Chromosomal translocation (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Chromosomal translocation" in English language version.

refsWebsite

Global rank English rank

48nih.gov

4^th place

34doi.org

2^nd place

12worldcat.org

5^th place

4harvard.edu

18^th place

17^th place

4mayoclinic.org

1,610^th place

1,279^th place

2nature.com

234^th place

397^th place

2springer.com

274^th place

309^th place

2cancer.gov

1,684^th place

1,350^th place

2medlineplus.gov

1,581^st place

1,299^th place

2spandidos-publications.com

low place

1web.archive.org

1^st place

1eurogentest.org

low place

1thermofisher.com

low place

1europepmc.org

8,929^th place

8,063^rd place

1wiley.com

222^nd place

297^th place

1webmd.com

1,169^th place

1,075^th place

1macmillan.org.uk

low place

1handle.net

102^nd place

76^th place

1who.int

195^th place

302^nd place

1cdc.gov

218^th place

212^th place

1chop.edu

low place

1rerf.jp

low place

1books.google.com

3^rd place

1semanticscholar.org

11^th place

8^th place

1atlasgeneticsoncology.org

low place

atlasgeneticsoncology.org

"t(1;12)(q21;p13) ETV6/ARNT". atlasgeneticsoncology.org. Retrieved March 12, 2025.

books.google.com

Burtis, Carl A.; Ashwood, Edward R.; Bruns, David E. (December 16, 2011). "44. Hematopoeitic malignancies". Tietz Textbook of Clinical Chemistry and Molecular Diagnostics. Elsevier Health Sciences. pp. 1371–1396. ISBN 978-1-4557-5942-2. Retrieved November 5, 2012.

cancer.gov

"Leukemia—Patient Version - NCI". www.cancer.gov. Retrieved April 11, 2025.
"Acute Myeloid Leukemia Treatment - NCI". www.cancer.gov. April 4, 2025. Retrieved April 11, 2025.

cdc.gov

CDC (December 26, 2024). "Down Syndrome". Birth Defects. Retrieved April 11, 2025.

chop.edu

Philadelphia, The Children's Hospital of. "Translocation Down Syndrome | Children's Hospital of Philadelphia". www.chop.edu. Retrieved April 2, 2025.

doi.org

Oviedo de Valeria, Jenny (August 2, 1994). "Problemas multiplicativos tip transformacion lineal: tareas de compra y venta". Educación matemática. 6 (2): 73–86. doi:10.24844/em0602.06. ISSN 2448-8089.
Rowley, Janet D. (June 1973). "A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa Staining". Nature. 243 (5405): 290–293. Bibcode:1973Natur.243..290R. doi:10.1038/243290a0. ISSN 1476-4687.
Therman, Eeva; Susman, Millard (1993), Therman, Eeva; Susman, Millard (eds.), "Reciprocal Translocations", Human Chromosomes: Structure, Behavior, and Effects, New York, NY: Springer US, pp. 273–287, doi:10.1007/978-1-4684-0529-3_26, ISBN 978-1-4684-0529-3, retrieved April 2, 2025
Wilch, Ellen S.; Morton, Cynthia C. (2018), Zhang, Yu (ed.), "Historical and Clinical Perspectives on Chromosomal Translocations", Chromosome Translocation, vol. 1044, Singapore: Springer, pp. 1–14, doi:10.1007/978-981-13-0593-1_1, ISBN 978-981-13-0593-1, PMID 29956287, retrieved April 2, 2025
Parslow, Malcolm; Chambers, Diana; Aftimos, Salim (1981). "An inherited reciprocal translocation—balanced or unbalanced?". Pathology. 13 (1): 174. doi:10.1016/S0031-3025(16)38470-7.
Chen, Chih-Ping; Wu, Pei-Chen; Lin, Chen-Ju; Chern, Schu-Rern; Tsai, Fuu-Jen; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Li-Feng; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen (March 2011). "Unbalanced reciprocal translocations at amniocentesis". Taiwanese Journal of Obstetrics and Gynecology. 50 (1): 48–57. doi:10.1016/j.tjog.2011.02.001. PMID 21482375.
Ali, Hanif; Daser, Angelika; Dear, Paul; Wood, Henry; Rabbitts, Pamela; Rabbitts, Terence (2013). "Nonreciprocal chromosomal translocations in renal cancer involve multiple DSBs and NHEJ associated with breakpoint inversion but not necessarily with transcription". Genes, Chromosomes and Cancer. 52 (4): 402–409. doi:10.1002/gcc.22038. ISSN 1098-2264. PMID 23341332.
Nikitin, Dmitri; Tosato, Valentina; Zavec, Apolonija Bedina; Bruschi, Carlo V. (July 15, 2008). "Cellular and molecular effects of nonreciprocal chromosome translocations in Saccharomyces cerevisiae". Proceedings of the National Academy of Sciences. 105 (28): 9703–9708. Bibcode:2008PNAS..105.9703N. doi:10.1073/pnas.0800464105. PMC 2474487. PMID 18599460.
Nambiar, Mridula; Kari, Vijayalakshmi; Raghavan, Sathees C. (December 2008). "Chromosomal translocations in cancer". Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1786 (2): 139–152. doi:10.1016/j.bbcan.2008.07.005. PMID 18718509.
E. Anton; J. Blanco; J. Egozcue; F. Vidal (April 29, 2004). "Sperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q10)". Human Reproduction. 19 (6): 1345–1351. doi:10.1093/humrep/deh232. ISSN 1460-2350. PMID 15117905.
Yip, Moh-Ying (April 2015). "Autosomal ring chromosomes in human genetic disorders". Translational Pediatrics. 4 (2): 164–174. doi:10.3978/j.issn.2224-4336.2015.03.04. PMC 4729093. PMID 26835370.
Agarwal, S.; Tafel, A. A.; Kanaar, R. (2006). "DNA double-strand break repair and chromosome translocations". DNA Repair. 5 (9–10): 1075–1081. doi:10.1016/j.dnarep.2006.05.029. PMID 16798112.
Bohlander, Stefan K.; Kakadia, Purvi M. (2015). "DNA Repair and Chromosomal Translocations". Chromosomal Instability in Cancer Cells. Recent Results in Cancer Research. Vol. 200. pp. 1–37. doi:10.1007/978-3-319-20291-4_1. ISBN 978-3-319-20290-7.
Steyer, Benjamin; Cory, Evan; Saha, Krishanu (August 2018). "Developing precision medicine using scarless genome editing of human pluripotent stem cells". Drug Discovery Today: Technologies. 28: 3–12. doi:10.1016/j.ddtec.2018.02.001. PMC 6136251. PMID 30205878. Non-homologous end joining (NHEJ)—an error prone DNA repair process where double strand breaks are directly ligated, commonly resulting in insertion or deletion mutations.
Rocha, P. P.; Chaumeil, J.; Skok, J. A. (2013). "Molecular biology. Finding the right partner in a 3D genome". Science. 342 (6164): 1333–1334. doi:10.1126/science.1246106. PMC 3961821. PMID 24337287.
Nambiar, Mridula; Raghavan, Sathees C. (August 2011). "How does DNA break during chromosomal translocations?". Nucleic Acids Research. 39 (14): 5813–5825. doi:10.1093/nar/gkr223. ISSN 1362-4962. PMC 3152359. PMID 21498543.
Jasin, Maria (June 1996). "Genetic manipulation of genomes with rare-cutting endonucleases". Trends in Genetics. 12 (6): 224–228. doi:10.1016/0168-9525(96)10019-6. PMID 8928227.
Povirk, Lawrence F. (September 2006). "Biochemical mechanisms of chromosomal translocations resulting from DNA double-strand breaks". DNA Repair. 5 (9–10): 1199–1212. doi:10.1016/j.dnarep.2006.05.016. PMID 16822725.
Qiu, Zhijun; Zhang, Zhenhua; Roschke, Anna; Varga, Tamas; Aplan, Peter D. (February 22, 2017). "Generation of Gross Chromosomal Rearrangements by a Single Engineered DNA Double Strand Break". Scientific Reports. 7 (1): 43156. Bibcode:2017NatSR...743156Q. doi:10.1038/srep43156. hdl:2437/288170. ISSN 2045-2322. PMC 5320478. PMID 28225067.
Streb, Patrick; Kowarz, Eric; Benz, Tamara; Reis, Jennifer; Marschalek, Rolf (June 2023). "How chromosomal translocations arise to cause cancer: Gene proximity, trans-splicing, and DNA end joining". iScience. 26 (6): 106900. Bibcode:2023iSci...26j6900S. doi:10.1016/j.isci.2023.106900. PMC 10291325. PMID 37378346.
Aplan, Peter D. (January 2006). "Causes of oncogenic chromosomal translocation". Trends in Genetics. 22 (1): 46–55. doi:10.1016/j.tig.2005.10.002. ISSN 0168-9525. PMC 1762911. PMID 16257470.
Zhang, Hong-Guo; Wang, Rui-Xue; Pan, Yuan; Zhang, Han; Li, Lei-Lei; Zhu, Hai-Bo; Liu, Rui-Zhi (January 25, 2018). "A report of nine cases and review of the literature of infertile men carrying balanced translocations involving chromosome 5". Molecular Cytogenetics. 11 (1): 10. doi:10.1186/s13039-018-0360-x. ISSN 1755-8166. PMC 5785882. PMID 29416565.
Gaviria, Anibal; Cadena-Ullauri, Santiago; Cevallos, Francisco; Guevara-Ramirez, Patricia; Ruiz-Pozo, Viviana; Tamayo-Trujillo, Rafael; Paz-Cruz, Elius; Zambrano, Ana Karina (September 5, 2022). "Clinical, cytogenetic, and genomic analyses of an Ecuadorian subject with Klinefelter syndrome, recessive hemophilia A, and 1;19 chromosomal translocation: a case report". Molecular Cytogenetics. 15 (1): 40. doi:10.1186/s13039-022-00618-w. PMC 9446752. PMID 36064723.
Semple CA, Devon RS, Le Hellard S, Porteous DJ (April 2001). "Identification of genes from a schizophrenia-linked translocation breakpoint region". Genomics. 73 (1): 123–6. doi:10.1006/geno.2001.6516. PMID 11352574.
Zheng, Jie (November 1, 2013). "Oncogenic chromosomal translocations and human cancer (Review)". Oncology Reports. 30 (5): 2011–2019. doi:10.3892/or.2013.2677. ISSN 1021-335X. PMID 23970180.
Li JY, Gaillard F, Moreau A, et al. (May 1999). "Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization". Am. J. Pathol. 154 (5): 1449–52. doi:10.1016/S0002-9440(10)65399-0. PMC 1866594. PMID 10329598.
Zheng, Jie (November 1, 2013). "Oncogenic chromosomal translocations and human cancer (Review)". Oncology Reports. 30 (5): 2011–2019. doi:10.3892/or.2013.2677. ISSN 1021-335X. PMID 23970180.
Kurzrock R, Kantarjian HM, Druker BJ, Talpaz M (May 2003). "Philadelphia chromosome-positive leukemias: from basic mechanisms to molecular therapeutics". Ann. Intern. Med. 138 (10): 819–30. doi:10.7326/0003-4819-138-10-200305200-00010. PMID 12755554. S2CID 25865321.
Eykelenboom, Jennifer E; Briggs, Gareth J; Bradshaw, Nicholas J; Soares, Dinesh C; Ogawa, Fumiaki; Christie, Sheila; Malavasi, Elise LV; Makedonopoulou, Paraskevi; Mackie, Shaun; Malloy, Mary P; Wear, Martin A; Blackburn, Elizabeth A; Bramham, Janice; McIntosh, Andrew M; Blackwood, Douglas H (April 30, 2012). "A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins". Human Molecular Genetics. 21 (15): 3374–3386. doi:10.1093/hmg/dds169. PMC 3392113. PMID 22547224.
Przybyl, Joanna; Sciot, Raf; Rutkowski, Piotr; Siedlecki, Janusz A.; Vanspauwen, Vanessa; Samson, Ignace; Debiec-Rychter, Maria (December 2012). "Recurrent and novel SS18-SSX fusion transcripts in synovial sarcoma: description of three new cases". Tumor Biology. 33 (6): 2245–2253. doi:10.1007/s13277-012-0486-0. PMC 3501176. PMID 22976541.
Eckel-Passow, Jeanette E.; Lachance, Daniel H.; Molinaro, Annette M.; Walsh, Kyle M.; Decker, Paul A.; Sicotte, Hugues; Pekmezci, Melike; Rice, Terri; Kosel, Matt L.; Smirnov, Ivan V.; Sarkar, Gobinda; Caron, Alissa A.; Kollmeyer, Thomas M.; Praska, Corinne E.; Chada, Anisha R. (June 25, 2015). "Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors". The New England Journal of Medicine. 372 (26): 2499–2508. doi:10.1056/NEJMoa1407279. ISSN 1533-4406. PMC 4489704. PMID 26061753.
Cairncross, Gregory; Jenkins, Robert (November 2008). "Gliomas With 1p/19q Codeletion:a.k.a. Oligodendroglioma". The Cancer Journal. 14 (6): 352–357. doi:10.1097/PPO.0b013e31818d8178. PMID 19060598.
Wu, Shuiyan; Lu, Jun; Su, Dongni; Yang, Fan; Zhang, Yongping; Hu, Shaoyan (March 2021). "The advantage of chimeric antigen receptor T cell therapy in pediatric acute lymphoblastic leukemia with E2A-HLF fusion gene positivity: a case series". Translational Pediatrics. 10 (3): 686–691. doi:10.21037/tp-20-323. ISSN 2224-4344. PMC 8041607. PMID 33880339.
Mohamed, Mustafa; Fisher, Cyril; Thway, Khin (June 2017). "Low-grade fibromyxoid sarcoma: Clinical, morphologic and genetic features". Annals of Diagnostic Pathology. 28: 60–67. doi:10.1016/j.anndiagpath.2017.04.001. PMID 28648941.

eurogentest.org

"EuroGentest: Chromosome Translocations". www.eurogentest.org. Archived from the original on January 24, 2018. Retrieved March 29, 2019.

europepmc.org

PMC, Europe. "Europe PMC". europepmc.org. Retrieved April 2, 2025.

handle.net

hdl.handle.net

Qiu, Zhijun; Zhang, Zhenhua; Roschke, Anna; Varga, Tamas; Aplan, Peter D. (February 22, 2017). "Generation of Gross Chromosomal Rearrangements by a Single Engineered DNA Double Strand Break". Scientific Reports. 7 (1): 43156. Bibcode:2017NatSR...743156Q. doi:10.1038/srep43156. hdl:2437/288170. ISSN 2045-2322. PMC 5320478. PMID 28225067.

harvard.edu

ui.adsabs.harvard.edu

Rowley, Janet D. (June 1973). "A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa Staining". Nature. 243 (5405): 290–293. Bibcode:1973Natur.243..290R. doi:10.1038/243290a0. ISSN 1476-4687.
Nikitin, Dmitri; Tosato, Valentina; Zavec, Apolonija Bedina; Bruschi, Carlo V. (July 15, 2008). "Cellular and molecular effects of nonreciprocal chromosome translocations in Saccharomyces cerevisiae". Proceedings of the National Academy of Sciences. 105 (28): 9703–9708. Bibcode:2008PNAS..105.9703N. doi:10.1073/pnas.0800464105. PMC 2474487. PMID 18599460.
Qiu, Zhijun; Zhang, Zhenhua; Roschke, Anna; Varga, Tamas; Aplan, Peter D. (February 22, 2017). "Generation of Gross Chromosomal Rearrangements by a Single Engineered DNA Double Strand Break". Scientific Reports. 7 (1): 43156. Bibcode:2017NatSR...743156Q. doi:10.1038/srep43156. hdl:2437/288170. ISSN 2045-2322. PMC 5320478. PMID 28225067.
Streb, Patrick; Kowarz, Eric; Benz, Tamara; Reis, Jennifer; Marschalek, Rolf (June 2023). "How chromosomal translocations arise to cause cancer: Gene proximity, trans-splicing, and DNA end joining". iScience. 26 (6): 106900. Bibcode:2023iSci...26j6900S. doi:10.1016/j.isci.2023.106900. PMC 10291325. PMID 37378346.

macmillan.org.uk

"Chemotherapy - What it is, types, treatment and side effects". www.macmillan.org.uk. Retrieved April 11, 2025.

mayoclinic.org

"Cancer - Symptoms and causes". Mayo Clinic. Retrieved April 11, 2025.
"Chronic myelogenous leukemia - Symptoms and causes". Mayo Clinic. Retrieved April 11, 2025.
"Ewing sarcoma - Symptoms and causes". Mayo Clinic. Retrieved April 11, 2025.
"A genetic disorder that affects females-Turner syndrome - Symptoms & causes". Mayo Clinic.

medlineplus.gov

"SRY gene" (PDF). medlineplus.gov.
"Emanuel syndrome: MedlinePlus Genetics".

nature.com

Rowley, Janet D. (June 1973). "A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa Staining". Nature. 243 (5405): 290–293. Bibcode:1973Natur.243..290R. doi:10.1038/243290a0. ISSN 1476-4687.
"Human Chromosome Translocations and Cancer | Learn Science at Scitable". www.nature.com. Retrieved April 2, 2025.

nih.gov

pubmed.ncbi.nlm.nih.gov

HROMAS, ROBERT; WILLIAMSON, ELIZABETH; LEE, SUK-HEE; NICKOLOFF, JAC (2016). "Preventing the Chromosomal Translocations That Cause Cancer". Transactions of the American Clinical and Climatological Association. 127: 176–195. PMC 5216476. PMID 28066052.
Wilch, Ellen S.; Morton, Cynthia C. (2018), Zhang, Yu (ed.), "Historical and Clinical Perspectives on Chromosomal Translocations", Chromosome Translocation, vol. 1044, Singapore: Springer, pp. 1–14, doi:10.1007/978-981-13-0593-1_1, ISBN 978-981-13-0593-1, PMID 29956287, retrieved April 2, 2025
Chen, Chih-Ping; Wu, Pei-Chen; Lin, Chen-Ju; Chern, Schu-Rern; Tsai, Fuu-Jen; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Li-Feng; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen (March 2011). "Unbalanced reciprocal translocations at amniocentesis". Taiwanese Journal of Obstetrics and Gynecology. 50 (1): 48–57. doi:10.1016/j.tjog.2011.02.001. PMID 21482375.
Ali, Hanif; Daser, Angelika; Dear, Paul; Wood, Henry; Rabbitts, Pamela; Rabbitts, Terence (2013). "Nonreciprocal chromosomal translocations in renal cancer involve multiple DSBs and NHEJ associated with breakpoint inversion but not necessarily with transcription". Genes, Chromosomes and Cancer. 52 (4): 402–409. doi:10.1002/gcc.22038. ISSN 1098-2264. PMID 23341332.
Nikitin, Dmitri; Tosato, Valentina; Zavec, Apolonija Bedina; Bruschi, Carlo V. (July 15, 2008). "Cellular and molecular effects of nonreciprocal chromosome translocations in Saccharomyces cerevisiae". Proceedings of the National Academy of Sciences. 105 (28): 9703–9708. Bibcode:2008PNAS..105.9703N. doi:10.1073/pnas.0800464105. PMC 2474487. PMID 18599460.
Nambiar, Mridula; Kari, Vijayalakshmi; Raghavan, Sathees C. (December 2008). "Chromosomal translocations in cancer". Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1786 (2): 139–152. doi:10.1016/j.bbcan.2008.07.005. PMID 18718509.
E. Anton; J. Blanco; J. Egozcue; F. Vidal (April 29, 2004). "Sperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q10)". Human Reproduction. 19 (6): 1345–1351. doi:10.1093/humrep/deh232. ISSN 1460-2350. PMID 15117905.
Yip, Moh-Ying (April 2015). "Autosomal ring chromosomes in human genetic disorders". Translational Pediatrics. 4 (2): 164–174. doi:10.3978/j.issn.2224-4336.2015.03.04. PMC 4729093. PMID 26835370.
Agarwal, S.; Tafel, A. A.; Kanaar, R. (2006). "DNA double-strand break repair and chromosome translocations". DNA Repair. 5 (9–10): 1075–1081. doi:10.1016/j.dnarep.2006.05.029. PMID 16798112.
Steyer, Benjamin; Cory, Evan; Saha, Krishanu (August 2018). "Developing precision medicine using scarless genome editing of human pluripotent stem cells". Drug Discovery Today: Technologies. 28: 3–12. doi:10.1016/j.ddtec.2018.02.001. PMC 6136251. PMID 30205878. Non-homologous end joining (NHEJ)—an error prone DNA repair process where double strand breaks are directly ligated, commonly resulting in insertion or deletion mutations.
Rocha, P. P.; Chaumeil, J.; Skok, J. A. (2013). "Molecular biology. Finding the right partner in a 3D genome". Science. 342 (6164): 1333–1334. doi:10.1126/science.1246106. PMC 3961821. PMID 24337287.
Nambiar, Mridula; Raghavan, Sathees C. (August 2011). "How does DNA break during chromosomal translocations?". Nucleic Acids Research. 39 (14): 5813–5825. doi:10.1093/nar/gkr223. ISSN 1362-4962. PMC 3152359. PMID 21498543.
Jasin, Maria (June 1996). "Genetic manipulation of genomes with rare-cutting endonucleases". Trends in Genetics. 12 (6): 224–228. doi:10.1016/0168-9525(96)10019-6. PMID 8928227.
Povirk, Lawrence F. (September 2006). "Biochemical mechanisms of chromosomal translocations resulting from DNA double-strand breaks". DNA Repair. 5 (9–10): 1199–1212. doi:10.1016/j.dnarep.2006.05.016. PMID 16822725.
Qiu, Zhijun; Zhang, Zhenhua; Roschke, Anna; Varga, Tamas; Aplan, Peter D. (February 22, 2017). "Generation of Gross Chromosomal Rearrangements by a Single Engineered DNA Double Strand Break". Scientific Reports. 7 (1): 43156. Bibcode:2017NatSR...743156Q. doi:10.1038/srep43156. hdl:2437/288170. ISSN 2045-2322. PMC 5320478. PMID 28225067.
Streb, Patrick; Kowarz, Eric; Benz, Tamara; Reis, Jennifer; Marschalek, Rolf (June 2023). "How chromosomal translocations arise to cause cancer: Gene proximity, trans-splicing, and DNA end joining". iScience. 26 (6): 106900. Bibcode:2023iSci...26j6900S. doi:10.1016/j.isci.2023.106900. PMC 10291325. PMID 37378346.
Aplan, Peter D. (January 2006). "Causes of oncogenic chromosomal translocation". Trends in Genetics. 22 (1): 46–55. doi:10.1016/j.tig.2005.10.002. ISSN 0168-9525. PMC 1762911. PMID 16257470.
Zhang, Hong-Guo; Wang, Rui-Xue; Pan, Yuan; Zhang, Han; Li, Lei-Lei; Zhu, Hai-Bo; Liu, Rui-Zhi (January 25, 2018). "A report of nine cases and review of the literature of infertile men carrying balanced translocations involving chromosome 5". Molecular Cytogenetics. 11 (1): 10. doi:10.1186/s13039-018-0360-x. ISSN 1755-8166. PMC 5785882. PMID 29416565.
Gaviria, Anibal; Cadena-Ullauri, Santiago; Cevallos, Francisco; Guevara-Ramirez, Patricia; Ruiz-Pozo, Viviana; Tamayo-Trujillo, Rafael; Paz-Cruz, Elius; Zambrano, Ana Karina (September 5, 2022). "Clinical, cytogenetic, and genomic analyses of an Ecuadorian subject with Klinefelter syndrome, recessive hemophilia A, and 1;19 chromosomal translocation: a case report". Molecular Cytogenetics. 15 (1): 40. doi:10.1186/s13039-022-00618-w. PMC 9446752. PMID 36064723.
Semple CA, Devon RS, Le Hellard S, Porteous DJ (April 2001). "Identification of genes from a schizophrenia-linked translocation breakpoint region". Genomics. 73 (1): 123–6. doi:10.1006/geno.2001.6516. PMID 11352574.
Zheng, Jie (November 1, 2013). "Oncogenic chromosomal translocations and human cancer (Review)". Oncology Reports. 30 (5): 2011–2019. doi:10.3892/or.2013.2677. ISSN 1021-335X. PMID 23970180.
Li JY, Gaillard F, Moreau A, et al. (May 1999). "Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization". Am. J. Pathol. 154 (5): 1449–52. doi:10.1016/S0002-9440(10)65399-0. PMC 1866594. PMID 10329598.
Zheng, Jie (November 1, 2013). "Oncogenic chromosomal translocations and human cancer (Review)". Oncology Reports. 30 (5): 2011–2019. doi:10.3892/or.2013.2677. ISSN 1021-335X. PMID 23970180.
Kurzrock R, Kantarjian HM, Druker BJ, Talpaz M (May 2003). "Philadelphia chromosome-positive leukemias: from basic mechanisms to molecular therapeutics". Ann. Intern. Med. 138 (10): 819–30. doi:10.7326/0003-4819-138-10-200305200-00010. PMID 12755554. S2CID 25865321.
Eykelenboom, Jennifer E; Briggs, Gareth J; Bradshaw, Nicholas J; Soares, Dinesh C; Ogawa, Fumiaki; Christie, Sheila; Malavasi, Elise LV; Makedonopoulou, Paraskevi; Mackie, Shaun; Malloy, Mary P; Wear, Martin A; Blackburn, Elizabeth A; Bramham, Janice; McIntosh, Andrew M; Blackwood, Douglas H (April 30, 2012). "A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins". Human Molecular Genetics. 21 (15): 3374–3386. doi:10.1093/hmg/dds169. PMC 3392113. PMID 22547224.
Przybyl, Joanna; Sciot, Raf; Rutkowski, Piotr; Siedlecki, Janusz A.; Vanspauwen, Vanessa; Samson, Ignace; Debiec-Rychter, Maria (December 2012). "Recurrent and novel SS18-SSX fusion transcripts in synovial sarcoma: description of three new cases". Tumor Biology. 33 (6): 2245–2253. doi:10.1007/s13277-012-0486-0. PMC 3501176. PMID 22976541.
Eckel-Passow, Jeanette E.; Lachance, Daniel H.; Molinaro, Annette M.; Walsh, Kyle M.; Decker, Paul A.; Sicotte, Hugues; Pekmezci, Melike; Rice, Terri; Kosel, Matt L.; Smirnov, Ivan V.; Sarkar, Gobinda; Caron, Alissa A.; Kollmeyer, Thomas M.; Praska, Corinne E.; Chada, Anisha R. (June 25, 2015). "Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors". The New England Journal of Medicine. 372 (26): 2499–2508. doi:10.1056/NEJMoa1407279. ISSN 1533-4406. PMC 4489704. PMID 26061753.
Cairncross, Gregory; Jenkins, Robert (November 2008). "Gliomas With 1p/19q Codeletion:a.k.a. Oligodendroglioma". The Cancer Journal. 14 (6): 352–357. doi:10.1097/PPO.0b013e31818d8178. PMID 19060598.
Wu, Shuiyan; Lu, Jun; Su, Dongni; Yang, Fan; Zhang, Yongping; Hu, Shaoyan (March 2021). "The advantage of chimeric antigen receptor T cell therapy in pediatric acute lymphoblastic leukemia with E2A-HLF fusion gene positivity: a case series". Translational Pediatrics. 10 (3): 686–691. doi:10.21037/tp-20-323. ISSN 2224-4344. PMC 8041607. PMID 33880339.
Mohamed, Mustafa; Fisher, Cyril; Thway, Khin (June 2017). "Low-grade fibromyxoid sarcoma: Clinical, morphologic and genetic features". Annals of Diagnostic Pathology. 28: 60–67. doi:10.1016/j.anndiagpath.2017.04.001. PMID 28648941.

ncbi.nlm.nih.gov

HROMAS, ROBERT; WILLIAMSON, ELIZABETH; LEE, SUK-HEE; NICKOLOFF, JAC (2016). "Preventing the Chromosomal Translocations That Cause Cancer". Transactions of the American Clinical and Climatological Association. 127: 176–195. PMC 5216476. PMID 28066052.
Nikitin, Dmitri; Tosato, Valentina; Zavec, Apolonija Bedina; Bruschi, Carlo V. (July 15, 2008). "Cellular and molecular effects of nonreciprocal chromosome translocations in Saccharomyces cerevisiae". Proceedings of the National Academy of Sciences. 105 (28): 9703–9708. Bibcode:2008PNAS..105.9703N. doi:10.1073/pnas.0800464105. PMC 2474487. PMID 18599460.
Yip, Moh-Ying (April 2015). "Autosomal ring chromosomes in human genetic disorders". Translational Pediatrics. 4 (2): 164–174. doi:10.3978/j.issn.2224-4336.2015.03.04. PMC 4729093. PMID 26835370.
Steyer, Benjamin; Cory, Evan; Saha, Krishanu (August 2018). "Developing precision medicine using scarless genome editing of human pluripotent stem cells". Drug Discovery Today: Technologies. 28: 3–12. doi:10.1016/j.ddtec.2018.02.001. PMC 6136251. PMID 30205878. Non-homologous end joining (NHEJ)—an error prone DNA repair process where double strand breaks are directly ligated, commonly resulting in insertion or deletion mutations.
Rocha, P. P.; Chaumeil, J.; Skok, J. A. (2013). "Molecular biology. Finding the right partner in a 3D genome". Science. 342 (6164): 1333–1334. doi:10.1126/science.1246106. PMC 3961821. PMID 24337287.
Nambiar, Mridula; Raghavan, Sathees C. (August 2011). "How does DNA break during chromosomal translocations?". Nucleic Acids Research. 39 (14): 5813–5825. doi:10.1093/nar/gkr223. ISSN 1362-4962. PMC 3152359. PMID 21498543.
Qiu, Zhijun; Zhang, Zhenhua; Roschke, Anna; Varga, Tamas; Aplan, Peter D. (February 22, 2017). "Generation of Gross Chromosomal Rearrangements by a Single Engineered DNA Double Strand Break". Scientific Reports. 7 (1): 43156. Bibcode:2017NatSR...743156Q. doi:10.1038/srep43156. hdl:2437/288170. ISSN 2045-2322. PMC 5320478. PMID 28225067.
Streb, Patrick; Kowarz, Eric; Benz, Tamara; Reis, Jennifer; Marschalek, Rolf (June 2023). "How chromosomal translocations arise to cause cancer: Gene proximity, trans-splicing, and DNA end joining". iScience. 26 (6): 106900. Bibcode:2023iSci...26j6900S. doi:10.1016/j.isci.2023.106900. PMC 10291325. PMID 37378346.
Aplan, Peter D. (January 2006). "Causes of oncogenic chromosomal translocation". Trends in Genetics. 22 (1): 46–55. doi:10.1016/j.tig.2005.10.002. ISSN 0168-9525. PMC 1762911. PMID 16257470.
Zhang, Hong-Guo; Wang, Rui-Xue; Pan, Yuan; Zhang, Han; Li, Lei-Lei; Zhu, Hai-Bo; Liu, Rui-Zhi (January 25, 2018). "A report of nine cases and review of the literature of infertile men carrying balanced translocations involving chromosome 5". Molecular Cytogenetics. 11 (1): 10. doi:10.1186/s13039-018-0360-x. ISSN 1755-8166. PMC 5785882. PMID 29416565.
Gilbert, Scott F. (2000). "Chromosomal Sex Determination in Mammals". Developmental Biology. 6th edition. Sinauer Associates.
Gaviria, Anibal; Cadena-Ullauri, Santiago; Cevallos, Francisco; Guevara-Ramirez, Patricia; Ruiz-Pozo, Viviana; Tamayo-Trujillo, Rafael; Paz-Cruz, Elius; Zambrano, Ana Karina (September 5, 2022). "Clinical, cytogenetic, and genomic analyses of an Ecuadorian subject with Klinefelter syndrome, recessive hemophilia A, and 1;19 chromosomal translocation: a case report". Molecular Cytogenetics. 15 (1): 40. doi:10.1186/s13039-022-00618-w. PMC 9446752. PMID 36064723.
Li JY, Gaillard F, Moreau A, et al. (May 1999). "Detection of translocation t(11;14)(q13;q32) in mantle cell lymphoma by fluorescence in situ hybridization". Am. J. Pathol. 154 (5): 1449–52. doi:10.1016/S0002-9440(10)65399-0. PMC 1866594. PMID 10329598.
Eykelenboom, Jennifer E; Briggs, Gareth J; Bradshaw, Nicholas J; Soares, Dinesh C; Ogawa, Fumiaki; Christie, Sheila; Malavasi, Elise LV; Makedonopoulou, Paraskevi; Mackie, Shaun; Malloy, Mary P; Wear, Martin A; Blackburn, Elizabeth A; Bramham, Janice; McIntosh, Andrew M; Blackwood, Douglas H (April 30, 2012). "A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins". Human Molecular Genetics. 21 (15): 3374–3386. doi:10.1093/hmg/dds169. PMC 3392113. PMID 22547224.
Przybyl, Joanna; Sciot, Raf; Rutkowski, Piotr; Siedlecki, Janusz A.; Vanspauwen, Vanessa; Samson, Ignace; Debiec-Rychter, Maria (December 2012). "Recurrent and novel SS18-SSX fusion transcripts in synovial sarcoma: description of three new cases". Tumor Biology. 33 (6): 2245–2253. doi:10.1007/s13277-012-0486-0. PMC 3501176. PMID 22976541.
Eckel-Passow, Jeanette E.; Lachance, Daniel H.; Molinaro, Annette M.; Walsh, Kyle M.; Decker, Paul A.; Sicotte, Hugues; Pekmezci, Melike; Rice, Terri; Kosel, Matt L.; Smirnov, Ivan V.; Sarkar, Gobinda; Caron, Alissa A.; Kollmeyer, Thomas M.; Praska, Corinne E.; Chada, Anisha R. (June 25, 2015). "Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors". The New England Journal of Medicine. 372 (26): 2499–2508. doi:10.1056/NEJMoa1407279. ISSN 1533-4406. PMC 4489704. PMID 26061753.
Wu, Shuiyan; Lu, Jun; Su, Dongni; Yang, Fan; Zhang, Yongping; Hu, Shaoyan (March 2021). "The advantage of chimeric antigen receptor T cell therapy in pediatric acute lymphoblastic leukemia with E2A-HLF fusion gene positivity: a case series". Translational Pediatrics. 10 (3): 686–691. doi:10.21037/tp-20-323. ISSN 2224-4344. PMC 8041607. PMID 33880339.

ghr.nlm.nih.gov

"Can changes in the structure of chromosomes affect health and development?". Genetics Home Reference. National Library of Medicine. Retrieved July 15, 2020.

rerf.jp

"Characteristics of chromosome groups: Karyotyping". rerf.jp. Radiation Effects Research Foundation. Retrieved June 30, 2014.

semanticscholar.org

api.semanticscholar.org

Kurzrock R, Kantarjian HM, Druker BJ, Talpaz M (May 2003). "Philadelphia chromosome-positive leukemias: from basic mechanisms to molecular therapeutics". Ann. Intern. Med. 138 (10): 819–30. doi:10.7326/0003-4819-138-10-200305200-00010. PMID 12755554. S2CID 25865321.

spandidos-publications.com

Zheng, Jie (November 1, 2013). "Oncogenic chromosomal translocations and human cancer (Review)". Oncology Reports. 30 (5): 2011–2019. doi:10.3892/or.2013.2677. ISSN 1021-335X. PMID 23970180.
Zheng, Jie (November 1, 2013). "Oncogenic chromosomal translocations and human cancer (Review)". Oncology Reports. 30 (5): 2011–2019. doi:10.3892/or.2013.2677. ISSN 1021-335X. PMID 23970180.

springer.com

link.springer.com

Therman, Eeva; Susman, Millard (1993), Therman, Eeva; Susman, Millard (eds.), "Reciprocal Translocations", Human Chromosomes: Structure, Behavior, and Effects, New York, NY: Springer US, pp. 273–287, doi:10.1007/978-1-4684-0529-3_26, ISBN 978-1-4684-0529-3, retrieved April 2, 2025
Wilch, Ellen S.; Morton, Cynthia C. (2018), Zhang, Yu (ed.), "Historical and Clinical Perspectives on Chromosomal Translocations", Chromosome Translocation, vol. 1044, Singapore: Springer, pp. 1–14, doi:10.1007/978-981-13-0593-1_1, ISBN 978-981-13-0593-1, PMID 29956287, retrieved April 2, 2025

thermofisher.com

Case, Sean (July 27, 2020). "History and Evolution of Cytogenetics". Behind the Bench. Retrieved March 13, 2025.

web.archive.org

"EuroGentest: Chromosome Translocations". www.eurogentest.org. Archived from the original on January 24, 2018. Retrieved March 29, 2019.

webmd.com

Mehta, Parang. "What Are Translocations?". WebMD. Retrieved April 2, 2025.

who.int

"Infertility". www.who.int. Retrieved April 11, 2025.

wiley.com

onlinelibrary.wiley.com

Ali, Hanif; Daser, Angelika; Dear, Paul; Wood, Henry; Rabbitts, Pamela; Rabbitts, Terence (2013). "Nonreciprocal chromosomal translocations in renal cancer involve multiple DSBs and NHEJ associated with breakpoint inversion but not necessarily with transcription". Genes, Chromosomes and Cancer. 52 (4): 402–409. doi:10.1002/gcc.22038. ISSN 1098-2264. PMID 23341332.

worldcat.org

search.worldcat.org

Oviedo de Valeria, Jenny (August 2, 1994). "Problemas multiplicativos tip transformacion lineal: tareas de compra y venta". Educación matemática. 6 (2): 73–86. doi:10.24844/em0602.06. ISSN 2448-8089.
Rowley, Janet D. (June 1973). "A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa Staining". Nature. 243 (5405): 290–293. Bibcode:1973Natur.243..290R. doi:10.1038/243290a0. ISSN 1476-4687.
Ali, Hanif; Daser, Angelika; Dear, Paul; Wood, Henry; Rabbitts, Pamela; Rabbitts, Terence (2013). "Nonreciprocal chromosomal translocations in renal cancer involve multiple DSBs and NHEJ associated with breakpoint inversion but not necessarily with transcription". Genes, Chromosomes and Cancer. 52 (4): 402–409. doi:10.1002/gcc.22038. ISSN 1098-2264. PMID 23341332.
E. Anton; J. Blanco; J. Egozcue; F. Vidal (April 29, 2004). "Sperm FISH studies in seven male carriers of Robertsonian translocation t(13;14)(q10;q10)". Human Reproduction. 19 (6): 1345–1351. doi:10.1093/humrep/deh232. ISSN 1460-2350. PMID 15117905.
Nambiar, Mridula; Raghavan, Sathees C. (August 2011). "How does DNA break during chromosomal translocations?". Nucleic Acids Research. 39 (14): 5813–5825. doi:10.1093/nar/gkr223. ISSN 1362-4962. PMC 3152359. PMID 21498543.
Qiu, Zhijun; Zhang, Zhenhua; Roschke, Anna; Varga, Tamas; Aplan, Peter D. (February 22, 2017). "Generation of Gross Chromosomal Rearrangements by a Single Engineered DNA Double Strand Break". Scientific Reports. 7 (1): 43156. Bibcode:2017NatSR...743156Q. doi:10.1038/srep43156. hdl:2437/288170. ISSN 2045-2322. PMC 5320478. PMID 28225067.
Aplan, Peter D. (January 2006). "Causes of oncogenic chromosomal translocation". Trends in Genetics. 22 (1): 46–55. doi:10.1016/j.tig.2005.10.002. ISSN 0168-9525. PMC 1762911. PMID 16257470.
Zhang, Hong-Guo; Wang, Rui-Xue; Pan, Yuan; Zhang, Han; Li, Lei-Lei; Zhu, Hai-Bo; Liu, Rui-Zhi (January 25, 2018). "A report of nine cases and review of the literature of infertile men carrying balanced translocations involving chromosome 5". Molecular Cytogenetics. 11 (1): 10. doi:10.1186/s13039-018-0360-x. ISSN 1755-8166. PMC 5785882. PMID 29416565.
Zheng, Jie (November 1, 2013). "Oncogenic chromosomal translocations and human cancer (Review)". Oncology Reports. 30 (5): 2011–2019. doi:10.3892/or.2013.2677. ISSN 1021-335X. PMID 23970180.
Zheng, Jie (November 1, 2013). "Oncogenic chromosomal translocations and human cancer (Review)". Oncology Reports. 30 (5): 2011–2019. doi:10.3892/or.2013.2677. ISSN 1021-335X. PMID 23970180.
Eckel-Passow, Jeanette E.; Lachance, Daniel H.; Molinaro, Annette M.; Walsh, Kyle M.; Decker, Paul A.; Sicotte, Hugues; Pekmezci, Melike; Rice, Terri; Kosel, Matt L.; Smirnov, Ivan V.; Sarkar, Gobinda; Caron, Alissa A.; Kollmeyer, Thomas M.; Praska, Corinne E.; Chada, Anisha R. (June 25, 2015). "Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors". The New England Journal of Medicine. 372 (26): 2499–2508. doi:10.1056/NEJMoa1407279. ISSN 1533-4406. PMC 4489704. PMID 26061753.
Wu, Shuiyan; Lu, Jun; Su, Dongni; Yang, Fan; Zhang, Yongping; Hu, Shaoyan (March 2021). "The advantage of chimeric antigen receptor T cell therapy in pediatric acute lymphoblastic leukemia with E2A-HLF fusion gene positivity: a case series". Translational Pediatrics. 10 (3): 686–691. doi:10.21037/tp-20-323. ISSN 2224-4344. PMC 8041607. PMID 33880339.