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  • 1
    Publication Date: 2002-10-12
    Description: A goal in visual neuroscience is to reveal how the visual system reconstructs the three-dimensional (3D) representation of the world from two-dimensional retinal images. Although the importance of texture gradient cues in the process of 3D vision has been pointed out, most studies concentrate on the neural process based on binocular disparity. We report the neural correlates of depth perception from texture gradient in the cortex. In the caudal part of the lateral bank of intraparietal sulcus, many neurons were selective to 3D surface orientation defined by texture gradient, and their response was invariant over different types of texture pattern. Most of these neurons were also sensitive to a disparity gradient, suggesting that they integrate texture and disparity gradient signals to construct a generalized representation of 3D surface orientation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tsutsui, Ken-Ichiro -- Sakata, Hideo -- Naganuma, Tomoka -- Taira, Masato -- New York, N.Y. -- Science. 2002 Oct 11;298(5592):409-12.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology, Nihon University School of Medicine, Tokyo 173-8610, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/12376700" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain Mapping ; Cues ; Depth Perception/*physiology ; Electrophysiology ; Form Perception/*physiology ; Learning ; Macaca ; Male ; Neurons/*physiology ; Parietal Lobe/*physiology ; Pattern Recognition, Visual ; Photic Stimulation ; Task Performance and Analysis ; Vision Disparity ; Visual Pathways/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 1999-05-15
    Description: The mammalian hippocampus contains the neural circuitry that is crucial for cognitive functions such as learning and memory. The development of such circuitry is dependent on the generation and correct placement of the appropriate number and types of neurons. Mice lacking function of the LIM homeobox gene Lhx5 showed a defect in hippocampus development. Hippocampal neural precursor cells were specified and proliferated, but many of them failed to either exit the cell cycle or to differentiate and migrate properly. Lhx5 is therefore essential for the regulation of precursor cell proliferation and the control of neuronal differentiation and migration during hippocampal development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhao, Y -- Sheng, H Z -- Amini, R -- Grinberg, A -- Lee, E -- Huang, S -- Taira, M -- Westphal, H -- New York, N.Y. -- Science. 1999 May 14;284(5417):1155-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Mammalian Genes and Development, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10325223" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Body Patterning ; Cell Differentiation ; Cell Division ; Cell Movement ; Crosses, Genetic ; Dentate Gyrus/cytology/embryology ; Female ; Gene Deletion ; Gene Expression ; *Genes, Homeobox ; Hippocampus/*cytology/*embryology ; Homeodomain Proteins/*genetics/physiology ; Interneurons/cytology ; LIM-Homeodomain Proteins ; Male ; Mice ; Morphogenesis ; Nerve Tissue Proteins/*genetics/physiology ; Neuroglia/cytology ; Neurons/*cytology ; Pyramidal Cells/cytology ; Stem Cells/*cytology ; Transcription Factors
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1993-04-02
    Description: A major challenge of current neuroscience is to elucidate the brain mechanisms that underlie cognitive function. There is no doubt that cognitive processing in the brain engages large populations of cells. This article explores the logic of investigating these problems by combining psychological studies in human subjects and neurophysiological studies of neuronal populations in the motor cortex of behaving monkeys. The results obtained show that time-varying psychological processes can be visualized in the time-varying activity of neuronal populations. Moreover, the functional interactions between cells in the motor cortex are very similar to those observed in a massively interconnected artificial network performing the same computation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Georgopoulos, A P -- Taira, M -- Lukashin, A -- NS17413/NS/NINDS NIH HHS/ -- PSMH48185/PS/NCHHSTP CDC HHS/ -- New York, N.Y. -- Science. 1993 Apr 2;260(5104):47-52.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉American Legion, Minneapolis, MN.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8465199" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/physiology ; Cognition/*physiology ; Electrophysiology ; Haplorhini ; Humans ; Macaca mulatta ; Mathematics ; Motor Activity/physiology ; Motor Cortex/*physiology ; Movement ; Neurons/physiology ; Space Perception/physiology ; Vision, Ocular/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1992-06-19
    Description: The relation of cellular activity in the motor cortex to the direction of two-dimensional isometric force was investigated under dynamic conditions in monkeys. A task was designed so that three force variables were dissociated: the force exerted by the subject, the net force, and the change in force. Recordings of neuronal activity in the motor cortex revealed that the activity of single cells was directionally tuned and that this tuning was invariant across different directions of a bias force. Cell activity was not related to the direction of force exerted by the subject, which changed drastically as the bias force changed. In contrast, the direction of net force, the direction of force change, and the visually instructed direction all remained quite invariant and congruent and could be the directional variables, alone or in combination, to which cell activity might relate.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Georgopoulos, A P -- Ashe, J -- Smyrnis, N -- Taira, M -- NS07226/NS/NINDS NIH HHS/ -- NS17413/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1992 Jun 19;256(5064):1692-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Brain Sciences Center, Department of Veterans Affairs Medical Center, Minneapolis, MN 55455.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1609282" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Electrophysiology ; Haplorhini ; Isometric Contraction/*physiology ; Motor Activity/physiology ; Motor Cortex/*physiology ; Motor Neurons/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 1980-02-01
    Description: Mouse interferons of three size classes (A, 35,000 to 40,000 daltons; B, 26,000 to 33,000 daltons; and C, 20,000 daltons) were purified from Ehrlich ascites tumor cells infected with Newcastle disease virus. The sequences of the first 24 amino acids (No. 17 has not been identified) of interferons A and B are identical. The sequence of the first 20 amino acids of interferon C differs from that of A and B in 18 positions. There is partial homology in amino terminal sequence between mouse interferons A (or B) and a human fibroblast interferon and between mouse interferon C and a human lymphoblastoid interferon.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Taira, H -- Broeze, R J -- Jayaram, B M -- Lengyel, P -- Hunkapiller, M W -- Hood, L E -- New York, N.Y. -- Science. 1980 Feb 1;207(4430):528-30.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7352261" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Biological Evolution ; Carcinoma, Ehrlich Tumor/analysis ; Cells, Cultured ; Glycoproteins/analysis ; *Interferons/genetics ; Mice ; Molecular Weight
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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