Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Veena G. Supramaniam"'
Autor:
Ana A. Baburamani, Regina T. Vontell, Alena Uus, Maximilian Pietsch, Prachi A. Patkee, Jo Wyatt-Ashmead, Evonne C. Chin-Smith, Veena G. Supramaniam, J. Donald Tournier, Maria Deprez, Mary A. Rutherford
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-17 (2020)
Abstract Down syndrome (DS) occurs with triplication of human chromosome 21 and is associated with deviations in cortical development evidenced by simplified gyral appearance and reduced cortical surface area. Radial glia are neuronal and glial proge
Externí odkaz:
https://doaj.org/article/73bbd642760f4d90af2068718d112266
Dysmaturation of Somatostatin Interneurons Following Umbilical Cord Occlusion in Preterm Fetal Sheep
Autor:
Maryam Ardalan, Pernilla Svedin, Ana A. Baburamani, Veena G. Supramaniam, Joakim Ek, Henrik Hagberg, Carina Mallard
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
IntroductionCerebral white matter injury is the most common neuropathology observed in preterm infants. However, there is increasing evidence that gray matter development also contributes to neurodevelopmental abnormalities. Fetal cerebral ischemia c
Externí odkaz:
https://doaj.org/article/28462e175d3446a69711f0b8ece19a1c
Autor:
Regina Vontell, Veena G. Supramaniam, Alice Davidson, Claire Thornton, Andreas Marnerides, Muriel Holder-Espinasse, Suzanne Lillis, Shu Yau, Mattias Jansson, Henrik E. Hagberg, Mary A. Rutherford
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Cytoplasmic Actin Gamma 1 (ACTG1) gene variant are autosomal dominant and can cause CNS anomalies (Baraitser Winter Malformation Syndrome; BWMS). ACTG1 anomalies in offspring include agenesis of the corpus callosum (ACC) and neuronal heterotopia whic
Externí odkaz:
https://doaj.org/article/c70e40fd5db3467286d5de2a9f649edb
Autor:
Regina, Vontell, Veena G, Supramaniam, Alice, Davidson, Claire, Thornton, Andreas, Marnerides, Muriel, Holder-Espinasse, Suzanne, Lillis, Shu, Yau, Mattias, Jansson, Henrik E, Hagberg, Mary A, Rutherford
Publikováno v:
Frontiers in Physiology
Cytoplasmic Actin Gamma 1 (ACTG1) gene variant are autosomal dominant and can cause CNS anomalies (Baraitser Winter Malformation Syndrome; BWMS). ACTG1 anomalies in offspring include agenesis of the corpus callosum (ACC) and neuronal heterotopia whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5cb498183d9610d37304abcaa38af3a6
https://pubmed.ncbi.nlm.nih.gov/31231230
https://pubmed.ncbi.nlm.nih.gov/31231230
Autor:
Ana A, Baburamani, Yasuka, Miyakuni, Regina, Vontell, Veena G, Supramaniam, Pernilla, Svedin, Mary, Rutherford, Pierre, Gressens, Carina, Mallard, Satoru, Takeda, Claire, Thornton, Henrik, Hagberg
Publikováno v:
Developmental Neuroscience
Apoptotic mechanisms are centre stage for the development of injury in the immature brain, and caspases have been shown to play a pivotal role during brain development and in response to injury. The inhibition of caspases using broad-spectrum agents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b57269984f89bead0e41bf7a88a1ccc
https://pubmed.ncbi.nlm.nih.gov/25823427
https://pubmed.ncbi.nlm.nih.gov/25823427
Autor:
Nicole O. Alers, Niel VanZyl, Tamara Yawno, Grant R Drummond, David W. Walker, Veena G. Supramaniam, Graham Jenkin, Euan M. Wallace, Jan Mi Loose, Tharani Sabaretnam, Suzanne L. Miller, Margie Castillo-Melendez
Publikováno v:
Journal of pineal research. 56(3)
Fetal intrauterine growth restriction (IUGR) is a serious pregnancy complication associated with increased rates of perinatal morbidity and mortality, and ultimately with long-term neurodevelopmental impairments. No intervention currently exists that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1021e39021e53c8b8f241807458d2dd8
https://pubmed.ncbi.nlm.nih.gov/24456220
https://pubmed.ncbi.nlm.nih.gov/24456220