Zobrazeno 1 - 10 of 101 pro vyhledávání: '"H.-H. Dahl"'
1
Typing of families with classical phenylketonuria using three alleles of the Hindlll linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe
Autor: G. Cobet, H.-H. Dahl, O. Riess, A. Speer, R. Hanke, R. G. H. Cotton, Ch. Coutelle
Publikováno v: Clinical Genetics. 29:491-495
A human phenylalanine hydroxylase cDNA clone was isolated from a human liver cDNA library. The size of the cDNA insert is approximately 2.4 kb and appears to be a near full length copy of a phenylalanine hydroxylase mRN A. This cDN A was used to prob
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::071238a73385dcaf22758b756f269d65
https://doi.org/10.1111/j.1399-0004.1986.tb00549.x
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3
Atomic force microscopy imaging of DNA-cationic liposome complexes optimised for gene transfection into neuronal cells
Autor: L A, Wangerek, H H, Dahl, T J, Senden, J B, Carlin, D A, Jans, D E, Dunstan, P A, Ioannou, R, Williamson, S M, Forrest
Publikováno v: The journal of gene medicine. 3(1)
Cationic liposomes represent an important gene delivery system due to their low immunogenicity, but are relatively inefficient, with optimisation of DNA-liposome complexes (lipoplexes) for transfection necessary for each cell type of interest. There
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::719428458559b5f061b060a73558cb96
https://pubmed.ncbi.nlm.nih.gov/11269338
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4
A simple PCR test to detect the common 35delG mutation in the connexin 26 gene
Autor: S A, Wilcox, A H, Osborn, H H, Dahl
Publikováno v: Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology. 5(1)
The most common form of nonsyndromic neurosensory autosomal recessive deafness, DFNB1, is caused by mutations in the connexin 26 gene (GJB2) on chromosome 13. One mutation, in which one guanosine (G) residue is deleted from a run of 6 Gs (35delG), is
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ead43665ce52f09a5be5c3615ae96fb5
https://pubmed.ncbi.nlm.nih.gov/10837093
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7
Temporal and tissue-specific interactions involving novel transcription factors and the proximal promoter of the mouse Pdha-2 gene
Autor: R C, Iannello, I, Kola, H H, Dahl
Publikováno v: The Journal of biological chemistry. 268(30)
We have determined by deletion analysis that the most proximal region of the Pdha-2 promoter between nucleotide position -187 to +22 harbors a transcriptionally active core. This "core" promoter directs high levels of CAT (chloramphenicol acetyltrans
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bee28a8c4e7986ab8f34806f35a16f86
https://pubmed.ncbi.nlm.nih.gov/7693672
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8
Pyruvate dehydrogenase deficiency caused by deletion of a 7-bp repeat sequence in the E1 alpha gene
Autor: H H, Dahl, C, Maragos, R M, Brown, L L, Hansen, G K, Brown
Publikováno v: American journal of human genetics. 47(2)
A 7-bp deletion in the X-chromosomal pyruvate dehydrogenase (PDH) E1 alpha gene was characterized in a female patient with the "cerebral" form of PDH deficiency. The mutation was localized using the chemical cleavage method and further characterized
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3dd34ad992fb404de7a49d4c5cd036b0
https://pubmed.ncbi.nlm.nih.gov/2378353
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9
Isolation and sequence of a cDNA clone which contains the complete coding region of rat phenylalanine hydroxylase. Structural homology with tyrosine hydroxylase, glucocorticoid regulation, and use of alternate polyadenylation sites
Autor: H H Dahl, J F Mercer
Publikováno v: Journal of Biological Chemistry. 261:4148-4153
Screening of a rat liver cDNA expression library constructed in the vector lambda gt11 with an affinity purified antiserum to rat phenylalanine hydroxylase has resulted in the isolation of two clones which contain the complete coding region (1362 bas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a7d7d8d75c572f674e5d5d4b6a03c960
https://doi.org/10.1016/s0021-9258(17)35638-7
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10
The human pyruvate dehydrogenase complex. Isolation of cDNA clones for the E1 alpha subunit, sequence analysis, and characterization of the mRNA
Autor: S M Hunt, G K Brown, H H Dahl, W M Hutchison
Publikováno v: Journal of Biological Chemistry. 262:7398-7403
cDNA clones corresponding to the entire length of mRNA for the alpha subunit of human pyruvate dehydrogenase (EC 1.2.4.1), the E1 component of the pyruvate dehydrogenase complex, have been isolated from liver cDNA libraries. Two classes of cDNA clone
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1925c3377e864d8d3afe811bdd9826f5
https://doi.org/10.1016/s0021-9258(18)48250-6
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