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The Journal of Clinical Investigation
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October 13, 2011
For Huda Zoghbi, collaboration is the key to unlocking the secrets of neurobiology. Interview by Kathryn Claiborn
Huda Zoghbi
Science (New York, N.Y.)
|
February 24, 2022
C. Thomas Caskey (1938-2022)
Andrea Ballabio, Huda Zoghbi
Biotechniques
|
October 1, 2013
Scientists. Curiosity and observation
Huda Zoghbi, Kristie Nybo
Current Opinion in Neurobiology
|
March 6, 2022
Editorial overview: Neurobiology of disease
Bart De Strooper, Huda Zoghbi
Science Translational Medicine
|
September 21, 2012
Childhood disorders of the synapse: challenges and opportunities
Virginia Hughes, Morgan Sheng, Huda Zoghbi
Gastroenterology
|
July 10, 2002
Prenylcysteine carboxylmethyltransferase is essential for the earliest stages of liver development in mice
Xi Lin, Joonil Jung, Dongcheul Kang, et al.
Molecular Cell
|
July 9, 2016
A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos
Irina Stancheva, Anne L Collins, Ingatia B Van den Veyver, et al.
Molecular Cell
|
October 11, 2003
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos
Irina Stancheva, Anne L Collins, Ingatia B Van den Veyver, et al.
Frontiers in Molecular Neuroscience
|
August 8, 2022
The Transcription Factor Pou3f1 Sheds Light on the Development and Molecular Diversity of Glutamatergic Cerebellar Nuclear Neurons in the Mouse
Joshua Po Han Wu, Joanna Yeung, Maryam Rahimi-Balaei, et al.
Neuron
|
August 6, 2002
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
Mona Shahbazian, Juan Young, Lisa Yuva-Paylor, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
The Journal of Clinical Investigation
|
October 13, 2011
For Huda Zoghbi, collaboration is the key to unlocking the secrets of neurobiology. Interview by Kathryn Claiborn
Huda Zoghbi
Science (New York, N.Y.)
|
February 24, 2022
C. Thomas Caskey (1938-2022)
Andrea Ballabio, Huda Zoghbi
Biotechniques
|
October 1, 2013
Scientists. Curiosity and observation
Huda Zoghbi, Kristie Nybo
Current Opinion in Neurobiology
|
March 6, 2022
Editorial overview: Neurobiology of disease
Bart De Strooper, Huda Zoghbi
Science Translational Medicine
|
September 21, 2012
Childhood disorders of the synapse: challenges and opportunities
Virginia Hughes, Morgan Sheng, Huda Zoghbi
Gastroenterology
|
July 10, 2002
Prenylcysteine carboxylmethyltransferase is essential for the earliest stages of liver development in mice
Xi Lin, Joonil Jung, Dongcheul Kang, et al.
Molecular Cell
|
July 9, 2016
A Mutant Form of MeCP2 Protein Associated with Human Rett Syndrome Cannot Be Displaced from Methylated DNA by Notch in Xenopus Embryos
Irina Stancheva, Anne L Collins, Ingatia B Van den Veyver, et al.
Molecular Cell
|
October 11, 2003
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos
Irina Stancheva, Anne L Collins, Ingatia B Van den Veyver, et al.
Frontiers in Molecular Neuroscience
|
August 8, 2022
The Transcription Factor Pou3f1 Sheds Light on the Development and Molecular Diversity of Glutamatergic Cerebellar Nuclear Neurons in the Mouse
Joshua Po Han Wu, Joanna Yeung, Maryam Rahimi-Balaei, et al.
Neuron
|
August 6, 2002
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
Mona Shahbazian, Juan Young, Lisa Yuva-Paylor, et al.
Page
of 2