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Akademický článek
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Autor:
A. Bittsánszky, R. P. Malone, Jozsef Kiss, L. Márton, Tamás Kőmíves, László Heszky, Gábor Gyulai, Gábor Gullner, M. Czakó
Publikováno v:
Acta Phytopathologica et Entomologica Hungarica. 42:235-243
As DNA methylation patterns are inherited (‘epigenetic memory’) gsh I transgenic poplar ( Populus × canescens ) clones (11 ggs and 6 Lgl ) were treated with the DNA demethylating drug DHAC (5,6-dihydro-5′-azacytidine hydrochloride) at 10 −4
Autor:
R. P. Marathe, G. J. Bishop, László Márton, D. J. Guerra, C. Xiang, M. Czakó, Jonathan D. G. Jones
Publikováno v:
Theoretical and Applied Genetics. 91:1242-1247
The potentials and limitations of negative-selection systems based on the human herpes simplex virus thymidine kinase type-1 (HSVtk) gene, which causes sensitivity to the nucleoside analog ganciclovir, were examined in tobacco as a model system. Ther
Publikováno v:
Genetic counseling (Geneva, Switzerland). 13(4)
We report on a female patient who had mosaic trisomy 9, presenting with severe scoliosis and mental retardation. Scoliosis is seldom reported in patients with mosaic trisomy 9 syndrome. FISH studies in our proband detected no trisomic cell line in th
Publikováno v:
Orvosi hetilap. 142(35)
Kennedy disease is an adult onset neuromuscular disease characterized by slowly progressive proximal and bulbar muscle weakness. The disease associates with gynecomastia, adult onset infertility and sensory neuropathy, and caused by pathologic expans
Publikováno v:
Clinical genetics. 58(5)
Velo-cardio-facial syndrome is a developmental disorder characterized by heart defects, specific facial features, cleft palate and learning disability. Most patients have a 3-Mb deletion in chromosomal region 22q11.2. This microdeletion has also been
Publikováno v:
Orvosi hetilap. 141(34)
Velo-cardio-facial syndrome includes the following clinical features: congenital heart anomaly, velo-pharyngeal malformations and dysmorphic facial features. In 80% of the patients microdeletion of the long arm of chromosome 22 can be detected. Many
Publikováno v:
Orvosi hetilap. 139(52)
Fragile X syndrome is the most common inherited from of familial mental retardation. It is caused by an expanded CGG repeat in the first exon of the fragile X mental retardation gene. A polymerase chain reaction based technique was used for the ident
Publikováno v:
Plant molecular biology. 34(6)
When Agrobacterium was used to transform Nicotiana plumbaginifolia protoplasts and Arabidopsis thaliana roots and seedlings, a large number of plants were found in which not only the T-region defined by the border repeat sequences but the entire bina