Evidence for multi-site closure of the neural tube in humans.
about
Towards a cellular and molecular understanding of neurulationRibonucleotide reductase subunit R1: a gene conferring sensitivity to valproic acid-induced neural tube defects in miceDynamic imaging of mammalian neural tube closureCongenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. IV: closure defects of the neural tube.Neural tube defects: recent advances, unsolved questions, and controversies.Further evidence for an intermittent pattern of neural tube closure in humansFetal valproate syndrome.Apparent lability of neural tube closure in laboratory animals and humans.Valproic acid use in psychiatry: issues in treating women of reproductive age.Spinal dysraphism: A challenge continued to be faced by neurosurgeons in developing countriesMethylmercury induced toxicogenomic response in C57 and SWV mouse embryos undergoing neural tube closureHuman prenatal craniofacial development related to brain development under normal and pathologic conditions.Testing the vulnerability of the phylotypic stage: on modularity and evolutionary conservation.Classifying sex biased congenital anomalies.The cerebellum in children with spina bifida and Chiari II malformation: Quantitative volumetrics by region.Visual fixation in Chiari type II malformationUpper limb motor function in young adults with spina bifida and hydrocephalusLooking for causes of neural tube defects: where does the environment fit in?Anti-epileptic drugs in pregnancy: current safety and other issues.A familial association between twinning and upper-neural tube defects.A Study on The Incidence of Neural Tube Defects in A Tertiary Care Hospital Over A Period of Five Years.Maternal Antenatal Bereavement and Neural Tube Defect in Live-Born Offspring: A Cohort Study.Human neural tube defects: developmental biology, epidemiology, and geneticsNeurulation in the cranial region--normal and abnormal.Biomechanical coupling facilitates spinal neural tube closure in mouse embryos.Clinical spectrum of neural tube defects with special reference to karyotyping study.Etiology, pathogenesis and prevention of neural tube defects.Multiple neural tube defects in a child: A rare developmental anomalyProfiling placental and fetal DNA methylation in human neural tube defects.The vestibulo-ocular reflex during active head motion in Chiari II malformation.Family-based association study between SLC2A1, HK1, and LEPR polymorphisms with myelomeningocele in Chile.Recent perspectives on the genetic background of neural tube defects with special regard to iniencephaly.Disruption of the MacMARCKS gene prevents cranial neural tube closure and results in anencephaly.Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and HumansHuman neural tube defects: genetic causes and prevention.A rare case of split pons with double encephalocoele, dermal sinus tract, and lipomeningomyelocele: a case report and review of literature.Genetic evidence in planar cell polarity signaling pathway in human neural tube defects.Stretching cell morphogenesis during late neurulation and mild neural tube defects.Prospective, declarative, and nondeclarative memory in young adults with spina bifida.Drug and environmental factors associated with adverse pregnancy outcomes. Part II: Improvement with folic acid.
P2860
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P2860
Evidence for multi-site closure of the neural tube in humans.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年学术文章
@wuu
1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
@yue
1993年學術文章
@zh
1993年學術文章
@zh-hant
name
Evidence for multi-site closure of the neural tube in humans.
@en
type
label
Evidence for multi-site closure of the neural tube in humans.
@en
prefLabel
Evidence for multi-site closure of the neural tube in humans.
@en
P2093
P356
P1476
Evidence for multi-site closure of the neural tube in humans.
@en
P2093
Chernoff GF
Chitayat D
Juriloff D
Kalousek DK
Langlois S
MacLeod PM
McGillivray BC
Van Allen MI
P2860
P304
P356
10.1002/AJMG.1320470528
P577
1993-10-01T00:00:00Z