Mutations disrupting primary cilia cause retinal, renal, and cerebellar defects, and misregulated Sonic hedgehog signaling. A new mouse mutant in the TTBK2 kinase fails to make cilia, and shows neural tube and Sonic hedgehog signaling defects. Ciliary targeting mutations in human TTBK2 are linked to spinocerebellar ataxia, suggesting cilia protect from neurodegeneration
SummaryNephronophthisis (NPHP), Joubert (JBTS), and Meckel-Gruber (MKS) syndromes are autosomal-rece...
Essential to development, primary cilia are microtubule-based cellular organelles that protrude from...
SummaryVertebrate hedgehog signaling is coordinated by the differential localization of the receptor...
Mutations disrupting primary cilia cause retinal, renal, and cerebellar defects, and misregulated So...
Spinocerebellar ataxia type 11 (SCA11) is a rare, dominantly inherited human ataxia characterized by...
Spinocerebellar ataxia type 11 (SCA11) is a rare, dominantly inherited human ataxia characterized by...
SummaryThe primary cilium has critical roles in human development and disease, but the mechanisms th...
AbstractOrganizing centers in the developing brain provide an assortment of instructive patterning c...
Recent recognition of the key role of primary cilia in orchestrating human development and of the di...
Primary cilia defects result in a group of related pleiotropic malformation syndromes known as cilio...
AbstractCilia are dynamic organelles that are essential for a vast array of developmental patterning...
Cilia are key subcellular organelles for the coordination of signaling pathways. The importance of c...
The Niemann-Pick type C1 (NPC1) disease is a neurodegenerative lysosomal storage disorder due to mut...
Previously, we showed that cholinergic interneurons of the dorsal striatum lose cilia in mice harbor...
SummaryRecent findings indicate that mammalian Sonic hedgehog (Shh) signal transduction occurs withi...
SummaryNephronophthisis (NPHP), Joubert (JBTS), and Meckel-Gruber (MKS) syndromes are autosomal-rece...
Essential to development, primary cilia are microtubule-based cellular organelles that protrude from...
SummaryVertebrate hedgehog signaling is coordinated by the differential localization of the receptor...
Mutations disrupting primary cilia cause retinal, renal, and cerebellar defects, and misregulated So...
Spinocerebellar ataxia type 11 (SCA11) is a rare, dominantly inherited human ataxia characterized by...
Spinocerebellar ataxia type 11 (SCA11) is a rare, dominantly inherited human ataxia characterized by...
SummaryThe primary cilium has critical roles in human development and disease, but the mechanisms th...
AbstractOrganizing centers in the developing brain provide an assortment of instructive patterning c...
Recent recognition of the key role of primary cilia in orchestrating human development and of the di...
Primary cilia defects result in a group of related pleiotropic malformation syndromes known as cilio...
AbstractCilia are dynamic organelles that are essential for a vast array of developmental patterning...
Cilia are key subcellular organelles for the coordination of signaling pathways. The importance of c...
The Niemann-Pick type C1 (NPC1) disease is a neurodegenerative lysosomal storage disorder due to mut...
Previously, we showed that cholinergic interneurons of the dorsal striatum lose cilia in mice harbor...
SummaryRecent findings indicate that mammalian Sonic hedgehog (Shh) signal transduction occurs withi...
SummaryNephronophthisis (NPHP), Joubert (JBTS), and Meckel-Gruber (MKS) syndromes are autosomal-rece...
Essential to development, primary cilia are microtubule-based cellular organelles that protrude from...
SummaryVertebrate hedgehog signaling is coordinated by the differential localization of the receptor...