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5 in total

Review 1. Active sugar transport in health and disease.

Authors: E M Wright; B A Hirayama; D F Loo
Journal: J Intern Med Date: 2007-01 Impact factor: 8.989

2. Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients.

Authors: Lei Yu; Ji-Cheng Lv; Xu-jie Zhou; Li Zhu; Ping Hou; Hong Zhang
Journal: Hum Genet Date: 2010-12-17 Impact factor: 4.132

3. Molecular analysis of the SGLT2 gene in patients with renal glucosuria.

Authors: René Santer; Martina Kinner; Christoph L Lassen; Reinhard Schneppenheim; Paul Eggert; Martin Bald; Johannes Brodehl; Markus Daschner; Jochen H H Ehrich; Markus Kemper; Salvatore Li Volti; Thomas Neuhaus; Flemming Skovby; Peter G F Swift; Jürgen Schaub; Dan Klaerke
Journal: J Am Soc Nephrol Date: 2003-11 Impact factor: 10.121

4. Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion.

Authors: Joaquim Calado; Yves Sznajer; Daniel Metzger; Ana Rita; Marie C Hogan; Antonis Kattamis; Mauro Scharf; Velibor Tasic; Johann Greil; Florian Brinkert; Markus J Kemper; René Santer
Journal: Nephrol Dial Transplant Date: 2008-07-12 Impact factor: 5.992

5. Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting.

Authors: J Calado; J Loeffler; O Sakallioglu; F Gok; K Lhotta; J Barata; J Rueff
Journal: Kidney Int Date: 2006-03 Impact factor: 10.612

5 in total

4 in total

A novel sodium-glucose co-transporter 2 gene (SGLT2) mutation contributes to the abnormal expression of SGLT2 in renal tissues in familial renal glucosuria.

Review 1. Active sugar transport in health and disease.

2. Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients.

3. Molecular analysis of the SGLT2 gene in patients with renal glucosuria.

4. Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion.

5. Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting.

Review 1. Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease.

2. Decreased expression and function of sodium-glucose co-transporter 2 from a novel C-terminal mutation: a case report.

3. Novel SLC5A2 mutation contributes to familial renal glucosuria: Abnormal expression in renal tissues.

4. SLC5A2 mutations, including two novel mutations, responsible for renal glucosuria in Chinese families.