Published in Front Cell Neurosci on January 12, 2015
De novo point mutations in patients diagnosed with ataxic cerebral palsy. Brain (2015) 0.98
Ex vivo imaging of active caspase 3 by a FRET-based molecular probe demonstrates the cellular dynamics and localization of the protease in cerebellar granule cells and its regulation by the apoptosis-inhibiting protein survivin. Mol Neurodegener (2016) 0.82
Hepatitis B and C virus-induced hepatitis: Apoptosis, autophagy, and unfolded protein response. World J Gastroenterol (2015) 0.81
Cell cycle analysis in the rat external granular layer evaluated by several bromodeoxyuridine immunoperoxidase staining protocols. Histochem Cell Biol (2017) 0.81
DNA Methylation Profiling at Single-Base Resolution Reveals Gestational Folic Acid Supplementation Influences the Epigenome of Mouse Offspring Cerebellum. Front Neurosci (2016) 0.77
Low Density Lipoprotein Receptor Related Proteins as Regulators of Neural Stem and Progenitor Cell Function. Stem Cells Int (2016) 0.77
Polycomb Ezh2 controls the fate of GABAergic neurons in the embryonic cerebellum. Development (2016) 0.76
Alterations of Cell Proliferation and Apoptosis in the Hypoplastic Reeler Cerebellum. Front Cell Neurosci (2016) 0.75
The role of the ubiquitin proteasome system in cerebellar development and medulloblastoma. Mol Brain (2015) 0.75
Epigenetics and Signaling Pathways in Glaucoma. Biomed Res Int (2017) 0.75
Overexpression of Human SOD1 Leads to Discrete Defects in the Cerebellar Architecture in the Mouse. Front Neuroanat (2017) 0.75
Effects of Transforming Growth Factor Beta 1 in Cerebellar Development: Role in Synapse Formation. Front Cell Neurosci (2016) 0.75
Radiation induces progenitor cell death, microglia activation, and blood-brain barrier damage in the juvenile rat cerebellum. Sci Rep (2017) 0.75
Notch signaling: cell fate control and signal integration in development. Science (1999) 28.83
Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice. Nature (2006) 24.39
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet (1999) 22.84
Loss of autophagy in the central nervous system causes neurodegeneration in mice. Nature (2006) 21.40
Origins and Mechanisms of miRNAs and siRNAs. Cell (2009) 20.77
Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice. Cell (2007) 14.63
Eaten alive: a history of macroautophagy. Nat Cell Biol (2010) 8.83
Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog. Neuron (1999) 7.80
The molecular machinery of autophagy: unanswered questions. J Cell Sci (2005) 6.67
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology (2001) 6.55
Cell death during development of the nervous system. Annu Rev Neurosci (1991) 6.37
Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration. Nature (2006) 5.07
Bmi1 is essential for cerebellar development and is overexpressed in human medulloblastomas. Nature (2004) 4.82
Programmed cell death and the control of cell survival: lessons from the nervous system. Science (1993) 4.63
Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain. J Comp Neurol (2009) 4.55
Cerebellar neurodegeneration in the absence of microRNAs. J Exp Med (2007) 4.48
ER chaperones in mammalian development and human diseases. FEBS Lett (2007) 4.40
Functional screening identifies miRNAs inducing cardiac regeneration. Nature (2012) 4.39
The role of autophagy in mammalian development: cell makeover rather than cell death. Dev Cell (2008) 4.25
Math1 is essential for genesis of cerebellar granule neurons. Nature (1997) 4.16
5-hmC-mediated epigenetic dynamics during postnatal neurodevelopment and aging. Nat Neurosci (2011) 4.15
Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS). Brain (2005) 3.99
Essential role for autophagy protein Atg7 in the maintenance of axonal homeostasis and the prevention of axonal degeneration. Proc Natl Acad Sci U S A (2007) 3.92
The bHLH protein PTF1-p48 is essential for the formation of the exocrine and the correct spatial organization of the endocrine pancreas. Genes Dev (1998) 3.42
Microglia promote the death of developing Purkinje cells. Neuron (2004) 3.42
A decrease of reelin expression as a putative vulnerability factor in schizophrenia. Proc Natl Acad Sci U S A (1998) 3.33
Mechanisms of neural patterning and specification in the developing cerebellum. Annu Rev Neurosci (1995) 3.26
An autoradiographic analysis of histogenesis in the mouse cerebellum. Exp Neurol (1961) 3.22
Induction of apoptosis in cerebellar granule neurons by low potassium: inhibition of death by insulin-like growth factor I and cAMP. Proc Natl Acad Sci U S A (1993) 3.18
Math1 is expressed in temporally discrete pools of cerebellar rhombic-lip neural progenitors. Neuron (2005) 3.17
MicroRNA expression in the adult mouse central nervous system. RNA (2008) 3.12
Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene. Nature (1997) 3.10
Chaperone-mediated autophagy in aging and disease. Curr Top Dev Biol (2006) 3.10
Genetic ablation reveals that the roof plate is essential for dorsal interneuron specification. Nature (2000) 3.06
Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA. Nucleic Acids Res (1992) 2.99
Math1 expression redefines the rhombic lip derivatives and reveals novel lineages within the brainstem and cerebellum. Neuron (2005) 2.93
GRP78/BiP is required for cell proliferation and protecting the inner cell mass from apoptosis during early mouse embryonic development. Mol Cell Biol (2006) 2.78
Sonic hedgehog signaling is required for expansion of granule neuron precursors and patterning of the mouse cerebellum. Dev Biol (2004) 2.77
Cerebellum implicated in sensory acquisition and discrimination rather than motor control. Science (1996) 2.71
The cells and molecules that make a cerebellum. Trends Neurosci (1998) 2.69
Ptf1a, a bHLH transcriptional gene, defines GABAergic neuronal fates in cerebellum. Neuron (2005) 2.66
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nat Genet (1995) 2.63
Transcription factors in glutamatergic neurogenesis: conserved programs in neocortex, cerebellum, and adult hippocampus. Neurosci Res (2006) 2.50
Genetic regulation of cerebellar development. Nat Rev Neurosci (2001) 2.47
Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy. Nat Genet (2005) 2.38
Neuropathological findings in autism. Brain (2004) 2.34
Consensus paper: pathological role of the cerebellum in autism. Cerebellum (2012) 2.32
Sequential phases of cortical specification involve Neurogenin-dependent and -independent pathways. EMBO J (2004) 2.30
Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. Proc Natl Acad Sci U S A (2007) 2.27
The midbrain-hindbrain phenotype of Wnt-1-/Wnt-1- mice results from stepwise deletion of engrailed-expressing cells by 9.5 days postcoitum. Cell (1992) 2.27
The developmental neurobiology of autism spectrum disorder. J Neurosci (2006) 2.21
Morphology, molecular codes, and circuitry produce the three-dimensional complexity of the cerebellum. Annu Rev Cell Dev Biol (2007) 2.19
Roles of Pax-genes in developing and adult brain as suggested by expression patterns. J Neurosci (1994) 2.19
PTF1 is an organ-specific and Notch-independent basic helix-loop-helix complex containing the mammalian Suppressor of Hairless (RBP-J) or its paralogue, RBP-L. Mol Cell Biol (2006) 2.13
Hypoplasia of cerebellar vermal lobules VI and VII in autism. N Engl J Med (1988) 2.12
Cognition, emotion and the cerebellum. Brain (2006) 2.10
Intracellular Ca2+ fluctuations modulate the rate of neuronal migration. Neuron (1996) 2.07
Neural plate patterning: upstream and downstream of the isthmic organizer. Nat Rev Neurosci (2001) 2.06
The gene disrupted in Marinesco-Sjögren syndrome encodes SIL1, an HSPA5 cochaperone. Nat Genet (2005) 2.05
Spatial pattern of sonic hedgehog signaling through Gli genes during cerebellum development. Development (2004) 2.04
Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP. Nat Genet (2005) 1.98
A mouse serine/threonine kinase homologous to C. elegans UNC51 functions in parallel fiber formation of cerebellar granule neurons. Neuron (1999) 1.95
Engrailed-1 as a target of the Wnt-1 signalling pathway in vertebrate midbrain development. Nature (1996) 1.91
Sonic hedgehog regulates Gli activator and repressor functions with spatial and temporal precision in the mid/hindbrain region. Development (2006) 1.89
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome. Nat Genet (2004) 1.88
Histogenesis of cortical layers in human cerebellum, particularly the lamina dissecans. J Comp Neurol (1970) 1.85
Epigenetic control. J Cell Physiol (2009) 1.85
T-brain-1: a homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex. Neuron (1995) 1.84
Role of Pax6 in development of the cerebellar system. Development (1999) 1.81
The translation of translational control by FMRP: therapeutic targets for FXS. Nat Neurosci (2013) 1.81
The role of free radicals and p53 in neuron apoptosis in vivo. J Neurosci (1995) 1.79
The major form of MeCP2 has a novel N-terminus generated by alternative splicing. Nucleic Acids Res (2004) 1.79
Specification of the anterior hindbrain and establishment of a normal mid/hindbrain organizer is dependent on Gbx2 gene function. Development (1997) 1.79
The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS. Nature (2000) 1.76
Notch1 is required for neuronal and glial differentiation in the cerebellum. Development (2002) 1.69
Molecular-clinical spectrum of the ATR-X syndrome. Am J Med Genet (2000) 1.68
Development of the deep cerebellar nuclei: transcription factors and cell migration from the rhombic lip. J Neurosci (2006) 1.64
Morphogenetic and cellular movements that shape the mouse cerebellum; insights from genetic fate mapping. Neuron (2005) 1.63
The human cerebro-cerebellar system: its computing, cognitive, and language skills. Behav Brain Res (1991) 1.59
In situ labeling of granule cells for apoptosis-associated DNA fragmentation reveals different mechanisms of cell loss in developing cerebellum. Neuron (1993) 1.58
Mash1 and neurogenin1 expression patterns define complementary domains of neuroepithelium in the developing CNS and are correlated with regions expressing notch ligands. J Neurosci (1997) 1.57
The fetal cerebellum: development and common malformations. J Child Neurol (2011) 1.55
Pax-2 expression defines a subset of GABAergic interneurons and their precursors in the developing murine cerebellum. J Neurobiol (1999) 1.53
Cerebellar development and disease. Curr Opin Neurobiol (2008) 1.53
Deletion of astroglial Dicer causes non-cell-autonomous neuronal dysfunction and degeneration. J Neurosci (2011) 1.52
Brainstem, cerebellar and limbic neuroanatomical abnormalities in autism. Curr Opin Neurobiol (1997) 1.49
The role of the rhombic lip in avian cerebellum development. Development (1999) 1.48
Structural and quantitative studies on the normal C3H and Lurcher mutant mouse. Philos Trans R Soc Lond B Biol Sci (1979) 1.48
The roof plate regulates cerebellar cell-type specification and proliferation. Development (2006) 1.46
Generation of cerebellar granule neurons in vivo by transplantation of BMP-treated neural progenitor cells. Nat Neurosci (1999) 1.46
Unipolar brush cells of the cerebellum are produced in the rhombic lip and migrate through developing white matter. J Neurosci (2006) 1.43
Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain development. Mech Dev (1999) 1.39
Cytodifferentiation of Bergmann glia and its relationship with Purkinje cells. Anat Sci Int (2002) 1.38
Morphological and electrophysiological properties of GABAergic and non-GABAergic cells in the deep cerebellar nuclei. J Neurophysiol (2006) 1.38
Predominant expression of human zic in cerebellar granule cell lineage and medulloblastoma. Cancer Res (1996) 1.36
Neurogenesis in the cerebellum. Neuroscientist (2007) 1.36
The midbrain--hindbrain boundary organizer. Curr Opin Neurobiol (2001) 1.35
Neuroepithelial stem cells from the embryonic spinal cord: isolation, characterization, and clonal analysis. Dev Biol (1997) 1.33
The rhombic lip and early cerebellar development. Curr Opin Neurobiol (2001) 1.33
Molecular mechanisms of cortical differentiation. Eur J Neurosci (2006) 1.33