Zobrazeno 1 - 10
of 217
pro vyhledávání: '"Craniorachischisis"'
Publikováno v:
National Journal of Clinical Anatomy, Vol 11, Iss 2, Pp 110-112 (2022)
Neural tube defects (NTDs) are the second most common cause of congenital anomaly worldwide (cardiac anomalies is the first). The 3rd and 4th week of gestation is the critical period for neural tube development. Multiple genetic and environmental fac
Externí odkaz:
https://doaj.org/article/a74e70c1384343ee8429fb1b69bcccee
Autor:
Faten Limaiem, Kaouther Dimassi
Publikováno v:
Clinical Case Reports, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Craniorachischisis totalis is an uncommon and severe form of neural tube defect. It is characterized by anencephaly and spina bifida throughout the vertebral column accompanied by herniation of neural tissue and meninges. Hepatic calcificati
Externí odkaz:
https://doaj.org/article/a037fac840c3457f8f66e3a6421c454f
Akademický článek
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Autor:
Hong-Ming Zhou, Simon J. Conway
Publikováno v:
Journal of Developmental Biology, Vol 10, Iss 2, p 19 (2022)
Pax3 and Pax7 transcription factors are paralogs within the Pax gene family that that are expressed in early embryos in partially overlapping expression domains and have distinct functions. Significantly, mammalian development is largely unaffected b
Externí odkaz:
https://doaj.org/article/5e4a6c22df4d49a094f7fa025fd47d24
Autor:
Jennifer N. Murdoch, Christine Damrau, Anju Paudyal, Debora Bogani, Sara Wells, Nicholas D. E. Greene, Philip Stanier, Andrew J. Copp
Publikováno v:
Disease Models & Mechanisms, Vol 7, Iss 10, Pp 1153-1163 (2014)
Neural tube defects (NTDs) are among the commonest and most severe forms of developmental defect, characterized by disruption of the early embryonic events of central nervous system formation. NTDs have long been known to exhibit a strong genetic dep
Externí odkaz:
https://doaj.org/article/97de87b50a4e4ca0a710889558ea52d5
Akademický článek
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Autor:
Pranadeep Reddy Inukollu
Thai Journal of Obstetrics and Gynaecology, 30, 2, 145-149
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fd75171f9aaf01a869074c2326fe987
Autor:
Gabriel L. Galea, Dawn Savery, Andrew J. Copp, Oleksandr Nychyk, Matteo A. Molè, Philip Stanier, Nicholas D. E. Greene
Publikováno v:
Disease Models & Mechanisms
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Planar cell polarity (PCP) signalling is vital for initiation of mouse neurulation, with diminished convergent extension (CE) cell movements leading to craniorachischisis, a severe neural tube defect (NTD). Some humans with NTDs also have PCP gene mu
Autor:
Diana M. Juriloff, Muriel J. Harris
Publikováno v:
Journal of Developmental Biology, Vol 6, Iss 3, p 22 (2018)
The human neural tube defects (NTD), anencephaly, spina bifida and craniorachischisis, originate from a failure of the embryonic neural tube to close. Human NTD are relatively common and both complex and heterogeneous in genetic origin, but the genet
Externí odkaz:
https://doaj.org/article/58d8fcfe97ea42498894ca30f11eacad
Autor:
Chih-Ping Chen, Yu-Peng Liu, Fuu-Jen Tsai, Chen-Yu Chen, Hung-Hung Lin, Pei-Chen Wu, Wayseen Wang
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 48, Iss 3, Pp 286-291 (2009)
Objective: To present the prenatal magnetic resonance imaging (MRI) findings of concomitant craniorachischisis and omphalocele, review the literature, and discuss the pathogenesis. Case Report: A 20-year-old, gravida 2, para 0, woman was referred to
Externí odkaz:
https://doaj.org/article/bb000d87501740519d90dfb906b3b885