Terms: = Leukemia AND PTPN11, CFC, Q06124, 5781, ENSG00000179295, SHP2, MGC14433, SHP-2, BPTP3, PTP-1D, SH-PTP3, NS1, SH-PTP2, PTP2C AND Diagnosis
94 results:
1. Triple Trouble.
Diwan A; Barsode S
J Assoc Physicians India; 2024 Mar; 72(3):97-99. PubMed ID: 38736127
[TBL] [Abstract] [Full Text] [Related]
2. Genomic Mutation Profiles of Patients with Acute Myeloid leukemia in Korea: a Single-Center Experience.
Han E; Ryu S; Kim D; Koh EH; Byun JH; Lee DH
Clin Lab; 2023 Nov; 69(11):. PubMed ID: 37948498
[TBL] [Abstract] [Full Text] [Related]
3. Biallelic inactivation of the NF1 tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workup.
Ramamoorthy S; Lebrecht D; Schanze D; Schanze I; Wieland I; Andrieux G; Metzger P; Hess M; Albert MH; Borkhardt A; Bresters D; Buechner J; Catala A; De Haas V; Dworzak M; Erlacher M; Hasle H; Jahnukainen K; Locatelli F; Masetti R; Stary J; Turkiewicz D; Vinci L; Wlodarski MW; Yoshimi A; Boerries M; Niemeyer CM; Zenker M; Flotho C
Br J Haematol; 2024 Feb; 204(2):595-605. PubMed ID: 37945316
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4. [Clinical features and prognosis of juvenile myelomonocytic leukemia: an analysis of 63 cases].
Yang WY; Liu LP; Liu F; Qi BQ; Chang LX; Zhang L; Chen XJ; Zou Y; Chen YM; Guo Y; Zhu XF
Zhongguo Dang Dai Er Ke Za Zhi; 2023 Mar; 25(3):265-271. PubMed ID: 36946161
[TBL] [Abstract] [Full Text] [Related]
5. Spectrum and clinical features of gene mutations in Chinese pediatric acute lymphoblastic leukemia.
Shen D; Liu L; Xu X; Song H; Zhang J; Xu W; Zhao F; Liang J; Liao C; Wang Y; Xia T; Wang C; Lou F; Cao S; Qin J; Tang Y
BMC Pediatr; 2023 Feb; 23(1):62. PubMed ID: 36739388
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6. Prediction of survival with intensive chemotherapy in acute myeloid leukemia.
Sasaki K; Ravandi F; Kadia T; DiNardo C; Borthakur G; Short N; Jain N; Daver N; Jabbour E; Garcia-Manero G; Khoury J; Konoplev S; Loghavi S; Patel K; Montalban-Bravo G; Masarova L; Konopleva M; Kantarjian H
Am J Hematol; 2022 Jul; 97(7):865-876. PubMed ID: 35384048
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7. Whole exome sequencing of pediatric leukemia reveals a novel InDel within FLT-3 gene in AML patient from Mizo tribal population, Northeast India.
Vanlallawma A; Lallawmzuali D; Pautu JL; Scaria V; Sivasubbu S; Kumar NS
BMC Genom Data; 2022 Mar; 23(1):23. PubMed ID: 35350997
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8. Comprehensive immunophenotypic study of acute myeloid leukemia with KMT2A (MLL) rearrangement in adults: A single-institution experience.
Konoplev S; Wang X; Tang G; Li S; Wang W; Xu J; Pierce SA; Jia F; Jorgensen JL; Ravandi F; Issa GC; Medeiros LJ; Wang SA
Cytometry B Clin Cytom; 2022 Mar; 102(2):123-133. PubMed ID: 34964255
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9. Mutational profiling of myeloid neoplasms associated genes may aid the diagnosis of acute myeloid leukemia with myelodysplasia-related changes.
Yu J; Du Y; Jalil A; Ahmed Z; Mori S; Patel R; Varela JC; Chang CC
Leuk Res; 2021 Nov; 110():106701. PubMed ID: 34481124
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10. The Prognostic Ability of RAS Pathway-Related Gene Mutations in Patients with Myeloid Neoplasms Treated with Hypomethylating Agents.
Park HS; Son BR; Shin KS; Byeon S; Kim HK; Yang Y; Jeong Y; Han HS; Lee KH; Kwon J
Acta Haematol; 2021; 144(6):649-659. PubMed ID: 34233332
[TBL] [Abstract] [Full Text] [Related]
11. What Is Abnormal in Normal Karyotype Acute Myeloid leukemia in Children? Analysis of the Mutational Landscape and Prognosis of the TARGET-AML Cohort.
Herlin MK; Yones SA; Kjeldsen E; Holmfeldt L; Hasle H
Genes (Basel); 2021 May; 12(6):. PubMed ID: 34064268
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12. Pediatric myelodysplastic syndrome with inflammatory manifestations: diagnosis, genetics, treatment, and outcome.
Yanir AD; Krauss A; Stein J; Steinberg-Shemer O; Gilad O; Lotan SN; Dgany O; Krasnov T; Kodman Y; Feuerstein T; Mardoukh J; Fishman H; Geron I; Yacobovich J; Tamary H; Birger Y; Avrahami G; Izraeli S; Birenboim SB
Pediatr Blood Cancer; 2021 Oct; 68(10):e29138. PubMed ID: 34019335
[TBL] [Abstract] [Full Text] [Related]
13. [Analysis of Gene Mutation and Clinical Characteristics in 19 Children with Juvenile Myelomonocytic leukemia].
Weng KZ; Zheng YZ; Zhuang SQ; Chen HY; LE SH
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2020 Dec; 28(6):1811-1818. PubMed ID: 33283703
[TBL] [Abstract] [Full Text] [Related]
14. Dasatinib response in acute myeloid leukemia is correlated with FLT3/ITD, ptpn11 mutations and a unique gene expression signature.
Tavor S; Shalit T; Chapal Ilani N; Moskovitz Y; Livnat N; Groner Y; Barr H; Minden MD; Plotnikov A; Deininger MW; Kaushansky N; Shlush LI
Haematologica; 2020 Dec; 105(12):2795-2804. PubMed ID: 33256378
[TBL] [Abstract] [Full Text] [Related]
15. Multiclonal complexity of pediatric acute lymphoblastic leukemia and the prognostic relevance of subclonal mutations.
Antić Ž; Yu J; Van Reijmersdal SV; Van Dijk A; Dekker L; Segerink WH; Sonneveld E; Fiocco M; Pieters R; Hoogerbrugge PM; Van Leeuwen FN; Van Kessel AG; Waanders E; Kuiper RP
Haematologica; 2021 Dec; 106(12):3046-3055. PubMed ID: 33147938
[TBL] [Abstract] [Full Text] [Related]
16. Immunophenotypic characteristics of juvenile myelomonocytic leukaemia and their relation with the molecular subgroups of the disease.
Frisanco Oliveira A; Tansini A; Toledo TR; Balceiro R; Onofre Vidal D; de Martino Lee ML; Lorand-Metze I; Lopes LF
Br J Haematol; 2021 Jan; 192(1):129-136. PubMed ID: 32966606
[TBL] [Abstract] [Full Text] [Related]
17. Prolonged thrombocytopenia in a neonate with Noonan syndrome: a case report.
Li M; Zhang J; Sun N
J Int Med Res; 2020 Aug; 48(8):300060520936445. PubMed ID: 32867556
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18. Genetic aberrations involved in relapse of pediatric acute myeloid leukemia: A literature review.
Zafar N; Ghias K; Fadoo Z
Asia Pac J Clin Oncol; 2021 Oct; 17(5):e135-e141. PubMed ID: 32573082
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19. RAS Pathway Mutation Patterns in Patients With Juvenile Myelomonocytic leukemia: A Developing Country Single-center Experience.
Hamdy N; Bokhary H; Elsayed A; Hozayn W; Soliman S; Salem S; Alsheshtawi K; Abdalla A; Hafez H; Hammad M
Clin Lymphoma Myeloma Leuk; 2020 Jul; 20(7):e368-e374. PubMed ID: 32209330
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20. Rapid detection by hydrops panel of Noonan syndrome with ptpn11 mutation (p.Thr73Ile) and persistent thrombocytopenia.
Schönfeld M; Selig M; Russo A; Lindner C; Kampmann C; Mildenberger E; Whybra C
Mol Genet Genomic Med; 2020 May; 8(5):e1174. PubMed ID: 32144894
[TBL] [Abstract] [Full Text] [Related]
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