scholarly article | Q13442814 |
P2093 | author name string | Qing Li | |
Shenandoah Robinson | |||
Mark L Cohen | |||
Anne Dechant | |||
P2860 | cites work | Origin of GABAergic neurons in the human neocortex | Q24299048 |
Laminar distribution of neuropeptide Y-immunoreactive neurons in human prefrontal cortex during development | Q24336771 | ||
BDNF-induced TrkB activation down-regulates the K+-Cl- cotransporter KCC2 and impairs neuronal Cl- extrusion | Q24673062 | ||
Mice lacking the 65 kDa isoform of glutamic acid decarboxylase (GAD65) maintain normal levels of GAD67 and GABA in their brains but are susceptible to seizures | Q28116644 | ||
Role of subplate neurons in functional maturation of visual cortical columns | Q28189581 | ||
Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes | Q28251621 | ||
Perinatal subplate neuron injury: implications for cortical development and plasticity | Q28274896 | ||
Neurologic and developmental disability at six years of age after extremely preterm birth | Q28301325 | ||
Decreased expression of vesicular glutamate transporter 1 and complexin II mRNAs in schizophrenia: further evidence for a synaptic pathology affecting glutamate neurons | Q28302622 | ||
Prenatal alteration and distribution of the GABA(B1) and GABA(B2) receptor subunit mRNAs during rat central nervous system development | Q28571368 | ||
Expression of the vesicular glutamate transporters during development indicates the widespread corelease of multiple neurotransmitters | Q28581851 | ||
Excitatory actions of gaba during development: the nature of the nurture | Q29617435 | ||
Microstructural brain development after perinatal cerebral white matter injury assessed by diffusion tensor magnetic resonance imaging | Q30636036 | ||
Correlation between the sequential ingrowth of afferents and transient patterns of cortical lamination in preterm infants | Q30690438 | ||
Distinct cortical migrations from the medial and lateral ganglionic eminences. | Q31816321 | ||
Outcomes of children of extremely low birthweight and gestational age in the 1990's | Q33544232 | ||
Neuropeptide Y: emerging evidence for a functional role in seizure modulation. | Q33544242 | ||
GABA expression dominates neuronal lineage progression in the embryonic rat neocortex and facilitates neurite outgrowth via GABA(A) autoreceptor/Cl- channels. | Q33939350 | ||
Recent advances in human perinatal white matter injury | Q34361149 | ||
Neurobiology of periventricular leukomalacia in the premature infant | Q34407686 | ||
Morphology of neuropeptide Y-immunoreactive neurons and fibers in human prefrontal cortex during prenatal and postnatal development | Q34419432 | ||
Proliferation and apoptosis in the developing human neocortex. | Q34747476 | ||
Differential response of cortical plate and ventricular zone cells to GABA as a migration stimulus. | Q34750391 | ||
Is there more to GABA than synaptic inhibition? | Q34810140 | ||
Increased anxiety and altered responses to anxiolytics in mice deficient in the 65-kDa isoform of glutamic acid decarboxylase. | Q35010483 | ||
New approaches to brain injury in preterm infants | Q35086205 | ||
Neurocognitive outcome after very preterm birth | Q35294356 | ||
The Scottish perinatal neuropathology study: clinicopathological correlation in early neonatal deaths | Q35295423 | ||
Late oligodendrocyte progenitors coincide with the developmental window of vulnerability for human perinatal white matter injury. | Q49071435 | ||
Abnormal cerebral structure is present at term in premature infants. | Q49086898 | ||
Periventricular leukomalacia of infancy. A form of neonatal anoxic encephalopathy. | Q51292054 | ||
Experimentally induced disorders of neuronal migration produce an increased propensity for electrographic seizures in rats. | Q51599337 | ||
Research in neonatology for the 21st century: executive summary of the National Institute of Child Health and Human Development-American Academy of Pediatrics workshop. Part I: academic issues. | Q52058704 | ||
The chemokine growth-regulated oncogene-alpha promotes spinal cord oligodendrocyte precursor proliferation. | Q52181496 | ||
School-age outcomes in children with birth weights under 750 g. | Q52214195 | ||
Periventricular white matter injury in the premature infant is followed by reduced cerebral cortical gray matter volume at term | Q57242179 | ||
Postnatal development of the α1 containing GABAA receptor subunit in rat hippocampus | Q60462291 | ||
Subplate neurons--missing link in brain injury of the premature infant? | Q70851754 | ||
Cajal-Retzius neurons in human cerebral cortex at midgestation show immunoreactivity for neurofilament and calcium-binding proteins | Q70890321 | ||
Immunohistochemical study of myelination and oligodendrocyte in infants with periventricular leukomalacia | Q71438477 | ||
Apoptosis and necrosis in the newborn piglet brain following transient cerebral hypoxia-ischaemia | Q73134624 | ||
Perinatal brain damage, cortical reorganization (acquired cortical dysplasias), and epilepsy | Q73224951 | ||
Clinical and aetiological aspects of epilepsy in children with cerebral palsy | Q73475926 | ||
Maturation-dependent vulnerability of oligodendrocytes to oxidative stress-induced death caused by glutathione depletion | Q77068020 | ||
Caspase-3 activation and caspase-like proteolytic activity in human perinatal hypoxic-ischemic brain injury | Q77630397 | ||
Longitudinal, 15-year follow-up of children born at less than 29 weeks' gestation after introduction of surfactant therapy into a region: neurologic, cognitive, and educational outcomes | Q78587934 | ||
Subplate neurons: bridging the gap to function in the cortex | Q79828833 | ||
Systemic prenatal insults disrupt telencephalon development: implications for potential interventions | Q35569038 | ||
Postnatal development of calcium-binding proteins immunoreactivity (parvalbumin, calbindin, calretinin) in the human entorhinal cortex. | Q35631857 | ||
Transient microcircuits formed by subplate neurons and their role in functional development of thalamocortical connections | Q35889364 | ||
Development of neurotransmitter systems during critical periods. | Q35924928 | ||
Age terminology during the perinatal period | Q35936113 | ||
Glutamate and GABA receptor signalling in the developing brain. | Q35979714 | ||
Subplate neuron ablation alters neurotrophin expression and ocular dominance column formation | Q36678564 | ||
Perinatal telencephalic leucoencephalopathy | Q37136670 | ||
Caspase inhibitor affords neuroprotection with delayed administration in a rat model of neonatal hypoxic-ischemic brain injury | Q37381665 | ||
Epilepsy, hyperalgesia, impaired memory, and loss of pre- and postsynaptic GABA(B) responses in mice lacking GABA(B(1)). | Q39576197 | ||
The subplate, a transient neocortical structure: its role in the development of connections between thalamus and cortex | Q40765992 | ||
Programmed cell death and the control of cell survival: lessons from the nervous system | Q40777905 | ||
Developmental history of the transient subplate zone in the visual and somatosensory cortex of the macaque monkey and human brain | Q41240472 | ||
Prenatal development of neurons in the human prefrontal cortex: I. A qualitative Golgi study | Q41278159 | ||
Developmental neuropathology and impact of perinatal brain damage. II: white matter lesions of the neocortex | Q41369282 | ||
Laminar and cellular distribution of AMPA, kainate, and NMDA receptor subunits in monkey sensory-motor cortex. | Q41650913 | ||
Ion channel expression by white matter glia: The O-2A glial progenitor cell | Q41892034 | ||
Cytokine immunoreactivity in cortical and subcortical neurons in periventricular leukomalacia: are cytokines implicated in neuronal dysfunction in cerebral palsy? | Q42436407 | ||
Age-related changes in calbindin-D28k, calretinin, and parvalbumin-immunoreactive neurons in the human cerebral cortex | Q42443528 | ||
Neurodevelopmental and functional outcomes of extremely low birth weight infants in the National Institute of Child Health and Human Development Neonatal Research Network, 1993-1994. | Q43522850 | ||
Constitutive expression of growth-related oncogene and its receptor in oligodendrogliomas | Q43588231 | ||
Selective Vulnerability of Subplate Neurons after Early Neonatal Hypoxia-Ischemia | Q43906832 | ||
Expression and distribution of metabotropic GABA receptor subtypes GABABR1 and GABABR2 during rat neocortical development | Q44039746 | ||
Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction. | Q44281916 | ||
Behavioral outcomes and evidence of psychopathology among very low birth weight infants at age 20 years. | Q44369954 | ||
Blockade of GABA(B) receptors alters the tangential migration of cortical neurons. | Q44539346 | ||
GABA-mediated trophic effect on oligodendrocytes requires Na-K-2Cl cotransport activity | Q44540590 | ||
Synaptic signaling between GABAergic interneurons and oligodendrocyte precursor cells in the hippocampus. | Q44683771 | ||
Hypoxia differentially reduces GABA(A) receptor density during embryonic chick optic lobe development | Q44852250 | ||
Distinct expression of phosphorylated N-methyl-D-aspartate receptor NR1 subunits by projection neurons and interneurons in the striatum of normal and amphetamine-treated rats | Q44918606 | ||
The GABAergic system of the developing neocortex has a reduced capacity to recover from in utero injury in experimental cortical dysplasia. | Q45205875 | ||
Constructing circuits: neurogenesis and migration in the developing neocortex | Q46228143 | ||
Disruption of interneuron development | Q46733519 | ||
Preferential origin and layer destination of GAD65-GFP cortical interneurons | Q47308563 | ||
Improved survival rates with increased neurodevelopmental disability for extremely low birth weight infants in the 1990s | Q47386422 | ||
Adverse neurodevelopmental outcomes among extremely low birth weight infants with a normal head ultrasound: prevalence and antecedents | Q47390154 | ||
Annual summary of vital statistics--2003. | Q47591806 | ||
Three distinct subpopulations of GABAergic neurons in rat frontal agranular cortex | Q48103983 | ||
Developmental neuropathology and impact of perinatal brain damage. III: gray matter lesions of the neocortex | Q48208663 | ||
Thalamocortical development of parvalbumin neurons in normal and periventricular leukomalacia brains | Q48223292 | ||
An immunohistochemical study of neurotransmitter profiles in developing human visual cortex | Q48280824 | ||
Knock-out mice reveal a critical antiepileptic role for neuropeptide Y. | Q48579930 | ||
Laminar organization of the human fetal cerebrum revealed by histochemical markers and magnetic resonance imaging | Q48632358 | ||
Ontogeny of GABA pathway in human fetal brains | Q48861681 | ||
Developmental changes revealed by immunohistochemical markers in human cerebral cortex | Q48878898 | ||
Effect of fetal hydrocephalus on the distribution patterns of calcium-binding proteins in the human occipital cortex | Q48935386 | ||
Developmental changes induced by graded prenatal systemic hypoxic-ischemic insults in rats | Q48985335 | ||
Axonal development in the cerebral white matter of the human fetus and infant | Q49014020 | ||
Retardation of neuronal maturation in premature infants compared with term infants of the same postconceptional age. | Q49068608 | ||
P433 | issue | 6 Suppl | |
P304 | page(s) | 396-408 | |
P577 | publication date | 2006-06-01 | |
P1433 | published in | Journal of Neurosurgery | Q15708886 |
P1476 | title | Neonatal loss of gamma-aminobutyric acid pathway expression after human perinatal brain injury | |
P478 | volume | 104 |
Q37385634 | 12/15-lipoxygenase expression is increased in oligodendrocytes and microglia of periventricular leukomalacia |
Q90044126 | Age-Dependency of Levetiracetam Effects on Exocytotic GABA Release from Nerve Terminals in the Hippocampus and Cortex in Norm and After Perinatal Hypoxia |
Q46795545 | Altered cortical inhibitory function in children with spastic diplegia: a TMS study |
Q37253850 | Brain injury in premature infants: a complex amalgam of destructive and developmental disturbances |
Q50680469 | Brain injury in premature neonates: A primary cerebral dysmaturation disorder? |
Q27022056 | Cerebral white and gray matter injury in newborns: new insights into pathophysiology and management |
Q47100497 | Combined fetal inflammation and postnatal hypoxia causes myelin deficits and autism-like behavior in a rat model of diffuse white matter injury |
Q34026944 | Complex pattern of interaction between in utero hypoxia-ischemia and intra-amniotic inflammation disrupts brain development and motor function. |
Q38610168 | Controversies in preterm brain injury |
Q37425303 | Cross-species analyses of the cortical GABAergic and subplate neural populations |
Q90056963 | Current Evidence on Cell Death in Preterm Brain Injury in Human and Preclinical Models |
Q64950856 | Dysmaturation of Somatostatin Interneurons Following Umbilical Cord Occlusion in Preterm Fetal Sheep. |
Q47113795 | Embracing oligodendrocyte diversity in the context of perinatal injury |
Q64107024 | Emerging Roles of miRNAs in Brain Development and Perinatal Brain Injury |
Q36520524 | Erythropoietin Modulates Cerebral and Serum Degradation Products from Excess Calpain Activation following Prenatal Hypoxia-Ischemia |
Q30851577 | Extensive migration of young neurons into the infant human frontal lobe |
Q33584268 | Functional connectivity for somatosensory and motor cortex in spastic diplegia |
Q38211328 | GABA receptors in brain development, function, and injury |
Q34051476 | GABA, resting-state connectivity and the developing brain |
Q35693647 | GABAergic regulation of cerebellar NG2 cell development is altered in perinatal white matter injury |
Q91806634 | Human 3D cellular model of hypoxic brain injury of prematurity |
Q33932727 | Human umbilical cord blood cells restore brain damage induced changes in rat somatosensory cortex |
Q64110346 | Impaired Interneuron Development in a Novel Model of Neonatal Brain Injury |
Q92205549 | Impaired αVβ8 and TGFβ signaling lead to microglial dysmaturation and neuromotor dysfunction |
Q39371592 | Interplay of brain structure and function in neonatal congenital heart disease |
Q92528660 | Intranasally Administered Exosomes from Umbilical Cord Stem Cells Have Preventive Neuroprotective Effects and Contribute to Functional Recovery after Perinatal Brain Injury |
Q35353268 | Late development of the GABAergic system in the human cerebral cortex and white matter |
Q24657688 | Long-term deficits of preterm birth: evidence for arousal and attentional disturbances |
Q35190435 | Loss of cation-chloride cotransporter expression in preterm infants with white matter lesions: implications for the pathogenesis of epilepsy |
Q59791427 | Loss of interneurons and disruption of perineuronal nets in the cerebral cortex following hypoxia-ischaemia in near-term fetal sheep |
Q34714096 | Microstructural and functional connectivity in the developing preterm brain |
Q45162312 | Modeling Encephalopathy of Prematurity Using Prenatal Hypoxia-ischemia with Intra-amniotic Lipopolysaccharide in Rats |
Q42183221 | Modeling the encephalopathy of prematurity in animals: the important role of translational research |
Q37095576 | Molecular mechanisms involved in injury to the preterm brain |
Q30847961 | Neonatal Hypoxia Ischaemia: Mechanisms, Models, and Therapeutic Challenges |
Q47216442 | Neonatal erythropoietin mitigates impaired gait, social interaction and diffusion tensor imaging abnormalities in a rat model of prenatal brain injury |
Q38187691 | Neurogenesis and maturation in neonatal brain injury |
Q35859815 | Neuron deficit in the white matter and subplate in periventricular leukomalacia |
Q34554583 | Neuronal damage in the preterm baboon: impact of the mode of ventilatory support |
Q30405077 | Oligodendroglial alterations and the role of microglia in white matter injury: relevance to schizophrenia |
Q33725429 | Perinatal hypoxia: different effects of the inhibitors of GABA transporters GAT1 and GAT3 on the initial velocity of [3H]GABA uptake by cortical, hippocampal, and thalamic nerve terminals. |
Q36768181 | Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants |
Q35956626 | Postnatal Erythropoietin Mitigates Impaired Cerebral Cortical Development Following Subplate Loss from Prenatal Hypoxia-Ischemia |
Q34569855 | Postnatal erythropoietin treatment mitigates neural cell loss after systemic prenatal hypoxic-ischemic injury |
Q35767540 | Potential neuronal repair in cerebral white matter injury in the human neonate |
Q38365734 | Preclinical Models of Encephalopathy of Prematurity |
Q36022351 | Prenatal Hypoxia-Ischemia Induces Abnormalities in CA3 Microstructure, Potassium Chloride Co-Transporter 2 Expression and Inhibitory Tone |
Q36410599 | Spatial contrast sensitivity vision loss in children with cortical visual impairment |
Q48107914 | Stem cells and cell-based therapies for cerebral palsy: A call for rigor |
Q42545076 | Subplate neurons: crucial regulators of cortical development and plasticity |
Q64260095 | The Potential of Stem Cell Therapy to Repair White Matter Injury in Preterm Infants: Lessons Learned From Experimental Models |
Q91790873 | The Roles of GABA in Ischemia-Reperfusion Injury in the Central Nervous System and Peripheral Organs |
Q34995998 | The developing oligodendrocyte: key cellular target in brain injury in the premature infant |
Q35894087 | The effect of preterm birth on thalamic and cortical development |
Q33516828 | The encephalopathy of prematurity--brain injury and impaired brain development inextricably intertwined |
Q35183938 | Vessel maturation schedule determines vulnerability to neuronal injuries of prematurity |
Q35595756 | Visual cortical function in very low birth weight infants without retinal or cerebral pathology |