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May 11, 2010
3DM: systematic analysis of heterogeneous superfamily data to discover protein functionalities
Remko K Kuipers, Henk-Jan Joosten, Willem J H van Berkel, et al.
Physiological Genomics
|
August 13, 2009
Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein
Hee Keun Lee, Mee Hyun Song, Myengmo Kang, et al.
Plos One
|
May 26, 2017
CorNet: Assigning function to networks of co-evolving residues by automated literature mining
Tom van den Bergh, Giorgio Tamo, Alberto Nobili, et al.
American Journal of Human Genetics
|
October 13, 2006
Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs
Jan A M Smeitink, Orly Elpeleg, Hana Antonicka, et al.
Disease Models & Mechanisms
|
August 3, 2016
The role of the dopamine D1 receptor in social cognition: studies using a novel genetic rat model
Judith R Homberg, Jocelien D A Olivier, Marie VandenBroeke, et al.
European Journal of Human Genetics : EJHG
|
August 21, 2014
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine
Se-Kyung Oh, Jeong-In Baek, Karl M Weigand, et al.
Proteins
|
March 31, 2015
Key challenges for the creation and maintenance of specialist protein resources
Gemma L Holliday, Amos Bairoch, Pantelis G Bagos, et al.
Structure (London, England : 1993)
|
October 18, 2011
A new generation of crystallographic validation tools for the protein data bank
Randy J Read, Paul D Adams, W Bryan Arendall, et al.
Journal of Applied Crystallography
|
April 6, 2012
PDB_REDO: automated re-refinement of X-ray structure models in the PDB
Robbie P Joosten, Jean Salzemann, Vincent Bloch, et al.
Nucleic Acids Research
|
May 14, 2010
The EMBRACE web service collection
Steve Pettifer, Jon Ison, Matús Kalas, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 108) with videos related to
Sort By:
Page
of 11
Proteins
|
May 11, 2010
3DM: systematic analysis of heterogeneous superfamily data to discover protein functionalities
Remko K Kuipers, Henk-Jan Joosten, Willem J H van Berkel, et al.
Physiological Genomics
|
August 13, 2009
Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein
Hee Keun Lee, Mee Hyun Song, Myengmo Kang, et al.
Plos One
|
May 26, 2017
CorNet: Assigning function to networks of co-evolving residues by automated literature mining
Tom van den Bergh, Giorgio Tamo, Alberto Nobili, et al.
American Journal of Human Genetics
|
October 13, 2006
Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs
Jan A M Smeitink, Orly Elpeleg, Hana Antonicka, et al.
Disease Models & Mechanisms
|
August 3, 2016
The role of the dopamine D1 receptor in social cognition: studies using a novel genetic rat model
Judith R Homberg, Jocelien D A Olivier, Marie VandenBroeke, et al.
European Journal of Human Genetics : EJHG
|
August 21, 2014
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine
Se-Kyung Oh, Jeong-In Baek, Karl M Weigand, et al.
Proteins
|
March 31, 2015
Key challenges for the creation and maintenance of specialist protein resources
Gemma L Holliday, Amos Bairoch, Pantelis G Bagos, et al.
Structure (London, England : 1993)
|
October 18, 2011
A new generation of crystallographic validation tools for the protein data bank
Randy J Read, Paul D Adams, W Bryan Arendall, et al.
Journal of Applied Crystallography
|
April 6, 2012
PDB_REDO: automated re-refinement of X-ray structure models in the PDB
Robbie P Joosten, Jean Salzemann, Vincent Bloch, et al.
Nucleic Acids Research
|
May 14, 2010
The EMBRACE web service collection
Steve Pettifer, Jon Ison, Matús Kalas, et al.
Page
of 11