MeSH Review:
Neural Tube Defects
- Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS). Gibbons, R.J., Pellagatti, A., Garrick, D., Wood, W.G., Malik, N., Ayyub, H., Langford, C., Boultwood, J., Wainscoat, J.S., Higgs, D.R. Nat. Genet. (2003)
- Regulation of repulsion versus adhesion by different splice forms of an Eph receptor. Holmberg, J., Clarke, D.L., Frisén, J. Nature (2000)
- Folate deficiency, neural tube defects, and cardiac disease in UK Indians and Pakistanis. Michie, C.A., Chambers, J., Abramsky, L., Kooner, J.S. Lancet (1998)
- Amniotic-fluid acetylcholinesterase as a possible diagnostic test for neural-tube defects in early pregnancy. Smith, A.D., Wald, N.J., Cuckle, H.S., Stirrat, G.M., Bobrow, M., Lagercrantz, H. Lancet (1979)
- Genetic effects on variation in red-blood-cell folate in adults: implications for the familial aggregation of neural tube defects. Mitchell, L.E., Duffy, D.L., Duffy, P., Bellingham, G., Martin, N.G. Am. J. Hum. Genet. (1997)
- The absence of a relation between the periconceptional use of vitamins and neural-tube defects. National Institute of Child Health and Human Development Neural Tube Defects Study Group. Mills, J.L., Rhoads, G.G., Simpson, J.L., Cunningham, G.C., Conley, M.R., Lassman, M.R., Walden, M.E., Depp, O.R., Hoffman, H.J. N. Engl. J. Med. (1989)
- Targeting Ras signaling through inhibition of carboxyl methylation: an unexpected property of methotrexate. Winter-Vann, A.M., Kamen, B.A., Bergo, M.O., Young, S.G., Melnyk, S., James, S.J., Casey, P.J. Proc. Natl. Acad. Sci. U.S.A. (2003)
- Glucose transporter gene expression in rat conceptus during high glucose culture. Takao, Y., Akazawa, S., Matsumoto, K., Takino, H., Akazawa, M., Trocino, R.A., Maeda, Y., Okuno, S., Kawasaki, E., Uotani, S. Diabetologia (1993)
- Therapy-related acute myelogenous leukemia associated with 11q23 chromosomal abnormalities and topoisomerase II inhibitors: report of four additional cases and brief commentary. Bredeson, C.N., Barnett, M.J., Horsman, D.E., Dalal, B.I., Ragaz, J., Phillips, G.L. Leuk. Lymphoma (1993)
- Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski-/- mice. Colmenares, C., Heilstedt, H.A., Shaffer, L.G., Schwartz, S., Berk, M., Murray, J.C., Stavnezer, E. Nat. Genet. (2002)
- Prevention of neural-tube defects with folic acid in China. China-U.S. Collaborative Project for Neural Tube Defect Prevention. Berry, R.J., Li, Z., Erickson, J.D., Li, S., Moore, C.A., Wang, H., Mulinare, J., Zhao, P., Wong, L.Y., Gindler, J., Hong, S.X., Correa, A. N. Engl. J. Med. (1999)
- HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3. Magnaghi, P., Roberts, C., Lorain, S., Lipinski, M., Scambler, P.J. Nat. Genet. (1998)
- Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene. Zhao, Q., Behringer, R.R., de Crombrugghe, B. Nat. Genet. (1996)
- Neural-tube defects and derangement of homocysteine metabolism. Steegers-Theunissen, R.P., Boers, G.H., Trijbels, F.J., Eskes, T.K. N. Engl. J. Med. (1991)
- Disruption of the csk gene, encoding a negative regulator of Src family tyrosine kinases, leads to neural tube defects and embryonic lethality in mice. Imamoto, A., Soriano, P. Cell (1993)
- Neutral-red uptake by amniotic-fluid macrophages in neural-tube defects: a rapid test. Polgár, K., Sipka, S., Abel, G., Papp, Z. N. Engl. J. Med. (1984)
- Transferrin and HLA: spontaneous abortion, neural tube defects, and natural selection. Weitkamp, L.R., Schacter, B.Z. N. Engl. J. Med. (1985)
- Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice. Neumann, P.E., Frankel, W.N., Letts, V.A., Coffin, J.M., Copp, A.J., Bernfield, M. Nat. Genet. (1994)
- Cellular and developmental control of O2 homeostasis by hypoxia-inducible factor 1 alpha. Iyer, N.V., Kotch, L.E., Agani, F., Leung, S.W., Laughner, E., Wenger, R.H., Gassmann, M., Gearhart, J.D., Lawler, A.M., Yu, A.Y., Semenza, G.L. Genes Dev. (1998)
- Multivitamin/folic acid supplementation in early pregnancy reduces the prevalence of neural tube defects. Milunsky, A., Jick, H., Jick, S.S., Bruell, C.L., MacLaughlin, D.S., Rothman, K.J., Willett, W. JAMA (1989)
- Preliminary results of treatment with filgrastim for relapse of leukemia and myelodysplasia after allogeneic bone marrow transplantation. Giralt, S., Escudier, S., Kantarjian, H., Deisseroth, A., Freireich, E.J., Andersson, B.S., O'Brien, S., Andreeff, M., Fisher, H., Cork, A. N. Engl. J. Med. (1993)
- Increased risk of myelodysplasia and leukaemia after etoposide, cisplatin, and bleomycin for germ-cell tumours. Pedersen-Bjergaard, J., Daugaard, G., Hansen, S.W., Philip, P., Larsen, S.O., Rørth, M. Lancet (1991)
- Detection of abnormal pretransplant clones in progenitor cells of patients who developed myelodysplasia after autologous transplantation. Abruzzese, E., Radford, J.E., Miller, J.S., Vredenburgh, J.J., Rao, P.N., Pettenati, M.J., Cruz, J.M., Perry, J.J., Amadori, S., Hurd, D.D. Blood (1999)
- Decreased phosphorylation of protein kinase B and extracellular signal-regulated kinase in neutrophils from patients with myelodysplasia. Fuhler, G.M., Drayer, A.L., Vellenga, E. Blood (2003)
- Transgenic rescue of congenital heart disease and spina bifida in Splotch mice. Li, J., Liu, K.C., Jin, F., Lu, M.M., Epstein, J.A. Development (1999)
- Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR. Goyette, P., Christensen, B., Rosenblatt, D.S., Rozen, R. Am. J. Hum. Genet. (1996)
- Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion. Boultwood, J., Rack, K., Kelly, S., Madden, J., Sakaguchi, A.Y., Wang, L.M., Oscier, D.G., Buckle, V.J., Wainscoat, J.S. Proc. Natl. Acad. Sci. U.S.A. (1991)
- Homozygosity for Waardenburg syndrome. Zlotogora, J., Lerer, I., Bar-David, S., Ergaz, Z., Abeliovich, D. Am. J. Hum. Genet. (1995)
- Crooked tail (Cd) model of human folate-responsive neural tube defects is mutated in Wnt coreceptor lipoprotein receptor-related protein 6. Carter, M., Chen, X., Slowinska, B., Minnerath, S., Glickstein, S., Shi, L., Campagne, F., Weinstein, H., Ross, M.E. Proc. Natl. Acad. Sci. U.S.A. (2005)
- The supportive effects of erythropoietin and mast cell growth factor on CD34+/CD36- sorted bone marrow cells of myelodysplasia patients. Brada, S., de Wolf, J., Hendriks, D., Esselink, M., Ruiters, M., Vellenga, E. Blood (1996)
- Inositol prevents folate-resistant neural tube defects in the mouse. Greene, N.D., Copp, A.J. Nat. Med. (1997)
- Amniotic fluid alpha-fetoprotein in the prenatal diagnosis of fetal neural tube defects. Summitt, R.L. JAMA (1980)
- Folate levels and neural tube defects. Implications for prevention. Daly, L.E., Kirke, P.N., Molloy, A., Weir, D.G., Scott, J.M. JAMA (1995)
- Idarubicin cardiotoxicity: a retrospective study in acute myeloid leukemia and myelodysplasia. Anderlini, P., Benjamin, R.S., Wong, F.C., Kantarjian, H.M., Andreeff, M., Kornblau, S.M., O'Brien, S., Mackay, B., Ewer, M.S., Pierce, S.A. J. Clin. Oncol. (1995)
- Automated two-site immunoradiometric assay of human alpha-fetoprotein in maternal serum. Kemp, H.A., Simpson, J.S., Woodhead, J.S. Clin. Chem. (1981)