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Human Molecular Genetics|September 22, 2010
Allele-specific DNA methylation: beyond imprintingBenjamin Tycko
Human Molecular Genetics|October 14, 2010
Identification of genes specific to mouse primordial germ cells through dynamic global gene expressionDavood Sabour, Marcos J Araúzo-Bravo, Karin Hübner, et al.
Human Molecular Genetics|September 23, 2010
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in miceAnne-Cécile Durieux, Alban Vignaud, Bernard Prudhon, et al.
Human Molecular Genetics|September 23, 2010
Sequestration of chaperones and proteasome into Lafora bodies and proteasomal dysfunction induced by Lafora disease-associated mutations of malinSudheendra N R Rao, Ranjan Maity, Jaiprakash Sharma, et al.
Human Molecular Genetics|February 9, 2011
The COPI vesicle complex binds and moves with survival motor neuron within axonsCyril Jayakumar Peter, Matthew Evans, Venugopal Thayanithy, et al.
Human Molecular Genetics|March 1, 2011
Mutant huntingtin causes defective actin remodeling during stress: defining a new role for transglutaminase 2 in neurodegenerative diseaseLise Munsie, Nicholas Caron, Randy Singh Atwal, et al.
Human Molecular Genetics|March 1, 2011
Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplicationsPengfei Liu, Ayelet Erez, Sandesh C Sreenath Nagamani, et al.
Human Molecular Genetics|February 8, 2011
The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathiesVandana Gupta, Genri Kawahara, Stacey R Gundry, et al.
Human Molecular Genetics|April 21, 2011
Molecular and cellular characterization of novel {alpha}-mannosidosis mutationsElina Kuokkanen, Hilde Monica Frostad Riise Stensland, Wesley Smith, et al.
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