Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ela Bar"'
Autor:
Ariel Nir Sade, Gilad Levy, Sari Schokoroy Trangle, Galit Elad Sfadia, Ela Bar, Omer Ophir, Inbar Fischer, May Rokach, Andrea Atzmon, Hadar Parnas, Tali Rosenberg, Asaf Marco, Orna Elroy Stein, Boaz Barak
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-17 (2023)
Abstract Gtf2i encodes the general transcription factor II-I (TFII-I), with peak expression during pre-natal and early post-natal brain development stages. Because these stages are critical for proper brain development, we studied at the single-cell
Externí odkaz:
https://doaj.org/article/4f6a8d1486f84e14ae32d70a925fdfed
Autor:
Omer Ophir, Gilad Levy, Ela Bar, Omri Kimchi Feldhorn, May Rokach, Galit Elad Sfadia, Boaz Barak
Publikováno v:
Biomedicines, Vol 11, Iss 8, p 2273 (2023)
Williams syndrome (WS) is a neurodevelopmental disorder characterized by distinctive cognitive and personality profiles which also impacts various physiological systems. The syndrome arises from the deletion of about 25 genes located on chromosome 7q
Externí odkaz:
https://doaj.org/article/7598d15b0fcd4806b1dfb7db76302c1f
Autor:
Inbar Fischer, Sophie Shohat, Gilad Levy, Ela Bar, Sari Schokoroy Trangle, Shai Efrati, Boaz Barak
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11077 (2022)
Autism spectrum disorder (ASD) is a multifactorial neurodevelopmental disorder (NDD) characterized by impaired social communication and repetitive behavior, among other symptoms. ASD is highly heritable, with SHANK3 being one of the high-risk genes f
Externí odkaz:
https://doaj.org/article/2a12e3ebd65f4172ae8bc48591656b9e
Autor:
Suzan Sweitat, Yulia Mitiagin, Ronit Galron, Ela Bar, Stav Cohen-Adiv, Sivan Kanner, Ari Barzilai, Hadar Levi
Publikováno v:
Glia. 70:536-557
Ataxia-telangiectasia (A-T) is a multisystem autosomal recessive disease caused by mutations in the ATM gene and characterized by cerebellar atrophy, progressive ataxia, immunodeficiency, male and female sterility, radiosensitivity, cancer predisposi
Autor:
Sari Schokoroy Trangle, Tali Rosenberg, Hadar Parnas, Gilad Levy, Ela Bar, Asaf Marco, Boaz Barak
Publikováno v:
Molecular psychiatry.
Williams syndrome (WS) is a neurodevelopmental disorder caused by a heterozygous micro-deletion in the WS critical region (WSCR) and is characterized by hyper-sociability and neurocognitive abnormalities. Nonetheless, whether and to what extent WSCR
Autor:
Ela Bar, Boaz Barak
Publikováno v:
Frontiers for Young Minds. 8
Williams syndrome is a neurodevelopmental disorder characterized by hypersociability and unique neurocognitive abnormalities. One of the characteristics of Williams syndrome is an inappropriate increase in social behavior. People with the syndrome ma
Autor:
Boaz Barak, Ela Bar
Publikováno v:
GliaREFERENCES. 67(11)
Microglia are the immune cells of the brain, involved in synapse formation, circuit sculpting, myelination, plasticity, and cognition. Being active players during early development as well as in adulthood, microglia affect other cells directly by the