Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Thomas Hildmann"'
Autor:
Vardhman K Rakyan, Thomas Hildmann, Karen L Novik, Jörn Lewin, Jörg Tost, Antony V Cox, T Dan Andrews, Kevin L Howe, Thomas Otto, Alexander Olek, Judith Fischer, Ivo G Gut, Kurt Berlin, Stephan Beck
Publikováno v:
PLoS Biology, Vol 2, Iss 12, p e405 (2004)
The Human Epigenome Project aims to identify, catalogue, and interpret genome-wide DNA methylation phenomena. Occurring naturally on cytosine bases at cytosine-guanine dinucleotides, DNA methylation is intimately involved in diverse biological proces
Externí odkaz:
https://doaj.org/article/2cf00ba41d244a9caba9210bb644349d
Autor:
Dieter Janz, Thomas Sander, Bettina Schmitz, M Rees, Magali Williamson, Gertrud Beck-Mannagetta, Ulrike Sailer, A. Scaramelli, Thomas Hildmann, G. Bauer, Amedeo Bianchi, F. V. Elmslie, Rebekka Kretz, RM Gardiner
Publikováno v:
Acta Neurologica Scandinavica. 96:1-7
INTRODUCTION: We tested the hypothesis that genetic variants within the GABA(A) alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15q11-q13 confer genetic susceptibility to common subtypes of idiopathic generalized epilepsy (IGE). MATERIAL
Autor:
Odej Kao, Thomas Hildmann
Publikováno v:
ICDCS Workshops
The conception and implementation of an on-premise cloud storage is a significant, but also necessary step in the development of modern data centers. Providing seamless access to data from multiple devices and from any network-connected location worl
Autor:
Emilie Dagand, Hans Lehrach, Hoang-My Christensen, Marie-Laure Yaspo, Thomas Hildmann, Xianging Kong, Lisa Riesselman, John T. O'Brien
Publikováno v:
Europe PubMed Central
Progress in complete genomic sequencing of human chromosome 21 relies on the construction of high-quality bacterial clone maps spanning large chromosomal regions. To achieve this goal, we have applied a strategy based on nonradioactive hybridizations
Autor:
Bockenkamp B, Olaf Riess, D. Janz, Jörg T. Epplen, Gertrud Beck-Mannagetta, Thomas F. Wienker, Thomas Sander, Rainer Blasczyk, Andreas Ziegler, Thomas Hildmann, Rebekka Kretz, Bettina Schmitz, Armin Volz
Publikováno v:
Neurology. 49:842-847
Juvenile myoclonic epilepsy (JME) is a genetically determined common subtype of idiopathic generalized epilepsy. Linkage to the HLA complex on chromosome 6p21.3 and an allelic association with HLA-DR13 and -DQB1 alleles suggest that a susceptibility
Publikováno v:
EUNIS 2013 Congress Proceedings; 2013: ICT Role for Next Generation Universities
Our students and researchers arrive nowadays at the university with a broad knowledge and expectations about the IT support and the IT technology. Notebooks, netbooks, smart phones together with a broad WiFi coverage enable a nearly unlimited freedom
Autor:
Dieter Janz, Amedeo Bianchi, Gertrud Beck-Mannagetta, Thomas Hildmann, Gerhard Bauer, Thomas Sander, Alejandro Scaramelli
Publikováno v:
Epilepsy Research. 25:139-145
Hereditary factors play a major role in the etiology of idiopathic generalized epilepsies (IGEs). The frequent neuropathological occurrence of microdysgeneses in the brain of IGE patients implies that genes regulating neural migration and cell adhesi
Autor:
Gertrud Beck-Mannagetta, Thomas F. Wienker, Thomas Hildmann, Keith J. Johnson, Ulrike Sailer, Thomas Sander, G. Bauer, Heidemarie Neitzel, Amedeo Bianchi, Mark G. Darlison, Mark E.S. Bailey, Dieter Janz, Alejandro Scaramelli, Bettina Schmitz
Publikováno v:
Epilepsy Research. 23:235-244
Hereditary factors play a major role in the etiology of idiopathic generalized epilepsies (IGEs). The pivotal function of ionotropic gamma-aminobutyric acid type A receptors (GABRs) in inhibitory neurotransmission in the mammalian central nervous sys
Autor:
Gertrud Beck-Mannagetta, Thomas Sander, Thomas Hildmann, Keith J. Johnson, G. Bauer, Christian Ramel, Amedeo Bianchi, D. Janz, Thomas F. Wienker, Martina Durner, Bettina Schmitz, Heidemarie Neitzel, Ulrike Sailer, Klaus Berek
Publikováno v:
American Journal of Medical Genetics. 67:31-39
Hereditary factors play a major role in the etiology of idiopathic generalized epilepsies (IGEs). A trait locus (EBN1) for a rare subtype of IGEs, the benign neonatal familial convulsions, and a susceptibility gene (EEGV1) for the common human low-vo
Autor:
Thomas Hildmann, Christopher Ritter
Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich. This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae530a9e8441da7b6cd4816ccb628ef1