DRAFT AGENDA
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Day 1, Monday, December 8, 2008 |
| 12:00 – 1:00 p.m. |
Registration |
| 1:00 – 1:10 p.m. |
Welcome and Introduction
Robert Star, National Institute of Diabetes and Digestive and Kidney Diseases |
| 1:10 – 2:00 p.m. |
Keynote Address: Anion Channels and Transporters All Mixed Up
Chris Miller, Brandeis University |
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| Session 1: Transporters |
| 2:00 – 2:25 p.m. |
SLC26a Family in Gut and Kidney
Manoocher Soleimani, University of Cincinnati |
| 2:25 – 2:50 p.m. |
Oxalate Transport Properties of SLC26A6 and SLC26 Polypeptide Orthologs From Human and Mouse
Seth Alper, Beth Israel Deaconess Medical Center, Harvard Medical School |
| 2:50 – 3:15 p.m. |
Regulation of Slc26a6
Hatim Hassan, The University of Chicago |
| 3:15 – 3:40 p.m. |
Physiological Characterization of Epithelial Oxalate Exchangers
David Mount, Brigham and Women’s Hospital |
| 3:40 – 4:00 p.m. |
BREAK |
| 4:00 – 4:25 p.m. |
The Sat1 (Slc26a1) Anion Transporter and Calcium Oxalate Urolithiasis
Daniel Markovich, University of Queensland |
| 4:25 – 4:50 p.m. |
Diverse Transport Modes by the Solute Carrier 26 Family of Anion Transporters
Shmuel Muallem, University of Texas Southwestern Medical Center |
| 4:50 – 5:15 p.m. |
Structure and Function of OxlT, the Oxalate Antiporter of Oxalobacter formigenes
Peter Maloney, The Johns Hopkins University Medical School |
| 5:15 – 5:30 p.m. |
siRNA Knockdown of Slc26a6 Reveals the Contribution and Some Properties of PAT-1 to Transepithelial Anion Transport, Particularly Oxalate, Across Caco-2 Monolayers
Robert Freel, University of Florida |
| 5:45 p.m. |
Reception |
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Day 2, Tuesday, December 9, 2008 |
| Session 2: Oxalate Homeostasis |
| 8:30 – 9:15 a.m. |
Keynote Address: Identification of Small Molecules to Modulate Membrane Transport
Alan Verkman, University of California, San Francisco |
| 9:15 – 9:40 a.m. |
Modulation of DRA Function and Expression by Gut Microbes
Pradeep Dudeja, University of Illinois at Chicago |
| 9:40 – 10:05 a.m. |
Gut Oxalate Intake and Processing in Human Subjects
Ross Holmes, Wake Forest University Medical School |
| 10:05 – 10:20 a.m. |
BREAK |
| 10:20 – 10:45 a.m. |
Oxalate Homeostasis—Insights From Knockout Mice
Peter Aronson, Yale University School of Medicine |
| 10:45 – 11:10 a.m. |
Oxalate in the Kidneys of Human Stone Forming Patients
Fred Coe, The University of Chicago |
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| Session 3: Clinical Applications – Altering Oxalate Homeostasis |
| 11:10 – 11:55 a.m. |
Keynote Address: What Can We Learn from Bacteria?
Jon Clardy, Ph.D., Harvard Medical School |
| 11:55 – 1:05 p.m. |
Lunch (on your own) |
| 1:05 – 1:30 p.m. |
Physiological Interactions Between Oxalobacter and the Transporting Mucosa
Marguerite Hatch, University of Florida |
| 1:30 – 1:55 p.m. |
Oxalobacter formigenes: A Potential New Therapy for Primary Hyperoxaluria
Dawn Milliner, Mayo Clinic |
| 1:55 – 2:20 p.m. |
Oxalate Degrading Enzyme in Clinical Trials
Kenneth Attie, Altus Pharmaceuticals |
| 2:20 – 2:30 p.m. |
Identification, Cloning, and Characterization of Human 2-Keto-4-Hydroxy-Glutarate Aldolase (KHGA), an Attractive Therapeutic Target to Block the Production of Glyoxylate From Hydroxyproline Catabolism
Travis Riedel, Wake Forest University School of Medicine |
| 2:30 – 2:55 p.m. |
The Epidemiology of Oxalobacter formigenes and Its Relation
to Kidney Stones
Judith Kelly, Boston University School of Medicine |
| 2:55 – 3:20 p.m. |
Human SLC26A6 Variation in Oxalate Homeostasis
Carla Monico, Mayo Clinic |
| 3:20 p.m. |
Adjournment |
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