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Human Mutation
|
November 6, 2007
Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation
Ellen Denayer, Annabel Parret, Magdalena Chmara, et al.
The Journal of Biological Chemistry
|
August 20, 2010
Structure and function of the hetero-oligomeric cysteine synthase complex in plants
Markus Wirtz, Hannah Birke, Corinna Heeg, et al.
Science (New York, N.Y.)
|
April 25, 2009
Catalytic core of a membrane-associated eukaryotic polyphosphate polymerase
Michael Hothorn, Heinz Neumann, Esther D Lenherr, et al.
Science (New York, N.Y.)
|
September 23, 2017
Crystal structure of the human lysosomal mTORC1 scaffold complex and its impact on signaling
Mariana E G de Araujo, Andreas Naschberger, Barbara G Fürnrohr, et al.
The Biochemical Journal
|
October 24, 2018
Structural basis for the bi-functionality of human oxaloacetate decarboxylase FAHD1
Alexander K H Weiss, Andreas Naschberger, Johannes R Loeffler, et al.
EMBO Reports
|
September 5, 2018
MacroH2A histone variants limit chromatin plasticity through two distinct mechanisms
Marek Kozlowski, David Corujo, Michael Hothorn, et al.
Journal of Proteome Research
|
February 15, 2018
Expression, Purification, and Biochemical Characterization of Human Afamin
Alessandra Altamirano, Andreas Naschberger, Barbara G Fürnrohr, et al.
The Journal of Cell Biology
|
October 11, 2017
LAMTOR/Ragulator is a negative regulator of Arl8b- and BORC-dependent late endosomal positioning
Przemyslaw A Filipek, Mariana E G de Araujo, Georg F Vogel, et al.
Cancer Cell
|
July 4, 2009
Proteasomal and genetic inactivation of the NF1 tumor suppressor in gliomagenesis
Lauren T McGillicuddy, Jody A Fromm, Pablo E Hollstein, et al.
Human Mutation
|
November 20, 2012
Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency
Martin H Berryer, Fadi F Hamdan, Laura L Klitten, et al.
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of 6
Search research articles
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Showing results (51-60 of 60) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 60 results.
Human Mutation
|
November 6, 2007
Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation
Ellen Denayer, Annabel Parret, Magdalena Chmara, et al.
The Journal of Biological Chemistry
|
August 20, 2010
Structure and function of the hetero-oligomeric cysteine synthase complex in plants
Markus Wirtz, Hannah Birke, Corinna Heeg, et al.
Science (New York, N.Y.)
|
April 25, 2009
Catalytic core of a membrane-associated eukaryotic polyphosphate polymerase
Michael Hothorn, Heinz Neumann, Esther D Lenherr, et al.
Science (New York, N.Y.)
|
September 23, 2017
Crystal structure of the human lysosomal mTORC1 scaffold complex and its impact on signaling
Mariana E G de Araujo, Andreas Naschberger, Barbara G Fürnrohr, et al.
The Biochemical Journal
|
October 24, 2018
Structural basis for the bi-functionality of human oxaloacetate decarboxylase FAHD1
Alexander K H Weiss, Andreas Naschberger, Johannes R Loeffler, et al.
EMBO Reports
|
September 5, 2018
MacroH2A histone variants limit chromatin plasticity through two distinct mechanisms
Marek Kozlowski, David Corujo, Michael Hothorn, et al.
Journal of Proteome Research
|
February 15, 2018
Expression, Purification, and Biochemical Characterization of Human Afamin
Alessandra Altamirano, Andreas Naschberger, Barbara G Fürnrohr, et al.
The Journal of Cell Biology
|
October 11, 2017
LAMTOR/Ragulator is a negative regulator of Arl8b- and BORC-dependent late endosomal positioning
Przemyslaw A Filipek, Mariana E G de Araujo, Georg F Vogel, et al.
Cancer Cell
|
July 4, 2009
Proteasomal and genetic inactivation of the NF1 tumor suppressor in gliomagenesis
Lauren T McGillicuddy, Jody A Fromm, Pablo E Hollstein, et al.
Human Mutation
|
November 20, 2012
Mutations in SYNGAP1 cause intellectual disability, autism, and a specific form of epilepsy by inducing haploinsufficiency
Martin H Berryer, Fadi F Hamdan, Laura L Klitten, et al.
Page
of 6