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The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
June 20, 2006
Detection of tripeptidyl peptidase I activity in living cells by fluorogenic substrates
Robert Steinfeld, Jens C Fuhrmann, Jutta Gärtner
Nature Cell Biology
|
November 2, 2004
Ion channels: function unravelled by dysfunction
Thomas J Jentsch, Christian A Hübner, Jens C Fuhrmann
Molecular and Cellular Neurosciences
|
December 27, 2005
The state of the actin cytoskeleton determines its association with gephyrin: role of ena/VASP family members
Melanie Bausen, Jens C Fuhrmann, Heinrich Betz, et al.
Annual Review of Physiology
|
February 16, 2005
Physiological functions of CLC Cl- channels gleaned from human genetic disease and mouse models
Thomas J Jentsch, Mallorie Poët, Jens C Fuhrmann, et al.
Nature
|
March 10, 2006
ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function
Philipp F Lange, Lena Wartosch, Thomas J Jentsch, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 8, 2009
Lysosomal degradation of endocytosed proteins depends on the chloride transport protein ClC-7
Lena Wartosch, Jens C Fuhrmann, Michaela Schweizer, et al.
Plos One
|
November 26, 2009
Metabolite profiling identifies candidate markers reflecting the clinical adaptations associated with Roux-en-Y gastric bypass surgery
David M Mutch, Jens C Fuhrmann, Dietrich Rein, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 5, 2002
Gephyrin interacts with Dynein light chains 1 and 2, components of motor protein complexes
Jens C Fuhrmann, Stefan Kins, Philippe Rostaing, et al.
Journal of Neuropathology and Experimental Neurology
|
November 26, 2010
Distinct neuropathologic phenotypes after disrupting the chloride transport proteins ClC-6 or ClC-7/Ostm1
Sarah N R Pressey, Kieran J O'Donnell, Tobias Stauber, et al.
The EMBO Journal
|
February 12, 2005
Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration
Dagmar Kasper, Rosa Planells-Cases, Jens C Fuhrmann, et al.
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of 2
Search research articles
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Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
June 20, 2006
Detection of tripeptidyl peptidase I activity in living cells by fluorogenic substrates
Robert Steinfeld, Jens C Fuhrmann, Jutta Gärtner
Nature Cell Biology
|
November 2, 2004
Ion channels: function unravelled by dysfunction
Thomas J Jentsch, Christian A Hübner, Jens C Fuhrmann
Molecular and Cellular Neurosciences
|
December 27, 2005
The state of the actin cytoskeleton determines its association with gephyrin: role of ena/VASP family members
Melanie Bausen, Jens C Fuhrmann, Heinrich Betz, et al.
Annual Review of Physiology
|
February 16, 2005
Physiological functions of CLC Cl- channels gleaned from human genetic disease and mouse models
Thomas J Jentsch, Mallorie Poët, Jens C Fuhrmann, et al.
Nature
|
March 10, 2006
ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function
Philipp F Lange, Lena Wartosch, Thomas J Jentsch, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
August 8, 2009
Lysosomal degradation of endocytosed proteins depends on the chloride transport protein ClC-7
Lena Wartosch, Jens C Fuhrmann, Michaela Schweizer, et al.
Plos One
|
November 26, 2009
Metabolite profiling identifies candidate markers reflecting the clinical adaptations associated with Roux-en-Y gastric bypass surgery
David M Mutch, Jens C Fuhrmann, Dietrich Rein, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 5, 2002
Gephyrin interacts with Dynein light chains 1 and 2, components of motor protein complexes
Jens C Fuhrmann, Stefan Kins, Philippe Rostaing, et al.
Journal of Neuropathology and Experimental Neurology
|
November 26, 2010
Distinct neuropathologic phenotypes after disrupting the chloride transport proteins ClC-6 or ClC-7/Ostm1
Sarah N R Pressey, Kieran J O'Donnell, Tobias Stauber, et al.
The EMBO Journal
|
February 12, 2005
Loss of the chloride channel ClC-7 leads to lysosomal storage disease and neurodegeneration
Dagmar Kasper, Rosa Planells-Cases, Jens C Fuhrmann, et al.
Page
of 2