Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ralph Oehlmann"'
Autor:
Marion Deuter, Francis Anthony Lai, Heiner Post, Paulina Wakula, Gottfried Brem, Urban Besenfelder, Burkert Pieske, Sabine Brauer, Jens Kockskämper, Ralph Oehlmann, Egbert Bisping
Publikováno v:
Journal of Pharmacological and Toxicological Methods. 63:180-185
Introduction Fundamental differences in Ca2+ homeostasis between mice and larger mammals require the validation of the mechanisms of arrhythmogenesis before translation into human pathophysiology. The purpose of this study was to create transgenic ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a9f9f95a5250f60195b8a3bee8c7be7
https://doi.org/10.1016/j.vascn.2010.09.007
https://doi.org/10.1016/j.vascn.2010.09.007
Autor:
Rolf D. Horstmann, Bertram Müller-Myhsok, Peter Vieregge, Ralph Oehlmann, Edito Fabrizio, Donald B. Calne, Benjamin Bereznai, Zbigniew K. Wszolek, Vincenzo Bonifati, Thomas Gasser
Publikováno v:
Nature Genetics. 18:262-265
Parkinson's disease (PD) is a common degenerative neurologic disorder, which is pathologically characterized by a selective degeneration of dopaminergic neurons of the substantia nigra pars compacta, and the presence of characteristic eosinophilic in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5370f262cd675087ace249fa526b2c8
https://doi.org/10.1038/ng0398-262
https://doi.org/10.1038/ng0398-262
Autor:
Farah Younus, Bertram Müller-Myhsok, S. Qasim Mehdi, Aisha Mohyuddin, Ralph Oehlmann, Andreas Gal, Andres Veske
Publikováno v:
Human molecular genetics. 5(1)
Autosomal recessive childhood-onset non-syndromic deafness is one of the most frequent forms of inherited hearing impairment. Recently five different chromosomal regions, 7q31, 11q13.5, 13q12, 14q and the pericentromeric region of chromosome 17, have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b59b02727a9f9fd31255f0e0c4cef9fb
https://pubmed.ncbi.nlm.nih.gov/8789456
https://pubmed.ncbi.nlm.nih.gov/8789456
Autor:
Farah Younus, Andreas Gal, Jutta Leutelt, L. Ingeborgh van den Born, S. Qasim Mehdi, James L. Weber, Ralph Oehlmann, Michael J. Denton
Publikováno v:
Clinical genetics. 47(3)
A large Pakistani family with several consanguineous marriages is described, in which autosomal recessive retinitis pigmentosa is segregating. Linkage studies revealed close linkage between the disease locus and six loci on chromosome 1q (D1S158, F13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a91ef362ff95dce28f1571566335f37
https://pubmed.ncbi.nlm.nih.gov/7634534
https://pubmed.ncbi.nlm.nih.gov/7634534
Autor:
Richard H. Rothman, Robert G. Knowlton, George Yeh, Maria Hervada-Page, Ralph Oehlmann, Eric J. Weaver, Sergio A. Jimenez, Gregg P. Summerville
Publikováno v:
American journal of medical genetics. 45(3)
We have studied a family with an autosomal dominant form of multiple epiphyseal dysplasia (MED) inherited through at least 5 generations. Bilateral deformity of the hips with subsequent degenerative arthritis was the most common and most severe chang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f49f7abd7e2eecd91eea6c4fd569c1c
https://pubmed.ncbi.nlm.nih.gov/8094597
https://pubmed.ncbi.nlm.nih.gov/8094597