Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Kapanadze Bi"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c38ce98a692485a920db71a7205c596
https://doi.org/10.1002/gcc.20046
https://doi.org/10.1002/gcc.20046
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9216886c5ba221d705a4eb534d8d5bea
https://doi.org/10.1016/j.gene.2003.08.007
https://doi.org/10.1016/j.gene.2003.08.007
Autor:
Stefan Einhorn, T. V. Tyazhelova, Kapanadze Bi, Dmitry Ivanov, E. A. Nikitin, Ancha Baranova, A. I. Vorobiev, N. V. Makeeva, N. K. Yankovsky, Dan Grandér, Olle Sangfelt, A. B. Semov
Publikováno v:
Russian Journal of Genetics. 37:1286-1292
Deletions in the region located between the STS markers D13S1168 and D13S25 on chromosome 13 are the most frequent genomic changes in patients with B-cell chronic lymphocytic leukemia (B-CLL). After sequencing of this region, two novel candidate gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51aaefb29e6cebb91ee843bab55d367d
https://doi.org/10.1023/a:1012561109880
https://doi.org/10.1023/a:1012561109880
Autor:
Kapanadze Bi, Larry L. Deaven, Eugene R. Zabarovsky, Fedorova Li, Omid Rasool, Rachel E. Ibbotson, Vladimir I. Kashuba, Alexander Syomov, Alexey Kazakov, Anna A. Baranova, Martin Corcoran, R. Z. Gizatullin, Charles H.C.M. Buys, A. B. Poltaraus, Anke van den Berg, Wim van Everdink, Dan Grandér, Alexander V. Zelenin, David Oscier, Natalia Syomova, Stephan Einhorn, Hans Lehrach, Vadim Brodyansky, Yie Liu, Galina Sulimova, N. K. Yankovsky
Publikováno v:
FEBS Letters, 426(2), 266-270. Wiley
B-cell chronic lymphocytic leukemia (B-CLL) is a human hematological neoplastic disease often associated with the toss of a chromosome 13 region between RB1 gene and locus D13S25, A new tumor suppressor gene (TSG) may be located in the region. A cosm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b4ea73ea92cf775b5a33b31b2f11600
https://doi.org/10.1016/s0014-5793(98)00357-3
https://doi.org/10.1016/s0014-5793(98)00357-3
Autor:
Kapanadze Bi, Ancha Baranova, Natalia Semova, Alexandre Semov, Martin Corcoran, Alexei Kutsenko
Publikováno v:
Genomics. 82(3)
IRLB was originally identified as a partial cDNA clone, encoding a 191-aa protein binding the interferon-stimulated response element (ISRE) in the P2 promoter of human MYC. Here, we cloned the full-size IRLB using different bioinformatics tools and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9dfe32ac348c273218e6c1752686d84
https://pubmed.ncbi.nlm.nih.gov/12906859
https://pubmed.ncbi.nlm.nih.gov/12906859
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeeeef488388e3dd76295a16b10f1cd0
https://pubmed.ncbi.nlm.nih.gov/11161783
https://pubmed.ncbi.nlm.nih.gov/11161783
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b11705a4c10eae148659ed27f02695b7
https://doi.org/10.1182/blood.v104.11.1540.1540
https://doi.org/10.1182/blood.v104.11.1540.1540
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