Pages that link to "Q28386748"

The following pages link to Defects of Lipid Synthesis Are Linked to the Age-Dependent Demyelination Caused by Lamin B1 Overexpression (Q28386748):

Displaying 19 items.

• Lamin B1 protein is required for dendrite development in primary mouse cortical neurons (Q27305619) (← links)
• The Goat (Capra hircus) Mammary Gland Mitochondrial Proteome: A Study on the Effect of Weight Loss Using Blue-Native PAGE and Two-Dimensional Gel Electrophoresis (Q28551096) (← links)
• Increasing N-acetylaspartate in the Brain during Postnatal Myelination Does Not Cause the CNS Pathologies of Canavan Disease. (Q33753200) (← links)
• Lamin B1 levels modulate differentiation into neurons during embryonic corticogenesis (Q33885092) (← links)
• Myelinating glia differentiation is regulated by extracellular matrix elasticity (Q37266987) (← links)
• Transcriptional Fingerprint of Hypomyelination in Zfp191null and Shiverer (Mbpshi) Mice (Q37303724) (← links)
• Inherited and acquired disorders of myelin: The underlying myelin pathology (Q38805611) (← links)
• Epigenetic control of oligodendrocyte development: adding new players to old keepers (Q38866793) (← links)
• Lamin B1 mediated demyelination: Linking Lamins, Lipids and Leukodystrophies (Q39010727) (← links)
• Mechanobiology of Chromatin and the Nuclear Interior. (Q39121085) (← links)
• The NIH Undiagnosed Diseases Program and Network: Applications to modern medicine (Q40929545) (← links)
• Reduced sterol regulatory element-binding protein (SREBP) processing through site-1 protease (S1P) inhibition alters oligodendrocyte differentiation in vitro (Q47098397) (← links)
• Mice overexpressing lamin B1 in oligodendrocytes recapitulate the age-dependent motor signs, but not the early autonomic cardiovascular dysfunction of autosomal-dominant leukodystrophy (ADLD). (Q47652245) (← links)
• Conditional depletion of GSK3b protects oligodendrocytes from apoptosis and lessens demyelination in the acute cuprizone model. (Q54109848) (← links)
• Duplication and deletion upstream of in autosomal dominant adult-onset leukodystrophy (Q61450666) (← links)
• Autosomal Dominant Leukodystrophy: A Disease of the Nuclear Lamina (Q64069814) (← links)
• Glucose metabolism in the brain in LMNB1-related autosomal dominant leukodystrophy. (Q64982596) (← links)
• Dynamic Lamin B1-Gene Association During Oligodendrocyte Progenitor Differentiation (Q89534202) (← links)
• A high-content drug screening strategy to identify protein level modulators for genetic diseases: a proof-of-principle in Autosomal Dominant LeukoDystrophy (ADLD) (Q103737163) (← links)