Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK063024-02
Application #
6691081
Study Section
Endocrinology Study Section (END)
Program Officer
Haft, Carol R
Project Start
2003-01-01
Project End
2007-12-31
Budget Start
2004-01-01
Budget End
2004-12-31
Support Year
2
Fiscal Year
2004
Total Cost
$259,875
Indirect Cost
Name
Northwestern University at Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Perone, Denise; Medeiros-Neto, Geraldo; Nogueira, CĂ©lia Regina et al. (2016) Analysis of the PAX8 gene in 32 children with thyroid dysgenesis and functional characterization of a promoter variant. J Pediatr Endocrinol Metab 29:193-201
Pesce, Liuska; Bizhanova, Aigerim; Caraballo, Juan Carlos et al. (2012) TSH regulates pendrin membrane abundance and enhances iodide efflux in thyroid cells. Endocrinology 153:512-21
Dossena, Silvia; Bizhanova, Aigerim; Nofziger, Charity et al. (2011) Identification of allelic variants of pendrin (SLC26A4) with loss and gain of function. Cell Physiol Biochem 28:467-76
Jacobson, Eric M; Concepcion, Erlinda; Ho, Kenneth et al. (2011) cDNA immunization of mice with human thyroglobulin generates both humoral and T cell responses: a novel model of thyroid autoimmunity. PLoS One 6:e19200
Bizhanova, Aigerim; Chew, Teng-Leong; Khuon, Satya et al. (2011) Analysis of cellular localization and function of carboxy-terminal mutants of pendrin. Cell Physiol Biochem 28:423-34
Bizhanova, Aigerim; Kopp, Peter (2009) Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid. Endocrinology 150:1084-90
Kopp, Peter; Pesce, Liuska; Solis-S, Juan Carlos (2008) Pendred syndrome and iodide transport in the thyroid. Trends Endocrinol Metab 19:260-8
Kopp, Peter (2007) Applications of molecular biology and genetics in endocrinology. Endocr Pract 13:534-41
Pfarr, Nicole; Borck, Guntram; Turk, Andrew et al. (2006) Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genes. J Clin Endocrinol Metab 91:2678-81
Gillam, M P; Bartolone, L; Kopp, P et al. (2005) Molecular analysis of the PDS gene in a nonconsanguineous Sicilian family with Pendred's syndrome. Thyroid 15:734-41

Showing the most recent 10 out of 12 publications