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Sarn Jiralerspong

Showing results (1-10 of 5) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 10, 2010
Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compoundsRui Zhang, Li Chen, Sarn Jiralerspong, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2008
The crystal structure and dimerization interface of GADD45gammaJoseph D Schrag, Sarn Jiralerspong, Myriam Banville, et al.
Human Mutation|October 13, 2011
Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3Brandon Itzkovitz, Sarn Jiralerspong, Graeme Nimmo, et al.
BMC Medical Genetics|August 17, 2012
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian populationSebastien Levesque, Charles Morin, Simon-Pierre Guay, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

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Pageof 1
Proceedings of the National Academy of Sciences of the United States of America|March 10, 2010
Recovery of PEX1-Gly843Asp peroxisome dysfunction by small-molecule compoundsRui Zhang, Li Chen, Sarn Jiralerspong, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2008
The crystal structure and dimerization interface of GADD45gammaJoseph D Schrag, Sarn Jiralerspong, Myriam Banville, et al.
Human Mutation|October 13, 2011
Functional characterization of novel mutations in GNPAT and AGPS, causing rhizomelic chondrodysplasia punctata (RCDP) types 2 and 3Brandon Itzkovitz, Sarn Jiralerspong, Graeme Nimmo, et al.
BMC Medical Genetics|August 17, 2012
A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian populationSebastien Levesque, Charles Morin, Simon-Pierre Guay, et al.
Neuron|January 29, 2013
Using whole-exome sequencing to identify inherited causes of autismTimothy W Yu, Maria H Chahrour, Michael E Coulter, et al.
Pageof 1