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| B.S. (honors) |
Biochemistry |
1989 |
SUNY Binghamton |
| Ph.D |
Biochemistry |
1994 |
University of Rochester |
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| 1994 - 1998 |
University of Rochester |
Center for Oral Biology |
Glycobiology |
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| 1994 - 1997 |
NIH Oral, Cell and Molecular Biology Postdoctoral
Training Grant |
| 1991 - 1994 |
NIH Mechanisms of Molecular Pathogenesis Pre-Doctoral
Training Grant |
| 1989 - 1991 |
Dean’s Fellowship, University of Rochester |
| 1985 - 1989 |
Presidential Fellowship, SUNY Binghamton |
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| Yeast tRNA Ligase
Mutants are Nonviable and Accumulate tRNA Splicing Intermediates.
J Biol Chem. 267, 4577-4582. |
| Overproduced Rho
Factor from p39AS has Lysine Replacing Glutamic Acid at Residue
155 in the Linker Region Between its RNA and ATP Binding Domains.
Nucleic Acids Res. 20, 6107. |
| NusG Alters Rho-Dependent
Termination of Transcription In Vitro Independent of Kinetic
Coupling. Gene Exp. 3, 119-133. |
| Evidence for the
Formation of a Quaternary Termination Complex: Rho, NusG, RNA
Polymerase and the Nascent Transcript. J Mol Biol. 243, 830-839 |
| REF2 Encodes a
Novel RNA-Binding Protein Directly Involved in Yeast mRNA 3'
End Formation. Mol Cell Biol. 15, 1689-1697 |
| Charge Distribution
of Flanking Amino Acids Influences O-Glycan Aquisition in Vivo.
J Biol Chem. 271, 7061-7065 |
| Biosynthesis of
a Low Molecular Mass Rat Submandibular Gland Mucin in COS7 Cells.
Biochem J. 323, 497-502 |
| Charge Distribution
of Flanking Amino Acids Inhibits O-Glycosylation of Several
Single Site Acceptors In Vivo. Glycobiology 7,1053-1060 |
| Isoform-specific
O-glycosylation by Murine UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase-T3,
in vivo. Glycobiology 8, 367-371 |
| cDNA Cloning and
Expression of UDP-N-acetyl-D-galactosamine:Polypeptide N-Acetylgalactosaminyltransferase
sequence homologs in Caenorhabditis elegans J Biol Chem. 273,
8268-8277 |
| C. elegans
ClC-type Chloride Channels: Novel Variants and Functional Expression.
Am J Physiol Cell Physiol., 279, C2052-C2066. |
| Defective Fluid
Secretion and NaCl Absorption by Parotid Glands in Mice Lacking
Na-H Exchange. J Biol Chem., 276, 27042-27050. |
| Targeted Disruption
of the Nhe1 Gene Fails to Inhibit b1-Adrenergic Receptor-Induced
Parotid Gland Hypertrophy. Am J Physiol Gastrointest Liver Physiol.,
280, G694-G700. |
| The Nck-interacting
kinase NIK phosphorylates the Na-H exchanger NHE1 and regulates
NHE1 activation by platelet-derived growth factor. J Biol Chem.,
276, 31349-31356 |
| Acute Inhibition
of Brain-Specific Na+/H+ Exchanger Isoform 5 by Protein Kinase
A, Protein Kinase C and Cell Shrinkage. Am J Physiol Cell Physiol.,
281, C1146-C1157 |
| Molecular and functional
characterization of a murine calcium-activated chloride channel
expressed in smooth muscle. J Biol Chem., 277, 18586-18591 |
| Saliva Secretion
and Cell Volume Regulation by Parotid Gland Acinar Cells from
Mice Lacking Expression of the Clcn2 Cl- Channel Gene. J Biol
Chem. 277:23604-23611 |
| The NHX family
of Na-H exchangers in Caenorhabditis elegans. J Biol Chem. 277:29036-29044 |
| Secretion and Cell
Volume Regulation by Salivary Acinar Cells from Mice Lacking
Expression of the Clcn3 Cl- Channel Gene. J Physiol. 545:207-216 |
| Altered GABAergic
function accompanies hippocampal degeneration in mice lacking
ClC-3 voltage-gated chloride channels. Brain Research 958:227-250. |
| Molecular identification
of the Ca2+-activated K+ channels in parotid acinar cells. Am
J Physiol Cell Physiol. 284:C535-C546. |
| Active K+ secretion
through multiple KCa-type channels and regulation by IKCa channels
in rat proximal colon. Am J Physiol Gastrointest Liver Physiol.
285:G185-G196 |
| The hSK4 (KCNN4)
isoform is the Ca2+-activated K+ channel (Gardos channel) in
human red blood cells. Proc Natl Acad Sci U S A. 100:7366-7371 |
| A reduction in
intestinal cell pHi due to loss of the C. elegans Na+/H+ exchanger
NHX-2 increases lifespan. J Biol Chem 278:44657-44666 |
| Genome-wide search
and identification of a novel gel-forming mucin MUC19/Muc19
in glandular tissues. Am J Respir Cell Mol Biol 30:155-165 |
| Alternative splicing
of N- and C-termini of a C. elegans ClC channel alters
gating and sensitivity to external Cl- and H+. J Physiol 555:
97-114. |
| Physiological roles
of the intermediate conductance, Ca2+-activated K channel, Kcnn4.
J Biol Chem. [Epub ahead of print]. |
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| Experimental Approaches
to Studying O-Glycosylation In Vivo. In: Techniques
in Glycobiology, Ed. R. Townsend and A. Hotchkiss.
Marcel Dekker. New York, NY. |
| Mucin Type O-Glycosylation
in C. elegans is Initiated by a Family of Glycosyltransferases.
Trends in Glycoscience and Glycotechnology,
13 (73): 463-479 |
| Ca2+-Activated
Cl- Currents in Salivary and Lacrimal Glands. In: Current
Topics in Membranes, vol. 53. Ed. C.M. Fuller. Academic
Press. San Diego, CA. |
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| Molecular identification
of the Ca2+-activated K+ channels in parotid acinar cells.Poster
presented at FASEB meeting, New Orleans, LA |
| Serine/threonine
phosphorylation signaling pathways regulate the C. elegans
ClC anion channel CLH-3. Poster presented at FASEB meeting,
New Orleans, LA |
| Biophysical
analysis of two C. elegans CLH-3 variants reveals a
role of intracellular amino- and carboxyl-termini in channel
gating and extracellular pH sensitivity. Poster presented
at FASEB meeting, New Orlean, LA |
| Regulation
of C. elegans CLH-3b activation kinetics by an Ste20-related
kinase. Poster presented at FASEB meeting, New Orleans,
LA |
| The C.
elegans intestinal Na+-H+ exchanger NHX-2 influences nutrient
uptake and aging. Poster presented at AGA national meeting,
Orlando, FL |
| A reduction
in intestinal cell pHi due to loss of the C. elegans Na+/H+
exchanger NHX-2 increases lifespan. Lecture presented at
the biennial International C. elegans meeting, Los
Angeles, CA |
| Acid-base transport
in C. elegans. Poster presented at FASEB meeting,
Washington, DC |
| Alternative
splicing of N- and C-termini of a C. elegans ClC channel
alters gating and sensitivity to external Cl- and H+. Poster
presented at FASEB meeting, Washington, DC |
| Molecular identification
of a kinase that interacts with and regulates cell volume-dependent
activity of a ClC anion channel. Poster presented at FASEB
meeting, Washington, DC |
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| Principal Investigator:
K. Nehrke |
| Dates of project:
04/01/01-03/31/03 |
| Principal Investigator:
K. Nehrke |
| Dates of project:
4/1/03-3/31/05 |
| Principal Investigator:
H.J. Federoff |
| Pilot Project-“Intestinal
Cellular pH as a Regulator of Longevity in C. elegans” |
| Dates of project:
7/1/04-6/30/05 |
| Principal Investigator:
K. Nehrke |
| Dates of project:
10/1/04-9/30/08 |
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| Graduate research
associate to Dr. Terry Platt, Department of Biochemistry, University
of Rochester. Research: RNA processing in E. coli and S. cerevisiae.
Relevant techniques: yeast genetics, yeast two-hybrid analysis,
classical enzyme kinetics, recombinant protein production, cell
fractionation and protein purification, transcriptional regulation
and RNA processing, molecular biology |
| Postdoctoral research
associate to Dr. Lawrence A. Tabak, Departmental Chair, Departments
of Dental Research and Biochemistry; Director, Center for Oral
Biology, University of Rochester. Research: Molecular
mechanisms of mucin biosynthesis and glycosylation.
Relevant techniques: cDNA library construction, molecular and
in silico gene identification/screening, expressional cloning
and purification of mammalian fusion proteins from E. coli,
S. cerevisiae, P. pastoris and tissue culture cells, yeast two-hybrid
analysis, oligosaccharide analysis, protein microsequencing,
immunoassays, molecular biology. |
| Assistant Research
Professor in the laboratory of Dr. James E. Melvin, Professor
and Director, Center for Oral Biology and Professor, Department
of Pharmacology and Physiology, University of Rochester. Research:
Ion Channel Function in Secretory Oral Epithelia. Relevant
techniques: C. elegans genetics, reverse genetics and
biochemistry, mouse targeted gene ablations, confocal microscopy,
immunohistochemistry, cellular physiology and real time fluorescent
imaging, electrophysiology, molecular biology. |
| Assistant Professor
of Medicine, Nephrology Unit, University of Rochester. Research:
i) Acid-Base Transport in C. elegans and ii)
Molecular Mechanisms of Calcium Homeostasis. |
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