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Ute Scholl

Showing results (1-10 of 9) with videos related to

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MMW Fortschritte Der Medizin|April 1, 2022
[Secondary hypertension]Markus van der Giet, Ute Scholl
Acta Neurologica Belgica|July 12, 2012
KCNJ10 gene mutation in an 8-year-old boy with seizuresBülent Kara, Barış Ekici, Belkıs Ipekçi, et al.
Journal of the American Society of Nephrology : JASN|September 9, 2008
Disease-causing dysfunctions of barttin in Bartter syndrome type IVAudrey G H Janssen, Ute Scholl, Constanze Domeyer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2006
Barttin modulates trafficking and function of ClC-K channelsUte Scholl, Simon Hebeisen, Audrey G H Janssen, et al.
Nature Communications|November 16, 2019
Elevated aldosterone and blood pressure in a mouse model of familial hyperaldosteronism with ClC-2 mutationJulia Schewe, Eric Seidel, Sofia Forslund, et al.
Nature Communications|May 27, 2022
Author Correction: Elevated aldosterone and blood pressure in a mouse model of familial hyperaldosteronism with ClC-2 mutationJulia Schewe, Eric Seidel, Sofia Forslund, et al.
Genes, Chromosomes & Cancer|June 27, 2012
Comprehensive DNA methylation analysis of benign and malignant adrenocortical tumorsAnnabelle L Fonseca, Johan Kugelberg, Lee F Starker, et al.
Nucleic Acids Research|April 28, 2020
VarFish: comprehensive DNA variant analysis for diagnostics and researchManuel Holtgrewe, Oliver Stolpe, Mikko Nieminen, et al.
American Journal of Human Genetics|August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndromeSaima Riazuddin, Saima Anwar, Martin Fischer, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
MMW Fortschritte Der Medizin|April 1, 2022
[Secondary hypertension]Markus van der Giet, Ute Scholl
Acta Neurologica Belgica|July 12, 2012
KCNJ10 gene mutation in an 8-year-old boy with seizuresBülent Kara, Barış Ekici, Belkıs Ipekçi, et al.
Journal of the American Society of Nephrology : JASN|September 9, 2008
Disease-causing dysfunctions of barttin in Bartter syndrome type IVAudrey G H Janssen, Ute Scholl, Constanze Domeyer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2006
Barttin modulates trafficking and function of ClC-K channelsUte Scholl, Simon Hebeisen, Audrey G H Janssen, et al.
Nature Communications|November 16, 2019
Elevated aldosterone and blood pressure in a mouse model of familial hyperaldosteronism with ClC-2 mutationJulia Schewe, Eric Seidel, Sofia Forslund, et al.
Nature Communications|May 27, 2022
Author Correction: Elevated aldosterone and blood pressure in a mouse model of familial hyperaldosteronism with ClC-2 mutationJulia Schewe, Eric Seidel, Sofia Forslund, et al.
Genes, Chromosomes & Cancer|June 27, 2012
Comprehensive DNA methylation analysis of benign and malignant adrenocortical tumorsAnnabelle L Fonseca, Johan Kugelberg, Lee F Starker, et al.
Nucleic Acids Research|April 28, 2020
VarFish: comprehensive DNA variant analysis for diagnostics and researchManuel Holtgrewe, Oliver Stolpe, Mikko Nieminen, et al.
American Journal of Human Genetics|August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndromeSaima Riazuddin, Saima Anwar, Martin Fischer, et al.
Pageof 1