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Cells
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November 26, 2022
Mutation of Tyrosine Sites in the Human Alpha-Synuclein Gene Induces Neurotoxicity in Transgenic Mice with Soluble Alpha-Synuclein Oligomer Formation
Louise Berkhoudt Lassen, Maj Schneider Thomsen, Elisa Basso, et al.
Molecular and Cellular Biology
|
September 5, 2013
SORLA-dependent and -independent functions for PACS1 in control of amyloidogenic processes
Tilman Burgert, Vanessa Schmidt, Safak Caglayan, et al.
Journal of Virology
|
February 5, 2010
Antisense transcription in gammaretroviruses as a mechanism of insertional activation of host genes
Mads Heilskov Rasmussen, Borja Ballarín-González, Jinghua Liu, et al.
Cell Stress & Chaperones
|
April 16, 2010
Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice
Jane H Christensen, Marit N Nielsen, Jakob Hansen, et al.
Molecular Pharmacology
|
July 12, 2007
A mouse model for studying the interaction of bisdioxopiperazines with topoisomerase IIalpha in vivo
Morten Grauslund, Annemette Vinding Thougaard, Annette Füchtbauer, et al.
Biological Chemistry
|
August 10, 2011
Septin9 is involved in septin filament formation and cellular stability
Annette Füchtbauer, Louise B Lassen, Astrid B Jensen, et al.
International Journal of Molecular Sciences
|
May 28, 2013
Loss of vps54 function leads to vesicle traffic impairment, protein mis-sorting and embryonic lethality
Páll Karlsson, Aida Droce, Jakob M Moser, et al.
Stem Cells and Development
|
June 11, 2009
Identification of distinct topographical surface microstructures favoring either undifferentiated expansion or differentiation of murine embryonic stem cells
Lotte D'Andrea Markert, Jette Lovmand, Morten Foss, et al.
Science Translational Medicine
|
February 14, 2014
Lysosomal sorting of amyloid-β by the SORLA receptor is impaired by a familial Alzheimer's disease mutation
Safak Caglayan, Shizuka Takagi-Niidome, Fan Liao, et al.
Scientific Reports
|
May 13, 2016
C4.4A gene ablation is compatible with normal epidermal development and causes modest overt phenotypes
Mette Camilla Kriegbaum, Benedikte Jacobsen, Annette Füchtbauer, et al.
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of 3
Search research articles
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Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Cells
|
November 26, 2022
Mutation of Tyrosine Sites in the Human Alpha-Synuclein Gene Induces Neurotoxicity in Transgenic Mice with Soluble Alpha-Synuclein Oligomer Formation
Louise Berkhoudt Lassen, Maj Schneider Thomsen, Elisa Basso, et al.
Molecular and Cellular Biology
|
September 5, 2013
SORLA-dependent and -independent functions for PACS1 in control of amyloidogenic processes
Tilman Burgert, Vanessa Schmidt, Safak Caglayan, et al.
Journal of Virology
|
February 5, 2010
Antisense transcription in gammaretroviruses as a mechanism of insertional activation of host genes
Mads Heilskov Rasmussen, Borja Ballarín-González, Jinghua Liu, et al.
Cell Stress & Chaperones
|
April 16, 2010
Inactivation of the hereditary spastic paraplegia-associated Hspd1 gene encoding the Hsp60 chaperone results in early embryonic lethality in mice
Jane H Christensen, Marit N Nielsen, Jakob Hansen, et al.
Molecular Pharmacology
|
July 12, 2007
A mouse model for studying the interaction of bisdioxopiperazines with topoisomerase IIalpha in vivo
Morten Grauslund, Annemette Vinding Thougaard, Annette Füchtbauer, et al.
Biological Chemistry
|
August 10, 2011
Septin9 is involved in septin filament formation and cellular stability
Annette Füchtbauer, Louise B Lassen, Astrid B Jensen, et al.
International Journal of Molecular Sciences
|
May 28, 2013
Loss of vps54 function leads to vesicle traffic impairment, protein mis-sorting and embryonic lethality
Páll Karlsson, Aida Droce, Jakob M Moser, et al.
Stem Cells and Development
|
June 11, 2009
Identification of distinct topographical surface microstructures favoring either undifferentiated expansion or differentiation of murine embryonic stem cells
Lotte D'Andrea Markert, Jette Lovmand, Morten Foss, et al.
Science Translational Medicine
|
February 14, 2014
Lysosomal sorting of amyloid-β by the SORLA receptor is impaired by a familial Alzheimer's disease mutation
Safak Caglayan, Shizuka Takagi-Niidome, Fan Liao, et al.
Scientific Reports
|
May 13, 2016
C4.4A gene ablation is compatible with normal epidermal development and causes modest overt phenotypes
Mette Camilla Kriegbaum, Benedikte Jacobsen, Annette Füchtbauer, et al.
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of 3