<p>Western blots showing the phosphorylation of PDK1 at Ser-241 in brain extracts of WT and KO mice, both female and male mice. After normalization of the phospho-PDK1 signals to β-actin, statistical analysis revealed no significant difference between the KO and WT extracts.</p
According to the Research Domain Criteria (RDoC), phenotypic differences among disorders may be expl...
According to the Research Domain Criteria (RDoC), phenotypic differences among disorders may be expl...
Fragile X syndrome (FXS) is an X-chromosome-linked dominant genetic disorder that causes a variable ...
<p>Panels A-C show Western blots of brain extracts from female mice for dynamin-1 (A), phosphorylati...
<p>Mouse sex for each lane is indicated at the bottom on panel C. Western blots used a mixture of an...
PDK1 functions as a master kinase, phosphorylating and activating PKB/Akt, S6K and RSK. To learn mor...
<p>(A) Representative Western blots of forebrain homogenate from control and Ptpn11<sup>D61Y</sup> m...
<p>Immunoblots for total and/or phosphorylated AKT, 4E-BP1, 4E-BP2, and S6K1 are presented for both ...
<p>(<b>A</b>) Western blot analysis of whole brain protein extracts from adult female and male wild-...
Baba et al. analyzed the transcriptomes from quadriceps type IIB fibers of untreated, gonadectomized...
<p>(<b>a</b>) Total DARPP32 from striatal homogenates of 3-month-old wt and RGS9-deficient mice was ...
PDK1 activates a group of kinases, including. protein kinase B (PKB)/Akt, p70 ribosomal S6 kinase (S...
<div><p>Isoaspartate (isoAsp) formation is a major source of protein damage that is kept in check by...
<p>To substantiate the NIA data we did mass spectometry to identify modified residues especially loo...
Fragile X syndrome (FXS) is an X-chromosome-linked dominant genetic disorder that causes a variable ...
According to the Research Domain Criteria (RDoC), phenotypic differences among disorders may be expl...
According to the Research Domain Criteria (RDoC), phenotypic differences among disorders may be expl...
Fragile X syndrome (FXS) is an X-chromosome-linked dominant genetic disorder that causes a variable ...
<p>Panels A-C show Western blots of brain extracts from female mice for dynamin-1 (A), phosphorylati...
<p>Mouse sex for each lane is indicated at the bottom on panel C. Western blots used a mixture of an...
PDK1 functions as a master kinase, phosphorylating and activating PKB/Akt, S6K and RSK. To learn mor...
<p>(A) Representative Western blots of forebrain homogenate from control and Ptpn11<sup>D61Y</sup> m...
<p>Immunoblots for total and/or phosphorylated AKT, 4E-BP1, 4E-BP2, and S6K1 are presented for both ...
<p>(<b>A</b>) Western blot analysis of whole brain protein extracts from adult female and male wild-...
Baba et al. analyzed the transcriptomes from quadriceps type IIB fibers of untreated, gonadectomized...
<p>(<b>a</b>) Total DARPP32 from striatal homogenates of 3-month-old wt and RGS9-deficient mice was ...
PDK1 activates a group of kinases, including. protein kinase B (PKB)/Akt, p70 ribosomal S6 kinase (S...
<div><p>Isoaspartate (isoAsp) formation is a major source of protein damage that is kept in check by...
<p>To substantiate the NIA data we did mass spectometry to identify modified residues especially loo...
Fragile X syndrome (FXS) is an X-chromosome-linked dominant genetic disorder that causes a variable ...
According to the Research Domain Criteria (RDoC), phenotypic differences among disorders may be expl...
According to the Research Domain Criteria (RDoC), phenotypic differences among disorders may be expl...
Fragile X syndrome (FXS) is an X-chromosome-linked dominant genetic disorder that causes a variable ...