Works matching DE "PROSENCEPHALON abnormalities"
Results: 36
Paradoxical inter-hemispheric transfer after section of the cerebral commissures.
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- Experimental Brain Research, 2009, v. 192, n. 3, p. 425, doi. 10.1007/s00221-008-1524-4
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- Article
Block CREB activity induces ischemic like neuron-glial degenration.
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- Journal of Chinese Clinical Medicine, 2010, v. 5, n. 4, p. 194
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Absence of Prenatal Forebrain Defects in the Dp(16)1Yey/+ Mouse Model of Down Syndrome.
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- Journal of Neuroscience, 2016, v. 36, n. 10, p. 2926, doi. 10.1523/JNEUROSCI.2513-15.2016
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- Article
Optogenetic Dissection of the Basal Forebrain Neuromodulatory Control of Cortical Activation, Plasticity, and Cognition.
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- Journal of Neuroscience, 2015, v. 35, n. 41, p. 13896, doi. 10.1523/JNEUROSCI.2590-15.2015
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- Article
EphA4-Mediated Ipsilateral Corticospinal Tract Misprojections Are Necessary for Bilateral Voluntary Movements But Not Bilateral Stereotypic Locomotion.
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- Journal of Neuroscience, 2014, v. 34, n. 15, p. 5211, doi. 10.1523/JNEUROSCI.4848-13.2014
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Cholinergic Neurons Excite Cortically Projecting Basal Forebrain GABAergic Neurons.
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- Journal of Neuroscience, 2014, v. 34, n. 8, p. 2832, doi. 10.1523/JNEUROSCI.3235-13.2014
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- Article
Vax1 Plays an Indirect Role in the Etiology of Murine Cleft Palate.
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- 2017
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- journal article
A mechanism for mutational inactivation of the homeodomain protein TGIF in holoprosencephaly.
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- FASEB Journal, 2007, v. 21, n. 2, p. 488, doi. 10.1096/fj.06-6423com
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A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
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- Human Genetics, 2002, v. 110, n. 5, p. 422, doi. 10.1007/s00439-002-0709-3
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- Article
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
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- Human Genetics, 2002, v. 110, n. 4, p. 297, doi. 10.1007/s00439-002-0695-5
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Forebrain Cholinergic Dysfunction and Systemic and Brain Inflammation in Murine Sepsis Survivors.
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- Frontiers in Immunology, 2017, p. 1, doi. 10.3389/fimmu.2017.01673
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- Article
Ethmocephaly caused by de novo translocation 18;21prenatal diagnosis.
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- Prenatal Diagnosis, 2003, v. 23, n. 10, p. 788, doi. 10.1002/pd.689
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Pretreatment with the ciclosporin derivative NIM811 reduces delayed neuronal death in the hippocampus after transient forebrain ischaemia.
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- Journal of Pharmacy & Pharmacology, 2010, v. 62, n. 4, p. 485, doi. 10.1211/jpp.62.04.0011
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- Article
Absent cavum septum pellucidum: a review with emphasis on associated commissural abnormalities.
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- Pediatric Radiology, 2015, v. 45, n. 7, p. 950, doi. 10.1007/s00247-015-3318-8
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- Article
Group I mGluR5 metabotropic glutamate receptors regulate proliferation of neuronal progenitors in specific forebrain developmental domains.
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- Journal of Neurochemistry, 2008, v. 104, n. 1, p. 155, doi. 10.1111/j.1471-4159.2007.04955.x
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Prospects for new restorative and neuroprotective treatments in Parkinson's disease.
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- Nature, 1999, v. 399, n. 6738, p. A32, doi. 10.1038/399a032
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Essential role of neocortical acetylcholine in spatial memory.
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- Nature, 1995, v. 375, n. 6531, p. 484, doi. 10.1038/375484a0
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Cyclopia and synophthalmia: congenital facial anomalies with neurological defects.
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- Orbit, 1997, v. 16, n. 1, p. 45, doi. 10.3109/01676839709076366
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The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephaly.
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- Cytogenetics & Cell Genetics, 2000, v. 89, n. 3/4, p. 220, doi. 10.1159/000015618
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The ups and downs of holoprosencephaly: dorsal versus ventral patterning forces.
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- Clinical Genetics, 2008, v. 73, n. 5, p. 413, doi. 10.1111/j.1399-0004.2008.00994.x
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Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literature.
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- Clinical Genetics, 2005, v. 68, n. 4, p. 349, doi. 10.1111/j.1399-0004.2005.00498.x
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Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function.
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- European Journal of Human Genetics, 2011, v. 19, n. 12, p. 1238, doi. 10.1038/ejhg.2011.121
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Ultrasound in Trisomy 18 and 13.
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- Journal of the Turkish-German Gynecological Association, 2009, v. 10, n. 4, p. 218
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- Article
Tauopathy in transgenic (SHR72) rats impairs function of central noradrenergic system and promotes neuroinflammation.
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- 2016
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- Publication type:
- journal article
Mutations in Hedgehog Acyltransferase (Hhat) Perturb Hedgehog Signaling, Resulting in Severe Acrania-Holoprosencephaly-Agnathia Craniofacial Defects.
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- PLoS Genetics, 2012, v. 8, n. 10, p. 1, doi. 10.1371/journal.pgen.1002927
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Deep brain stimulation of the nucleus basalis of Meynert in Alzheimer's dementia.
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- Molecular Psychiatry, 2015, v. 20, n. 3, p. 353, doi. 10.1038/mp.2014.32
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- Article
Circumscribed lesion of the medial forebrain bundle area causes structural impairment of lymphoid organs and severe depression of immune function in rats.
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- Molecular Psychiatry, 1998, v. 3, n. 5, p. 397, doi. 10.1038/sj.mp.4000426
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Basal forebrain activation controls contrast sensitivity in primary visual cortex.
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- BMC Neuroscience, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2202-14-55
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Familial Cebocephaly.
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- Clinical Pediatrics, 1970, v. 9, n. 8, p. 491
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Determination of the connectivity of newborn neurons in mammalian olfactory circuits.
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- Cellular & Molecular Life Sciences, 2017, v. 74, n. 5, p. 849, doi. 10.1007/s00018-016-2367-y
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Neural Progenitors of the Postnatal and Adult Mouse Forebrain Retain the Ability to Self-Replicate, Form Neurospheres, and Undergo Multipotent Differentiation In Vivo.
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- Stem Cells, 2009, v. 27, n. 3, p. 714, doi. 10.1634/stemcells.2008-0985
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Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.
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- Nature Genetics, 2002, v. 32, n. 3, p. 359, doi. 10.1038/ng1009
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Early Reactive Changes in Astrocytes in the Paranigral Nucleus of the Midbrain after Forebrain Ischemia and Treatment with the Cerebroprotective Agent Ropren in Rats.
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- Neuroscience & Behavioral Physiology, 2015, v. 45, n. 1, p. 5, doi. 10.1007/s11055-014-0032-1
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Defects in Embryonic Neurogenesis and Initial Synapse Formation in the Forebrain of the Ts65Dn Mouse Model of Down Syndrome.
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- Journal of Neuroscience, 2007, v. 27, n. 43, p. 11483, doi. 10.1523/JNEUROSCI.3406-07.2007
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Zic1 and Zic3 Regulate Medial Forebrain Development through Expansion of Neuronal Progenitors.
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- Journal of Neuroscience, 2007, v. 27, n. 20, p. 5461, doi. 10.1523/JNEUROSCI.4046-06.2007
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Holoprosencephaly and Diabetes Insipidus in a 3-Month-Old Infant.
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- Journal of Child Neurology, 2008, v. 23, n. 1, p. 118, doi. 10.1177/0883073807308708
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