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The Slc26a4 transporter functions as an electroneutral Cl−/I−/HCO3− exchanger: role of Slc26a4 and Slc26a6 in I− and HCO3− secretion and in regulation of CFTR in the parotid duct

The Journal of physiology, 2008-08, Vol.586 (16), p.3813-3824

2008

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Pendrin, Encoded by the Pendred Syndrome Gene, Resides in the Apical Region of Renal Intercalated Cells and Mediates Bicarbonate Secretion

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (7), p.4221-4226

2001

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The pendred syndrome gene encodes a chloride-iodide transport protein

Nature genetics, 1999-04, Vol.21 (4), p.440-443

1999

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Regulated transport of sulfate and oxalate by SLC26A2/DTDST

American Journal of Physiology: Cell Physiology, 2010-06, Vol.298 (6), p.C1363-C1375

2010

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Regulation of anion exchanger Slc26a6 by protein kinase C

American Journal of Physiology: Cell Physiology, 2007-04, Vol.292 (4), p.C1485-C1492

2007

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Immunolocalization of sat-1 sulfate/oxalate/bicarbonate anion exchanger in the rat kidney

American journal of physiology. Renal physiology, 1998-07, Vol.275 (1), p.F79-F87

1998

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Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

American Journal of Physiology: Cell Physiology, 2000-01, Vol.278 (1), p.C207-C211

2000

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Functional expression and cellular distribution of diastrophic dysplasia sulfate transporter (DTDST) gene mutations in HEK cells

Human molecular genetics, 2004-10, Vol.13 (19), p.2165-2171

KARNISKI, Lawrence P

2004

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Mutations in the diastrophic dysplasia sulfate transporter (DTSTt) gene : correlation between sulfate transport activity and chondrodysplasia phenotype

Human molecular genetics, 2001-07, Vol.10 (14), p.1485-1490

KARNISKI, Lawrence P

2001

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Protein localization of SLC26A2 (DTDST) in rat kidney

Histochemistry and cell biology, 2010-05, Vol.133 (5), p.541-547

2010

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Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4)

Human molecular genetics, 2000-07, Vol.9 (11), p.1709-1715

2000

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A compound heterozygote harboring novel and recurrent DTDST mutations with intermediate phenotype between atelosteogenesis type II and diastrophic dysplasia

American journal of medical genetics. Part A, 2006-06, Vol.140A (11), p.1143-1147

2006

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Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein

American journal of physiology. Renal physiology, 2002-11, Vol.283 (5), p.F952-F956

2002

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The Pendred syndrome gene encodes a chloride-iodide transport protein

Nature genetics, 1999-04, Vol.21 (4), p.440-443

1999

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Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations

Human mutation, 2001-05, Vol.17 (5), p.403-411

2001

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Effects of sulfate and chloride on three separate oxalate transporters reconstituted from rabbit renal cortex

American journal of physiology. Renal physiology, 1998-01, Vol.274 (1), p.F189-F196

Karniski, L P

1998

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Protein localization of SLC26A2 (DTDST) in rat kidneys

The FASEB journal, 2007, Vol.21 (6), p.A1333-A1333

2007

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Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype–phenotype correlations

Human mutation, 2001-05, Vol.17 (5), p.403-411

2001

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Regulated transport of sulfate and oxalate by SLC26A2/DTDST

American Journal of Physiology: Cell Physiology, 2010, Vol.67 (6)

2010

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The Slc26a4 transporter functions as an electroneutral Cl − /I − /HCO 3 − exchanger: role of Slc26a4 and Slc26a6 in I − and HCO 3 − secretion and in regulation of CFTR in the parotid duct

The Journal of physiology, 2008-08, Vol.586 (16), p.3813-3824

2008

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The Slc26a4 transporter functions as an electroneutral Clâ/Iâ/HCO3â exchanger: role of Slc26a4 and Slc26a6 in Iâ and HCO3â secretion and in regulation of CFTR in the parotid duct

The Journal of physiology, 2008-08, Vol.586 (16), p.3813

2008

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Regulation of anion exchanger SIc26a6 by protein kinase C

American Journal of Physiology: Cell Physiology, 2007-04, Vol.292 (4), p.C1485

2007

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Regulation of anion exchanger Slc26a6 by protein kinase C

American Journal of Physiology: Cell Physiology, 2007, Vol.61 (4)

2007

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Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

American Journal of Physiology: Cell Physiology, 2000-01, Vol.47 (1), p.C207

2000

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The Slc26a4 transporter functions as an electroneutral Cl−/I−/HCO3− exchanger: role of Slc26a4 and Slc26a6 in I− and HCO3− secretion and in regulation of CFTR in the parotid duct

Pendrin, Encoded by the Pendred Syndrome Gene, Resides in the Apical Region of Renal Intercalated Cells and Mediates Bicarbonate Secretion

The pendred syndrome gene encodes a chloride-iodide transport protein

Regulated transport of sulfate and oxalate by SLC26A2/DTDST

Regulation of anion exchanger Slc26a6 by protein kinase C

Immunolocalization of sat-1 sulfate/oxalate/bicarbonate anion exchanger in the rat kidney

Hypo-Functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

Functional expression and cellular distribution of diastrophic dysplasia sulfate transporter (DTDST) gene mutations in HEK cells

Mutations in the diastrophic dysplasia sulfate transporter (DTSTt) gene : correlation between sulfate transport activity and chondrodysplasia phenotype

Protein localization of SLC26A2 (DTDST) in rat kidney

Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4)

A compound heterozygote harboring novel and recurrent DTDST mutations with intermediate phenotype between atelosteogenesis type II and diastrophic dysplasia

Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein

The Pendred syndrome gene encodes a chloride-iodide transport protein

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations

Effects of sulfate and chloride on three separate oxalate transporters reconstituted from rabbit renal cortex

Protein localization of SLC26A2 (DTDST) in rat kidneys

Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype–phenotype correlations

Regulated transport of sulfate and oxalate by SLC26A2/DTDST

The Slc26a4 transporter functions as an electroneutral Cl − /I − /HCO 3 − exchanger: role of Slc26a4 and Slc26a6 in I − and HCO 3 − secretion and in regulation of CFTR in the parotid duct

The Slc26a4 transporter functions as an electroneutral Clâ/Iâ/HCO3â exchanger: role of Slc26a4 and Slc26a6 in Iâ and HCO3â secretion and in regulation of CFTR in the parotid duct

Regulation of anion exchanger SIc26a6 by protein kinase C

Regulation of anion exchanger Slc26a6 by protein kinase C

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

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