Pages that link to "Q24657241"
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The following pages link to Cerebellar development and disease (Q24657241):
Displayed 50 items.
- Joubert Syndrome and related disorders (Q21202880) (← links)
- Joubert syndrome Arl13b functions at ciliary membranes and stabilizes protein transport in Caenorhabditis elegans (Q24614362) (← links)
- Congenital basis of posterior fossa anomalies (Q26798344) (← links)
- Polyglutamine neurodegeneration: expanded glutamines enhance native functions (Q27026773) (← links)
- Inferior cerebellar hypoplasia resembling a Dandy-Walker-like malformation in purebred Eurasier dogs with familial non-progressive ataxia: a retrospective and prospective clinical cohort study (Q27315776) (← links)
- Hypoxic preconditioning differentially affects GABAergic and glutamatergic neuronal cells in the injured cerebellum of the neonatal rat (Q27319945) (← links)
- The c-Ski family member and transcriptional regulator Corl2/Skor2 promotes early differentiation of cerebellar Purkinje cells (Q28505535) (← links)
- Congenital hydrocephalus in genetically engineered mice (Q28506486) (← links)
- Semaphorin 4C and 4G are ligands of Plexin-B2 required in cerebellar development (Q28506606) (← links)
- Reciprocal actions of ATF5 and Shh in proliferation of cerebellar granule neuron progenitor cells (Q28507031) (← links)
- Nuclear factor one X regulates the development of multiple cellular populations in the postnatal cerebellum (Q28585345) (← links)
- ZFP423 coordinates Notch and bone morphogenetic protein signaling, selectively up-regulating Hes5 gene expression (Q28592502) (← links)
- FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation (Q28941244) (← links)
- Model organisms inform the search for the genes and developmental pathology underlying malformations of the human hindbrain (Q30479819) (← links)
- Head Tilting Elicited by Head Turning in Three Dogs with Hypoplastic Cerebellar Nodulus and Ventral Uvula (Q30829420) (← links)
- Looking at cerebellar malformations through text-mined interactomes of mice and humans (Q33515271) (← links)
- Novel approaches to studying the genetic basis of cerebellar development (Q33553583) (← links)
- DAMD to epigenetic silence (Q33591779) (← links)
- Prospective motion correction of high-resolution magnetic resonance imaging data in children (Q33602510) (← links)
- Human genetic disorders of axon guidance (Q33693788) (← links)
- Deletion of the Chd6 exon 12 affects motor coordination (Q33751230) (← links)
- The p53 inhibitor MDM2 facilitates Sonic Hedgehog-mediated tumorigenesis and influences cerebellar foliation (Q33855554) (← links)
- A Boolean probabilistic model of metabolic adaptation to oxygen in relation to iron homeostasis and oxidative stress (Q33871673) (← links)
- Lmx1a regulates fates and location of cells originating from the cerebellar rhombic lip and telencephalic cortical hem (Q33934835) (← links)
- The fetal cerebellum: development and common malformations (Q34033639) (← links)
- Nos2 inactivation promotes the development of medulloblastoma in Ptch1(+/-) mice by deregulation of Gap43-dependent granule cell precursor migration (Q34205933) (← links)
- Phenotypic and genetic analysis of the cerebellar mutant tmgc26, a new ENU-induced ROR-alpha allele (Q34283380) (← links)
- CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592 (Q34329675) (← links)
- Cellular commitment in the developing cerebellum (Q34460069) (← links)
- Gene delivery in mouse auditory brainstem and hindbrain using in utero electroporation (Q34464219) (← links)
- Foxc1 dependent mesenchymal signalling drives embryonic cerebellar growth (Q34802747) (← links)
- Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient mice (Q35200183) (← links)
- Sun1 deficiency leads to cerebellar ataxia in mice (Q35923450) (← links)
- Twitch-related and rhythmic activation of the developing cerebellar cortex. (Q36064799) (← links)
- The cerebellum as a target for estrogen action (Q36392945) (← links)
- The apical complex protein Pals1 is required to maintain cerebellar progenitor cells in a proliferative state (Q36497241) (← links)
- Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins (Q36585455) (← links)
- Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations (Q36661862) (← links)
- Common partner Smad-independent canonical bone morphogenetic protein signaling in the specification process of the anterior rhombic lip during cerebellum development (Q36826828) (← links)
- Besides Purkinje cells and granule neurons: an appraisal of the cell biology of the interneurons of the cerebellar cortex (Q37234482) (← links)
- The cerebellum, cerebellar disorders, and cerebellar research--two centuries of discoveries (Q37293902) (← links)
- SHH pathway and cerebellar development (Q37395399) (← links)
- Optimized immunohistochemical analysis of cerebellar purkinje cells using a specific biomarker, calbindin d28k. (Q37420116) (← links)
- The metamorphosis of the developing cerebellar microcircuit (Q37847374) (← links)
- Cellular and molecular basis of cerebellar development (Q38117366) (← links)
- Sonic hedgehog patterning during cerebellar development (Q38616153) (← links)
- WNT/β-catenin pathway activation in Myc immortalised cerebellar progenitor cells inhibits neuronal differentiation and generates tumours resembling medulloblastoma. (Q39289215) (← links)
- Identification of a novel ARL13B variant in a Joubert syndrome-affected patient with retinal impairment and obesity (Q39774231) (← links)
- MRI analysis of cerebellar and vestibular developmental phenotypes in Gbx2 conditional knockout mice (Q40816269) (← links)
- Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome (Q41928299) (← links)