Zobrazeno 1 - 10
of 130
pro vyhledávání: '"K. Grade"'
Autor:
R. Kath, E. Bender, Siegfried Scherneck, Burkhard Jandrig, Anita Nothnagel, Peter M. Schlag, Manuela Müller, Beate Waindzoch, Susanne Seitz, Klaus Rohde, Klaus Höffken, K. Grade
Publikováno v:
International Journal of Cancer. 68:188-192
We analyzed germline mutations of the BRCA1 gene in 20 German breast/ovarian-cancer families. BRCA1 mutations co-segregating with breast-cancer susceptibility were identified in 3 of these families. All mutations were found to generate a premature st
Publikováno v:
Human Genetics. 94:19-24
A pilot project offering voluntary heterozygote screening for the delta F508 mutation causing cystic fibrosis (CF) to 638 pregnant women attending two antenatal clinics in the eastern part of Berlin was carried out from 1990-1993. Participation was i
Publikováno v:
eLS
Position effect variegation (PEV) is the mosaic pattern of expression shown by genes placed within or near heterochromatic environments. Research on several model organisms has identified molecular mechanisms that account for PEV. These studies sugge
Autor:
Laura E, Norwood, Stephanie K, Grade, Diane E, Cryderman, Karrie A, Hines, Nicholas, Furiasse, Rafael, Toro, Yuhong, Li, Archana, Dhasarathy, Michael P, Kladde, Mary J C, Hendrix, Dawn A, Kirschmann, Lori L, Wallrath
Publikováno v:
Gene. 336(1)
Heterochromatin protein 1 Hsalpha (HP1(Hsalpha)) is one of three human proteins that share sequence similarity with Drosophila HP1. HP1 proteins are enriched at centric heterochromatin and play a role in chromatin packaging and gene regulation. In hu
Autor:
Xiaoyi Yao, Agnieszka Niewmierzycka, Peter A. Rubenstein, Steven Clarke, Stephanie K. Grade, Kym F. Faull, Hamid Reza Kalhor
Publikováno v:
Archives of biochemistry and biophysics. 370(1)
To identify a protein histidine methyltransferase from Saccharomyces cerevisiae, we examined purified actin for the presence of the highly conserved 3-methylhistidine residue at position 73 by amino acid analysis of the whole protein and by amino aci
Publikováno v:
Human mutation. 8(4)
Publikováno v:
Human mutation. 4(1)
Cystic fibrosis, a common recessive disorder of exocrine glands, is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. We describe the identification of a 32-bp deletion within the coding region of CFTR that i
Publikováno v:
Journal of medical genetics. 30(11)
More than 30% of Duchenne and Becker muscular dystrophy (DMD/BMD) patients have no gross DNA rearrangements like deletions or duplications. The large size of the coding sequence of the dystrophin gene (11 kilobases) complicates systematic identificat
Autor:
K. Grade, H. Matthies
Publikováno v:
Zeitschrift für Chemie. 3:229-229
Autor:
K. Grade
Publikováno v:
Zeitschrift für Chemie. 1:158-158