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Anion Transporters and Oxalate Homeostasis: From Genes to Diseases  -  December 8-9, 2008

DRAFT AGENDA

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

   
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
   

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
   
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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