Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice
Fragile X syndrome (FXS) is a common inherited form of mental retardation that is caused, in
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice
L Liao, SK Park, T Xu, P Vanderklish… - Proceedings of the …, 2008 - cir.nii.ac.jp
抄録< jats: p> Fragile X syndrome (FXS) is a common inherited form of mental retardation
that is caused, in the vast majority of cases, by the transcriptional silencing of a single …
that is caused, in the vast majority of cases, by the transcriptional silencing of a single …
Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice
L Liao, SK Park, T Xu… - Proceedings of the …, 2008 - pubmed.ncbi.nlm.nih.gov
Fragile X syndrome (FXS) is a common inherited form of mental retardation that is caused, in
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice
L Liao, SK Park, T Xu, P Vanderklish… - Proceedings of the …, 2008 - ui.adsabs.harvard.edu
Fragile X syndrome (FXS) is a common inherited form of mental retardation that is caused, in
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
[PDF][PDF] Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice
L Liao, SK Park, T Xu, P Vanderklish, JR Yates III - PNAS, 2008 - researchgate.net
Results Stable Isotope Labeling of Primary Cortical Neurons from Mice. The overall strategy
combining SILAC techniques for labeling of cellular proteins, isolation of synaptic fractions …
combining SILAC techniques for labeling of cellular proteins, isolation of synaptic fractions …
Quantitative Proteomic Analysis of Primary Neurons Reveals Diverse Changes in Synaptic Protein Content in fmr1 Knockout Mice
L Liao, SK Park, T Xu, P Vanderklish… - Proceedings of the …, 2008 - JSTOR
Fragile X syndrome (FXS) is a common inherited form of mental retardation that is caused, in
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
[HTML][HTML] Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice
L Liao, SK Park, T Xu, P Vanderklish… - Proceedings of the …, 2008 - ncbi.nlm.nih.gov
Fragile X syndrome (FXS) is a common inherited form of mental retardation that is caused, in
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice.
L Liao, SK Park, T Xu, P Vanderklish… - Proceedings of the …, 2008 - europepmc.org
Fragile X syndrome (FXS) is a common inherited form of mental retardation that is caused, in
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
Quantitative proteomic analysis of primary neurons reveals diverse changes in synaptic protein content in fmr1 knockout mice.
L Liao, SK Park, T Xu, P Vanderklish… - Proceedings of the …, 2008 - europepmc.org
Fragile X syndrome (FXS) is a common inherited form of mental retardation that is caused, in
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …
the vast majority of cases, by the transcriptional silencing of a single gene, fmr1. The …