T. Hildmann

发表

DNA Methylation Profiling of the Human Major Histocompatibility Complex: A Pilot Study for the Human Epigenome Project

Antony V. Cox, A. Cox, I. Gut, 2004, PLoS biology.

Comparative DNA methylation analysis in normal and tumour tissues and in cancer cell lines using differential methylation hybridisation.

C. Lofton-Day, T. Rujan, F. Eckhardt, 2007, The international journal of biochemistry & cell biology.

A contiguous 3-Mb sequence-ready map in the S3-MX region on 21q22.2 based on high- throughput nonisotopic library screenings.

J. O'Brien, H. Lehrach, E. Dagand, 1999, Genome research.

Linkage analysis between idiopathic generalized epilepsies and the GABAA receptor α5, β3 and γ3 subunit gene cluster on chromosome 15

Rm Gardiner, M Rees, Thomas Hildmann, 1997 .

Lack of linkage between idiopathic generalized epilepsies and the gene encoding the neural cell adhesion molecule

T. Sander, D. Janz, A. Bianchi, 1996, Epilepsy Research.

General roles of abscisic and jasmonic acids in gene activation as a result of mechanical wounding.

L. Willmitzer, S. Prat, J. Sánchez-Serrano, 1992, The Plant cell.

Quantitative DNA methylation analysis based on four-dye trace data from direct sequencing of PCR amplificates

Jörn Lewin, Christian Piepenbrock, Péter Adorján, 2004, Bioinform..

Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism.

T. Wienker, B. Schmitz, T. Sander, 1997, American journal of medical genetics.

Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alpha5, beta3 and gamma3 subunit gene cluster on chromosome 15.

F. Elmslie, B. Schmitz, T. Sander, 1997, Acta neurologica Scandinavica.

Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies

T. Wienker, A. Ziegler, C. Ross, 1995, Neurology.

Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor α1 and γ2 subunit gene cluster on chromosome 5

T. Wienker, B. Schmitz, T. Sander, 1996, Epilepsy Research.

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

T. Wienker, A. Ziegler, O. Riess, 1997, Neurology.

Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.

T. Wienker, B. Schmitz, T. Sander, 1996, American journal of medical genetics.

The phenotypic spectrum related to the human epilepsy susceptibility gene “EJM1”

T. Wienker, B. Schmitz, T. Sander, 1995, Annals of neurology.

The gene encoding the α 1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy

T. Wienker, O. Riess, J. Epplen, 1998, Epilepsy Research.

The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.

T. Wienker, O. Riess, J. Epplen, 1998, Epilepsy Research.