Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Abnormalities and PAX5[original query] |
---|
PAX5 mutations occur frequently in adult B-cell progenitor acute lymphoblastic leukemia and PAX5 haploinsufficiency is associated with BCR-ABL1 and TCF3-PBX1 fusion genes: a GRAALL study. Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2009 Jul . Familiades J, Bousquet M, Lafage-Pochitaloff M, Béné MC, Beldjord K, De Vos J, Dastugue N, Coyaud E, Struski S, Quelen C, Prade-Houdellier N, Dobbelstein S, Cayuela JM, Soulier J, Grardel N, Preudhomme C, Cavé H, Blanchet O, Lhéritier V, Delannoy A, Chalandon Y, Ifrah N, Pigneux A, Brousset P, Macintyre EA, Huguet F, Dombret H, Broccardo C, Delabesse E |
Outcome in children with Down's syndrome and acute lymphoblastic leukemia: role of IKZF1 deletions and CRLF2 aberrations. Leukemia 2012 Oct 26 (10): 2204-11. Buitenkamp T D, Pieters R, Gallimore N E, van der Veer A, Meijerink J P P, Beverloo H B, Zimmermann M, de Haas V, Richards S M, Vora A J, Mitchell C D, Russell L J, Schwab C, Harrison C J, Moorman A V, van den Heuvel-Eibrink M M, den Boer M L, Zwaan C |
A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients. Genes, chromosomes & cancer 2015 May 54 (5): 326-33. Dirse Vaidas, Bertasiute Agne, Gineikiene Egle, Zvirblis Tadas, Dambrauskiene Ruta, Gerbutavicius Rolandas, Juozaityte Elona, Malciute Ligita, Paulsson Kajsa, Griskevicius Laimon |
[Significance of PAX5 deletion in childhood B-lineage acute lymphoblastic leukemia without reproducible chromosomal abnormalities]. Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics 2016 Apr 18 (4): 287-91. Liu Xiao-Ming, Zhang Li, Ruan Min, Liu Tian-Feng, Zhang Jia-Yuan, Liu Fang, Qi Ben-Quan, Chen Xiao-Juan, Wang Shu-Chun, Yang Wen-Yu, Guo Ye, Zou Yao, Chen Yu-Mei, Zhu Xiao-F |
Copy number abnormality of acute lymphoblastic leukemia cell lines based on their genetic subtypes. International journal of hematology 2018 May . Tomoyasu Chihiro, Imamura Toshihiko, Tomii Toshihiro, Yano Mio, Asai Daisuke, Goto Hiroaki, Shimada Akira, Sanada Masashi, Iwamoto Shotaro, Takita Junko, Minegishi Masayoshi, Inukai Takeshi, Sugita Kanji, Hosoi Haji |
High frequency of intermediate and poor risk copy number abnormalities in pediatric cohort of B-ALL correlate with high MRD post induction. Leukemia research 2018 2 66 79-84. Singh Minu, Bhatia Prateek, Trehan Amita, Varma Neelam, Sachdeva Manupdesh Singh, Bansal Deepak, Jain Richa, Naseem Sha |
Microarray testing as an efficient tool to redefine hyperdiploid paediatric B-cell precursor acute lymphoblastic leukaemia patients. Leukemia research 2019 May 83 106163. Lejman Monika, Zawitkowska Joanna, Styka Borys, Babicz Mariusz, Winnicka Dorota, Zaucha-Pra?mo Agnieszka, Pastorczak Agata, Taha Joanna, M?ynarski Wojciech, Kowalczyk Jerzy |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: