Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Marianne, Hammarsund"'
Autor:
Mikael Lerner, Marianne Hammarsund, Monika Jansson, Martin Corcoran, Olle Sangfelt, Stefan Einhorn, Chaoyong Zhu, Mats Merup, Dan Grandér, Gösta Gahrton, Hanneke C. Kluin-Nelemans
Publikováno v:
Human Molecular Genetics, 13(23), 2925-2936. Oxford University Press
Karyotypical alteration of chromosome 5 and in particular band 5q13 is a frequent finding in hairy cell leukemia (HCL). We have previously identified a number of candidate genes localized in close proximity to a constitutional inv(5)(p13.1q13.3) brea
Autor:
Martin Corcoran, Olle Sangfelt, Mikael Lerner, Dan Grandér, Marianne Hammarsund, Lars Forsberg, Chaoyong Zhu, Rachel E. Ibbotson, Kapanadze Bi, Stefan Einhorn, Catharina Larsson, David Oscier, Bill Wilson
Publikováno v:
Genes, Chromosomes and Cancer. 40:285-297
Our group previously identified two novel genes, RFP2/LEU5 and DLEU2, within a 13q14.3 genomic region of loss seen in various malignancies. However, no specific inactivating mutations were found in these or other genes in the vicinity of the deletion
Autor:
Anna Pestova, Rachel E. Ibbotson, Ancha Baranova, Francesco Gorreta, N. V. Makeeva, Stefan Einhorn, Marianne Hammarsund, Tariq Alsheddi, Martin Corcoran, Dmitry A. Shagin, Eugene R. Zabarovsky, T. V. Tyazhelova, Nikitin Ea, Andrey Ivanovich Vorobiev, Dmitry Ivanov, Kapanadze Bi, Mikhail Skoblov, N. K. Yankovsky, Karen Schlauch, Olle Sangfelt, Tatiana Borodina, Vikas Chandhoke, A. B. Poltaraus, Dan Grandér, Svetlana Nazarenko, David Oscier, Sergey Lukianov
Publikováno v:
Gene. 321:103-112
In the present study, we describe the human and mouse RFP2 gene structure, multiple RFP2 mRNA isoforms in the two species that have different 5' UTRs and a human-specific antisense transcript RFP2OS. Since the human RFP2 5' UTR is not conserved in mo
Autor:
Martin M, Corcoran, Marianne, Hammarsund, Chaoyong, Zhu, Mikael, Lerner, Bagrat, Kapanadze, Bill, Wilson, Catharina, Larsson, Lars, Forsberg, Rachel E, Ibbotson, Stefan, Einhorn, David G, Oscier, Dan, Grandér, Olle, Sangfelt
Publikováno v:
Genes, chromosomescancer. 40(4)
Our group previously identified two novel genes, RFP2/LEU5 and DLEU2, within a 13q14.3 genomic region of loss seen in various malignancies. However, no specific inactivating mutations were found in these or other genes in the vicinity of the deletion
Characterization of a novel B-CLL candidate gene--DLEU7--located in the 13q14 tumor suppressor locus
Autor:
William Wilson, Dan Grandér, Marianne Hammarsund, Stefan Einhorn, Chaoyong Zhu, Martin Corcoran, Olle Sangfelt
Publikováno v:
FEBS letters. 556(1-3)
Deletion of chromosome 13q14 is the most frequent genetic aberration in B-cell chronic lymphocytic leukemia (CLL), found in more than 50% of cases, indicating that this region contains a gene(s) involved in the development of CLL. However, the pathog
Autor:
Dan Grandér, Mats Merup, Marianne Hammarsund, William Wilson, Martin Corcoran, Olle Sangfelt, Stefan Einhorn
Publikováno v:
Human genetics. 109(5)
Rapid progress in the sequencing of the genome of man and other species allows for the comparative analysis of their genetic structure and content. We have used a combined biochemical and computer-based approach to characterize a 146 kb human genomic
Autor:
Niclas Jareborg, Marianne Hammarsund, T. Dan Grander, Olga Vorontsova, Eugene R. Zabarovsky, N. K. Yankovsky, Olle Sangfelt, Ancha Baranova, Mats Merup, Stefan Einhorn, Kapanadze Bi, Monika Jansson, Martin Corcoran, N. V. Makeeva, David Oscier, Gösta Gahrton
Publikováno v:
Genomics. 70(3)
Previous studies have indicated the presence of a putative tumor suppressor gene on human chromosome 13q14, commonly deleted in patients with B-cell chronic lymphocytic leukemia (B-CLL). We have recently identified a minimally deleted region encompas
Autor:
Stefan Einhorn, Olle Sangfelt, David Oscier, Dan Grandér, Lars Forsberg, Mikael Lerner, Marianne Hammarsund, Martin Corcoran, Rachel E. Ibbotson, Chaoyong Zhu, Kapanadze Bi, Catharina Larsson
Publikováno v:
Blood. 104:1540-1540
Our group previously identified two novel genes, RFP2/LEU5 and DLEU2, within a 13q14.3 genomic region of loss seen in various malignancies, including chronic lymphocytic leukemia and mantle cell lymphoma. However, no specific inactivating mutations w
Autor:
Stefan Einhorn, Mats Merup, Mikael Lerner, Marianne Hammarsund, G. Gahrton, Dan Grandér, Monika Jansson, Hanneke C. Kluin-Nelemans, Martin Corcoran, Olle Sangfelt, Chaoyong Zhu
Publikováno v:
Blood. 104:1538-1538
Chromosomal aberrations on chromosome 5 and in particular band 5q13 is frequently seen in Hairy Cell Leukemia (HCL). Detailed characterization of a constitutional inv (5)(p13.1q13.3) breakpoint in one HCL patient yielded a number of candidate genes t