Results 81 to 90 of about 2,665 (161)
BMC Medicine, 2004 Background Pendred syndrome, a common autosomal-recessive disorder characterized by congenital deafness and goiter, is caused by mutations of SLC26A4, which codes for pendrin.
Wall Susan M +11 more
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Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status [PDF]
, 2002 Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status.BackgroundPendrin belongs to a superfamily of Cl-/anion exchangers and is expressed in the inner ear, the thyroid gland, and the kidney.
Finberg, Karin E. +6 more
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EMBO Molecular Medicine, 2012 The V‐ATPase is a multisubunit complex that transports protons across membranes. Mutations of its B1 or a4 subunit are associated with distal renal tubular acidosis and deafness.
J. Christopher Hennings +9 more
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Expression of pendrin in kidneys of WT and NCC KO mice.
, 2016 Expression of pendrin by (a) Northern hybridization and (b) Immunofluorescence labeling in kidneys of WT and NCC KO mice. Northern hybridizations showed significant increase in pendrin expression in NCC KO mice vs.
Jie Xu (34477) +5 more
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Cellular Physiology and Biochemistry, 2014 Background: Molecular dynamics (MD) simulations provide valuable information on the conformational changes that accompany time-dependent motions in proteins.
Alok K. Sharma +2 more
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A Role for Iodide and Thyroglobulin in Modulating the Function of Human Immune Cells
Frontiers in Immunology, 2017 Iodine is an essential element required for the function of all organ systems. Although the importance of iodine in thyroid hormone synthesis and reproduction is well known, its direct effects on the immune system are elusive.
Mahmood Y. Bilal +9 more
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, 2017 Introduction: To assess the pendrin expression density in placental bed biopsies from preeclampsia cases in comparison with healthy term controls. Material and Methods: A prospective case-control study with 106 placental bed biopsies obtained during ...
Canan Fırat +9 more
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Human pendrin expressed inXenopus laevisoocytes mediates chloride/formate exchange
, 2000 Pendred syndrome, characterized by congenital sensorineural hearing loss and goiter, is one of the most common forms of syndromic deafness. The gene causing Pendred syndrome ( PDS) encodes a protein designated pendrin, which is expressed in the thyroid ...
Lawrence P. Karniski, Daryl A. Scott
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Cellular Physiology and Biochemistry, 2013 Ion transporters are the molecular basis for ion homeostasis of the cell and the whole organism. The anion exchanger pendrin is only one of a number of examples where a complete or partial loss of function and/or deregulation of expression of ion ...
Silvia Dossena +4 more
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Onset of pendrin expression in the cochlea.
, 2013 Pendrin (red) was visualized by immunocytochemistry. F-actin (green) and nuclei (blue) were labeled. A: Diagram of the inner ear. B–G: Cross-sections of the cochlear duct in the hook region (B), basal turn (C, E and G) and upper turn (D and F) of Slc26a4+
Hyoung-Mi Kim (237178) +1 more
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