Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Hindbrain formation"'
Autor:
Houda Kilani, Aljazi Al-Maraghi, Sahar I. Da'as, Alya Al-Kurbi, Waleed Aamer, Khalid A. Fakhro, Mitchell A. Stotland, Khaled Zamel, Jehan AlRayahi, Waseem Hasan
Publikováno v:
Cells
Volume 9
Issue 8
Cells, Vol 9, Iss 1782, p 1782 (2020)
Volume 9
Issue 8
Cells, Vol 9, Iss 1782, p 1782 (2020)
Recessive mutations in Post-GPI attachment to proteins 3 (PGAP3) cause the rare neurological disorder hyperphosphatasia with mental retardation syndrome 4 type (HPMRS4). Here, we report a novel homozygous nonsense mutation in PGAP3 (c.265C>
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Publikováno v:
The International Journal of Developmental Biology. 62:767-774
Hox proteins have long been known to function as transcriptional regulators during development of the vertebrate hindbrain. In particular, these factors are thought to play key roles in assigning distinct fates to the rhombomere segments arising in t
Publikováno v:
World neurosurgery. 135
Background Chiari malformations include a large spectrum of anomalies of hindbrain formation that appear at different stages of development of the central nervous system. Chiari described these malformations as congenital anomalies of the hindbrain c
Publikováno v:
Neural Development
Neural Development, Vol 13, Iss 1, Pp 1-24 (2018)
Neural Development, Vol 13, Iss 1, Pp 1-24 (2018)
Background Previous work aimed at understanding the gene regulatory networks (GRNs) governing caudal hindbrain formation identified morphogens such as Retinoic Acid (RA) and Fibroblast growth factors (FGFs), as well as transcription factors like hoxb
Autor:
Ronald D. G. McKay, Ioannis Karampelas, Marannia Saridaki, Nikolaos Mandalos, Eumorphia Remboutsika, Mark L. Cohen
The cerebellum, a derivative of the hindbrain, plays a crucial role in balance and posture as well as in higher cognitive and locomotive processes. Cerebellar development is initiated during the segmental phase of hindbrain formation. Here, we descri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1534dfd520cf8b3d774aff65fc4fb947
https://europepmc.org/articles/PMC6295446/
https://europepmc.org/articles/PMC6295446/
Autor:
Satoshi Shimozono, Shin-ichi Higashijima, Atsushi Miyawaki, Tadahiro Iimura, Tetsuya Kitaguchi
Publikováno v:
Nature. 496:363-366
In vertebrate development, the body plan is determined by primordial morphogen gradients that suffuse the embryo. Retinoic acid (RA) is an important morphogen involved in patterning the anterior-posterior axis of structures, including the hindbrain a
Autor:
Yuval Ebenstein, Deepak Kumar Sinha, Carole Gauron, Zhiping Feng, Arbel D. Tadmor, David Bensimon, Shuo Lin, Sophie Vriz, Bertrand Ducos, Lijun Xu, Thomas Le Saux, Shimon Weiss, Ludovic Jullien
Publikováno v:
Development. 139:3355-3362
All-trans retinoic acid (RA) is a key player in many developmental pathways. Most methods used to study its effects in development involve continuous all-trans RA activation by incubation in a solution of all-trans RA or by implanting all-trans RA-so
Autor:
Ori Scott, Helly Goez
Publikováno v:
Journal of Child Neurology. 26:1311-1315
Studies in animal models have established that intra-uterine vitamin A deficiency can hinder hindbrain formation; however, reports of such a phenomenon in humans had not been published until recently, when our group presented the case of an infant di
Autor:
Hiroyuki Takeda, Kyo Yamasu, Yuri Kuroyanagi, Akiko Ishioka, Tomoko Jindo, Mst. Shahnaj Parvin, Toshihiro Kawanabe, Masataka Nikaido, Kohei Hatta
Publikováno v:
Developmental Biology. 350:154-168
Zebrafish hoxb1b is expressed during epiboly in the posterior neural plate, with its anterior boundary at the prospective r4 region providing a positional cue for hindbrain formation. A similar function and expression is known for Hoxa1 in mice, sugg
Autor:
Yoni E. Gutkovich, Rachel Ofir, Charna Dibner, Dale Frank, Yaniv M. Elkouby, Aharon Gefen, Sarah Elias
Publikováno v:
Developmental Biology, Vol. 338, No 1 (2010) pp. 50-62
In Xenopus embryos, XMeis3 protein activity is required for normal hindbrain formation. Our results show that XMeis3 protein knock down also causes a loss of primary neuron and neural crest cell lineages, without altering expression of Zic, Sox or Pa