Terms: = Leukemia AND FANCD2, FANCD, 2177, ENSG00000144554, FLJ23826, FAD, FACD, FA4, FA-D2, FAD2, DKFZp762A223 AND Diagnosis
10 results:
1. Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia.
Behera CK; Gyandeep G; Mishra R; Mohanty RP; Pal A; Behera J; Samal S; Das B
Mol Biol Rep; 2023 Jan; 50(1):931-936. PubMed ID: 36369330
[TBL] [Abstract] [Full Text] [Related]
2. Fluorescence spectral detection of acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML): A novel photodiagnosis strategy.
Masilamani V; Devanesan S; AlSalhi MS; AlQahtany FS; Farhat KH
Photodiagnosis Photodyn Ther; 2020 Mar; 29():101634. PubMed ID: 31870897
[TBL] [Abstract] [Full Text] [Related]
3. Prospective, longitudinal assessment of quality of life in children from diagnosis to 3 months off treatment for standard risk acute lymphoblastic leukemia: Results of Children's Oncology Group study AALL0331.
Mitchell HR; Lu X; Myers RM; Sung L; Balsamo LM; Carroll WL; Raetz E; Loh ML; Mattano LA; Winick NJ; Devidas M; Hunger SP; Maloney K; Kadan-Lottick NS
Int J Cancer; 2016 Jan; 138(2):332-9. PubMed ID: 26235006
[TBL] [Abstract] [Full Text] [Related]
4. Utility of next-generation sequencing technologies for the efficient genetic resolution of haematological disorders.
Zhang J; Barbaro P; Guo Y; Alodaib A; Li J; Gold W; Adès L; Keating BJ; Xu X; Teo J; Hakonarson H; Christodoulou J
Clin Genet; 2016 Feb; 89(2):163-72. PubMed ID: 25703294
[TBL] [Abstract] [Full Text] [Related]
5. Fanconi anemia.
Soulier J
Hematology Am Soc Hematol Educ Program; 2011; 2011():492-7. PubMed ID: 22160080
[TBL] [Abstract] [Full Text] [Related]
6. Management of poor peripheral blood stem cell mobilization: incidence, predictive factors, alternative strategies and outcome. A retrospective analysis on 2177 patients from three major Italian institutions.
Perseghin P; Terruzzi E; Dassi M; Baldini V; Parma M; Coluccia P; Accorsi P; Confalonieri G; Tavecchia L; Verga L; Ravagnani F; Iacone A; Pogliani EM; Pioltelli P
Transfus Apher Sci; 2009 Aug; 41(1):33-7. PubMed ID: 19540167
[TBL] [Abstract] [Full Text] [Related]
7. Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.
Ali AM; Kirby M; Jansen M; Lach FP; Schulte J; Singh TR; Batish SD; Auerbach AD; Williams DA; Meetei AR
Hum Mutat; 2009 Jul; 30(7):E761-70. PubMed ID: 19405097
[TBL] [Abstract] [Full Text] [Related]
8. [Fanconi anemia: genes and function(s) revisited].
Papadopoulo D; Moustacchi E
Med Sci (Paris); 2005; 21(8-9):730-6. PubMed ID: 16115458
[TBL] [Abstract] [Full Text] [Related]
9. Cytogenetic characteristics of patients with signs and symptoms of myelodysplastic syndromes in the State of Pará, Brazil.
Pinto GR; Overal DJ; Moraes LS; Van Den Berg AV; Lemos JA; Smith Mde A; Burbano RR
Genet Mol Res; 2005 Mar; 4(1):18-30. PubMed ID: 15841432
[TBL] [Abstract] [Full Text] [Related]
10. The molecular biology of Fanconi anemia.
Tamary H; Bar-Yam R; Zemach M; Dgany O; Shalmon L; Yaniv I
Isr Med Assoc J; 2002 Oct; 4(10):819-23. PubMed ID: 12389351
[TBL] [Abstract] [Full Text] [Related]
