Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
C Delépine, H Meziane, J Nectoux… - Human molecular …, 2016 - academic.oup.com
Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by
normal post-natal development followed by a sudden deceleration in brain growth with …
normal post-natal development followed by a sudden deceleration in brain growth with …
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.
C Delépine, H Meziane, J Nectoux, M Opitz… - Human Molecular …, 2015 - europepmc.org
Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by
normal post-natal development followed by a sudden deceleration in brain growth with …
normal post-natal development followed by a sudden deceleration in brain growth with …
[HTML][HTML] Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
C Delépine, H Meziane, J Nectoux, M Opitz… - Human Molecular …, 2016 - ncbi.nlm.nih.gov
Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by
normal post-natal development followed by a sudden deceleration in brain growth with …
normal post-natal development followed by a sudden deceleration in brain growth with …
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
C Delepine, H Meziane, J Nectoux, M Opitz… - Human Molecular …, 2016 - hal.science
Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by
normal post-natal development followed by a sudden deceleration in brain growth with …
normal post-natal development followed by a sudden deceleration in brain growth with …
[引用][C] Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
C Delépine, H Meziane, J Nectoux, M Opitz… - Human Molecular …, 2015 - cir.nii.ac.jp
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient
astrocytes | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 …
astrocytes | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 …
[PDF][PDF] Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
M Opitz, AB Smith10, C Ballatore10… - Human Molecular …, 2016 - researchgate.net
Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by
normal post-natal development followed by a sudden deceleration in brain growth with …
normal post-natal development followed by a sudden deceleration in brain growth with …
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.
C Delépine, H Meziane, J Nectoux… - Human Molecular …, 2016 - search.ebscohost.com
Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by
normal post-natal development followed by a sudden deceleration in brain growth with …
normal post-natal development followed by a sudden deceleration in brain growth with …
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes
C Delépine, H Meziane, J Nectoux… - Human molecular …, 2016 - pubmed.ncbi.nlm.nih.gov
Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by
normal post-natal development followed by a sudden deceleration in brain growth with …
normal post-natal development followed by a sudden deceleration in brain growth with …
Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.
C Delépine, H Meziane, J Nectoux, M Opitz… - Human Molecular …, 2015 - europepmc.org
Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder, characterized by
normal post-natal development followed by a sudden deceleration in brain growth with …
normal post-natal development followed by a sudden deceleration in brain growth with …