Found: 7
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Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsy.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 2, p. 128, doi. 10.1007/s100380050053
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- Article
A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia.
- Published in:
- Journal of Human Genetics, 1998, v. 43, n. 2, p. 135, doi. 10.1007/s100380050055
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- Article
Prenatal diagnosis of non-ketotic hyperglycinaemia: enzymatic diagnosis in 28 families and DNA diagnosis detecting prevalent Finnish and Israeli-Arab mutations.
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- Prenatal Diagnosis, 1999, v. 19, n. 8, p. 717, doi. 10.1002/(SICI)1097-0223(199908)19:8<717::AID-PD625>3.0.CO;2-L
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- Article
Role of Central Angiotensin II in Interleukin-1-Induced Fever in Rats.
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- Annals of the New York Academy of Sciences, 1997, v. 813, n. 1, p. 314, doi. 10.1111/j.1749-6632.1997.tb51712.x
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- Article
Human glycine decarboxylase gene (GLDC) and its highly conserved processed pseudogene (ψGLDC): their structure and expression, and the identification of a large deletion in a family with nonketotic hyperglycinemia.
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- Human Genetics, 2000, v. 106, n. 3, p. 298, doi. 10.1007/s004390051041
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- Article
In vivo optical recordings of synaptic transmission and intracellular Ca<sup>2+</sup> and Cl<sup>–</sup> in the superior colliculus of fetal rats.
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- European Journal of Neuroscience, 2006, v. 23, n. 6, p. 1405, doi. 10.1111/j.1460-9568.2006.04683.x
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- Article
Asphyxia induced by umbilical cord occlusion alters glutamatergic and GABAergic synaptic transmission in neurons of the superior colliculus in fetal rats.
- Published in:
- International Journal of Developmental Neuroscience, 2013, v. 31, n. 4, p. 274, doi. 10.1016/j.ijdevneu.2013.03.001
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- Article