Human Genome Epidemiology Literature Finder
|
Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and BAALC[original query] |
|---|
| Wilms' tumor 1 gene mutations independently predict poor outcome in adults with cytogenetically normal acute myeloid leukemia: a cancer and leukemia group B study. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2008 Oct 26 (28): 4595-602. Paschka Peter, Marcucci Guido, Ruppert Amy S, Whitman Susan P, Mrózek Krzysztof, Maharry Kati, Langer Christian, Baldus Claudia D, Zhao Weiqiang, Powell Bayard L, Baer Maria R, Carroll Andrew J, Caligiuri Michael A, Kolitz Jonathan E, Larson Richard A, Bloomfield Clara |
| RUNX1 mutations are associated with poor outcome in younger and older patients with cytogenetically normal acute myeloid leukemia and with distinct gene and MicroRNA expression signatures. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012 Sep 30 (25): 3109-18. Mendler Jason H, Maharry Kati, Radmacher Michael D, Mrózek Krzysztof, Becker Heiko, Metzeler Klaus H, Schwind Sebastian, Whitman Susan P, Khalife Jihane, Kohlschmidt Jessica, Nicolet Deedra, Powell Bayard L, Carter Thomas H, Wetzler Meir, Moore Joseph O, Kolitz Jonathan E, Baer Maria R, Carroll Andrew J, Larson Richard A, Caligiuri Michael A, Marcucci Guido, Bloomfield Clara |
| A stem cell-like gene expression signature associates with inferior outcomes and a distinct microRNA expression profile in adults with primary cytogenetically normal acute myeloid leukemia. Leukemia 2013 Oct 27 (10): 2023-31. Metzeler K H, Maharry K, Kohlschmidt J, Volinia S, Mrózek K, Becker H, Nicolet D, Whitman S P, Mendler J H, Schwind S, Eisfeld A-K, Wu Y-Z, Powell B L, Carter T H, Wetzler M, Kolitz J E, Baer M R, Carroll A J, Stone R M, Caligiuri M A, Marcucci G, Bloomfield C |
| Implication of higher BAALC expression in combination with other gene mutations in adult cytogenetically normal acute myeloid leukemia. Leukemia & lymphoma 2014 Jan 55 (1): 110-20. Yoon Jae-Ho, Kim Hee-Je, Shin Seung-Hwan, Yahng Seung-Ah, Lee Sung-Eun, Cho Byung-Sik, Eom Ki-Seong, Kim Yoo-Jin, Lee Seok, Min Chang-Ki, Cho Seok-Goo, Kim Dong-Wook, Lee Jong-Wook, Min Woo-Sung, Park Chong-Won, Lim Ji-Hya |
| Evaluation of rs62527607 [GT] single nucleotide polymorphism located in BAALC gene in children with acute leukemia using mismatch PCR-RFLP. Cancer genetics 2016 Jun . Nadimi Motahareh, Rahgozar Soheila, Moafi Alireza, Tavassoli Manoochehr, Mesrian Tanha Hamz |
| Combining gene mutation with gene expression analysis improves outcome prediction in acute promyelocytic leukemia. Blood 2019 Jul . Lucena-Araujo Antonio R, Coelho-Silva Juan L, Pereira-Martins Diego A, Silveira Douglas R, Koury Luisa Corrêa de Araujo, Melo Raul A M, Bittencourt Rosane, Pagnano Katia, Pasquini Ricardo, Nunes Elenaide C, Fagundes Evandro M, Gloria Ana B, Kerbauy Fabio R, Chauffaille Maria de Lourdes, Bendit Israel, Rocha Vanderson, Keating Armand, Tallman Martin S, Ribeiro Raul C, Dillon Richard, Ganser Arnold, Löwenberg Bob, Valk Peter, Lo Coco Francesco, Sanz Miguel A, Berliner Nancy, Rego Eduardo |
Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.
The pharmacogenomics journal 2019 Dec . de Las Fuentes L, Sung Y J, Sitlani C M, Avery C L, Bartz T M, Keyser C de, Evans D S, Li X, Musani S K, Ruiter R, Smith A V, Sun F, Trompet S, Xu H, Arnett D K, Bis J C, Broeckel U, Busch E L, Chen Y-D I, Correa A, Cummings S R, Floyd J S, Ford I, Guo X, Harris T B, Ikram M A, Lange L, Launer L J, Reiner A P, Schwander K, Smith N L, Sotoodehnia N, Stewart J D, Stott D J, Stürmer T, Taylor K D, Uitterlinden A, Vasan R S, Wiggins K L, Cupples L A, Gudnason V, Heckbert S R, Jukema J W, Liu Y, Psaty B M, Rao D C, Rotter J I, Stricker B, Wilson J G, Whitsel E |
| Prognostic Impact of Blood MN1 Copy Numbers Before Allogeneic Stem Cell Transplantation in Patients With Acute Myeloid Leukemia. HemaSphere 2019 11 3 (1): e167. Jentzsch Madlen, Bill Marius, Grimm Juliane, Schulz Julia, Beinicke Stefanie, Häntschel Janine, Goldmann Karoline, Pönisch Wolfram, Franke Georg-Nikolaus, Vucinic Vladan, Cross Michael, Behre Gerhard, Lange Thoralf, Niederwieser Dietger, Schwind Sebasti |
| RUNX1 variant as a genetic predisposition factor for acute myeloid leukemia. Experimental and molecular pathology 2020 Apr 104440. Javadlar Masoumeh, Dastar Saba, Gharesouran Jalal, Ghafouri-Fard Soudeh, Hosseinzadeh Hassan, Moradi Mohsen, Mazraeh Shamsi Abdi, Nasiri Ganjineh Ketab Fereshteh, Rezamand Azim, Hiradfar Amirataollah, Taheri Mohammad, Rezazadeh Mary |
| Prognostic significance of combined BAALC and MN1 gene expression level in acute myeloid leukemia with normal karyotype. International journal of laboratory hematology 2020 11 43 (3): 433-440. Marjanovic Irena, Karan-Djurasevic Teodora, Kostic Tatjana, Virijevic Marijana, Vukovic Nada Suvajdzic, Pavlovic Sonja, Tosic Nata |
| Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes.
Progress in neuro-psychopharmacology & biological psychiatry 2021 Jul 110393. Wang Kesheng, Xu Chun, Smith Amanda, Xiao Danqing, Navia R Osvaldo, Lu Yongke, Xie Changchun, Piamjariyakul Ubolrat, |
- Page last reviewed:Feb 1, 2024
- Content source: