, T. Conway, S. Lal, 1991, Plant Molecular Biology.

The effect of amino acid analogues and heat shock on gene expression in chicken embryo fibroblasts

M. Schlesinger, P. M. Kelley, 1978, Cell.

The M34T allele variant of connexin 26.

G. Green, G. Van Camp, P. M. Kelley, 2000, Genetic testing.

Maize pyruvate decarboxylase mRNA is induced anaerobically

P. M. Kelley, 1989, Plant Molecular Biology.

Differential Induction of mRNAs for the Glycolytic and Ethanolic Fermentative Pathways by Hypoxia and Anoxia in Maize Seedlings

D. MacAlpine, B. Cobb, D. Andrews, 1994, Plant physiology.

Coordinate induction of alcohol dehydrogenase 1, aldolase, and other anaerobic RNAs in maize.

S. Hake, M. Freeling, W. Taylor, 1985, The Journal of biological chemistry.

Anaerobic expression of maize glucose phosphate isomerase I.

M. Freeling, P. M. Kelley, 1984, The Journal of biological chemistry.

Anaerobic expression of maize fructose-1,6-diphosphate aldolase.

M. Freeling, P. M. Kelley, 1984, The Journal of biological chemistry.

Nerve Growth Factor Regulates Neurolymphatic Remodeling during Corneal Inflammation and Resolution

M. Hollingsworth, P. M. Kelley, Darci M. Fink, 2014, PloS one.

temperature-sensitive auditory neuropathy allele Running Title : A potential OTOF temperature-sensitive allele

A. Starr, C. Berlin, B. Keats, 2005 .

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

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

Lymphatic vessel memory stimulated by recurrent inflammation.

P. M. Kelley, R. Tempero, Alicia L. Connor, 2013, The American journal of pathology.

The response of cells to heat shock

G. Aliperti, M. Schlesinger, P. M. Kelley, 1982 .

Purification and differential expression of enolase from maize

S. Lal, P. M. Kelley, T. Elthon, 1994 .

Molecular approaches to the genetic analysis of specific reading disability.

Shelley D. Smith, S. Smith, A. Brower, 1998, Human biology.

DIFFERENCES IN THE STRUCTURE, FUNCTION, AND FORMATION OF TWO ISOZYMES OF ESCHERICHIA COLI ALKALINE PHOSPHATASE

M. Schlesinger, P. M. Kelley, W. Bloch, 1975 .

Amino acid sequence of Escherichia coli alkaline phosphatase. Amino- and carboxyl-terminal sequences and variations between two isozymes.

R. Bradshaw, M. Schlesinger, P. M. Kelley, 1973, Biochemistry.

Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12.

J. W. Askew, W. Kimberling, S. Smith, 1999, Genomics.

Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation.

W. Kimberling, P. M. Kelley, S. Usami, 2001, American journal of medical genetics.

Lymphatic vessel hypertrophy in inflamed human tonsils.

P. M. Kelley, R. Tempero, 2010, Lymphatic research and biology.

The Genetics of Auditory Neuropathy

P. M. Kelley, E. Cohn, R. Rogers, 2002 .

The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41.

E. Zabarovsky, G. Klein, W. Kimberling, 1996, Genomics.

Development of a genotyping microarray for Usher syndrome

C. Cremers, M. Bitner-Glindzicz, E. van Wijk, 2006, Journal of Medical Genetics.

Calcium Regulates Molecular Interactions of Otoferlin with Soluble NSF Attachment Protein Receptor (SNARE) Proteins Required for Hair Cell Exocytosis*

B. Morley, P. M. Kelley, N. A. Ramakrishnan, 2014, The Journal of Biological Chemistry.

Invariant asymmetry renews the lymphatic vasculature during homeostasis

P. M. Kelley, R. Tempero, A. Connor, 2016, Journal of Translational Medicine.

Glucocorticoids Suppress Corneal Lymphangiogenesis

P. M. Kelley, R. Tempero, M. M. Steele, 2011, Cornea.

Lymphatic endothelial lineage assemblage during corneal lymphangiogenesis

P. M. Kelley, R. Tempero, A. Connor, 2015, Laboratory Investigation.

Tietz syndrome (hypopigmentation/deafness) caused by mutation ofMITF

Shelley D. Smith, P. M. Kelley, J. Kenyon, 2000, Journal of medical genetics.

Differential induction of heat shock, SOS, and oxidation stress regulons and accumulation of nucleotides in Escherichia coli

F. Neidhardt, R. Vanbogelen, P. M. Kelley, 1987, Journal of bacteriology.

Searching for evidence of DFNB2.

J. W. Askew, W. Kimberling, M. D. Weston, 2002, American journal of medical genetics.

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

G Van Camp, P Van de Heyning, C. Cremers, 1999, Human molecular genetics.

Mutations in the KCNQ 4 gene are responsible for autosomal dominant deafness in four DFNA 2 families

C. Cremers, P. Heyning, S. Bhasin, 1999 .

GJB2 mutations and degree of hearing loss: a multicenter study.

Mustafa Tekin, Umberto Ambrosetti, Nikolaus Blin, 2005, American journal of human genetics.

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.

J. W. Askew, D. Harris, W. Kimberling, 1998, American journal of human genetics.

Identification of a new connexin gene GJA11 (Cx59) using degenerate PCR primers

P. Willems, P. Coucke, P. M. Kelley, 2000 .

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss

J. W. Askew, K. Beisel, Z. Talebizadeh, 1999, Human mutation.

Prevalent connexin 26 gene (GJB2) mutations in Japanese

W. Kimberling, P. M. Kelley, S. Usami, 2000, Journal of medical genetics.

Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinoma.

D. Birnbaum, J. Grosgeorge, C. Theillet, 1997, Cytogenetics and cell genetics.

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

G. B. Schaefer, D. Harris, W. Kimberling, 1999, Pediatrics.

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

S. Leal, A. Starr, B. Keats, 2003, Journal of medical genetics.

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

B J Keats, L J Hood, C I Berlin, 2005, Journal of Medical Genetics.

Calcium Regulates Molecular Interactions of Otoferlin with SNARE Proteins Required for Hair Cell Exocytosis

B. Morley, P. M. Kelley, N. A. Ramakrishnan, 2013 .

Molecular Cloning and Domain Structure of Human Myosin-VIIa , the Gene Product Defective in Usher Syndrome 1 B

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

Detergent (sodium dodecyl sulfate) shock proteins in Escherichia coli

M. Adamowicz, K. Nickerson, P. M. Kelley, 1991, Journal of bacteriology.

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.

Regressed lymphatic vessels develop during corneal repair

P. M. Kelley, R. Tempero, M. M. Steele, 2011, Laboratory Investigation.

Reading Disability and Chromosome 6p21.3

J. W. Askew, R. Olson, Shelley D. Smith, 2001, Journal of learning disabilities.

In vitro synthesis of heat-shock proteins by mRNAs from chicken embryo fibroblasts.

G. Aliperti, M. Schlesinger, P. M. Kelley, 1980, The Journal of biological chemistry.

Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5q

C. Cremers, C. Möller, W. Kimberling, 2000, Journal of medical genetics.

The complete amino Acid sequence for the anaerobically induced aldolase from maize derived from cDNA clones.

P. M. Kelley, D. Tolan, Philip M. Kelley, 1986, Plant physiology.

Connexin 26: required for normal auditory function

W. Kimberling, P. M. Kelley, E. Cohn, 2000, Brain Research Reviews.

Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss.

P. M. Kelley, E. Cohn, Edward S. Cohn, 1999, American journal of medical genetics.

Is hearing loss due to mutations in the Connexin 26 gene progressive?

W. Jesteadt, W. Kimberling, P. M. Kelley, 2008, International journal of audiology.

Analysis of DNA elements that modulate myosin VIIA expression in humans

S. Jacobson, M. D. Weston, P. M. Kelley, 1999, Human mutation.

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

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

Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32.

W. Kimberling, M. Ma-Edmonds, M. D. Weston, 1997, Genomics.

β1 integrin regulates MMP-10 dependant tubulogenesis in human lymphatic endothelial cells.

P. M. Kelley, R. Tempero, M. M. Steele, 2011, Matrix biology : journal of the International Society for Matrix Biology.

Characterization of the maize pyruvate decarboxylase gene

S. Lal, M. Alleman, P. M. Kelley, 1991, Plant Molecular Biology.

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

A. Starr, C. Berlin, W. Kimberling, 2005, Journal of Medical Genetics.

Lymphatic vessel memory stimulated by recurrent inflammation.

P. M. Kelley, R. Tempero, A. Connor, 2013, The American journal of pathology.