نتایج جستجو برای: exencephaly
تعداد نتایج: 186 فیلتر نتایج به سال:
The srbi gene encodes a lipoprotein receptor with high affinity for high density lipoprotein that is mainly expressed in the liver and in steroidogenic tissues. Disruption of this gene in mice and mutations in humans lead to alterations in lipoprotein metabolism and/or fertility. During murine development, scavenger receptor class B member I (SR-BI) is present in the yolk sac and the placenta a...
Dimethyl sulphoxide (DMSO) is a relatively simple organic compound with a molecular weight of 78. It has been reported to be exceptionally non-toxic and has been used extensively in biological systems as a cell preservative, including freeze storage (Porterfield & Ashwood-Smith, 1962; Dougherty, 1962), and as a radioprotective agent against X-irradiation in mice (Ashwood-Smith, 1961). Recent cl...
Genetic variations affecting neural tube closure along the head result in malformations of the face and brain. Neural tube defects (NTDs) are among the most common birth defects in humans. We previously reported a mouse mutant called tuft that arose spontaneously in our wild-type 3H1 colony. Adult tuft mice present midline craniofacial malformations with or without an anterior cephalocele. In a...
The utility of an in vitro system to search for molecular targets and markers of developmental toxicity was explored, using microarrays to detect genes susceptible to deregulation by the teratogen valproic acid (VPA) in the pluripotent mouse embryonal carcinoma cell line P19. Total RNA extracted from P19 cells cultured in the absence or presence of 1, 2.5, or 10mM VPA for 1.5, 6, or 24 h was su...
BACKGROUND Folic acid supplementation prevents the occurrence and recurrence of neural tube defects (NTDs), but the causal metabolic pathways underlying folic acid-responsive NTDs have not been established. Serine hydroxymethyltransferase (SHMT1) partitions folate-derived one-carbon units to thymidylate biosynthesis at the expense of cellular methylation, and therefore SHMT1-deficient mice are ...
BACKGROUND Exposure of pregnant outbred CD-1 mice to methanol during the period of gastrulation results in exencephaly, cleft palate, and cervical vertebra malformations [Rogers and Mole, Teratology 55: 364, 1997], while inbred C57BL/6J mice are sensitive to the teratogenicity of ethanol. C57BL/6J fetuses exhibit the holoprosencephaly spectrum of malformations after maternal exposure to ethanol...
The studies show that there are some embryonic malformation in maternal diabetic rats. This malformation may be manifestation in other embryonic organs such as skeletal cardiovascular or centeral nervus system. In this study the effects of the maternal hyperglicemia on the processes of embryonic evolution, during rat,s pregna...
Cyclophosphamide (CP) is a drug commonly used to treat neoplastic disease and some autoimmune diseases. It is also a well-known and well-studied teratogen causing a variety of birth defects in fetuses of pregnant women treated with the drug. There are many reports that show the adverse effects of CP can be decreased by use of antioxidant drugs. It appears that, quercetin has antioxidant effect....
Background and purpose: Ëpilepsy is a chronic nervous disease, inflicting about 1٪ of the world population. Toxic effects of antiepileptic drugs are significant and controversial issues. Since these drugs are used by millions of people, the least abnormalities could be presented as a hazardous defect. Âim of this study was to investigate the toxic effects of phenytoin and Phenobarbital. Âmong...
Craniofacial malformations, ranging from cleft lip and palate to complex disorders including holoprosencephaly (HPE), affect 84 in 10,000 people worldwide (WHO, 2003). These defects, which can be caused by genetic mutations, environmental factors or combinations of the two, have a mechanistic basis in the alteration of cellular processes during development. For example, mutations in Treacle (TC...
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