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William E Balch

Showing results (51-60 of 122) with videos related to

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Nature Communications|April 18, 2024
Tracing genetic diversity captures the molecular basis of misfolding diseasePei Zhao, Chao Wang, Shuhong Sun, et al.
The EMBO Journal|November 12, 2002
Rab-alphaGDI activity is regulated by a Hsp90 chaperone complexToshiaki Sakisaka, Timo Meerlo, Jeanne Matteson, et al.
Critical Reviews in Biochemistry and Molecular Biology|February 25, 2012
Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic interventionJames P Solomon, Lesley J Page, William E Balch, et al.
Journal of Molecular Biology|November 5, 2003
Gelsolin domain 2 Ca2+ affinity determines susceptibility to furin proteolysis and familial amyloidosis of finnish typeMary E Huff, Lesley J Page, William E Balch, et al.
The Journal of Biological Chemistry|April 22, 2011
Di-acidic motifs in the membrane-distal C termini modulate the transport of angiotensin II receptors from the endoplasmic reticulum to the cell surfaceXiaoping Zhang, Chunmin Dong, Qiong J Wu, et al.
Biochemical and Biophysical Research Communications|September 1, 2004
Ca2+ binding protects against gelsolin amyloidosisLesley J Page, Mary E Huff, Jeffery W Kelly, et al.
Trends in Biochemical Sciences|April 7, 2007
Functional amyloid--from bacteria to humansDouglas M Fowler, Atanas V Koulov, William E Balch, et al.
Protein Science : a Publication of the Protein Society|July 22, 2009
A general strategy for the bacterial expression of amyloidogenic peptides using BCL-XL-1/2 fusionsIsaac T Yonemoto, Malcolm R Wood, William E Balch, et al.
Cell Reports. Medicine|January 14, 2025
Spatial covariance reveals isothiocyanate natural products adjust redox stress to restore function in alpha-1-antitrypsin deficiencyShuhong Sun, Chao Wang, Junyan Hu, et al.
Molecular & Cellular Proteomics : MCP|September 2, 2017
Quantitative Analysis of the Proteome Response to the Histone Deacetylase Inhibitor (HDACi) Vorinostat in Niemann-Pick Type C1 diseaseKanagaraj Subramanian, Navin Rauniyar, Mathieu Lavalleé-Adam, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
Nature Communications|April 18, 2024
Tracing genetic diversity captures the molecular basis of misfolding diseasePei Zhao, Chao Wang, Shuhong Sun, et al.
The EMBO Journal|November 12, 2002
Rab-alphaGDI activity is regulated by a Hsp90 chaperone complexToshiaki Sakisaka, Timo Meerlo, Jeanne Matteson, et al.
Critical Reviews in Biochemistry and Molecular Biology|February 25, 2012
Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic interventionJames P Solomon, Lesley J Page, William E Balch, et al.
Journal of Molecular Biology|November 5, 2003
Gelsolin domain 2 Ca2+ affinity determines susceptibility to furin proteolysis and familial amyloidosis of finnish typeMary E Huff, Lesley J Page, William E Balch, et al.
The Journal of Biological Chemistry|April 22, 2011
Di-acidic motifs in the membrane-distal C termini modulate the transport of angiotensin II receptors from the endoplasmic reticulum to the cell surfaceXiaoping Zhang, Chunmin Dong, Qiong J Wu, et al.
Biochemical and Biophysical Research Communications|September 1, 2004
Ca2+ binding protects against gelsolin amyloidosisLesley J Page, Mary E Huff, Jeffery W Kelly, et al.
Trends in Biochemical Sciences|April 7, 2007
Functional amyloid--from bacteria to humansDouglas M Fowler, Atanas V Koulov, William E Balch, et al.
Protein Science : a Publication of the Protein Society|July 22, 2009
A general strategy for the bacterial expression of amyloidogenic peptides using BCL-XL-1/2 fusionsIsaac T Yonemoto, Malcolm R Wood, William E Balch, et al.
Cell Reports. Medicine|January 14, 2025
Spatial covariance reveals isothiocyanate natural products adjust redox stress to restore function in alpha-1-antitrypsin deficiencyShuhong Sun, Chao Wang, Junyan Hu, et al.
Molecular & Cellular Proteomics : MCP|September 2, 2017
Quantitative Analysis of the Proteome Response to the Histone Deacetylase Inhibitor (HDACi) Vorinostat in Niemann-Pick Type C1 diseaseKanagaraj Subramanian, Navin Rauniyar, Mathieu Lavalleé-Adam, et al.
Pageof 13