Terms: = Leukemia AND RAD21, HR21, 5885, ENSG00000164754, KIAA0078, FLJ25655, hHR21, MCD1, O60216, NXP1, HRAD21, FLJ40596, SCC1
45 results:
1. Role of chromosomal cohesion and separation in aneuploidy and tumorigenesis.
Pati D
Cell Mol Life Sci; 2024 Feb; 81(1):100. PubMed ID: 38388697
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2. IKZF3 polymorphisms contribute to the increased risk of acute lymphoblastic leukemia in children.
Yang X; Yang L; Luo A; Liu S; Zhang X; Liu X; Liu X; Luo A; Cai M; Yan Y; Wu X; Huang K; Xu L; Jiang H
Cancer; 2024 Mar; 130(6):973-984. PubMed ID: 38018448
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3. Alterations of cohesin complex genes in acute myeloid leukemia: differential co-mutations, clinical presentation and impact on outcome.
Eckardt JN; Stasik S; Röllig C; Sauer T; Scholl S; Hochhaus A; Crysandt M; Brümmendorf TH; Naumann R; Steffen B; Kunzmann V; Einsele H; Schaich M; Burchert A; Neubauer A; Schäfer-Eckart K; Schliemann C; Krause SW; Herbst R; Hänel M; Hanoun M; Kaiser U; Kaufmann M; Rácil Z; Mayer J; Cerqueira T; Kroschinsky F; Berdel WE; Serve H; Müller-Tidow C; Platzbecker U; Baldus CD; Schetelig J; Siepmann T; Bornhäuser M; Middeke JM; Thiede C
Blood Cancer J; 2023 Jan; 13(1):18. PubMed ID: 36693840
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4. PTPN11 mutations in adult acute myeloid leukaemia: Prevalence and clinical implications in the context of NPM1 mutation.
Liu J; Qin W; Wang B; Wang Z; Hua H; Zhou F; Jia Z; Wu P; Chao H; Lu X
Leuk Res; 2022 Jul; 118():106859. PubMed ID: 35617714
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5. Recurrent Germline Variant in
Schedel A; Friedrich UA; Morcos MNF; Wagener R; Mehtonen J; Watrin T; Saitta C; Brozou T; Michler P; Walter C; Försti A; Baksi A; Menzel M; Horak P; Paramasivam N; Fazio G; Autry RJ; Fröhling S; Suttorp M; Gertzen C; Gohlke H; Bhatia S; Wadt K; Schmiegelow K; Dugas M; Richter D; Glimm H; Heinäniemi M; Jessberger R; Cazzaniga G; Borkhardt A; Hauer J; Auer F
Int J Mol Sci; 2022 May; 23(9):. PubMed ID: 35563565
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6. The Dawn of next generation DNA sequencing in myelodysplastic syndromes- experience from Pakistan.
Anwar N; Memon FA; Shahid S; Shakeel M; Irfan M; Arshad A; Naz A; Ujjan ID; Shamsi T
BMC Genomics; 2021 Dec; 22(1):903. PubMed ID: 34915860
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7. Clonal dynamics in pediatric B-cell precursor acute lymphoblastic leukemia with very early relapse.
Antić Ž; Yu J; Bornhauser BC; Lelieveld SH; van der Ham CG; van Reijmersdal SV; Morgado L; Elitzur S; Bourquin JP; Cazzaniga G; Eckert C; Camós M; Sutton R; Cavé H; Moorman AV; Sonneveld E; Geurts van Kessel A; van Leeuwen FN; Hoogerbrugge PM; Waanders E; Kuiper RP
Pediatr Blood Cancer; 2022 Jan; 69(1):e29361. PubMed ID: 34597466
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8. Mutational patterns and their correlation to CHIP-related mutations and age in hematological malignancies.
Stengel A; Baer C; Walter W; Meggendorfer M; Kern W; Haferlach T; Haferlach C
Blood Adv; 2021 Nov; 5(21):4426-4434. PubMed ID: 34570179
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9. Cohesin mutations in myeloid malignancies.
Jann JC; Tothova Z
Blood; 2021 Aug; 138(8):649-661. PubMed ID: 34157074
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10. Integrative study of EZH2 mutational status, copy number, protein expression and H3K27 trimethylation in AML/MDS patients.
Stomper J; Meier R; Ma T; Pfeifer D; Ihorst G; Blagitko-Dorfs N; Greve G; Zimmer D; Platzbecker U; Hagemeijer A; Schmitt-Graeff I; Lübbert M
Clin Epigenetics; 2021 Apr; 13(1):77. PubMed ID: 33845873
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11. Whole Exome Sequencing Identifies Cohesin Component STAG1 Mutation in de novo Acute Myeloid leukemia (FAB M2): A Pilot Study with Cytogenetics, Clinical and Prognostic Implications.
Sakthivel KM; Geetha N; Raj TVA; Chandran RK; Krishna KMNJ; Sreedharan H
J Environ Pathol Toxicol Oncol; 2021; 40(1):51-64. PubMed ID: 33639073
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12. Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia.
Moura-Castro LH; Peña-Martínez P; Castor A; Galeev R; Larsson J; Järås M; Yang M; Paulsson K
Genes Chromosomes Cancer; 2021 Jun; 60(6):410-417. PubMed ID: 33368842
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13. Cohesin mutations are synthetic lethal with stimulation of WNT signaling.
Chin CV; Antony J; Ketharnathan S; Labudina A; Gimenez G; Parsons KM; He J; George AJ; Pallotta MM; Musio A; Braithwaite A; Guilford P; Hannan RD; Horsfield JA
Elife; 2020 Dec; 9():. PubMed ID: 33284104
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14. Machine learning derived genomics driven prognostication for acute myeloid leukemia with
Shaikh AF; Kakirde C; Dhamne C; Bhanshe P; Joshi S; Chaudhary S; Chatterjee G; Tembhare P; Prasad M; Roy Moulik N; Gokarn A; Bonda A; Nayak L; Punatkar S; Jain H; Bagal B; Shetty D; Sengar M; Narula G; Khattry N; Banavali S; Gujral S; P G S; Patkar N
Leuk Lymphoma; 2020 Dec; 61(13):3154-3160. PubMed ID: 32757686
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15. Dysregulation of NIPBL leads to impaired RUNX1 expression and haematopoietic defects.
Mazzola M; Pezzotta A; Fazio G; Rigamonti A; Bresciani E; Gaudenzi G; Pelleri MC; Saitta C; Ferrari L; Parma M; Fumagalli M; Biondi A; Cazzaniga G; Marozzi A; Pistocchi A
J Cell Mol Med; 2020 Jun; 24(11):6272-6282. PubMed ID: 32323916
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16. Clinical impact of clonal hematopoiesis in patients with lymphoma undergoing ASCT: a national population-based cohort study.
Husby S; Favero F; Nielsen C; Sørensen BS; Bæch J; Grell K; Hansen JW; Rodriguez-Gonzalez FG; Haastrup EK; Fischer-Nielsen A; Andersen P; Arboe B; Sækmose SG; Hansen PB; Christiansen I; Clasen-Linde E; Meldgaard L; Ebbesen LH; Segel EK; Josefsson P; Thorsgaard M; El-Galaly TC; Brown P; Weischenfeldt J; Larsen TS; Grønbæk K
Leukemia; 2020 Dec; 34(12):3256-3268. PubMed ID: 32203146
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17. The clinical mutatome of core binding factor leukemia.
Opatz S; Bamopoulos SA; Metzeler KH; Herold T; Ksienzyk B; Bräundl K; Tschuri S; Vosberg S; Konstandin NP; Wang C; Hartmann L; Graf A; Krebs S; Blum H; Schneider S; Thiede C; Middeke JM; Stölzel F; Röllig C; Schetelig J; Ehninger G; Krämer A; Braess J; Görlich D; Sauerland MC; Berdel WE; Wörmann BJ; Hiddemann W; Spiekermann K; Bohlander SK; Greif PA
Leukemia; 2020 Jun; 34(6):1553-1562. PubMed ID: 31896782
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18. Uncovering the Genomic Landscape in Newly Diagnosed and Relapsed Pediatric Cytogenetically Normal FLT3-ITD AML.
Buelow DR; Pounds SB; Wang YD; Shi L; Li Y; Finkelstein D; Shurtleff S; Neale G; Inaba H; Ribeiro RC; Palumbo R; Garrison D; Orwick SJ; Blachly JS; Kroll K; Byrd JC; Gruber TA; Rubnitz JE; Baker SD
Clin Transl Sci; 2019 Nov; 12(6):641-647. PubMed ID: 31350825
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19. Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome.
Aoi H; Mizuguchi T; Ceroni JR; Kim VEH; Furquim I; Honjo RS; Iwaki T; Suzuki T; Sekiguchi F; Uchiyama Y; Azuma Y; Hamanaka K; Koshimizu E; Miyatake S; Mitsuhashi S; Takata A; Miyake N; Takeda S; Itakura A; Bertola DR; Kim CA; Matsumoto N
J Hum Genet; 2019 Oct; 64(10):967-978. PubMed ID: 31337854
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20. Genetic characterization of ABT-199 sensitivity in human AML.
Bisaillon R; Moison C; Thiollier C; Krosl J; Bordeleau ME; Lehnertz B; Lavallée VP; MacRae T; Mayotte N; Labelle C; Boucher G; Spinella JF; Boivin I; D'Angelo G; Lavallée S; Marinier A; Lemieux S; Hébert J; Sauvageau G
Leukemia; 2020 Jan; 34(1):63-74. PubMed ID: 31300747
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