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Showing results (961-970 of 978) with videos related to

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Nature Biotechnology|February 24, 2009
A conditional transposon-based insertional mutagenesis screen for genes associated with mouse hepatocellular carcinomaVincent W Keng, Augusto Villanueva, Derek Y Chiang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2017
Transposon insertional mutagenesis in mice identifies human breast cancer susceptibility genes and signatures for stratificationLiming Chen, Piroon Jenjaroenpun, Andrea Mun Ching Pillai, et al.
Cancer Research|October 22, 2009
Whole-body sleeping beauty mutagenesis can cause penetrant leukemia/lymphoma and rare high-grade glioma without associated embryonic lethalityLara S Collier, David J Adams, Christopher S Hackett, et al.
Neuron|November 1, 1996
Familial Alzheimer's disease-linked presenilin 1 variants elevate Abeta1-42/1-40 ratio in vitro and in vivoD R Borchelt, G Thinakaran, C B Eckman, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2012
Sleeping Beauty mutagenesis reveals cooperating mutations and pathways in pancreatic adenocarcinomaKaren M Mann, Jerrold M Ward, Christopher Chin Kuan Yew, et al.
Nature Genetics|August 19, 2003
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)Wei Li, Qing Zhang, Naoki Oiso, et al.
Nature Genetics|January 28, 2003
Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6Qing Zhang, Baohui Zhao, Wei Li, et al.
Nature|September 4, 2009
Response and resistance to MEK inhibition in leukaemias initiated by hyperactive RasJennifer O Lauchle, Doris Kim, Doan T Le, et al.
Plos One|April 16, 2011
Dopaminergic neuronal loss, reduced neurite complexity and autophagic abnormalities in transgenic mice expressing G2019S mutant LRRK2David Ramonet, João Paulo L Daher, Brian M Lin, et al.
Nature Medicine|April 4, 2006
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1Marion G Ott, Manfred Schmidt, Kerstin Schwarzwaelder, et al.
Pageof 98

Showing results (961-970 of 978) with videos related to

Sort By:
Pageof 98
Nature Biotechnology|February 24, 2009
A conditional transposon-based insertional mutagenesis screen for genes associated with mouse hepatocellular carcinomaVincent W Keng, Augusto Villanueva, Derek Y Chiang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2017
Transposon insertional mutagenesis in mice identifies human breast cancer susceptibility genes and signatures for stratificationLiming Chen, Piroon Jenjaroenpun, Andrea Mun Ching Pillai, et al.
Cancer Research|October 22, 2009
Whole-body sleeping beauty mutagenesis can cause penetrant leukemia/lymphoma and rare high-grade glioma without associated embryonic lethalityLara S Collier, David J Adams, Christopher S Hackett, et al.
Neuron|November 1, 1996
Familial Alzheimer's disease-linked presenilin 1 variants elevate Abeta1-42/1-40 ratio in vitro and in vivoD R Borchelt, G Thinakaran, C B Eckman, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 17, 2012
Sleeping Beauty mutagenesis reveals cooperating mutations and pathways in pancreatic adenocarcinomaKaren M Mann, Jerrold M Ward, Christopher Chin Kuan Yew, et al.
Nature Genetics|August 19, 2003
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)Wei Li, Qing Zhang, Naoki Oiso, et al.
Nature Genetics|January 28, 2003
Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6Qing Zhang, Baohui Zhao, Wei Li, et al.
Nature|September 4, 2009
Response and resistance to MEK inhibition in leukaemias initiated by hyperactive RasJennifer O Lauchle, Doris Kim, Doan T Le, et al.
Plos One|April 16, 2011
Dopaminergic neuronal loss, reduced neurite complexity and autophagic abnormalities in transgenic mice expressing G2019S mutant LRRK2David Ramonet, João Paulo L Daher, Brian M Lin, et al.
Nature Medicine|April 4, 2006
Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1Marion G Ott, Manfred Schmidt, Kerstin Schwarzwaelder, et al.
Pageof 98