Zobrazeno 1 - 10
of 538
pro vyhledávání: '"H Hoehn"'
Autor:
H Hoehn, Sven Mahner, V Docheva, J Reichenbach, J Jueckstock, Fabian Trillsch, M Burgmann, Uwe Hasbargen
Publikováno v:
Geburtshilfe und Frauenheilkunde.
Autor:
H. Hoehn, Rudolf Happle
Publikováno v:
Clinical Genetics. 4:17-24
Chromosomal investigations were performed on fibroblast cultures established from tumour tissue of six patients with multiple basal cell carcinoma, and from one patient with a solitary basal cell carcinoma. In four instances, fibroblast cultures from
Autor:
Eric Steiner, Markus Maeurer, Marcus Schmidt, H Hoehn, Berno Tanner, Henryk Pilch, Rudolf Seufert
Publikováno v:
Zentralblatt für Gynäkologie. 124:406-412
Objective In response to antigenic stimulation, naive MHC-class I restricted and antigen-specific CD8+CD45RA+CD28+T-cells undergo clonal expansion and differentiate into CD8+CD45RO+ memory T-cells. Upon re- encounter with the nominal antigen, CD45RO+
Publikováno v:
Melanoma Research. 2:241-246
A model system for testing the efficacy of chemotherapy protocols for metastatic melanoma was established using cell cultures from two brain and three lymph node metastases of melanoma from five different patients. Continuously growing cultures which
Publikováno v:
American Journal of Physiology-Cell Physiology. 261:C964-C972
The aims of the present study were to characterize the phenotype, growth kinetics, and proliferative activation in culture of a population of poorly differentiated homogeneously small (HS) keratinocytes. These slow-cycling cells were separated by uni
Autor:
J.F. Tait, R. Espinosa, T. Ishida, R.S. Lemons, H.G. Schwarzacher, R.E. Magenis, T. Tobe, N.-H. Choi, S. Minoshima, M. Hirai, D.L. Foote, A. Herzog, A. Schedle, M.R. Rosner, S. Yamase, M.L. Little, M.H. Thorne, M. Tsukasaki, P.K. Tucker, T. Hori, E. Schurr, R. Shiang, T.R. King, C.M. Disteche, E. Takahashi, A. Stahl, David Patterson, B.K. Lee, S. Sonta, W.-L. Kuo, E.M. Eicher, H. Hoehn, M M Le Beau, E. Skamene, F. Wachtler, B.L. Sheldon, D.W. Hale, I. Gonzales, J. Sylvester, M. Hartung, M.T. Davisson, P. Gros, D.A. Frankenberry, P.A. Hunt, D.A. Adler, J.E. Wiley, B. Weber, C. Schöfer, J.T. Eppig, M. Tomita, L.L. Washburn, Robert M. Gemmill, M.R. Hayden, E.C. Akeson, N. Shimizu, R.K. Perlman, Harry A. Drabkin, J. Meyne, J.C. Murray, M. Yamada, L. Allen
Publikováno v:
Cytogenetic and Genome Research. 57:I-IV
Publikováno v:
Genes and immunity. 10(2)
Alternative splicing results in multiple protein isoforms derived from a single gene. The magnitude of this process ranges from a complete loss of function to gain of new function. We examined, as a paradigm, alternative splicing of the non-redundant
Publikováno v:
Genome dynamics. 1
Fanconi anemia (FA) is a rare recessive disease that reflects the cellular and phenotypic consequences of genetic instability: growth retardation, congenital malformations, bone marrow failure, high risk of neoplasia, and premature aging. At the cell
Autor:
D. Schindler, H. Hoehn
Publikováno v:
Monographs in Human Genetics ISBN: 9783805582773
Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging
Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::021a6499a4a049d56f8c60aaab7803d9
https://doi.org/10.1159/isbn.978-3-318-01461-7
https://doi.org/10.1159/isbn.978-3-318-01461-7
The recessive disease Fanconi anemia (FA) is a prototype chromosome instability syndrome which shows a high level of spontaneous and induced chromosomal aberrations in combination with a significant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::474448ab215a8a370088296f702c7ccc
https://doi.org/10.1159/000102546
https://doi.org/10.1159/000102546