Zobrazeno 1 - 10
of 111
pro vyhledávání: '"F H, Herrmann"'
Autor:
Erwin Klumpp, Manfred Stähli, Mika Korkiakoski, Nina Gottselig, Roland Bol, C. Hernández-Crespo, Hjalmar Laudon, Annalea Lohila, Wulf Amelung, Nunzio Romano, Jan Siemens, Kim Pilegaard, Maria-Teresa Sebastià, Steven J. Granger, Meelis Mölder, Irene Lehner, Werner Eugster, Harry Vereecken, Christoph Müller, Stefan Löfgren, Jan Jacob Keizer, Paolo Nasta, Eugénie Paul-Limoges, Marc Voltz, Christopher J.A. Macleod, Volker Nischwitz, James W. Kirchner, M. C. Pierret, Falko F. H. Herrmann
Publikováno v:
Global Biogeochemical Cycles. 31:1592-1607
Biogeochemical cycling of elements largely occurs in dissolved state, but many elements may also be bound to natural nanoparticles (NNP, 1-100 nm) and fine colloids (100-450 nm). We examined the hypothesis that the size and composition of stream wate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1f4217b66605ed35c3ff248c4c2a815
https://doi.org/10.1002/2017gb005657
https://doi.org/10.1002/2017gb005657
Autor:
F H, Herrmann, K, Wulff, G, Auerswald, S, Schulman, J, Astermark, A, Batorova, W, Kreuz, H, Pollmann, A, Ruiz-Saez, N, De Bosch, L, Salazar-Sanchez, A, Boadas
Publikováno v:
Haemophilia. 15:267-280
The congenital FVII deficiency (FVIID) is a rare haemorrhagic disorder with an autosomal recessive pattern of inheritance. Data on phenotype and the genotype from 717 subjects in Central Europe (six countries), Latin America (Costa Rica, Venezuela) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f2a273f310b43fbb7308c8720d30981
https://doi.org/10.1111/j.1365-2516.2008.01910.x
https://doi.org/10.1111/j.1365-2516.2008.01910.x
Autor:
K. Wulff, F. H. Herrmann
Publikováno v:
Hämostaseologie. 24:94-107
ZusammenfassungIn einer Übersicht werden einige molekulargenetische Aspekte der Gerinnungsfaktoren VII, VIII, IX und X dargestellt. Das Spektrum der Mutationen wird charakterisiert, das zu den genetisch bedingten Defekten Hämophilie A und B, Faktor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e67b76bb1bf89370c242b86226c21160
https://doi.org/10.1055/s-0037-1619618
https://doi.org/10.1055/s-0037-1619618
Autor:
Madhumita Roy Chowdhury, H. K. Kumbnani, P. S. N. Menon, Ishwar C. Verma, Mark Layton, W. Schroder, C. T. Lambert, M. R. A. Lalloz, Madhulika Kabra, F. H. Herrmann
Publikováno v:
Haemophilia. 6:625-630
Little is known about the heterozygous frequency of factor VIII gene markers in the Asian Indian population. The objective of this study was to establish the heterozygous frequency of polymorphic markers within and flanking the factor VIII gene in In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::218c0c21e1a3507c5b711eb9e8ff01fd
https://doi.org/10.1046/j.1365-2516.2000.00442.x
https://doi.org/10.1046/j.1365-2516.2000.00442.x
Publikováno v:
Histopathology. 34:234-240
Aims Little information is available about stage- or site-specific chromosomal aberrations in head and neck squamous cell carcinoma (HNSCC). We tried to identify whether different patterns of chromosomal gain or loss in squamous cell carcinomas were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a87b22d732c17df2ece3fd37fbeea938
https://doi.org/10.1046/j.1365-2559.1999.00607.x
https://doi.org/10.1046/j.1365-2559.1999.00607.x
Autor:
J. F. Jackson, G. J. de Klerk, K. S. Ramulu, J. Sybenga, G. Wenzel, G. Seidlitz, L. Bünger, R. C. Agoha, E. Günther, D. L. Mulcahy, J. A. M. Van der Mey, R. L. M. Pierik, F. H. Herrmann, P. Eberle
Publikováno v:
Theoretical and Applied Genetics. :1017-1022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3ab924ded2b330b126e7d2a51135025
https://doi.org/10.1007/bf00227419
https://doi.org/10.1007/bf00227419
Autor:
F. H. Herrmann, G. Machill, G. Seidlitz, John J. Hopwood, M. Zschiesche, J. Bielicki, L. Petruschka
Publikováno v:
Journal of Inherited Metabolic Disease. 17:89-92
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25443595cfba2cf896e792eb4b2cdf77
https://doi.org/10.1007/bf00735402
https://doi.org/10.1007/bf00735402
Publikováno v:
Journal of Inherited Metabolic Disease. 16:17-26
An immunoquantification protocol based on an enzyme-linked immunosorbent assay was developed to measure the abundance of the microsomal enzyme steroid sulphatase (STS). The two-step sandwich immunoassay is sufficiently sensitive to detect 100-200 pg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1ef97535fb78e7f6d478cec5cbede09
https://doi.org/10.1007/bf00711310
https://doi.org/10.1007/bf00711310
Publikováno v:
37th Hemophilia Symposium ISBN: 9783540735342
FVII is a vitamin K-dependent coagulation protease essential for the initiation phase of normal hemostasis. Hereditary FVII deficiency is a rare autosomal recessive bleeding disorder with a variable phenotype. There is a poor correlation between FVII
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e0f4bea9134ea3d93fa93a9d91f00c9
https://doi.org/10.1007/978-3-540-73535-9_53
https://doi.org/10.1007/978-3-540-73535-9_53
Publikováno v:
37th Hemophilia Symposium ISBN: 9783540735342
Resistance to activated protein C (APC resistance) was identified as the cause of familial thrombophilia by Dahlback et al. in 1993 [4]. Only one year later the underlying genetic defect of the APC resistance has been demonstrated by Bertina and coll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88c9ae5951014f684a874176a5eb6fa6
https://doi.org/10.1007/978-3-540-73535-9_40
https://doi.org/10.1007/978-3-540-73535-9_40