Hydrocephalus in the Otx2+/−Mutant Mouse
Tài liệu tham khảo
Acampora, 1996, Forebrain and midbrain regions are deleted in Otx2−/−, Development, 121, 3279, 10.1242/dev.121.10.3279
Berry, 1961, The inheritance and pathogenesis of hydrocephalus-3 in the mouse, J. Pathol. Bacteriol., 81, 157, 10.1002/path.1700810119
Boncinelli, 1993, Emx and Otx homeobox genes in the developing mouse brain, J. Neurobiol., 24, 1356, 10.1002/neu.480241008
Frantz, 1994, Otx1 and Otx2 define layers and regions in developing cerebral cortex and cerebellum, J. Neurosci., 14, 5725, 10.1523/JNEUROSCI.14-10-05725.1994
Harvey, 1979, Familial communicating hydrocephalus, posterior cerebellar agenesis, mega cisterna magna, and prt-wine nevi, M. Neurosurg., 51, 862, 10.3171/jns.1979.51.6.0862
James, 1992, Hydrocephalus in infancy and childhood, Am. Fam. Physician, 45, 733
Juet, 1994, X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations with L1 gene, Nat. Genet., 7, 402, 10.1038/ng0794-402
Kelly, 1983, A modified differential stain for cartilage and bone in whole mout preparations of mammalian fetuses and small vertebrates, Stain Technol., 58, 131, 10.3109/10520298309066773
Lawson, 1973, Hydrocephalus-3, a murine mutant. I. Alterations in fine structure of choroid plexus and ependyma, Surg. Neurol., 1, 115
Madeline, 1995, Postnatal development of the central skull base: Normal variants, Radiology, 196, 757, 10.1148/radiology.196.3.7644640
Matsuo, 1996, Mouse Otx2 functions in the formation and patterning of rostral head, Genes Dev., 9, 2646, 10.1101/gad.9.21.2646
McLone, 1973, Hydrocephalus-3, a murine mutant. II. Changes in the brain extracellular space, Surg. Neurol., 1, 233
Prockop, 1989, Hydrocephalus
Raimondi, 1973, The pathophysiology and morphology of murine hydrocephalus in hy-3 and ch mutants, Surg. Neurol., 1, 50
Schrander-Stumpel, 1990, MASA syndrome: new clinical features and linkage analysis using DNA probes, J. Med. Genet., 27, 688, 10.1136/jmg.27.11.688
Simeone, 1992, Nested expression domains of four homeobox genes indeveloping rostral brain, Nature, 358, 687, 10.1038/358687a0
Sofer, 1979, Cockayne syndrome: Unusual pathological findings and review of the literature, Ann. Neurol., 6, 340, 10.1002/ana.410060407
Yagi, 1993, A novel ES cell line, TT2, with high germline-differentiating potency, Anal. Biochem., 214, 70, 10.1006/abio.1993.1458