المؤلفون: Akdemir, Kadir C, Le, Victoria T, Chandran, Sahaana, Li, Yilong, Verhaak, Roel G, Beroukhim, Rameen, Campbell, Peter J, Chin, Lynda, Dixon, Jesse R, Futreal, P Andrew

المساهمون: Borg, Åke, Creator, Ringnér, Markus, Creator, Staaf, Johan, Creator

المصدر: Nature Genetics. 52(3):294-305

مصطلحات موضوعية: Chromatin/genetics, Gene Expression Regulation, Neoplastic, Gene Rearrangement/genetics, Genome, Human/genetics, Genomic Structural Variation, Humans, Neoplasms/genetics, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

URL الوصول: https://lup.lub.lu.se/record/1228fbf0-3db4-4126-a102-77440ce7e8cd
http://dx.doi.org/10.1038/s41588-019-0564-y

المؤلفون: Rodriguez-Martin, Bernardo, Alvarez, Eva G, Baez-Ortega, Adrian, Zamora, Jorge, Supek, Fran, Demeulemeester, Jonas, Santamarina, Martin, Ju, Young Seok, Temes, Javier, Garcia-Souto, Daniel, Detering, Harald, Li, Yilong, Rodriguez-Castro, Jorge, Dueso-Barroso, Ana, Bruzos, Alicia L, Dentro, Stefan C, Blanco, Miguel G, Contino, Gianmarco, Ardeljan, Daniel, Tojo, Marta, Roberts, Nicola D, Zumalave, Sonia, Edwards, Paul A, Weischenfeldt, Joachim, Puiggròs, Montserrat, Chong, Zechen, Chen, Ken, Lee, Eunjung Alice, Wala, Jeremiah A, Raine, Keiran M, Butler, Adam, Waszak, Sebastian M, Navarro, Fabio C P, Schumacher, Steven E, Monlong, Jean, Maura, Francesco, Bolli, Niccolo, Bourque, Guillaume, Gerstein, Mark, Park, Peter J, Wedge, David C, Beroukhim, Rameen, Torrents, David, Korbel, Jan O, Martincorena, Iñigo, Fitzgerald, Rebecca C, Van Loo, Peter, Kazazian, Haig H, Burns, Kathleen H, Campbell, Peter J, Tubio, Jose M C

المساهمون: Borg, Åke, Creator, Ringnér, Markus, Creator, Staaf, Johan, Creator

المصدر: Nature Genetics. 52(3):306-319

مصطلحات موضوعية: Carcinogenesis/genetics, Gene Rearrangement/genetics, Genome, Human/genetics, Humans, Long Interspersed Nucleotide Elements/genetics, Neoplasms/genetics, Retroelements/genetics, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

URL الوصول: https://lup.lub.lu.se/record/2d5c311f-b39f-44a5-82d2-efba3c9160b6
http://dx.doi.org/10.1038/s41588-019-0562-0

المؤلفون: Li, Yilong, Roberts, Nicola D, Wala, Jeremiah A, Shapira, Ofer, Schumacher, Steven E, Kumar, Kiran, Khurana, Ekta, Waszak, Sebastian, Korbel, Jan O, Haber, James E, Imielinski, Marcin, Weischenfeldt, Joachim, Beroukhim, Rameen, Campbell, Peter J

المساهمون: Borg, Åke, Creator, Ringnér, Markus, Creator, Staaf, Johan, Creator

المصدر: Nature. 578(7793):112-121

مصطلحات موضوعية: Gene Rearrangement/genetics, Genetic Variation, Genome, Human/genetics, Genomics, Humans, Mutagenesis, Insertional, Neoplasms/genetics, Telomerase/genetics, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

URL الوصول: https://lup.lub.lu.se/record/5ad43c7f-63e9-4e76-bae5-7ba7012fa3df
http://dx.doi.org/10.1038/s41586-019-1913-9

المؤلفون: Ana Rita Soares, Gabriela Soares, Manuela Mota-Freitas, Natália Oliva-Teles, Ana Maria Fortuna

المصدر: Acta Médica Portuguesa, Vol 32, Iss 7-8 (2019)

مصطلحات موضوعية: Intellectual Disability/genetics, Subtelomeric Rearrangements Gene Rearrangement/genetics, Telomere/genetics, Medicine, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/11466; https://doaj.org/toc/0870-399X; https://doaj.org/toc/1646-0758

URL الوصول: https://doaj.org/article/724086fa16534922a3d9add6cb9ca66a

المؤلفون: Rodriguez-Martin, B., Alvarez, E.G., Baez-Ortega, A., Zamora, J., Supek, F., Demeulemeester, J., Santamarina, M., Ju, Y.S., Temes, J., Garcia-Souto, D., Detering, H., Li, Y., Rodriguez-Castro, J., Dueso-Barroso, A., Bruzos, A.L., Dentro, S.C., Blanco, M.G., Contino, G., Ardeljan, D., Tojo, M., Roberts, N.D., Zumalave, S., Edwards, P.A., Weischenfeldt, J., Puiggròs, M., Chong, Z., Chen, K., Lee, E.A., Wala, J.A., Raine, K., Butler, A., Waszak, S.M., Navarro, F.C.P., Schumacher, S.E., Monlong, J., Maura, F., Bolli, N., Bourque, G., Gerstein, M., Park, P.J., Wedge, D.C., Beroukhim, R., Torrents, D., Korbel, J.O., Martincorena, I., Fitzgerald, R.C., Van Loo, P., Kazazian, H.H., Burns, K.H., Akdemir, K.C., Boutros, P.C., Bowtell, D.D.L., Brors, B., Campbell, P.J., Chan, K., Cortés-Ciriano, I., Dunford, A.J., Estivill, X., Etemadmoghadam, D., Feuerbach, L., Fink, J.L., Frenkel-Morgenstern, M., Garsed, D.W., Gordenin, D.A., Haan, D., Haber, J.E., Hess, J.M., Hutter, B., Imielinski, M., Jones, D.T.W., Kazanov, M.D., Klimczak, L.J., Koh, Y., Kumar, K., Lee, J.J.-K., Lynch, A.G., Macintyre, G., Markowetz, F., Martinez-Fundichely, A., Meyerson, M., Miyano, S., Nakagawa, H., Ossowski, S., Pearson, J.V., Rippe, K., Roberts, S.A., Scully, R., Shackleton, M., Sidiropoulos, N., Sieverling, L., Stewart, C., Tubio, J.M.C., Villasante, I., Waddell, N., Yang, L., Yao, X., Yoon, S.-S., Zhang, C.-Z.

المساهمون: University of St Andrews. School of Medicine, University of St Andrews. Statistics, University of St Andrews. Sir James Mackenzie Institute for Early Diagnosis, University of St Andrews. Cellular Medicine Division

المصدر: Nature Genetics
Nature Genetics, 52, 306-319
Rodriguez-Martin, B, Alvarez, E G, Baez-Ortega, A, Zamora, J, Supek, F, Demeulemeester, J, Santamarina, M, Ju, Y S, Temes, J, Garcia-Souto, D, Detering, H, Li, Y, Rodriguez-Castro, J, Dueso-Barroso, A, Bruzos, A L, Dentro, S C, Blanco, M G, Contino, G, Ardeljan, D, Tojo, M, Roberts, N D, Zumalave, S, Edwards, P A, Weischenfeldt, J, Puiggròs, M, Chong, Z, Chen, K, Lee, E A, Wala, J A, Raine, K, Butler, A, Waszak, S M, Navarro, F C P, Schumacher, S E, Monlong, J, Maura, F, Bolli, N, Bourque, G, Gerstein, M, Park, P J, Wedge, D C, Beroukhim, R, Torrents, D, Korbel, J O, Martincorena, I, Fitzgerald, R C, Van Loo, P, Kazazian, H H, Burns, K H, Akdemir, K C, Alvarez, E G, Baez-Ortega, A, Beroukhim, R, Boutros, P C, Bowtell, D D L, Brors, B, Burns, K H, Campbell, P J, Chan, K, Chen, K, Cortés-Ciriano, I, Dueso-Barroso, A, Dunford, A J, Edwards, P A, Estivill, X, Etemadmoghadam, D, Feuerbach, L, Fink, J L, Frenkel-Morgenstern, M, Garsed, D W, Gerstein, M, Gordenin, D A, Haan, D, Haber, J E, Hess, J M, Hutter, B, Imielinski, M, Jones, D T W, Ju, Y S, Kazanov, M D, Klimczak, L J, Koh, Y, Korbel, J O, Kumar, K, Lee, E A, Lee, JJ-K, Li, Y, Lynch, A G, Macintyre, G, Markowetz, F, Martincorena, I, Martinez-Fundichely, A, Meyerson, M, Miyano, S, Nakagawa, H, Navarro, F C P, Ossowski, S, Park, P J, Pearson, J V, Puiggròs, M, Rippe, K, Roberts, N D, Roberts, S A, Rodriguez-Martin, B, Schumacher, S E, Scully, R, Shackleton, M, Sidiropoulos, N, Sieverling, L, Stewart, C, Torrents, D, Tubio, J M C, Villasante, I, Waddell, N, Wala, J A, Weischenfeldt, J, Yang, L, Yao, X, Yoon, S-S, Zamora, J, Zhang, C-Z, Campbell, P J & Tubio, J M C 2020, ' Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition ', Nature Genetics, vol. 52, no. 3, pp. 306-319 . https://doi.org/10.1038/s41588-019-0562-0
Rodriguez-Martin, B, Alvarez, E G, Baez-Ortega, A, Zamora, J, Supek, F, Demeulemeester, J, Santamarina, M, Ju, Y S, Temes, J, Garcia-Souto, D, Detering, H, Li, Y, Rodriguez-Castro, J, Dueso-Barroso, A, Bruzos, A L, Dentro, S C, Blanco, M G, Contino, G, Ardeljan, D, Tojo, M, Roberts, N D, Zumalave, S, Edwards, P A W, Weischenfeldt, J, Puiggròs, M, Chong, Z, Chen, K, Lee, E A, Wala, J A, Raine, K, Butler, A, Waszak, S M, Navarro, F C P, Schumacher, S E, Monlong, J, Maura, F, Bolli, N, Bourque, G, Gerstein, M, Park, P J, Wedge, D C, Beroukhim, R, Torrents, D, Korbel, J O, Martincorena, I, Fitzgerald, R C, Van Loo, P, Kazazian, H H, Sidiropoulos, N, Weischenfeldt, J, PCAWG Structural Variation Working Group & PCAWG Consortium 2020, ' Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition ', Nature Genetics, vol. 52, no. 3, pp. 306-319 . https://doi.org/10.1038/s41588-019-0562-0
Nature Genetics, 52, 3, pp. 306-319

مصطلحات موضوعية: Somatic cell, Carcinogenesis, QH301 Biology, Retrotransposon, medicine.disease_cause, Genoma humà, Genome, 0302 clinical medicine, Neoplasms, ELEMENTS, Carcinogènesi, Cancer, Genetics, Gene Rearrangement, Genetics & Heredity, 0303 health sciences, Women's cancers Radboud Institute for Molecular Life Sciences [Radboudumc 17], Manchester Cancer Research Centre, 3rd-DAS, Genomics, Neoplasms/genetics, SOMATIC RETROTRANSPOSITION, Women's cancers Radboud Institute for Health Sciences [Radboudumc 17], 3. Good health, READ ALIGNMENT, 030220 oncology & carcinogenesis, Retroelements/genetics, Life Sciences & Biomedicine, Retroelements, INSTABILITY, L1 RETROTRANSPOSITION, QH426 Genetics, Biology, Article, Structural variation, RC0254, 03 medical and health sciences, QH301, SDG 3 - Good Health and Well-being, medicine, Humans, QH426, 030304 developmental biology, Tumors, Science & Technology, LANDSCAPE, RC0254 Neoplasms. Tumors. Oncology (including Cancer), Genome, Human, ResearchInstitutes_Networks_Beacons/mcrc, DELETION, Gene rearrangement, DNA, Gene Rearrangement/genetics, Long interspersed nuclear element, Reordenament genètic, Long Interspersed Nucleotide Elements, Long Interspersed Nucleotide Elements/genetics, Genome, Human/genetics, Carcinogenesis/genetics, Genètica

وصف الملف: Print-Electronic; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1bee2c01b8278d49bbe8813c2939cf
https://lirias.kuleuven.be/handle/123456789/651107

المؤلفون: Elena V Moroz, Olga O. Bochkareva, Mikhail S. Gelfand, Iakov I. Davydov

المصدر: BMC Genomics, Vol 19, Iss 1, Pp 1-17 (2018)
BMC Genomics
BMC genomics, vol. 19, no. 1, pp. 965

مصطلحات موضوعية: 0301 basic medicine, lcsh:QH426-470, Burkholderia, lcsh:Biotechnology, 030106 microbiology, Genome rearrangements, Context (language use), Pan-genome, Genome, 03 medical and health sciences, Multi-chromosome bacteria, Phylogenetics, lcsh:TP248.13-248.65, Databases, Genetic, Genetics, Gene, Phylogeny, 030304 developmental biology, Gene Rearrangement, Comparative genomics, Phase variation, 0303 health sciences, biology, 030306 microbiology, Chromosome, Chromosomes, Bacterial, biology.organism_classification, Positive selection, Strain phylogeny, lcsh:Genetics, 030104 developmental biology, Burkholderia/classification, Burkholderia/genetics, Gene Rearrangement/genetics, Adaptation, Research Article, Biotechnology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd364774e0ff551b24f0609083f016a2

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تسجيل الدخول للوصول الكامل.

المؤلفون: A.W. Langerak, M. van Grotel, E.M.M. (Esther) van Lieshout, Rob Pieters, M. Passier, M. M. van Noesel, Jessica G.C.A.M. Buijs-Gladdines, Jules P.P. Meijerink, E. R. Van Wering, N. B. Burger, Willem Kamps, H B Beverloo, Anjo J.P. Veerman

المساهمون: Obstetrics and gynaecology, Pediatric surgery, CCA - Disease profiling, Medical Microbiology and Infection Prevention, Obstetrics and Gynaecology, 04 Woman - Child, Intensive Care Medicine, Amsterdam institute for Infection and Immunity, Other Research, Rehabilitation medicine, Pediatrics, Immunology, Clinical Genetics, Surgery

المصدر: Leukemia, 22(1), 124-131. Nature Publishing Group
Leukemia, 22(1), 124-31. Nature Publishing Group
van Grotel, M, Meijerink, J P, van Wering, E R, Langerak, A W, Beverloo, HB, Buijs-Gladdines, J G, Burger, N B, Passier, M, van Lieshout, E M, Kamps, W A, Veerman, A J P, van Noesel, M M & Pieters, R 2008, ' Prognostic significance of molecular-cytogenetic abnormalities in pediatric T-ALL is not explained by immunophenotypic differences ', Leukemia, vol. 22, no. 1, pp. 124-131 . https://doi.org/10.1038/sj.leu.2404957
Leukemia, 22, 124-131. Nature Publishing Group

مصطلحات موضوعية: RNA, Messenger/genetics, Male, Oncology, Cancer Research, Pathology, Oncogene Proteins, Fusion, THYMOCYTE DIFFERENTIATION, Receptors, Antigen, T-Cell, alpha-beta, Leukemia-Lymphoma, CHILDREN, FUSION, Immunophenotyping, NOTCH1, RESIDUAL DISEASE, Receptors, Basic Helix-Loop-Helix Transcription Factors, Leukemia-Lymphoma, Adult T-Cell, RNA, Neoplasm, Receptor, Notch1, Child, In Situ Hybridization, Fluorescence, In Situ Hybridization, T-Cell Acute Lymphocytic Leukemia Protein 1, RNA, Neoplasm/genetics, Gene Rearrangement, Oncogene Proteins, Hematology, gamma-delta/genetics, Reverse Transcriptase Polymerase Chain Reaction, PROTEIN LMO2, Receptors, Antigen, T-Cell, gamma-delta, Adult T-Cell/diagnosis, Fusion/genetics, LINEAGE, Prognosis, immunophenotype, Leukemia, HOX11L2 EXPRESSION, Antigen, outcome, Female, Neoplasm Recurrence, Local/genetics, alpha-beta/genetics, Receptor, medicine.medical_specialty, Lineage (genetic), Mutation/genetics, Receptors, Antigen, T-Cell, alpha-beta/genetics, Biology, Fluorescence, Local/genetics, Proto-Oncogene Proteins, Acute lymphocytic leukemia, Internal medicine, Leukemia-Lymphoma, Adult T-Cell/diagnosis, medicine, Humans, SUBGROUPS, Cell Lineage, Clinical significance, RNA, Messenger, CLINICAL-SIGNIFICANCE, ACUTE LYMPHOBLASTIC-LEUKEMIA, Homeodomain Proteins, Receptor, Notch1/genetics, TAL1, Basic Helix-Loop-Helix Transcription Factors/genetics, Neoplasm/genetics, Cytogenetics, Cancer, pediatric T-ALL, T-Cell, medicine.disease, Gene Rearrangement/genetics, Receptors, Antigen, T-Cell, gamma-delta/genetics, Notch1/genetics, Proto-Oncogene Proteins/genetics, Neoplasm Recurrence, Mutation, Oncogene Proteins, Fusion/genetics, RNA, Messenger/genetics, Neoplasm Recurrence, Local, Homeodomain Proteins/genetics

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf7c3d7d583d3e32649d57e5ac7b7637
https://doi.org/10.1038/sj.leu.2404957

المؤلفون: Sjogren, H., Orndal, C., Tingby, O., Meis-Kindblom, J. M., Kindblom, L. G., Stenman, Göran, 1953

المصدر: International Journal of Oncology. 24(6):1385-91

مصطلحات موضوعية: Cell and Molecular Biology, Cell- och molekylärbiologi, Adolescent, Adult, Aged, Bone Neoplasms/*genetics/pathology, Child, Chondroblastoma/*genetics/pathology, Chondrosarcoma/*genetics/pathology, *Chromosome Aberrations, Chromosome Banding, Chromosomes, Human, Pair 18/genetics, Pair 2/genetics, Pair 3/genetics, Pair 6/genetics, Diploidy, Female, Gene Rearrangement/genetics, Humans, In Situ Hybridization, Fluorescence, Inversion, Chromosome, Male, Middle Aged, Neoplasms/genetics/pathology, Osteosarcoma/*genetics/pathology, *Spectral Karyotyping

URL الوصول: https://gup.ub.gu.se/publication/88037

المؤلفون: Evgeny M. Zdobnov, Guillaume Bourque, Pavel A. Pevzner, Peer Bork, Glenn Tesler

المصدر: Genome Research, Vol. 15, No 1 (2005) pp. 98-110

مصطلحات موضوعية: Chickens/genetics, Synteny/genetics, Lineage (evolution), Biology, Synteny, Genome, Chromosomes, Evolution, Molecular, Mice, Molecular evolution, Gene orders, Genetics, Chromosomes, Human, Animals, Humans, Genes/genetics, Gene, Genetics (clinical), Gene Rearrangement, Whole genome sequencing, Chromosomes/genetics, Genetic Variation, Chromosomes, Human/genetics, Gene rearrangement, Gene Rearrangement/genetics, Rats, Genes, Genetic Variation/genetics, Human genome, Chicken Special/Letters, Chickens

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c47614a0b78e22db27ca398719af903f
https://archive-ouverte.unige.ch/unige:30558