Terms: = Leukemia AND MLH1, COCA2, 4292, ENSG00000076242, hMLH1, FCC2, HNPCC2, P40692, MGC5172, HNPCC
112 results:
1. Constitutional Mismatch Repair Deficiency Syndrome as a Cause of Numerous Malignancies in a Teenage Patient-A Case Report.
Samborska M; Galli D; Achkar R; Thambyrajah S; Derwich K
J Pediatr Hematol Oncol; 2023 Oct; 45(7):e917-e920. PubMed ID: 37526375
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2. Immune evasion phenotype is common in Richter transformation diffuse large B-cell lymphoma variant.
El Hussein S; Medeiros LJ; Gruschkus SK; Wei P; Schlette E; Fang H; Jelloul FZ; Wang W; Fiskus W; Kanagal-Shamanna R; Loghavi S; Yang H; Li S; Xu J; Tang Z; Thakral B; Jain N; Wierda WG; Patel K; Bhalla KN; Khoury JD
Virchows Arch; 2023 Jun; 482(6):1011-1019. PubMed ID: 36864257
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3. 10-Year-Old Pakistani Boy With Multiple Malignancies: Loss Of Pms2-Constitutional Mismatch Repair Deficiency.
Rehman P; Wali RM
J Ayub Med Coll Abbottabad; 2022; 34(Suppl 1)(3):S727-S729. PubMed ID: 36414603
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4. Methylation of DNA Repair Genes as a Prognostic Biomarker in AML of a TCGA-LAML Cohort.
Park S; So MK; Huh J
Clin Lab; 2022 Jul; 68(7):. PubMed ID: 35975527
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5. Tuberous sclerosis complex: a complex case.
Powell RM; Pattison S; Moravec JC; Bhat B; Guirguis N; Markie D; Jones GT; Copedo J; Print CG; Morison IM; Gavryushkin A; Gray B; Wyeth LJ; Eccles MR; Macaulay EC
Cold Spring Harb Mol Case Stud; 2022 Apr; 8(3):. PubMed ID: 35483879
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6. Microsatellite Instability Assessment by Immunohistochemistry in Acute Myeloid leukemia: A Reappraisal and Review of the Literature.
El Hussein S; Daver N; Liu JL; Kornblau S; Fang H; Konoplev S; Kantarjian H; Khoury JD
Clin Lymphoma Myeloma Leuk; 2022 Jun; 22(6):e386-e391. PubMed ID: 34980577
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7. The Challenge of Diagnosing Constitutional Mismatch Repair Deficiency Syndrome in Brain Malignancies from Young Individuals.
Carrato C; Sanz C; Muñoz-Mármol AM; Blanco I; Pineda M; Del Valle J; Dámaso E; Esteller M; Musulen E
Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33924881
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8. Characteristics and outcome of patients with acute myeloid leukaemia and t(8;16)(p11;p13): results from an International Collaborative Study.
Kayser S; Hills RK; Langova R; Kramer M; Guijarro F; Sustkova Z; Estey EH; Shaw CM; Ráčil Z; Mayer J; Zak P; Baer MR; Brunner AM; Szotkowski T; Cetkovsky P; Grimwade D; Walter RB; Burnett AK; Ho AD; Ehninger G; Müller-Tidow C; Platzbecker U; Thiede C; Röllig C; Schulz A; Warsow G; Brors B; Esteve J; Russell NH; Schlenk RF; Levis MJ
Br J Haematol; 2021 Mar; 192(5):832-842. PubMed ID: 33529373
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9. Giant-cell arteritis associated with myelodysplastic syndrome: French multicenter case control study and literature review.
Roupie AL; de Boysson H; Thietart S; Carrat F; Seguier J; Terriou L; Versini M; Queyrel V; Groh M; Benhamou Y; Maurier F; Decaux O; d'Aveni M; Rossignol J; Galland J; Solary E; Willems L; Schleinitz N; Ades L; Dellal A; Samson M; Aouba A; Fenaux P; Fain O; Mekinian A;
Autoimmun Rev; 2020 Feb; 19(2):102446. PubMed ID: 31838164
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10. Metachronous Wilms Tumor, Glioblastoma, and T-cell leukemia in an Child With Constitutional Mismatch Repair Deficiency syndrome due to Novel Mutation in MSH6 (c.2590G>T).
Citak EC; Sagcan F; Gundugan BD; Bozdogan ST; Yilmaz EB; Avci E; Balci Y; Karabulut YY
J Pediatr Hematol Oncol; 2021 Mar; 43(2):e198-e202. PubMed ID: 31815888
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11. Gene mutation profile and risk stratification in AML1‑ETO‑positive acute myeloid leukemia based on next‑generation sequencing.
Yu G; Yin C; Wu F; Jiang L; Zheng Z; Xu D; Zhou J; Jiang X; Liu Q; Meng F
Oncol Rep; 2019 Dec; 42(6):2333-2344. PubMed ID: 31638252
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12. RPL22L1 induction in colorectal cancer is associated with poor prognosis and 5-FU resistance.
Rao S; Peri S; Hoffmann J; Cai KQ; Harris B; Rhodes M; Connolly DC; Testa JR; Wiest DL
PLoS One; 2019; 14(10):e0222392. PubMed ID: 31581233
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13. Genetic and genomic basis of the mismatch repair system involved in Lynch syndrome.
Tamura K; Kaneda M; Futagawa M; Takeshita M; Kim S; Nakama M; Kawashita N; Tatsumi-Miyajima J
Int J Clin Oncol; 2019 Sep; 24(9):999-1011. PubMed ID: 31273487
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14. mlh1 deficiency increases the risk of hematopoietic malignancy after simulated space radiation exposure.
Patel R; Zhang L; Desai A; Hoenerhoff MJ; Kennedy LH; Radivoyevitch T; Ban Y; Chen XS; Gerson SL; Welford SM
Leukemia; 2019 May; 33(5):1135-1147. PubMed ID: 30275527
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15. Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD).
Leenders EKSM; Westdorp H; Brüggemann RJ; Loeffen J; Kratz C; Burn J; Hoogerbrugge N; Jongmans MCJ
Eur J Hum Genet; 2018 Oct; 26(10):1417-1423. PubMed ID: 29904176
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16. Microsatellite Instability and Promoter Hypermethylation of DNA repair genes in Hematologic Malignancies: a forthcoming direction toward diagnostics.
Bhattacharya P; Patel TN
Hematology; 2018 Mar; 23(2):77-82. PubMed ID: 28728506
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17. Biallelic PMS2 Mutation and Heterozygous DICER1 Mutation Presenting as Constitutional Mismatch Repair Deficiency With Corpus Callosum Agenesis: Case Report and Review of Literature.
Cheyuo C; Radwan W; Ahn J; Gyure K; Qaiser R; Tomboc P
J Pediatr Hematol Oncol; 2017 Oct; 39(7):e381-e387. PubMed ID: 28562508
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18. Hypertriglyceridemia during asparaginase treatment in children with acute lymphoblastic leukemia correlates with antithrombin activity in adolescents.
Persson L; Harila-Saari A; Hed Myrberg I; Heyman M; Nilsson A; Ranta S
Pediatr Blood Cancer; 2017 Oct; 64(10):. PubMed ID: 28440015
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19. Loss of mutL homolog-1 (mlh1) expression promotes acquisition of oncogenic and inhibitor-resistant point mutations in tyrosine kinases.
Springuel L; Losdyck E; Saussoy P; Turcq B; Mahon FX; Knoops L; Renauld JC
Cell Mol Life Sci; 2016 Dec; 73(24):4739-4748. PubMed ID: 27436342
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20. Acute lymphoblastic leukemia and lymphoma in the context of constitutional mismatch repair deficiency syndrome.
Ripperger T; Schlegelberger B
Eur J Med Genet; 2016 Mar; 59(3):133-42. PubMed ID: 26743104
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