IntroductionProtein O-linked mannose β1,2-N-acetylglucosaminyltransferase 1 (POMGNT1) is crucial for the elongation of O-mannosyl glycans. Mutations in POMGNT1 cause muscle-eye-brain (MEB) disease, one of the main features of which is anatomical aberrations in the brain. A growing number of studies have shown that defects in POMGNT1 affect neuronal migration and distribution, disrupt basement membranes, and misalign Cajal-Retzius cells. Several studies have examined the distribution and expression of POMGNT1 in the fetal or neonatal brain for neurodevelopmental studies in the mouse or human brain. However, little is known about the neuroanatomical distribution and expression of POMGNT1 in the normal adult mouse brain.MethodsWe analyzed the ...
The protein O-mannose beta-1,2-N-acetylglucosaminyltransferase 1 (POMGNT1) gene is one of 18 genes i...
Protein O-mannosylation is a post-translational modification essential for correct development of ma...
Mutations in the POMT1 gene, encoding a protein O-mannosyltransferase essential for alpha-dystroglyc...
Purpose: The POMGNT1 gene, encoding protein O-linked-mannose β-1,2-N-acetylglucosaminyltransferase 1...
AbstractMuscle-eye-brain disease (MEB) is an autosomal recessive disorder characterized by congenita...
Protein O-mannosylation is a post-translational modification essential for correct development of ma...
Mammalian O-mannosylation, although an uncommon type of protein modification, is essential for norma...
Muscle-eye-brain disease (MEB) is an autosomal recessive disorder characterized by congenital muscul...
Walker-Warburg syndrome (WWS) is the most severe of a group of congenital disorders that have in com...
O-Mannosylation is an important protein modification in brain. During the last years, a few mammalia...
O-mannosylation is an important protein modification in eukaryotes that is initiated by an evolution...
O-Mannosylation is an important protein modification in brain. During the last years, a few mammalia...
Walker-Warburg syndrome (WWS) is an autosomal recessive developmental disorder characterized by cong...
Resumen del póster presentado al XXXIX Congreso anual de la Sociedad Española de Bioquímica y Biolog...
15 p.Hypoglycosylation of α-dystroglycan (cx-DG) resulting from deficiency of protein O-mannosyltran...
The protein O-mannose beta-1,2-N-acetylglucosaminyltransferase 1 (POMGNT1) gene is one of 18 genes i...
Protein O-mannosylation is a post-translational modification essential for correct development of ma...
Mutations in the POMT1 gene, encoding a protein O-mannosyltransferase essential for alpha-dystroglyc...
Purpose: The POMGNT1 gene, encoding protein O-linked-mannose β-1,2-N-acetylglucosaminyltransferase 1...
AbstractMuscle-eye-brain disease (MEB) is an autosomal recessive disorder characterized by congenita...
Protein O-mannosylation is a post-translational modification essential for correct development of ma...
Mammalian O-mannosylation, although an uncommon type of protein modification, is essential for norma...
Muscle-eye-brain disease (MEB) is an autosomal recessive disorder characterized by congenital muscul...
Walker-Warburg syndrome (WWS) is the most severe of a group of congenital disorders that have in com...
O-Mannosylation is an important protein modification in brain. During the last years, a few mammalia...
O-mannosylation is an important protein modification in eukaryotes that is initiated by an evolution...
O-Mannosylation is an important protein modification in brain. During the last years, a few mammalia...
Walker-Warburg syndrome (WWS) is an autosomal recessive developmental disorder characterized by cong...
Resumen del póster presentado al XXXIX Congreso anual de la Sociedad Española de Bioquímica y Biolog...
15 p.Hypoglycosylation of α-dystroglycan (cx-DG) resulting from deficiency of protein O-mannosyltran...
The protein O-mannose beta-1,2-N-acetylglucosaminyltransferase 1 (POMGNT1) gene is one of 18 genes i...
Protein O-mannosylation is a post-translational modification essential for correct development of ma...
Mutations in the POMT1 gene, encoding a protein O-mannosyltransferase essential for alpha-dystroglyc...