Zobrazeno 1 - 10
of 69
pro vyhledávání: '"H, van Kamp"'
Autor:
H. van Kamp, S. J. Halkes
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 84:904-917
The synthesis is described of 6-methyl-9β,10α-4-en-3-ones, which were dehydrogenated to some of their 1-dehydro, 6-dehydro and 1,6-bisdehydro derivatives. N.M.R. spectra reveal that ring B in 6α-methyl-9β,10α-4-en-3-ones has a boat conformation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0be3defe4455e7da480b496150f5c4dd
https://doi.org/10.1002/recl.19650840711
https://doi.org/10.1002/recl.19650840711
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 83:509-512
The synthesis is described of 9β,10α-progesterone and of 6-dehydro-9β,10α-progesterone and of 6-dehydro–β,10α-progesterone both tritiated at C4.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee23ff8a7ef8df5d72b1d3adf6dca6f7
https://doi.org/10.1002/recl.19640830510
https://doi.org/10.1002/recl.19640830510
Autor:
H. van Kamp
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 84:853-862
The synthesis is reported of 20α-hydroxy and 20β-hydroxy-9β,10α-pregna-4,6-dien-3-one and their corresponding 6,7-dihydro derivatives. The assignment of the configuration at C-20 is based on alternative synthesis by Baeyer-Villiger oxidation of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ddf805551221298a562bc0a6e0c6cca
https://doi.org/10.1002/recl.19650840707
https://doi.org/10.1002/recl.19650840707
Autor:
Ph. M. Kluin, R E Kibbelaar, H. Van Kamp, H.L. Haak, J. W. Wessels, Willem E. Fibbe, E.J. Dreef, J.W.R. Mulder, Geoffrey C. Beverstock
Publikováno v:
Blood. 82:904-913
Fluorescence in situ hybridization (FISH) is a powerful tool for detection of numerical and structural chromosomal aberrations. We have compared conventional banding techniques and FISH for the detection of monosomy 7 (-7) and trisomy 8 (+8) in 89 pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1b8a30d074171e54586d506779255b8
https://doi.org/10.1182/blood.v82.3.904.904
https://doi.org/10.1182/blood.v82.3.904.904
Autor:
R E, Kibbelaar, J W, Mulder, E J, Dreef, H, van Kamp, W E, Fibbe, J W, Wessels, G C, Beverstock, H L, Haak, P M, Kluin
Publikováno v:
Blood. 82:904-913
Fluorescence in situ hybridization (FISH) is a powerful tool for detection of numerical and structural chromosomal aberrations. We have compared conventional banding techniques and FISH for the detection of monosomy 7 (-7) and trisomy 8 (+8) in 89 pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282dcda1bfa261ed41f23f07cff27e16
https://doi.org/10.1182/blood.v82.3.904.bloodjournal823904
https://doi.org/10.1182/blood.v82.3.904.bloodjournal823904
Autor:
R. Willemze, J. E. Landegent, H. Van Kamp, R. Mout, M. J. P. L. Kroef, J. W. Wessels, W. E. Fibbe, R. P. M. Jansen, H.L. Haak
Publikováno v:
Blood. 81:1849-1854
Interstitial deletions of the long arm of chromosome 5 are among the most characteristic abnormalities observed in myeloid disorders. To assess the lineage involvement of peripheral blood cells from patients with a 5q--anomaly, purified neutrophils,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c920929802005a02680ddf6497ceb1a6
https://doi.org/10.1182/blood.v81.7.1849.1849
https://doi.org/10.1182/blood.v81.7.1849.1849
Autor:
M J, Kroef, W E, Fibbe, R, Mout, R P, Jansen, H L, Haak, J W, Wessels, H, Van Kamp, R, Willemze, J E, Landegent
Publikováno v:
Blood. 81:1849-1854
Interstitial deletions of the long arm of chromosome 5 are among the most characteristic abnormalities observed in myeloid disorders. To assess the lineage involvement of peripheral blood cells from patients with a 5q--anomaly, purified neutrophils,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::564dcd78a602b310bf96dc101aefccb8
https://doi.org/10.1182/blood.v81.7.1849.bloodjournal8171849
https://doi.org/10.1182/blood.v81.7.1849.bloodjournal8171849
Publikováno v:
Blood. 80:1774-1780
To determine the clonal nature of hematopoiesis and to assess lineage involvement in patients with myelodysplastic syndromes (MDS), we used restriction fragment length polymorphisms of the X-linked genes phosphoglycerate kinase (PGK1) and hypoxanthin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abb39537daa270e6d17bff07b1544d55
https://doi.org/10.1182/blood.v80.7.1774.bloodjournal8071774
https://doi.org/10.1182/blood.v80.7.1774.bloodjournal8071774
Autor:
Willem E. Fibbe, E. De Graaff, H. Van Kamp, R. P. M. Jansen, J. E. Landegent, M. Van Der Keur, Roelof Willemze
Publikováno v:
Blood. 80:1774-1780
To determine the clonal nature of hematopoiesis and to assess lineage involvement in patients with myelodysplastic syndromes (MDS), we used restriction fragment length polymorphisms of the X-linked genes phosphoglycerate kinase (PGK1) and hypoxanthin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1712c010efc1dda0148bc8e40a1daf78
https://doi.org/10.1182/blood.v80.7.1774.1774
https://doi.org/10.1182/blood.v80.7.1774.1774
Autor:
Johanna Kluin-Nelemans, Philippus Kluin, E.J. Dreef, Willem E. Fibbe, Geoffrey C. Beverstock, R E Kibbelaar, G de Groot-Swings, H. Van Kamp
Publikováno v:
Blood. 79:1823-1828
Clonality of myeloid and lymphoid cell fractions obtained from peripheral blood (PB) or bone marrow (BM) of five patients with a myelodysplastic syndrome (MDS), was studied by combined immunophenotypic analysis and DNA in situ hybridization. This nov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a91206b393e70f8bb8b16ba6f51e272a
https://doi.org/10.1182/blood.v79.7.1823.1823
https://doi.org/10.1182/blood.v79.7.1823.1823